It is clear that in order to satisfy global energy demands whilst maintaining sustainable levels of atmospheric greenhouse gases, alternative energy sources are required. Due to its high chemical energy density and the benign by-product of its combustion reactions, hydrogen is one of the most promising of these. However, methods of hydrogen storage such as gas compression or liquefaction are not suitable for portable or automotive applications due to their low hydrogen storage densities. Accordingly, much research activity has been focused on finding higher density hydrogen storage methods. One such method is to generate hydrogen via the hydrolysis of aqueous sodium borohydride (NaBH4) solutions, and this has been heavily studied since the turn of the century due to its high theoretical hydrogen storage capacity (10.8 wt%) and relatively safe operation in comparison to other chemical hydrides. This makes it very attractive for use as a hydrogen generator, in particular for portable applications. Major factors affecting the hydrolysis reaction of aqueous NaBH4 include the performance of the catalyst, reaction temperature, NaBH4 concentration, stabilizer concentration, and the volume of the reaction solution. Catalysts based on noble metals, in particular ruthenium (Ru) and platinum (Pt), have been shown to be particularly efficient at rapid generation of hydrogen from aqueous NaBH4 solutions. However, given the scarcity and expense of such metals, a transition metal-based catalyst would be a desirable alternative, and thus much work has been conducted using cobalt (Co) and nickel (Ni)-based materials to attempt to source a practical option. “Metal free” NaBH4 hydrolysis can also be achieved by the addition of aqueous acids such as hydrochloric acid (HCl) to solid NaBH4. This review summarizes the various catalysts which have been reported in the literature for the hydrolysis of NaBH4.


In recent years, global energy demand has grown at an unprecedented rate, and this trend is expected to continue long into the future [1]. At the same time, the cost of traditional energy sources such as coal, oil, and gas continues to increase. There is thus an acute need for alternative sources of energy.

One of the more widely studied alternative energy sources is hydrogen [2]. The chemical energy per unit mass of hydrogen (142 MJ kg−1) is at least three times larger than that of any other fuel (e.g., the chemical energy per unit mass of hydrocarbons is only 47 MJ kg−1) [3]. The combustion of hydrogen generates only water as a by-product, and is thus environmentally benign, and its adoption as fuel in internal combustion engines, for example, would lead to a significant reduction in atmospheric pollution. However, due to its very low density, hydrogen is difficult to store in the gaseous state under standard conditions and must be heavily compressed to be stored in useful quantities on board a vehicle. Compressed gases must be stored in heavy steel containers, partially nullifying the benefit in terms of high gravimetric energy density of using hydrogen in the first place. Alternatively, hydrogen can be stored in cryogenic containers, but these are costly and accumulate considerable “boil off” losses [4]. Both of these approaches are also hazardous and present considerable risks to the user and the public at large.

Hence alternative higher capacity methods of storing hydrogen need to be found. Materials currently under investigation for this purpose can largely be grouped into four categories, namely (a) large surface area materials onto which hydrogen molecules are absorbed, (b) intermetallic hydrides into which hydrogen molecules are absorbed by dissociation into hydrogen atoms, (c) complex metal hydrides where hydrogen atoms are chemically bonded within molecular structures and (d) chemical hydrides which react with water or alcohols to produce hydrogen [2, 5-10]. A brief description of each of these hydrogen storage methods, some example materials, and their advantages and disadvantages with respect to one another in terms of hydrogen storage is given in the following four subsections.

Hydrogen storage on large surface area materials

Carbon-based nanostructured materials such as fullerenes [11], graphene [12, 13], and nanotubes [14], mesporous silica [15, 16], metal organic frameworks [17-19], and clathrate hydrates [20] all belong in this category. These materials can offer high gravimetric hydrogen storage densities and good reversibility cycles (of hydrogen adsorption and desorption), but typically operate at temperatures lower (below 298 K) than that is desirable for practical application.

Hydrogen storage in intermetallic hydrides

Intermetallic hydrides, also known as interstitial hydrides, absorb and liberate hydrogen under nearly ambient conditions [9, 21-23]. The hydrogen is stored in interstitial sites and thus does not affect the host lattice [5]. They are often grouped by their structure type into four categories, namely AB5 (e.g., LaNi5), AB (e.g., FeTi), A2B (Mg2Ni), and AB2 (TiMn2) [5]. However, the gravimetric hydrogen storage densities of such systems are too low (<5 wt%) for portable applications.

Hydrogen storage in complex metal hydrides

Complex metal hydrides (e.g., NaAlH4 [24-26], LiAlH4 [27, 28], LiBH4 [29, 30]) generally have the formula AxByHn, where A is an alkali metal cation and B is a metal or metalloid to which the hydrogen atoms are covalently bonded. Certain binary metal hydrides such as MgH2 [31-33] and AlH3 [34-36] also have covalently bonded hydrogen atoms and are thus more similar to complex metal hydrides than intermetallic hydrides in their hydrogen storage properties. Complex metal hydrides are particularly promising due to their high theoretical gravimetric and volumetric hydrogen storage densities. However, they suffer from slow uptake and release kinetics, meaning that much of the stored hydrogen is not practically accessible due to the time it would take to release it.

Hydrogen storage in chemical hydrides

Chemical hydrides (e.g., NaBH4 [37], LiAlH4 [38-40], NH3BH3 [41-43]) have high gravimetric hydrogen storage densities and release hydrogen by reaction with water. In effect, the hydrogen is stored both in the chemical hydride itself and the water. These reactions tend not to be easily reversible and the by-products must be extracted from the spent fuel mixture to be regenerated. However, as the reactions can be controlled by control of parameters such as rate of water addition, pH, and the use of catalysts, chemical hydrides are particularly attractive for use in portable applications, where easy “on-off” control is crucial. A particularly attractive option is hydrogen generation from the hydrolysis of aqueous sodium borohydride (NaBH4) solutions. This brings several advantages over other potential materials such as lithium aluminum hydride, including nonflammability (of sodium borohydride solutions), stability in air, and low reactivity of reaction by-products which can (at least theoretically) be recycled.

Hydrogen Storage in Sodium Borohydride

Sodium borohydride can be classified as both a complex metal hydride and a chemical hydride as it can release hydrogen by two methods: thermolysis, where the stored hydrogen is released by heating, and hydrolysis, where the stored hydrogen is released by reaction with water. The former is not attractive for portable applications since sodium borohydride is stable up to 400°C [44]. The latter is particularly attractive for three major reasons. Firstly, hydrolysis of sodium borohydride is a spontaneous, exothermic (−210 kJ mol−1) [45] process that can be easily accelerated by the simple addition of a metal catalyst. Secondly, as can be seen from equation 1, half of the hydrogen comes from the water, giving sodium borohydride a relatively high theoretical hydrogen storage capacity of 10.8 wt%. Finally, the hydrolysis reaction can produce pure hydrogen at temperatures as low as 298 K.



However, hydrogen generation by hydrolysis of sodium borohydride is not without problems. A major issue is the volume of water required. Equation 1 shows the stoichiometric chemical reaction, but in reality at least 4 molar equivalents of water are required for each mole of sodium borohydride in the reaction. This is for two reasons. Firstly, as shown in Equation 2, sodium metaborate (NaBO2) is rapidly hydrated. Secondly, the solubility of sodium borohydride in water is relatively low (55 g per 100 g at 25°C), requiring more water than that required by stoichiometry to ensure the sodium borohydride remains in solution (although sodium borohydride does have a considerably higher solubility than ammonia borane (33.6 g per 100 g at 25°C) [41], and other hydrolysis materials such as aluminum [46, 47] and silicon [48], which are insoluble).This is further compounded by the even lower solubility of sodium metaborate (28 g per 100 g of water at 25°C), which means that the concentration of sodium borohydride must be kept below 16 g per 100 g of water to ensure that sodium metaborate does not precipitate from the reaction mixture and foul the catalyst and reaction vessel. All of these considerations mean that in reality the gravimetric hydrogen storage capacity of sodium borohydride is far lower than the theoretical value of 10.8 wt%, and has led to a “no-go” recommendation from the United States Department of Energy for use in automotive applications [49]. Nevertheless, sodium borohydride hydrolysis remains very attractive for smaller scale portable applications such as chargers for mobile phones, tablets, and laptop computers.

Another significant problem is the rate of reaction. Sodium borohydride undergoes self-hydrolysis upon the addition of water, and is thus typically stabilized by the addition of sodium hydroxide (the self-hydrolysis reaction rate drops to negligible above pH 13) [50]. The mechanism of self-hydrolysis has been described as follows [51]:

Step 3: BH3(aq) + 3H2O(l) → B(OH)3(aq) + 3H2(g)

The decrease in the amount of protons in basic media results in Step 2 of the self-hydrolysis being disfavored and the hydrogen generation process thus slowed. By increasing the amount of protons and thus accelerating Step 2, the addition of homogenous acid catalysts to aqueous sodium borohydride solutions results in an increase in the rate of hydrolysis.

Heterogeneous catalysts can be added to reduce the activation energy and accelerate the generation of hydrogen. Removal of the catalyst leads to an increase in the activation energy and a stabilization of the reaction. Various kinetic models have been used to describe the process of metal catalyzed hydrolysis and these have been well summarized by Rangel et al. [51]. The “on-off” control obtained by adjusting the pH or the contact with a heterogeneous catalyst makes sodium borohydride a very attractive hydrogen storage material for portable applications. In the past 15 years a host of different heterogeneous catalyst systems have been reported for sodium borohydride hydrolysis, the majority of them based on ruthenium and cobalt. The mechanism of many of these reactions is still poorly understood, and thus this remains a rich field of research. Acids can be used as homogenous catalysts for the hydrolysis reaction as they lower the pH and destabilize the sodium borohydride solution.

The physical form of heterogeneous catalysts also plays a large role in controlling the sodium borohydride hydrolysis process. In particular, the “on-off” functionality required for portable applications is far more difficult to achieve with loose powder catalysts than with supported catalysts as it is easier to remove the latter from solution (though powders can be pelletized to overcome this). However, supported catalysts are generally more susceptible to being blocked by a layer of sodium metaborate by-product, and can have lower accessible catalyst surface than powders.

Reactions of sodium borohydride with water vapor have been reported [52-54]. This hydrolysis method is promising as it increases the gravimetric hydrogen storage capacity by decreasing the amount of water required, and also do not require catalytic activation. However, the hydrogen yields are much poorer than those of liquid phase hydrolysis and the reactions must be carried out with water temperatures of above 110°C, and thus vapor phase hydrolysis of sodium borohydride has not been heavily investigated.

Noble Metal Catalysts: Ruthenium (Ru) and Platinum (Pt)

Several ruthenium-based catalysts giving high initial rates of hydrogen generation have been reported. The most active catalyst in terms of initial hydrogen generation rate was reported by Ozkar et al. [55], who achieved maximum hydrogen generation rates of 96,800 mL min−1 (g catalyst)−1 using water dispersible ruthenium(0) nanoclusters at ambient temperatures. The next highest performing ruthenium-based catalyst in terms of hydrogen generation rate is a ruthenium catalyst generated from a ruthenium salt by reduction with sodium borohydride, followed by an annealing step. In powder form this gave a maximum hydrogen generation rate of 18,600 mL min−1 (g catalyst)−1 [56].

A number of immobilized ruthenium-based catalysts have also been reported, though none can match the activity of Ozkars nanoclusters. Liang et al. [57] attached ruthenium(0) to graphite powder via an aminosilane chain. Though in this case a powder was used, if the same methodology could be employed to functionalize graphite rods then a viable “on/off” mechanism could easily be envisaged. This system achieved hydrogen generation rates of 969 mL min−1 (g catalyst)−1. Supported catalyst systems have also been very popular due to their practicality. A higher performing system (in terms of hydrogen generation rate) using carbon as the support was reported by Li et al. [58], who converted Ni/C to Ru-RuO2/C by galvanic replacement, generating hydrogen at a rate of 2800 mL min−1 (g catalyst)−1. Park et al. [59] used sodium borohydride to reduce various metal salts to form catalytic alloys on activated carbon fiber (ACF) in situ. A tertiary alloy of composition Ru60Co20Fe20 showed the highest hydrogen release of 5030 mL min−1 (g catalyst)−1.

Several catalysts formed of ruthenium on support materials such as carbon papers and polymer beads have been reported [60-67], but most of these suffer from poor catalytic performance in terms of hydrogen generation rate (see Table 1). Amendola et al. [61] dispersed a ruthenium boride catalyst onto various anionic and cationic resin beads, which they then dispersed in solutions of sodium borohydride stabilized with sodium hydroxide. IRA 400 resin beads were found to be the highest performing, giving hydrogen generation rate of 189 mL H2 min−1 (g catalyst−1). Chen et al. [63] obtained a higher hydrogen generation rate of 216 mL H2 min−1 (g catalyst−1) by depositing ruthenium(0) nanoparticles onto monodisperse polystyrene microspheres, though it was only tested in a 1 wt% solution of sodium borohydride (rather than the 20 wt% solution of Amendola et al.) and could thus perhaps be capable of producing hydrogen at a faster rate if placed in a more concentrated solution. Higher rates of hydrogen generation have been obtained using ruthenium catalysts supported on carbon. For example, Fisher et al. [65] obtained commercially available Ru/C catalyst powder and found that grinding it to a particle size of 35 μm minimized internal diffusion effects to give a maximum hydrogen generation rate of 770 mL H2 min−1 (g catalyst−1).

Table 1. Noble metal catalysts for sodium borohydride hydrolysis
Catalyst Form Activity (mL H2 min−1 (g catalyst−1) NaBH4 conc./wt% NaOH conc./wt% Temperature/°C Year Reference
Ru Supported on IRA 400 resin 189 20 10 25 2000 [61]
Pt-LiCoO2 Powder 3100 20 10 22 2002 [70]
Pt/C Powder 23,090 10 5 Not stated 2004 [69]
Ru NPs Powder 96,800 0.75 0 25 2005 [55]
Pt/Ru-LiCoO2 Catalyst dispersed on a nickel mesh 2400 5 5 25 2005 [72]
Pt/C Powder 23,000 10 5 25 2006 [68]
Ru(0) nanoclusters Powder 4 0.57 10 25 2006 [75]
Pt/C Powder 6000 9 Not stated 25 2007 [76]
Pt/Pd-CNT Supported on CNT paper 126 0.1 0.4 29 2007 [73]
Pt/C Powder 170 5 5 30 2007 [77]
Ru/C Powder 770 1 3.75 25 2007 [65]
Ru60Co20Fe20 alloy Supported on activated carbon fibers 5030 10 4 25 2008 [59]
Ru Powder 18,600 5 5 60 2008 [56]
Pt-Ru Powder 150 2 4 20 2008 [64]
Pt/Ru-LiCoO2 Catalyst bed 3000 10 5 25 2008 [78]
Ru Supported on ion exchange resin beads 132 5 1 25 2008 [67]
Ru Supported on polymer beads 216 1 1 Not stated 2009 [63]
Ru(0) nanoclusters confined in zeolites Powder 130 1.1 5 25 2009 [79]
Ru on graphite Supported on graphite 969 10 5 30 2010 [57]
Rh/TiO2 Immobilized onto titanium dioxide support to form a catalyst bed 210 15 5 23 2010 [80]
Alumina carrier Ru composite Supported on alumina 68.2 12.5 1 25 2012 [81]
Ru/C Powder 570 10 4 25 2012 [66]
Ru-RuO2/C Powder 2800 5 1 30 2013 [58]
Table 2. Nonnoble metal catalysts for sodium borohydride hydrolysis
Catalyst Form Activity (mL H2 min−1 (g catalyst−1) NaBH4 conc. (wt%) NaOH conc. (wt%) T/°C Year Reference
Ni-B Powder 330 1.5 20 25 2003 [119]
Co-B Powder 2970 2 5 15 2005 [120]
Co-B Powder 875 20 5 20 2005 [121]
Raney Ni Powder 228.5 1 10 20 2006 [122]
Raney Co Powder 267.5 1 10 20 2006 [122]
Co-B/Ni foam Dip coated 7200 25 3 20 2007 [123]
Co-B Thin film prepared by pulsed laser deposition 3300 0.1 Not stated 25 2007 [124]
Ni-Co-B Powder 2608 2.7 15 28 2007 [125]
Co-B Powder 2400 20 5 20 2007 [126]
Co-B Supported on carbon black 2073 0.75 8 25 2007 [114]
Co-P Electroplated on copper 954 10 1 30 2007 [127]
Co-B Powder 26,000 15 5 30 2008 [86]
Ni-B Powder 1300 10 5 60 2008 [56]
Co-B Powder 6000 5 5 60 2008 [56]
Co-W-B/Ni foam Electrolessly plated 15,000 20 5 30 2008 [91]
Co-B/Ni foam Electrolessly plated 11,000 20 10 30 2008 [128]
Co-B/MWCNTs Powder 5100 20 3 30 2008 [113]
Co-B Thin film prepared by pulsed laser deposition 5016 0.1 4 25 2008 [129]
Co/PPX-Cl Metallized films 4250 2.5 10 25 2008 [130]
Ni(0) nanoclusters Stabilized on PVP 4250 0.57 0 25 2008 [131]
Co-B/Pd Dry dip coated 2875 20 4 30 2008 [132]
Co on activated C Powder 3600 5 1 30 2008 [133]
Co-B Carbon supported 166 1 5 25 2008 [134]
Co-B Powder 39,000 5 0 40 2009 [85]
Co-P-B Powder 2120 0.95 1 25 2009 [135]
Co-Cr-B Powder 3400 0.95 1 25 2009 [136]
Co-Ni-P Electrodeposited 2479 10 10 30 2009 [104]
Co-Ni-P-B Powder 2400 0.95 1 25 2009 [105]
Co-B Electrolessly plated 1640 10 5 25 2009 [137]
Co-Ni-B Powder 1175 0.95 1 25 2009 [138]
Ni-Ru Electrolessly plated 400 10 5 35 2009 [62]
Co-Fe-B Powder 1300 0.95 1 25 2010 [139]
Fe-Co-B/Ni foam Electrolessly plated 22,000 15 5 30 2010 [90]
Co-P-B Thin film prepared by pulsed laser deposition 4320 0.95 1 25 2010 [140]
Co-P/Ni foam Electrolessly plated 3584 10 1 30 2010 [141]
Co-W-B Powder 2570 0.95 1 25 2010 [139]
Co-Mo-B Powder 2875 0.95 1 25 2010 [139]
Co-Cu-B Powder 2210 0.95 1 25 2010 [139]
Co-P on Cu sheet Electrolessly plated 1846 5 1 25 2010 [142]
Co-B Supported on attapulgite clay 3350 5 10 25 2010 [143]
Co-alumina on Cu plates Electrodeposited 383 3 1 80 2010 [144]
Co-B CoCl2 solution added to a solid powder mixture of NaOH and NaBH4 23,333 50 5 Unregulated 2011 [87]
Co NPs embedded on a B thin film Pulsed laser deposition 3375 0.095 0 25 2011 [106]
Co-B Powder 9000 10 5 Unregulated 2011 [145]
Co-B NPs Powder 4928 3 5 25 2011 [146]
Co-B NPS Supported on hydrogels 120 0.19 5 30 2011 [147]
Co-Ni-P/Pd-TiO2 Electrolessly plated 460 1.13 10 25 2011 [102]
Co-B NPs Supported on TiO2 12,500 1 3.75 30 2012 [99]
Co-B NPs Supported on Al2O3 11,650 1 3.75 30 2012 [99]
Co-B NPs Supported on CeO2 10,390 1 3.75 30 2012 [99]
Co Supported on collodial carbon spheres 1911 1 10 20 2012 [112]
Co-B Impregnation onto carbon supports 1358 1 8 27 2012 [111]
CoO nanocrystals Powder 8333 10 10 30 2012 [116]
Co–Pd–B Powder 2920 0.57 5 25 2012 [89]
Co–Mo–Pd–B Powder 6023 0.57 5 25 2012 [89]
Co-W-P on Cu substrates Electrolessly plated 5000 10 10 30 2012 [103]
Co-B Solution plasma process 4380 2 7 25 2012 [148]
Co-B Powder 4300 0.76 0.1 30 2012 [149]
Ni-B Powder 3400 0.76 0.1 30 2012 [149]
Co-ZIF-9 Solvothermal 182 0.5 5 30 2012 [150]
Ni-Fe-B Powder 2910 5 4 25 2012 [151]
Co-Mn-B Powder 35,000 7 7 70 2012 [97]
Co(II)-Cu(II)-based complex catalyst Powder 188 2.5 5 30 2012 [152]
Fe-Co NPs Powder 1433 5 0 30 2012 [153]
Co-Mo-B Powder 19,000 5 5 30 2013 [92]
Co NPS on aerogels Powder 2010 1 10 25 2013 [107]
Co-P Electrodeposition 5965 10 10 30 2013 [154]
Co-Ni-P Electrolessly plated 3636 10 10 30 2013 [155]
Zr/Co Impregnation onto carbon supports 1708 5 2 Not stated 2013 [156]
Co-La-Zr-B Powder 1500 10 2 40 2013 [94]
Co-La-Zr-B Powder 133 5 0 20 2013 [93]
Co-B Supported on carbon black 8034 10 5 25 2014 [115]
Co-B-TiO2 framework Powder 1980 5 1.5 30 2014 [157]
Ni-Co-P Supported on alumina 6600 2 4 55 2014 [158]
PAN/CoCl2-CNT nanofibers Electrospun 1255 1 0 25 2014 [159]
Oleic acid stabilized Co-La-Zr-B nanoparticle Powders 102 5 2 20 2014 [160]
Co-B/Ni foam Electrolessly plated 24,400 15 5 30 2014 [98]
Co/Ni foam Magnetron sputtered 2650 3.8 4.5 23 2014 [161]
Co3O4 Solution combustion synthesized powder 1240 0.6 0 20 2014 [162]
Co NPs Supported on a polyacrylamide hydrogel network 537 3.8 5 30 2014 [163]
Co-Ru-B Powder 8075 0.57 0.4 25 2014 [95]
Au/Ni NPs Powder 2597 0.11 Not stated 30 2014 [164]

Several platinum-based catalysts with high hydrogen generation rates have also been reported. Wu et al. [68, 69] utilized Pt/C powders to obtain hydrogen generation rates of ~23,000 mL min−1 (g catalyst−1). Kojima et al. coated Pt(0) onto LiCoO2 and used the resultant powder to generate hydrogen at a maximum rate of 3100 mL min−1 (g catalyst−1) [70]. This system was subsequently coated onto a honeycomb monolith and incorporated into a 10 kW scale hydrogen generator [71]. Another promising adaptation of this catalytic system was reported by Krishnan et al. [72]. They dispersed the catalyst onto a nickel mesh which could then be dipped in and out of solution in response to the demand for hydrogen generation. Pena-Alonso et al. [73] have also reported a promising system in which they deposited platinum and palladium atoms onto carbon nanotubes and achieved hydrogen generation rates of 126 mL min−1 (g catalyst−1). Saha et al. [74] have recently reported a highly stable graphene-Pt-Co nanohybrid catalyst which shows exceptional stability and a very high catalytic activity (TOF = 107 min−1). These catalysts are synthesized in a fairly simple manner and show great promise.

Nonnoble Metal Catalysts: Cobalt (Co) and Nickel (Ni)

Noble metals are scarce and expensive. Hence the use of catalyst systems based on the cheaper transition metals is highly desirable. Specifically, cobalt and nickel have been the most commonly employed transition metals to date due to their low cost and abundance compared to noble metals, whilst an increasing amount of research is being carried out on iron-based systems.

Cobalt borides (Co-B) have been heavily studied as catalysts for sodium borohydride hydrolysis reactions. The exact structure of these compounds and the mechanism of hydrogen generation remains a subject of debate. The current state of the art in terms of our understanding of the catalyst structure and mechanism has been well summarized by Demirci and Miele [37, 82, 83]. Cobalt boride-based catalysts are generally formed by reduction in cobalt(II) salts in aqueous solution with sodium borohydride, and it has been reported that the critical factor contributing to their catalytic activity is that the cobalt ought to be fully reduced [84]. The highest performing Co-B catalyst reported to date had a hydrogen generation rate of 39,000 mL min−1 (g catalyst−1), though given that this value was obtained in the absence of stabilizing sodium hydroxide and at an elevated temperature of 40°C, it is difficult to make a direct comparison with other systems [85]. Liu et al. [86] obtained a maximum HGR of 26,000 mL min−1 (g catalyst−1) in a sodium hydroxide stabilized solution of sodium borohydride with a super fine Co-B catalyst obtained via the formation of a colloidal Co(OH)2 intermediate.

An adaptation of these systems used cobalt chloride (CoCl2) in aqueous solution as catalyst, but with aluminum powder as well as sodium borohydride to accelerate the rate of generation of hydrogen [87]. However, after only three cycles the hydrogen generation rate had dropped to 20% of the maximum rate. The authors attributed this loss to the buildup of reaction by-products on the surface of the powder mixture. Bic have patented a fuel cartridge design which overcomes this problem, and allows the on-demand generation of hydrogen from an aqueous sodium hydroxide stabilized solution of sodium borohydride using CoCl2 as catalyst without excessive surface by-product build up [88].

Various alloy systems based on Co-B have been reported, such as Co-Mo-Pd-B [89], Co-Pd-B [53], Co-Fe-B [90], Co-W-B [91], Co-Mo-B [92],Co-La-Zr-B [93, 94], Co-Ru-B [95], Co-Cr-B [96], and Co-Cu-B [89]. The best performance of this type of catalyst reported to date is a Co-Mn-B powder, giving an HGR of 35,000 mL min−1 (g catalyst)−1 [97]. There have been several reports of highly performing Co-B-based catalysts being deposited on Ni foam by electroless plating. This highly porous structure is ideal for conferring on/off functionality to the hydrogen generation reaction by simply dipping and removing the catalyst into and out from the aqueous borohydride solution. Co-B/Ni foam gave a maximum hydrogen generation rate of 24,400 mL min−1 (g catalyst)−1 [98], whilst Co-Fe-B/Ni foam was used to obtain a maximum hydrogen generation rate of 22,000 mL min−1 (g catalyst)−1 [90]. Other substrates have also shown promising hydrogen generation rates, and could be deployed in a similar way for “on/off” hydrogen generation. Nanosized Co-B catalyst has also been prepared on TiO2, giving an HGR of 12,500 mL min−1 (g catalyst)−1. The authors [99] noted that supported Co-B catalysts perform better in the sodium borohydride hydrolysis reaction than unsupported catalysts. Chen et al. have investigated the effects of varying different synthesis conditions on the effect of catalyst activity of Co-B deposited on ion exchange resins [100]. They found that a slower reduction time gives a higher surface area, more active catalytic Co-B species.

A series of Co-P systems have also been reported, such as Co-P [101], Co-Ni-P [102], and Co-W-P [103], and also some mixed Co-P-B systems such as Co-P-B [104] and Co-Ni-P-B [105], but in general these systems have been poorer performing then the boron alloys in terms of hydrogen generation rates.

Cobalt nanoparticles have also been reported to be effective at catalyzing hydrogen generation. These are typically deposited initially as Co(II) ions on a support material and then reduced chemically to Co(0). Patel et al. [106] used pulsed layer deposition to coat a boron sheet with cobalt nanoparticles, obtaining an HGR of 3375 mL min−1 (g catalyst)−1. Zhu et al. [107] deposited cobalt nanoparticles onto carbon-based aerogels using an impregnation-reduction method, obtaining an HGR of 2010 mL min−1 (g catalyst)−1. Jaworkski et al. [108] impregnated a hydroxyapatite support with cobalt nanoparticles which showed reasonably good durability, attaining 75% of their maximum performance after 3 weeks of use. This system was improved further by Rakap et al. [109], who synthesized a hydroxyapatite-supported cobalt nanoparticle catalyst providing 25,600 turnovers in the hydrolysis of basic sodium borohydride. Bennici et al. [110]. have reported a better performing polyanion complex (in terms of hydrogen generation rate) as a support for cobalt nanoparticles, but the large weight of the support per g of cobalt metal would probably render such systems unsuitable for portable applications which are becoming increasingly popular at present.

Several carbon-supported cobalt nanoparticle catalysts have been reported, which have the advantage of being relatively low in cost. Niu et al. [111] observed a HGR of 1358 mL min−1 (g catalyst)−1 with such a system, whereas Zhu et al. [112] impregnated colloidal carbon spheres obtained from glucose with cobalt with a greater HGR of 1911 mL min−1 (g catalyst)−1. Cobalt boride has also been synthesized on carbon supports [113, 114], and these were found to be more highly performing than the carbon-supported Co NP systems; for example, Baydaroglu et al. attained a HGR of 8034 mL min−1 (g catalyst)−1 at room temperature [115]. Cobalt oxide (CoO) nanocrystals have also been found to be an effective catalyst [116], with an HGR of 8333 mL min−1 (g catalyst−1).

Cobalt, nickel, and iron are all ferromagnetic materials, and it has been suggested that this property could be used as a catalytic “on/off” switch by using a magnet to remove the catalyst from the solution when hydrogen generation is no longer required. In a recent study [117], cobalt, nickel, and iron were deposited onto SiO2 by an impregnation/chemical reduction process. These catalysts gave HGR values of 8700, 300, and 130 mL min−1 (g metal)−1, respectively. Silicon dioxide is a very attractive catalyst support material due to its low molecular mass, low cost and chemical stability.

Various other nickel-based catalysts have been reported [118], but cobalt-based catalysts have generally been found to be superior in terms of maximum hydrogen generation rate, rendering cobalt the catalyst of choice for sodium borohydride hydrolysis.

Acid catalysis

Acid homogenous catalysis of sodium borohydride to generate hydrogen was first reported as long ago as 1953 [165]. Unlike metal catalyzed hydrolysis of sodium borohydride, which is typically carried out in an aqueous alkaline solution, acid hydrolysis of sodium borohydride is usually conducted by adding aqueous acid solution drop wise onto solid sodium borohydride powder. The major advantages of these methods include the generation of very dry hydrogen gas, the easy control of hydrogen production and the pH neutral, environmentally benign nature of the waste products formed during the reaction. This is counterbalanced by the significant disadvantages of having to carry a reservoir of reasonably strong acid, and adding complications to the reactor design.

For example, Javed et al. [166] reported a system which used 6 mol/L hydrochloric acid (HCl) solution delivered at a flow rate of 1 μL min−1. A similar system was reported by Prosini et al. [167]. Such corrosive solutions are far from ideal for portable applications. Murugesan et al. [168] tested sulfuric, nitric, phosphoric, formic and acetic acids as catalysts for sodium borohydride. Even at high concentrations, nitric and phosphoric acid were incapable of yielding more than half of the theoretical hydrogen yield. Hydrochloric and sulfuric acid gave in excess of 95% of the theoretical hydrogen yield, but at concentrations of 3 N, which is still higher than desirable for portable applications. Even at concentrations as high as 12 N, formic and acetic acid gave only around three quarters of the theoretical hydrogen yield.

However, Akdim et al. [169] conducted further studies of acetic acid as an alternative to HCl and found that under the right conditions (specifically a temperature of 60°C and an acid/borohydride ratio of 2), acetic acid was found to catalyze the release of hydrogen as rapidly and to the same extent as HCl (60°C and an acid/borohydride ratio of 1). Tellingly, however, a like for like comparison of HCl and acetic acid at 60°C with an acid/borohydride ratio of 2, acetic acid yields only two-thirds of the amount of hydrogen that HCl does. More interestingly, Akdim et al. claim that hydrochloric and formic acid catalyzed hydrolysis produces more milliliters of hydrogen per minute than catalysis by the highest performing (in terms of hydrogen generation rate) cobalt catalysts, though direct comparisons are difficult given the nature of the two systems. If this be the case, acid hydrolysis becomes far more attractive.

Kim et al. [170] observed that when operating a PEM fuel cell using hydrogen generated by metal catalysis from an alkaline sodium borohydride solution, there is a rapid degradation in performance. They ascribe this at least in part to the presence of sodium ions in the water vapor in the hydrogen stream. They found that there were no detectable water vapor or sodium ions after condensation of the hydrogen feed generated from various organic acids, and that the cell performance degradation observed when using hydrogen generated by metal catalyzed hydrolysis was no longer observed. It is perhaps surprising that the promise of these studies has not resulted in further investigations in this area.


The highest performing heterogeneous catalyst for sodium borohydride hydrolysis was reported by Ozkar et al. [55], who achieved a maximum hydrogen generation rate of 96,800 mL min−1 (g catalyst)−1 using water dispersible ruthenium(0) nanoclusters at ambient temperatures. However, due to the scarcity and expense of noble metal catalysts such as ruthenium, recent research efforts in this field have been focused on developing catalyst systems based on transition metals. Of these, cobalt boride catalysts have proved the most popular, due to their high activity (a hydrogen generation rate of 39,000 mL min−1 (g catalyst)−1 is the highest yet reported [84]), low cost and ease of synthesis. Immobilized cobalt boride-based catalysts are particularly promising as they offer simple reaction control, giving the “on/off” functionality required for portable applications. At present there are comparatively fewer studies of the use of homogenous catalysts such as HCl on the hydrolysis of aqueous sodium borohydride solutions. However, due to the ease of reaction control and the formation of environmentally benign reaction by-products, both of which are very attractive properties for portable applications, it seems likely that this is an area which will attract more attention in the future.

Concluding Remarks

Over the last 15 years, a great deal of effort has been directed at the synthesis and characterization of catalyst systems for sodium borohydride hydrolysis. Cobalt-based systems, in particular cobalt borides, have emerged as the catalyst of choice due to their low cost, ease of synthesis and high activity leading to high maximum hydrogen generation rates. However, several significant issues must be addressed before the widespread deployment of hydrogen generators using sodium borohydride is feasible, such as the requirement for a large stoichiometric excess of water to ensure the sodium metaborate by-product does not foul the reactor or cover the surface of the heterogeneous catalyst and reduce the rate of reaction.


The authors thank the EPSRC and Intelligent Energy Ltd for funding and PB also thanks the SCI for the award of a scholarship.

Conflict of Interest

None declared.


  1. BP. 2014. BP statistical review of world energy. Available at http://www.bp.com/en/global/corporate/about-bp/energy-economics/statistical-review-of-world-energy.html (accessed Feb 25, 2015).
  2. Dalebrook, A. F., W. Gan, M. Grasemann, S. Moret, and G. Laurenczy. 2013. Hydrogen storage: beyond conventional methods. Chem. Commun. (Camb.)49:8735–8751.
  3. Schlapbach, L., and A. Züttel. 2001. Hydrogen-storage materials for mobile applications. Nature414:353–358.
  4. Sarkar, A., and R. Banerjee. 2005. Net energy analysis of hydrogen storage options. Int. J. Hydrogen Energy30:867–877.
  5. Pukazhselvan, D., V. Kumar, and S. K. Singh. 2012. High capacity hydrogen storage: basic aspects, new developments and milestones. Nano Energy1:566–589.
  6. David, W. I. F.2011. Effective hydrogen storage: a strategic chemistry challenge. Faraday Discuss.151:399.
  7. Durbin, D. J., and C. Malardier-Jugroot. 2013. Review of hydrogen storage techniques for on board vehicle applications. Int. J. Hydrogen Energy38:14595–14617.
  8. Eberle, U., M. Felderhoff, and F. Schüth. 2009. Chemical and physical solutions for hydrogen storage. Angew. Chem. Int. Ed. Engl.48:6608–6630.
  9. Jena, P.2011. Materials for hydrogen storage: past, present, and future. J. Phys. Chem. Lett.2:206–211.
  10. Van den Berg, A. W. C., and Areán C. O. 2008. Materials for hydrogen storage: current research trends and perspectives. Chem. Commun.668–681.
  11. Gao, P., Y. Wang, S. Yang, Y. Chen, Z. Xue, L. Wang et al. 2012. Mechanical alloying preparation of fullerene-like Co3C nanoparticles with high hydrogen storage ability. Int. J. Hydrogen Energy37:17126–17130.
  12. Wang, Y., J. Liu, K. Wang, T. Chen, X. Tan, and C. M. Li. 2011. Hydrogen storage in Ni–B nanoalloy-doped 2D graphene. Int. J. Hydrogen Energy36:12950–12954.
  13. Ganji, M. D., S. N. Emami, A. Khosravi, and M. Abbasi. 2015. M. Si-decorated graphene: a promising media for molecular hydrogen storage. Appl. Surf. Sci.332: 105–111.
  14. Barghi, S. H., T. T. Tsotsis, and M. Sahimi. 2014. Chemisorption, physisorption and hysteresis during hydrogen storage in carbon nanotubes. Int. J. Hydrogen Energy39:1390–1397.
  15. Kalantzopoulos, G. N., A. Enotiadis, E. Maccallini, M. Antoniou, K. Dimos, A. Policicchio, et al. 2014. Hydrogen storage in ordered and disordered phenylene-bridged mesoporous organosilicas. Int. J. Hydrogen Energy39:2104–2114.
  16. Owens, D., A. Han, L. Sun, and Y. Mao. 2015. Synthesis of VTMS(X)-HMS-3 mesoporous ordered silica for hydrogen storage. Int. J. Hydrogen Energy40:2736–2741.
  17. Hirscher, M., B. Panella, and B. Schmitz. 2010. Metal-organic frameworks for hydrogen storage. Microporous Mesoporous Mater.129:335–339.
  18. Langmi, H. W., J. Ren, B. North, M. Mathe, and D. Bessarabov. 2014. Hydrogen storage in metal-organic frameworks: a review. Electrochim. Acta128:368–392.
  19. Yan, Y., S. Yang, A. J. Blake, and M. Schroder. 2014. Studies on metal-organic frameworks of Cu (II) with isophthalate linkers for hydrogen storage. Acc. Chem. Res.47:296–307.
  20. Lee, H., J. Lee, D. Y. Kim, J. Park, and Y. Seo. 2005. Tuning clathrate hydrates for hydrogen storage. Nature434:2003–2006.
  21. Lototskyy, M. V., V. A. Yartys, B. G. Pollet, and R. C. Bowman. 2014. Metal hydride hydrogen compressors: a review. Int. J. Hydrogen Energy39:5818–5851.
  22. Sakintuna, B., F. Lamaridarkrim, and M. Hirscher. 2007. Metal hydride materials for solid hydrogen storage: a review. Int. J. Hydrogen Energy32:1121–1140.
  23. Pickering, L., Reed D., Bevan A. I., and Book D. 2014. Ti–V–Mn based metal hydrides for hydrogen compression applications. J. Alloys Compd. doi:10.1016/j.jallcom.2014.12.098, in press.
  24. Frankcombe, T. J. 2012. Proposed mechanisms for the catalytic activity of Ti in NaAlH4Chem. Rev.112:2164–2178.
  25. Lin, S. S.-Y., J. Yang, and H. H. Kung. 2012. Transition metal-decorated activated carbon catalysts for dehydrogenation of NaAlH4. Int. J. Hydrogen Energy37:2737–2741.
  26. Li, L., Y. Wang, F. Qiu, Y. Wang, Y. Xu, C An, et al. 2013. Reversible hydrogen storage properties of NaAlH4 enhanced with TiN catalyst. J. Alloys Compd.566:137–141.
  27. Fu, J., M. Tegel, and B. Kieback. 2014. Dehydrogenation properties of doped LiAlH4 compacts for hydrogen generator applications. Int. J. Hydrogen Energy39:16362–16371.
  28. Varin, R. A., Zbroniec L., Czujko T., and Wronski Z. S.. 2011. The effects of nanonickel additive on the decomposition of complex metal hydride LiAlH4 (lithium alanate). Int. J. Hydrogen Energy36, 1167–1176.
  29. Remhof, A. P. Mauron, A. Zu, J. P. Embs, L. Zbigniew, P. Ngene, et al. 2013. Hydrogen dynamics in nanoconfined lithiumborohydride. J. Phys. Chem. C117: 3789–3798.
  30. Borgschulte, A. A. Jain, A. J. Ramirez-Cuesta, P. Martelli, A. Remhof, O. Friedrichs, et al. 2011. Mobility and dynamics in the complex hydrides LiAlH4 and LiBH4. Faraday Discuss.151:213.
  31. Jain, I. P., C. Lal, and A. Jain. 2010. Hydrogen storage in Mg: a most promising material. Int. J. Hydrogen Energy35:5133–5144.
  32. Shao, H., G. Xin, J. Zheng, X. Li, and E. Akiba. 2012. Nanotechnology in Mg-based materials for hydrogen storage. Nano Energy1:590–601.
  33. Gabis, I., Dobrotvorskiy M., Evard E., and Voyt A. 2011. Kinetics of dehydrogenation of MgH2 and AlH3. J. Alloys Compd.509, S671–S674.
  34. Graetz, J., J. J. Reilly, V. A. Yartys, J. P. Maehlen, B. M. Bulychev, V. E. Antonov, et al. 2011. Aluminum hydride as a hydrogen and energy storage material: past, present and future. J. Alloys Compd.509:S517–S528.
  35. Grew, K. N., Z. B. Brownlee, K. C. Shukla, and D. Chu. 2012. Assessment of alane as a hydrogen storage media for portable fuel cell power sources. J. Power Sources217:417–430.
  36. Zidan, R, B. L. Garcia-Diaz, C. S. Fewox, A. C. Stowe, J. R. Gray, and A. G. Harter. 2009. Aluminium hydride: a reversible material for hydrogen storage. Chem. Commun.3717–3719.
  37. Demirci, U. B., and P. Miele. 2014. Reaction mechanisms of the hydrolysis of sodium borohydride: a discussion focusing on cobalt-based catalysts. Comptes Rendus Chim.17:707–716.
  38. Eickhoff, S., C. Zhang, and T. Cui. 2013. The effects of hydride chemistry, particle size, and void fraction on micro fuel cell performance. J. Power Sources243:562–568.
  39. Eickhoff, S., C. Zhang, and T. Cui. 2013. Micro fuel cell utilizing fuel cell water recovery and pneumatic valve. J. Power Sources240:1–7.
  40. Moghaddam, S., E. Pengwang, R. I. Masel, and M. Shannon. 2010. An enhanced microfluidic control system for improving power density of a hydride-based micro fuel cell. J. Power Sources195:1866–1871.
  41. Demirci, U. B., and P. Miele. 2009. Sodium borohydride versus ammonia borane, in hydrogen storage and direct fuel cell applications. Energy Environ. Sci.2:627–637.
  42. Figen, K. A. 2013. Dehydrogenation characteristics of ammonia borane via boron-based catalysts (Co–B, Ni–B, Cu–B) under different hydrolysis conditions. Int. J. Hydrogen Energy38:9186–9197.
  43. Lai, S.-W., H.-L. Lin, Y.-P. Lin, and T. L. Yu. 2013. Hydrolysis of ammonia–borane catalyzed by an iron–nickel alloy on an SBA-15 support. Int. J. Hydrogen Energy38:4636–4647.
  44. Santos, D. M. F., and Sequeira C. A.. 2011. Sodium borohydride as a fuel for the future. Renew. Sustain. Energy Rev.15: 3980–4001.
  45. Demirci, U. B., O. Akdim, J. Andrieux, J. Hannauer, R. Chamoun, and P. Miele. 2010. Sodium borohydride hydrolysis as hydrogen generator: issues, state of the art and applicability upstream from a fuel cell. Fuel Cells10:335–350.
  46. Elitzur, S., V. Rosenband, and A. Gany. 2014. Study of hydrogen production and storage based on aluminum-water reaction. Int. J. Hydrogen Energy39:6328–6334.
  47. Rosenband, V., and A. Gany. 2010. Application of activated aluminum powder for generation of hydrogen from water. Int. J. Hydrogen Energy35:10898–10904.
  48. Erogbogbo, F., T. Lin, P. M. Tucciarone, K. M. LaJoie, L. Lai, G. D. Patki, et al. 2013. On-demand hydrogen generation using nanosilicon: splitting water without light, heat, or electricity. Nano Lett.13:451–456.
  49. Demirci, U. B., O. Akdim, and P. Miele. 2009. Ten-year efforts and a no-go recommendation for sodium borohydride for on-board automotive hydrogen storage. Int. J. Hydrogen Energy34:2638–2645.
  50. Bartkus, T. P., J. S. T'ien, and C.-J. Sung. 2013. A semi-global reaction rate model based on experimental data for the self-hydrolysis kinetics of aqueous sodium borohydride. Int. J. Hydrogen Energy38:4024–4033.
  51. Retnamma, R., A. Q. Novais, and C. M. Rangel. 2011. Kinetics of hydrolysis of sodium borohydride for hydrogen production in fuel cell applications: a review. Int. J. Hydrogen Energy36:9772–9790.
  52. Marreroalfonso, E., J. Gray, T. Davis, and M. Matthews. 2007. Hydrolysis of sodium borohydride with steam. Int. J. Hydrogen Energy32:4717–4722.
  53. Liu, H., C. M. Boyd, A. M. Beaird, and M. A. Matthews. 2011. Vapor phase batch hydrolysis of NaBH4 at elevated temperature and pressure. Int. J. Hydrogen Energy36:6472–6477.
  54. Yu, L., and M. A. Matthews. 2014. A reactor model for hydrogen generation from sodium borohydride and water vapor. Int. J. Hydrogen Energy39:3830–3836.
  55. Özkar, S., and M. Zahmakıran. 2005. Hydrogen generation from hydrolysis of sodium borohydride using Ru(0) nanoclusters as catalyst. J. Alloys Compd.404–406:728–731.
  56. Walter, J. C., A. Zurawski, D. Montgomery, M. Thornburg, and S. Revankar. 2008. Sodium borohydride hydrolysis kinetics comparison for nickel, cobalt, and ruthenium boride catalysts. J. Power Sources179:335–339.
  57. Liang, Y., H.-B. Dai, L.-P. Ma, P. Wang, and H.-M. Cheng. 2010. Hydrogen generation from sodium borohydride solution using a ruthenium supported on graphite catalyst. Int. J. Hydrogen Energy35:3023–3028.
  58. Li, Y., Q. Zhang, N. Zhang, L. Zhu, J. Zheng, and B. H. Chen. 2013. Ru–RuO2/C as an efficient catalyst for the sodium borohydride hydrolysis to hydrogen. Int. J. Hydrogen Energy38:13360–13367.
  59. Park, J., P. Shakkthivel, H. Kim, M.-K. Han, J. Jang, Y. Kim, et al. 2008. Investigation of metal alloy catalyst for hydrogen release from sodium borohydride for polymer electrolyte membrane fuel cell application. Int. J. Hydrogen Energy33:1845–1852.
  60. Amendola, S. C., S. L. Sharp-Goldman, M. S. Janjua, N. C. Spencer, M. T. Kelly, P. J. Petillo, et al. 2000. A safe, portable, hydrogen gas generator using aqueous borohydride solution and Ru catalyst. Int. J. Hydrogen Energy25:969–975.
  61. Amendola, S. C., S. L. Sharp-Goldman, M. S. Janjua, M. T. Kelly, P. J. Petillo, and M. Binder. 2000. An ultrasafe hydrogen generator: Aqueous, alkaline borohydride solutions and Ru catalyst. J. Power Sources85:186–189.
  62. Liu, C.-H., B.-H. Chen, C.-L. Hseuh, J.-R. Ku, M.-S. Jeng, and F. Tsau. 2009. Hydrogen generation from hydrolysis of sodium borohydride using Ni–Ru nanocomposite as catalysts. Int. J. Hydrogen Energy34:2153–2163.
  63. Chen, C.-W., C.-Y. Chen, and Y.-H. Huang. 2009. Method of preparing Ru-immobilized polymer-supported catalyst for hydrogen generation from NaBH4 solution. Int. J. Hydrogen Energy34:2164–2173.
  64. Demirci, U. B., and F. Garin. 2008. Ru-based bimetallic alloys for hydrogen generation by hydrolysis of sodium tetrahydroborate. J. Alloys Compd.463:107–111.
  65. Zhang, J. S., W. N. Delgass, T. S. Fisher, and J. P. Gore. 2007. Kinetics of Ru-catalyzed sodium borohydride hydrolysis. J. Power Sources164:772–781.
  66. Crisafulli, C., S. Scirè, R. Zito, and C. Bongiorno. 2012. Role of the support and the Ru precursor on the performance of ru/carbon catalysts towards H2 production through NaBH4 hydrolysis. Catal. Letters142:882–888.
  67. Hsueh, C.-L., C.-Y. Chen, J.-R. Ku, S.-F. Tsai, Y.-Y. Hsu, F. Tsau, et al. 2008. Simple and fast fabrication of polymer template-Ru composite as a catalyst for hydrogen generation from alkaline NaBH4 solution. J. Power Sources177:485–492.
  68. Bai, Y., C. Wu, F. Wu, and B. Yi. 2006. Carbon-supported platinum catalysts for on-site hydrogen generation from NaBH4 solution. Mater. Lett.60:2236–2239.
  69. Wu, C., H. Zhang, and B. Yi. 2004. Hydrogen generation from catalytic hydrolysis of sodium borohydride for proton exchange membrane fuel cells. Catal. Today93–95:477–483.
  70. Kojima, Y., K.-I. Suzuki, K. Fukumoto, M. Sasaki, T. Yamamoto, Y. Kawai, et al. 2002. Hydrogen generation using sodium borohydride solution and metal catalyst coated on metal oxide. Int. J. Hydrogen Energy27:1029–1034.
  71. Kojima, Y., Y. Kawai, H. Nakanishi, and S. Matsumoto. 2004. Compressed hydrogen generation using chemical hydride. J. Power Sources135:36–41.
  72. Krishnan, P., T.-H. Yang, W.-Y. Lee, and C.-S. Kim. 2005. PtRu-LiCoO2—an efficient catalyst for hydrogen generation from sodium borohydride solutions. J. Power Sources143:17–23.
  73. Peña-Alonso, R., A. Sicurelli, E. Callone, G. Carturan, and R. Raj. 2007. A picoscale catalyst for hydrogen generation from NaBH4 for fuel cells. J. Power Sources165:315–323.
  74. Saha, S., V. Basak, A. Dasgupta, S. Ganguly, D. Banerjee, and K. Kargupta. 2014. Graphene supported bimetallic G-Co-Pt nanohybrid catalyst for enhanced and cost effective hydrogen generation. Int. J. Hydrogen Energy39:11566–11577.
  75. Zahmakıran, M., and S. Özkar. 2006. Water dispersible acetate stabilized ruthenium(0) nanoclusters as catalyst for hydrogen generation from the hydrolysis of sodium borohyride. J. Mol. Catal. A Chem.258:95–103.
  76. Guella, G., B. Patton, and A. Miotello. 2007. 11 B kinetic features of the platinum catalyzed hydrolysis of sodium borohydride from NMR measurements. J. Phys. Chem. C111:18744–18750.
  77. Xu, D., H. Zhang, and W. Ye. 2007. Hydrogen generation from hydrolysis of alkaline sodium borohydride solution using Pt/C catalyst. Catal. Commun.8:1767–1771.
  78. Liu, Z., B. Guo, S. H. Chan, E. H. Tang, and L. Hong. 2008. Pt and Ru dispersed on LiCoO2 for hydrogen generation from sodium borohydride solutions. J. Power Sources176:306–311.
  79. Zahmakiran, M., and S. Ozkar. 2009. Zeolite-confined ruthenium(0) nanoclusters catalyst: Record catalytic activity, reusability, and lifetime in hydrogen generation from the hydrolysis of sodium borohydride. Langmuir25:2667–2678.
  80. Larichev, Y. V., O. V. Netskina, O. V. Komova, and V. I. Simagina. 2010. Comparative XPS study of Rh/Al2O3 and Rh/TiO2 as catalysts for NaBH4 hydrolysis. Int. J. Hydrogen Energy35:6501–6507.
  81. Huang, Y.-H., C.-C. Su, S.-L. Wang, and M.-C. Lu. 2012. Development of Al2O3 carrier-Ru composite catalyst for hydrogen generation from alkaline NaBH4 hydrolysis. Energy46:242–247.
  82. Demirci, U. B., and P. Miele. 2010. Cobalt in NaBH4 hydrolysis. Phys. Chem. Chem. Phys.12:14651–14665.
  83. Demirci, U. B., and P. Miele. 2014. Cobalt-based catalysts for the hydrolysis of NaBH4 and NH3BH3. Phys. Chem. Chem. Phys.16:6872–6885.
  84. Manna, J., B. Roy, M. Vashistha, and P. Sharma. 2014. Effect of Co+2/BH− 4 ratio in the synthesis of Co-B catalysts on sodium borohydride hydrolysis. Int. J. Hydrogen Energy39:406–413.
  85. Akdim, O., U. B. Demirci, D. Muller, and P. Miele. 2009. Cobalt (II) salts, performing materials for generating hydrogen from sodium borohydride. Int. J. Hydrogen Energy34:2631–2637.
  86. Liu, B., and Q. Li. 2008. A highly active Co-B catalyst for hydrogen generation from sodium borohydride hydrolysis. Int. J. Hydrogen Energy33:7385–7391.
  87. Dai, H.-B., G.-L. Ma, X.-D. Kang, and P. Wang. 2011. Hydrogen generation from coupling reactions of sodium borohydride and aluminum powder with aqueous solution of cobalt chloride. Catal. Today170:50–55.
  88. Rosenzweig, A., P. Adams, A. J. Curello, F. Fairbanks, A. Sgroi, and C. R. Stepan. 2012. Hydrogen generating fuel cell cartridges, US Patent no: US 8,118,893 B2.
  89. Zhao, Y., Z. Ning, J. Tian, H. Wang, X. Liang, S. Nie, et al. 2012. Hydrogen generation by hydrolysis of alkaline NaBH4 solution on Co–Mo–Pd–B amorphous catalyst with efficient catalytic properties. J. Power Sources207:120–126.
  90. Liang, Y., P. Wang, and H.-B. Dai. 2010. Hydrogen bubbles dynamic template preparation of a porous Fe–Co–B/Ni foam catalyst for hydrogen generation from hydrolysis of alkaline sodium borohydride solution. J. Alloys Compd.491:359–365.
  91. Dai, H., Y. Liang, P. Wang, X. D. Yao, T. Rufford, M. Lu, et al. 2008. High-performance cobalt–tungsten–boron catalyst supported on Ni foam for hydrogen generation from alkaline sodium borohydride solution. Int. J. Hydrogen Energy33:4405–4412.
  92. Zhuang, D.-W., Q. Kang, S. S. Muir, X. Yao, H.-B. Dai, G.-L. Ma, et al. 2013. Evaluation of a cobalt–molybdenum–boron catalyst for hydrogen generation of alkaline sodium borohydride solution–aluminum powder system. J. Power Sources224:304–311.
  93. Loghmani, M. H., and A. F. Shojaei. 2013. Synthesis and characterization of Co–La–Zr–B quaternary amorphous nano alloy: Kinetic study for hydrogen generation from hydrolysis of sodium borohydride. J. Alloys Compd.580:61–66.
  94. Loghmani, M. H., and A. F. Shojaei. 2013. Hydrogen generation from hydrolysis of sodium borohydride by cubic Co–La–Zr–B nano particles as novel catalyst. Int. J. Hydrogen Energy38:10470–10478.
  95. Wang, W., Y. Zhao, D. Chen, X. Wang, X. Peng, and J. Tian. 2014. Promoted Mo incorporated Co-Ru-B catalyst for fast hydrolysis of NaBH4 in alkaline solutions. Int. J. Hydrogen Energy39:16202–16211.
  96. Fernandes, R., N. Patel, A. Miotello, R. Jaiswal, D. C. Kothari. 2011. Stability, durability, and reusability studies on transition metal-doped Co–B alloy catalysts for hydrogen production. Int. J. Hydrogen Energy36:13379–13391.
  97. Yuan, X., C. Jia, X.-L. Ding, and Z.-F. Ma. 2012. Effects of heat-treatment temperature on properties of Cobalt–Manganese–Boride as efficient catalyst toward hydrolysis of alkaline sodium borohydride solution. Int. J. Hydrogen Energy37:995–1001.
  98. Muir, S. S., Z. Chen, B. J. Wood, L. Wang, G. Q. Lu, and X. Yao. 2014. New electroless plating method for preparation of highly active Co-B catalysts for NaBH4 hydrolysis. Int. J. Hydrogen Energy39:414–425.
  99. Lu, Y.-C., M.-S. Chen, and Y.-W. Chen. 2012. Hydrogen generation by sodium borohydride hydrolysis on nanosized CoB catalysts supported on TiO2, Al2O3 and CeO2. Int. J. Hydrogen Energy37:4254–4258.
  100. Chen, Y., and C. Pan. 2014. Effect of various Co–B catalyst synthesis conditions on catalyst surface morphology and NaBH4 hydrolysis reaction kinetic parameters. Int. J. Hydrogen Energy39:1648–1663.
  101. Oh, T. H., and S. Kwon. 2013. Performance evaluation of hydrogen generation system with electroless-deposited Co–P/Ni foam catalyst for NaBH4 hydrolysis. Int. J. Hydrogen Energy38:6425–6435.
  102. Rakap, M., E. E. Kalu, and S. Özkar. 2011. Cobalt–nickel–phosphorus supported on Pd-activated TiO2 (Co–Ni–P/Pd-TiO2) as cost-effective and reusable catalyst for hydrogen generation from hydrolysis of alkaline sodium borohydride solution. J. Alloys Compd.509:7016–7021.
  103. Guo, Y., Z. Dong, Z. Cui, X. Zhang, and J. Ma. 2012. Promoting effect of W doped in electrodeposited Co–P catalysts for hydrogen generation from alkaline NaBH4 solution. Int. J. Hydrogen Energy37:1577–1583.
  104. Kim, D.-R., K.-W. Cho, Y.-I. Choi, and C.-J. Park. 2009. Fabrication of porous Co–Ni–P catalysts by electrodeposition and their catalytic characteristics for the generation of hydrogen from an alkaline NaBH4 solution. Int. J. Hydrogen Energy34:2622–2630.
  105. Fernandes, R., N. Patel, and Miotello A. 2009. Efficient catalytic properties of Co–Ni–P–B catalyst powders for hydrogen generation by hydrolysis of alkaline solution of NaBH4. Int. J. Hydrogen Energy34:2893–2900.
  106. Patel, N., A. Miotello, and V. Bello. 2011. Pulsed Laser Deposition of Co-nanoparticles embedded on B-thin film: A very efficient catalyst produced in a single-step process. Appl. Catal. B Environ.103:31–38.
  107. Zhu, J., R. Li, W. Niu, Y. Wu, and X. Gou. 2013. Fast hydrogen generation from NaBH4 hydrolysis catalyzed by carbon aerogels supported cobalt nanoparticles. Int. J. Hydrogen Energy38:10864–10870.
  108. Jaworski, J. W., S. Cho, Y. Kim, J. H. Jung, H. S. Jeon, B. K. Min, et al. 2013. Hydroxyapatite supported cobalt catalysts for hydrogen generation. J. Colloid Interface Sci.394:401–408.
  109. Rakap, M., and S. Özkar. 2012. Hydroxyapatite-supported cobalt(0) nanoclusters as efficient and cost-effective catalyst for hydrogen generation from the hydrolysis of both sodium borohydride and ammonia-borane. Catal. Today183:17–25.
  110. Bennici, S., H. Yu, E. Obeid, and A. Auroux. 2011. Highly active heteropolyanions supported Co catalysts for fast hydrogen generation in NaBH4 hydrolysis. Int. J. Hydrogen Energy36:7431–7442.
  111. Niu, W., D. Ren, Y. Han, Y. Wu, and X. Gou. 2012. Optimizing preparation of carbon supported cobalt catalyst for hydrogen generation from NaBH4 hydrolysis. J. Alloys Compd.543:159–166.
  112. Zhu, J., R. Li, W. Niu, Y. Wu, and X. Gou. 2012. Facile hydrogen generation using colloidal carbon supported cobalt to catalyze hydrolysis of sodium borohydride. J. Power Sources211:33–39.
  113. Huang, Y., Y. Wang, R. Zhao, P. Shen, and Z. Wei. 2008. Accurately measuring the hydrogen generation rate for hydrolysis of sodium borohydride on multiwalled carbon nanotubes/Co–B catalysts. Int. J. Hydrogen Energy33:7110–7115.
  114. Zhao, J., H. Ma, and J. Chen. 2007. Improved hydrogen generation from alkaline NaBH4 solution using carbon-supported Co–BCo–B as catalysts. Int. J. Hydrogen Energy32:4711–4716.
  115. Baydaroglu, F., E. Ozdemir, A. Hasimoglu, and E. Özdemir. 2014. An effective synthesis route for improving the catalytic activity of carbon-supported Co-B catalyst for hydrogen generation through hydrolysis of NaBH4. Int. J. Hydrogen Energy39:1516–1522.
  116. Lu, A., Y. Chen, J. Jin, G.-H. Yue, and D.-L. Peng. 2012. CoO nanocrystals as a highly active catalyst for the generation of hydrogen from hydrolysis of sodium borohydride. J. Power Sources220:391–398.
  117. Shih, Y.-J., C.-C. Su, Y.-H. Huang, and M.-C. Lu. 2013. SiO2-supported ferromagnetic catalysts for hydrogen generation from alkaline NaBH4 (sodium borohydride) solution. Energy54:263–270.
  118. Chinnappan, A., and H. Kim. 2012. Nanocatalyst: Electrospun nanofibers of PVDF – Dicationic tetrachloronickelate (II) anion and their effect on hydrogen generation from the hydrolysis of sodium borohydride. Int. J. Hydrogen Energy37:18851–18859.
  119. Hua, D., Y. Hanxi, A. Xinping, and C. Chuansin. 2003. Hydrogen production from catalytic hydrolysis of sodium borohydride solution using nickel boride catalyst. Int. J. Hydrogen Energy28:1095–1100.
  120. Wu, C., F. Wu, Y. Bai, B. Yi, and H. Zhang. 2005. Cobalt boride catalysts for hydrogen generation from alkaline NaBH4 solution. Mater. Lett.59:1748–1751.
  121. Jeong, S. U., R. K. Kim, E. A. Cho, H.-J. Kim, S.-W. Nam, I.-H. Oh, et al. 2005. A study on hydrogen generation from NaBH4 solution using the high-performance Co-B catalyst. J. Power Sources144:129–134.
  122. Liu, B. H., Z. P. Li, and S. Suda. 2006. Nickel- and cobalt-based catalysts for hydrogen generation by hydrolysis of borohydride. J. Alloys Compd.415:288–293.
  123. Lee, J., K.-Y. Kong, C. R. Jung, E. Cho, S. P. Yoon, J. Han, et al. 2007. A structured Co–B catalyst for hydrogen extraction from NaBH4 solution. Catal. Today120:305–310.
  124. Patel, N., G. Guella, A. Kale, A. Miotello, B. Patton, C. Zanchetta, et al. 2007. Thin films of Co–B prepared by pulsed laser deposition as efficient catalysts in hydrogen producing reactions. Appl. Catal. A Gen.323:18–24.
  125. Ingersoll, J. C., Mani N., Thenmozhiyal J. C., and Muthaiah A. 2007. Catalytic hydrolysis of sodium borohydride by a novel nickel–cobalt–boride catalyst. J. Power Sources173, 450–457 (2007).
  126. Jeong, S. U., E. A. Cho, S. W. Nam, I. H. Oh, U. H. Jung, and S. H. Kim. 2007. Effect of preparation method on Co–B catalytic activity for hydrogen generation from alkali NaBH4 solution. Int. J. Hydrogen Energy32:1749–1754.
  127. Cho, K. W., and H. S. Kwon. 2007. Effects of electrodeposited Co and Co–P catalysts on the hydrogen generation properties from hydrolysis of alkaline sodium borohydride solution. Catal. Today120:298–304.
  128. Dai, H.-B., Y. Liang, P. Wang, and H.-M. Cheng. 2008. Amorphous cobalt–boron/nickel foam as an effective catalyst for hydrogen generation from alkaline sodium borohydride solution. J. Power Sources177:17–23.
  129. Patel, N., R. Fernandes, G. Guella, A. Kale, A. Miotello, B. Patton, et al. 2008. Structured and nanoparticle assembled Co - B thin films prepared by pulsed laser deposition: a very efficient catalyst for hydrogen production. J. Phys. Chem. C112:6968–6976.
  130. Malvadkar, N., S. Park, M. Urquidi-MacDonald, H. Wang, and M. C. Demirel. 2008. Catalytic activity of cobalt deposited on nanostructured poly(p-xylylene) films. J. Power Sources182:323–328.
  131. Metin, Ö., and S. Özkar. 2008. Synthesis and characterization of poly(N-vinyl-2-pyrrolidone)-stabilized water-soluble nickel(0) nanoclusters as catalyst for hydrogen generation from the hydrolysis of sodium borohydride. J. Mol. Catal. A Chem.295:39–46.
  132. Liang, J., Y. Li, Y. Huang, J. Yang, H. Tang, Z. Wei, et al. 2008. Sodium borohydride hydrolysis on highly efficient Co–B/Pd catalysts. Int. J. Hydrogen Energy33:4048–4054.
  133. Xu, D., P. Dai, Q. Guo, and X. Yue. 2008. Improved hydrogen generation from alkaline NaBH4 solution using cobalt catalysts supported on modified activated carbon. Int. J. Hydrogen Energy33:7371–7377.
  134. Xu, D., P. Dai, X. Liu, C. Cao, and Q. Guo. 2008. Carbon-supported cobalt catalyst for hydrogen generation from alkaline sodium borohydride solution. J. Power Sources182:616–620.
  135. Patel, N., R. Fernandes, and A. Miotello. 2009. Hydrogen generation by hydrolysis of NaBH4 with efficient Co–P–B catalyst: A kinetic study. J. Power Sources188:411–420.
  136. Fernandes, R., N. Patel, and A. Miotello. 2009. Hydrogen generation by hydrolysis of alkaline NaBH4 solution with Cr-promoted Co–B amorphous catalyst. Appl. Catal. B Environ.92:68–74.
  137. Krishnan, P., S. G. Advani, and A. K. Prasad. 2009. Thin-film CoB catalyst templates for the hydrolysis of NaBH4 solution for hydrogen generation. Appl. Catal. B Environ.86:137–144.
  138. Fernandes, R., N. Patel, A. Miotello, and M. Filippi. 2009. Studies on catalytic behavior of Co–Ni–B in hydrogen production by hydrolysis of NaBH4. J. Mol. Catal. A Chem.298:1–6.
  139. Patel, N., R. Fernandes, and A. Miotello. 2010. Promoting effect of transition metal-doped Co–B alloy catalysts for hydrogen production by hydrolysis of alkaline NaBH4 solution. J. Catal.271:315–324.
  140. Patel, N., R. Fernandes, N. Bazzanella, and A. Miotello. 2010. Co–P–B catalyst thin films prepared by electroless and pulsed laser deposition for hydrogen generation by hydrolysis of alkaline sodium borohydride: A comparison. Thin Solid Films518:4779–4785.
  141. Eom, K., and H. Kwon. 2010. Effects of deposition time on the H2 generation kinetics of electroless-deposited cobalt–phosphorous catalysts from NaBH4 hydrolysis, and its cyclic durability. Int. J. Hydrogen Energy35:5220–5226.
  142. Zhang, X., J. Zhao, F. Cheng, J. Liang, Z. Tao, and J. Chen. 2010. Electroless-deposited Co–P catalysts for hydrogen generation from alkaline NaBH4 solution. Int. J. Hydrogen Energy35:8363–8369.
  143. Tian, H., Q. Guo, and D. Xu. 2010. Hydrogen generation from catalytic hydrolysis of alkaline sodium borohydride solution using attapulgite clay-supported Co-B catalyst. J. Power Sources195:2136–2142.
  144. Chamoun, R., U. B. Demirci, D. Cornu, Y. Zaater, A. Khoury, R. Khoury, et al. 2010. Cobalt-supported alumina as catalytic film prepared by electrophoretic deposition for hydrogen release applications. Appl. Surf. Sci.256:7684–7691.
  145. Dai, H.-B., G.-L. Ma, H.-J. Xia, and P. Wang. 2011. Combined usage of sodium borohydride and aluminum powder for high-performance hydrogen generation. Fuel Cells11:424–430.
  146. Wu, Z., and S. Ge. 2011. Facile synthesis of a Co–B nanoparticle catalyst for efficient hydrogen generation via borohydride hydrolysis. Catal. Commun.13:40–43.
  147. Sahiner, N., O. Ozay, E. Inger, and N. Aktas. 2011. Superabsorbent hydrogels for cobalt nanoparticle synthesis and hydrogen production from hydrolysis of sodium boron hydride. Appl. Catal. B Environ.102:201–206.
  148. Tong, D. G., W. Chu, P. Wu, and L. Zhang. 2012. Honeycomb-like Co–B amorphous alloy catalysts assembled by a solution plasma process show enhanced catalytic hydrolysis activity for hydrogen generation. RSC Adv.2:2369.
  149. Vernekar, A. A., S. T. Bugde, and S. Tilve. 2012. Sustainable hydrogen production by catalytic hydrolysis of alkaline sodium borohydride solution using recyclable Co–Co2B and Ni–Ni3B nanocomposites. Int. J. Hydrogen Energy37:327–334.
  150. Li, Q., and H. Kim. 2012. Hydrogen production from NaBH4 hydrolysis via Co-ZIF-9 catalyst. Fuel Process. Technol.100:43–48.
  151. Nie, M., Y. C. Zou, Y. M. Huang, and J. Q. Wang. 2012. Ni–Fe–B catalysts for NaBH4 hydrolysis. Int. J. Hydrogen Energy37:1568–1576.
  152. Kılınç, D., C. Saka, and Ö. Şahin. 2012. Hydrogen generation from catalytic hydrolysis of sodium borohydride by a novel Co(II)–Cu(II) based complex catalyst. J. Power Sources217:256–261.
  153. Tsai, C. W., H. M. Chen, R. S. Liu, J.-F. Lee, S. M. Chang, and B. J. Weng. 2012. Magnetically recyclable Fe@Co core-shell catalysts for dehydrogenation of sodium borohydride in fuel cells. Int. J. Hydrogen Energy37:3338–3343.
  154. Guo, Y., Q. Feng, Z. Dong, and J. Ma. 2013. Electrodeposited amorphous Co–P catalyst for hydrogen generation from hydrolysis of alkaline sodium borohydride solution. J. Mol. Catal. A Chem.378:273–278.
  155. Guo, Y., Q. Feng, and J. Ma. 2013. The hydrogen generation from alkaline NaBH4 solution by using electroplated amorphous Co–Ni–P film catalysts. Appl. Surf. Sci.273:253–256.
  156. Zhang, X., Z. Wei, Q. Guo, and H. Tian. 2013. Kinetics of sodium borohydride hydrolysis catalyzed via carbon nanosheets supported Zr/Co. J. Power Sources231:190–196.
  157. Cheng, J., C. Xiang, Y. Zou, H. Chu, S. Qiu, H. Zhang, et al. 2015. Highly active nanoporous Co-B-TiO2 framework for hydrolysis of NaBH4. Ceram. Int.41:899–905.
  158. Li, Z., H. Li, L. Wang, T. Liu, T. Zhang, G. Wang, et al. 2014. Hydrogen generation from catalytic hydrolysis of sodium borohydride solution using supported amorphous alloy catalysts (Ni-Co-P/g-Al2O3). Int. J. Hydrogen Energy39:14935–14941.
  159. Li, F., E. Evans, D. La, Q. Li, and H. Kim. 2014. Immobilization of CoCl2 (cobalt chloride) on PAN (polyacrylonitrile) composite nano fiber mesh filled with carbon nanotubes for hydrogen production from hydrolysis of NaBH4 (sodium borohydride). Energy71:32–39.
  160. Loghmani, M. H., and A. F. Shojaei. 2014. Hydrogen production through hydrolysis of sodium borohydride: oleic acid stabilized Co-La-Zr-B nanoparticle as a novel catalyst. Energy68:152–159.
  161. Paladini, M., G. M. Arzac, V. Godinho, M. C. J. De Haro, and A. Fernández. 2014. Supported Co catalysts prepared as thin films by magnetron sputtering for sodium borohydride and ammonia borane hydrolysis. Appl. Catal. B Environ.159:400–409.
  162. Pfeil, T. L., T. L. Pourpoint, and L. J. Groven. 2014. Effects of crystallinity and morphology of solution combustion synthesized Co3O4 as a catalyst precursor in hydrolysis of sodium borohydride. Int. J. Hydrogen Energy39:2149–2159.
  163. Seven, F., and N. Sahiner. 2014. Enhanced catalytic performance in hydrogen generation from NaBH4 hydrolysis by super porous cryogel supported Co and Ni catalysts. J. Power Sources272:128–136.
  164. Wang, X., S. Sun, Z. Huang, and H. Zhang. 2014. Preparation and catalytic activity of PVP-protected Au/Ni bimetallic nanoparticles for hydrogen generation from hydrolysis of basic NaBH4 solution. Int. J. Hydrogen Energy39:905–916.
  165. Schlesinger, H. I., et al. 1953. Sodium borohydride, its hydrolysis and its use as a reducing agent and in the generation of hydrogen. J. Am. Chem. Soc.75:215–219.
  166. Javed, U., and Subramanian V. R.. 2009. Hydrogen generation using a borohydride-based semi-continuous milli-scale reactor?: Effects of physicochemical parameters on hydrogen yield. Energy Fuels408–413 (2009).
  167. Prosini, P. P., and P. Gislon. 2006. A hydrogen refill for cellular phone. J. Power Sources161:290–293.
  168. Murugesan, S., and V. Subramanian. 2009. Effects of acid accelerators on hydrogen generation from solid sodium borohydride using small scale devices. J. Power Sources187:216–223.
  169. Akdim, O., U. B. Demirci, and P. Miele. 2009. Acetic acid, a relatively green single-use catalyst for hydrogen generation from sodium borohydride. Int. J. Hydrogen Energy34:7231–7238.
  170. Kim, H. J., K.-J. Shin, H.-J. Kim, M. K. Han, H. Kim, Y.-G. Shul, et al. 2010. Hydrogen generation from aqueous acid-catalyzed hydrolysis of sodium borohydride. Int. J. Hydrogen Energy35:12239–12245.
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