Issue 7, 2019

Surface reconstruction of cobalt phosphide nanosheets by electrochemical activation for enhanced hydrogen evolution in alkaline solution

Abstract

Transition metal phosphides exhibit promising catalytic performance for the hydrogen evolution reaction (HER); however their surface structure evolution during electrochemical operation has rarely been studied. In this work, we investigate the surface reconstruction of CoP nanosheets by an in situ electrochemical activation method. After remodeling, CoP nanosheets experience an irreversible and significant evolution of the morphology and composition, and low-valence Co complexes consisting of Co(OH)x species are formed on the surface of CoP nanosheets, and they largely accelerate the dissociation of water. Benefiting from the synergistic effect of CoP and Co(OH)x, the working electrode shows a remarkably enhanced HER activity of 100 mV at 10 mA cm−2 with a Tafel slope of 76 mV dec−1, which is better than that of most transition metal phosphide catalysts. This work would provide a deep understanding of surface reconstruction and a novel perspective for rational design of high performance transition metal phosphide electrocatalysts for water related electrolysis.

Graphical abstract: Surface reconstruction of cobalt phosphide nanosheets by electrochemical activation for enhanced hydrogen evolution in alkaline solution

Supplementary files

Article information

Article type
Edge Article
Submitted
15 اکتوٗبر 2018
Accepted
06 دسمبر 2018
First published
06 دسمبر 2018
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2019,10, 2019-2024

Surface reconstruction of cobalt phosphide nanosheets by electrochemical activation for enhanced hydrogen evolution in alkaline solution

L. Su, X. Cui, T. He, L. Zeng, H. Tian, Y. Song, K. Qi and B. Y. Xia, Chem. Sci., 2019, 10, 2019 DOI: 10.1039/C8SC04589E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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