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2D coordination polymer-derived CoSe2–NiSe2/CN nanosheets: the dual-phase synergistic effect and ultrathin structure to enhance the hydrogen evolution reaction.

Authors :
Jiang, Weifeng
Sun, Jianpeng
Lu, Kebin
Jiang, Chuanhai
Xu, Huakai
Huang, Zhaodi
Cao, Ning
Dai, Fangna
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry; 7/28/202, Vol. 50 Issue 28, p9934-9941, 8p
Publication Year :
2021

Abstract

The evolution of cost-effective hydrogen evolution reaction (HER) electrocatalysts is of great significance for the development of clean energy. Exploring effective synthesis strategies to optimize the performance of non-noble metal electrocatalysts has always attracted our attention. Herein, ultrathin coordination polymers were used as precursors to controllably synthesize two-dimensional (2D) ultrathin dual-phase transition metal selenide (TMSs)/carbon–nitrogen (CN) composites (CoSe<subscript>2</subscript>–NiSe<subscript>2</subscript>/CN) by a two-step method (first a low temperature hydrothermal method for selenization, and then high temperature calcination selenization). Benefiting from its large specific surface area (49 m<superscript>2</superscript> g<superscript>−1</superscript>), abundant catalytically active sites and synergistic effects, CoSe<subscript>2</subscript>–NiSe<subscript>2</subscript>/CN can significantly enhance the HER catalytic activity and exhibits good electrocatalytic activity with an overpotential of 150 mV at −10 mA cm<superscript>−2</superscript>, and a small Tafel slope of 42 mV dec<superscript>−1</superscript> in an acidic electrolyte for the HER. This work provides a new strategy for optimizing the HER catalytic activity of TMSs by preparing 2D ultrathin dual-phase TMS composite materials. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
50
Issue :
28
Database :
Complementary Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
151505217
Full Text :
https://doi.org/10.1039/d1dt01487k