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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Sequential Phase Conversion-Induced Phosphides Heteronanorod Arrays for Superior Hydrogen Evolution Performance to Pt
Hongyuan Yang1, Peifang Guo1, Ruirui Wang1
1Department of Materials Science, Fudan University, Shanghai, 200433, P. R. China.
Abstract:
Developing an efficient and non-precious pH-universal hydrogen evolution reaction electrocatalyst is highly desirable for hydrogen production by electrochemical water splitting but remains a significant challenge. Herein, a hierarchical structure composed of heterostructured Ni2 P-Ni12 P5 nanorod arrays rooted on Ni3 S2 film (Ni2 P-Ni12 P5 @Ni3 S2 ) via a simultaneous corrosion and sulfidation is built followed by a phosphidation treatment toward the metallic nickel foam. The combination of theoretical calculations with in/ex situ characterizations unveils that such a unique sequential phase conversion strategy ensures the strong interfacial coupling between Ni2 P and Ni12 P5 as well as the robust stabilization of 1D heteronanorod arrays by Ni3 S2 film, resulting in the promoted water adsorption/dissociation energy, the optimized hydrogen adsorption energy, and the enhanced electron/proton transfer ability accompanied with an excellent stability. Consequently, Ni2 P-Ni12 P5 @Ni3 S2 /NF requires only 32, 46, and 34 mV overpotentials to drive 10 mA cm-2 in 1.0 m KOH, 0.5 m H2 SO4 , and 1.0 m phosphate-buffered saline electrolytes, respectively, exceeding almost all the previously reported non-noble metal-based electrocatalysts. This work may pave a new avenue for the rational design of non-precious electrocatalysts toward pH-universal hydrogen evolution catalysis.

