钼
合金
材料科学
催化作用
电化学
单层
电催化剂
化学工程
金属
吸附
分解水
氢
无机化学
纳米技术
物理化学
化学
电极
冶金
有机化学
工程类
光催化
作者
Qiufang Gong,Liang Cheng,Changhai Liu,Mei Zhang,Qingliang Feng,Hualin Ye,Min Zeng,Liming Xie,Zhuang Liu,Yanguang Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2015-03-02
卷期号:5 (4): 2213-2219
被引量:530
摘要
The development of non precious metal based electrocatalysts for the hydrogen evolution reaction (HER) holds a decisive key to a spectrum of energy conversion technologies. Previous studies have established layered molybdenum chalcogenides as promising candidates. In this work, we prepared ultrathin MoS2(1–x)Se2x alloy nanoflakes with monolayer or few-layer thickness and fully tunable chemical composition for maximum HER activity. Spectroscopic characterizations corroborate the progressive evolution of their structures and properties as x increases from 0 to 1 without any noticeable phase separation. In particular, it is evidenced that the introduction of selenium continuously modulates the d band electronic structure of molybdenum, probably leading to tuned hydrogen adsorption free energy and consequently electrocatalytic activity. Electrochemical measurements show that all MoS2(1–x)Se2x nanoflakes are highly active and durable for HER with small overpotentials in the range of 80–100 mV and negligible activity loss up to 10000 cycles. Most importantly, alloyed nanoflakes, especially with the chemical composition of MoSSe, exhibit improved performance in comparison to either MoS2 or MoSe2. Given their overall similar nanoflake morphologies, we believe such improvements reflect the higher intrinsic activity of alloyed catalysts with the hydrogen adsorption free energy closer to thermoneutral.
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