2018 AIChE Annual Meeting
(544bp) Addressing Electronic Conductivity Limitations in Non-Precious Metal Alloy Electrocatalysts
Authors
Prior approaches for synthesis and processing of highly active NiâMo HER electrocatalysts relied on electrodeposition or thermal reduction of catalyst precursors directly on conducting substrates [1,2]. By contrast, deposition of unsupported NiâMo nanopowders on Ni or Ti substrates yields very low HER performance unless the deposition is followed by a thermal annealing step in a reducing environment [3]. We have now shown that this thermal annealing step can be eliminated by incorporating carbon black into the NiâMo nanopowder precursor mixture. Further studies of catalyst composition, morphology, and carbon loading give clear evidence that the advantageous role of carbon is to improve electrical conductivity, which is otherwise limited by the spontaneous formation of resistive surface oxides on NiâMo nanoparticles upon handling in air. Moreover, well-mixed NiâMo/C composites yield HER specific activity (normalized to NiâMo mass) that is several times greater than carbon-free catalysts prepared under otherwise identical conditions. These catalyst composites can be processed into coatings in the same way as commercial Pt/C, thereby providing a pathway to use nonprecious catalysts as drop-in replacements for noble metals in AAEM electrolyzers.
References:
[1] I. A. Raj and K. I. Vasu, âTransition metal-based hydrogen electrodes in alkaline solution - electrocatalysis on nickel based binary alloy coatings,â J. Appl. Electrochem., vol. 20, no. 1, pp. 32â38, Jan. 1990.
[2] D. E. Brown, M. N. Mahmood, M. C. M. Man, and A. K. Turner, âPreparation and characterization of low cvervoltage tranistion metal alloy electro-catalysts for hydrogen evolution in alkaline solutions, Electrochemica Acta, vol. 29, no. 11, pp. 1551-1586, 1984â
[3] J. R. McKone, B. F. Sadtler, C. A. Werlang, N. S. Lewis, and H. B. Gray, âNi-Mo nanopowders for efficient electrochemical hydrogen evolution,â ACS Catal., 2013.