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Research Article

Flexible cobalt phosphide network electrocatalyst for hydrogen evolution at all pH values

Jianwen Huang1,2Yanrong Li1Yufei Xia2Juntong Zhu2Qinghua Yi2Hao Wang2Jie Xiong1( )Yinghui Sun2 ( )Guifu Zou2( )
State Key Laboratory of Electronic Thin Film and Integrated DevicesUniversity of Electronic Science and Technology of ChinaChengdu610054China
College of Physics, Optoelectronics and EnergyInstitute of Chemical Power Sources & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow UniversitySuzhou215006China
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Abstract

High-performance electrocatalysts for water splitting at all pH values have attracted considerable interest in the field of sustainable hydrogen evolution. Herein, we report an efficient electrocatalyst with a nanocrystalline cobalt phosphide (CoP) network for water splitting in the pH range of 0-14. The novel flexible electrocatalyst is derived from a desirable nanocrystalline CoP network grown on a conductive Hastelloy belt. This kind of self-supported CoP network is directly used as an electrocatalytic cathode for hydrogen evolution. The nanocrystalline network structure results in superior performance with a low onset overpotential of ~45 mV over a broad pH range of 0 to 14 and affords a catalytic current density of 100 mA·cm-2 even in neutral media. The CoP network exhibits excellent catalytic properties not only at extreme pH values (0 and 14) but also in neutral media (pH = 7), which is comparable to the behavior of state-of-the-art platinum-based metals. The system exhibits an excellent flexible property and maintains remarkable catalytic stability during continuous 100-h-long electrolysis even after 100 cycles of bending/extending from 100° to 250°.

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Nano Research
Pages 1010-1020

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Cite this article:
Huang J, Li Y, Xia Y, et al. Flexible cobalt phosphide network electrocatalyst for hydrogen evolution at all pH values. Nano Research, 2017, 10(3): 1010-1020. https://doi.org/10.1007/s12274-016-1360-y

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Received: 26 August 2016
Revised: 19 October 2016
Accepted: 04 November 2016
Published: 18 January 2017
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2016