Application of Electrochemically Deposited Cobalt Films in a Hydrogen Evolution Reaction

催化作用 硼氢化钠 水溶液 无机化学 化学 贵金属 制氢 水煤气变换反应 化学工程 材料科学 有机化学 工程类
作者
Tarek M. Abdel‐Fattah,Clay Huff,Thomas Dushatinski
出处
期刊:Meeting abstracts 卷期号:MA2016-02 (47): 3483-3483
标识
DOI:10.1149/ma2016-02/47/3483
摘要

Hydrogen gas production is a rapidly growing field of research due to its desirable properties from a sustainability viewpoint. The burning of hydrogen gas provides an environmental incentive as well, due to the lack of carbon-based byproducts [1-2]. Hydrogen gas is often evolved from water but is an energy intensive process. Solid chemical storage has been implemented through the use of metal hydrides, such as sodium borohydride. The oxidation reaction of sodium borohydride in water slowly evolves 4 moles of hydrogen gas. While a slow reaction is favorable for reduction, the use of NaBH 4 to produce hydrogen gas necessitates the use of catalysis to accelerate the reaction to an appreciable rate. A great deal of research has been conducted searching for catalysts of such reactions, often finding noble metals to be the most efficient. While less efficient than noble metals, cobalt materials have also demonstrated catalytic properties in a variety of hydrogen evolution reactions. Cobalt is more abundant in the earth’s crust than the noble metals, which makes it an arguably more attractive catalytic material due to a relatively lower cost and easier scalability [3-5]. Cobalt films deposited from aqueous (H 2 O/CoCl) and non-aqueous precursor (Ch:Ch/EG/CoCl) solutions were tested for catalytic activity in the hydrogen evolution reaction of aqueous NaBH 4 . The evolved gas was measured through the use of a water-displacement system, Ohaus microbalance, and mass logging software. The non-aqueously deposited films initially showed a higher reaction rate, but voids in the surface could prevent disassociation of the hydrogen, reducing the catalytic surface. The aqueously deposited films were largely amorphous, providing better active sites for the reaction than its non-aqueous counterpart. Both Co films outperformed the copper substrate (Cu). Catalytic Surface Rate Constant (10 -3 min -1 ) Aqueous Co Deposition 4.9 Non-aqueous Co Deposition 4.6 Original Copper Substrate 3.3 References: Schlesinger, H.; Brown, H.; Finholt, A.; Gilbreath, J.; Hoekstra, H.; Hyde, E. Sodium Borohydride, Its Hydrolysis and its Use as a Reducing Agent and in the Generation of Hydrogen. 1952, J. Am. Chem. Soc. 75(1) 215-219 Chinnappan, A.; Kang, H.; Kim, H. Preparation of PVDF nanofiber composites for hydrogen generationfrom sodium borohydride. 2011, Energy 36(2) 755-759 Dushatinski, T.; Huff, C.; Abdel-Fattah, T. Synthesis and Characterizations of Cobalt Films Electrochemically Deposited from Aqueous and Non-Aqueous Media. 2014, ECS Trans. 64(4) 487-491 Dushatinski, T.; Huff, C.; Abdel-Fattah, T. Optical Properties of Cobalt Films Electrochemically Deposited from Aqueous and Non-Aqueous Ionic Liquids. 2014, ECS Trans. 61(10) 43-46 5. Damiano, B.; Wixtrom, A.; Abdel-Fattah, T. Electrochemical Deposition of Cobalt onto the Surface of Copper Using a Choline Chloride-Based Ionic Liquid. 2012, ECS Trans. 50(11) 277-281

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