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Iron molybdenum selenide supported on reduced graphene oxide as an efficient hydrogen electrocatalyst in acidic and alkaline media.

Authors :
Zhu, Min
Bai, Xiaojing
Yan, Qing
Yan, Yongde
Zhu, Kai
Ye, Ke
Yan, Jun
Cao, Dianxue
Huang, Xiaomei
Wang, Guiling
Source :
Journal of Colloid & Interface Science. Nov2021, Vol. 602, p384-393. 10p.
Publication Year :
2021

Abstract

[Display omitted] • FeSe 2 -MoSe 2 (1-1)/rGO has good HER activity in both acidic and alkaline media. • FeSe 2 -MoSe 2 (1-1)/rGO has well stability in both acidic and alkaline media. • On the morphology, FeSe 2 -MoSe 2 nanoparticles uniformly decorate the rGO matrix. • DFT results verify the FeSe 2 -MoSe 2 (1-1)/rGO owns small work function. It is of great significance to develop inexpensive and high-efficiency electrocatalysts for the hydrogen evolution reaction (HER). In this work, we synthesized iron molybdenum selenide (FeSe 2 -MoSe 2) loaded on reduced graphene oxide (FeSe 2 -MoSe 2 /rGO) by a one-step hydrothermal method. We further optimized the Fe/Mo ratio and determined the best ratio to be 1-1. In acidic (or alkaline) solution, the optimized FeSe 2 -MoSe 2 (1-1)/rGO has a small Tafel slope of 55 (or 80) mV dec−1 and needs an overpotential of 101 (or 178) mV to achieve 10 mA cm−2. These good properties are mainly due to the structure of bimetallic selenides combining rGO. Moreover, rGO enhances the electrical conductivity. Furthermore, the synergistic effect between FeSe 2 -MoSe 2 (1-1) and rGO results in better HER performance. Density functional theory (DFT) calculation proves that FeSe 2 -MoSe 2 (1-1)/rGO has a small work function. Based on our reasonable design and analysis, FeSe 2 -MoSe 2 (1-1)/rGO is expected to be an efficient and robust catalyst for large-scale applications. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
602
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
152201270
Full Text :
https://doi.org/10.1016/j.jcis.2021.06.038