塔菲尔方程
材料科学
石墨烯
过电位
化学工程
氧化物
催化作用
纳米技术
分解水
电催化剂
电极
化学
电化学
物理化学
冶金
工程类
生物化学
光催化
作者
Xiaojiao Fang,Zegao Wang,Shifei Kang,Liwei Zhao,Zaixing Jiang,Mingdong Dong
标识
DOI:10.1016/j.ijhydene.2019.11.059
摘要
Abstract CoSe2 is considered as a promising candidate among non-noble metal electrocatalysts for the hydrogen evolution reaction (HER) due to its intrinsic metallicity and low Gibbs free energy for hydrogen adsorption. Recently, the hexagonal CoSe2 becoming increasingly popular owing to its chemically favorable basal plane, which provides more active sites, but remains limited by the poor stability. In this study, we design a small-molecule-amine-assisted hydrothermal method to in situ anchor the hexagonal CoSe2 nanosheets (NSs) on nitrogen-doped reduced graphene oxides (RGO) as an advanced electrode material for HER. Due to the existence of abundant functional groups and high specific surface area of RGO, the hexagonal CoSe2 NSs could be stably formed on RGO. As a result, only a small overpotential of 172 mV is needed for the optimized sample to drive a current density of 10 mA cm−2 in 0.5 M H2SO4 and the Tafel slope is 35.2 mV dec−1, which is comparable with the state-of-the-art Pt catalyst (32.3 mV dec−1). Therefore, the facile and low-cost method for synthesizing hexagonal TMDs with robust electrical and chemical coupling developed in this work is promising in promoting the large-scale application of non-precious electrocatalysts.
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