分解水
化学
电催化剂
材料科学
化学工程
电化学
电极
催化作用
物理化学
生物化学
光催化
工程类
作者
Tzu Yin Chen,Yung Huang Chang,Chang Lung Hsu,Kung-Hwa Wei,Chia-Ying Chiang,Lain-Jong Li
标识
DOI:10.1016/j.ijhydene.2013.07.021
摘要
Abstract Replacing Pt by earth abundant catalysts is one of the most important tasks toward potential large-scale HER applications. Among many potential candidates, low cost and earth abundant transition metal dichalcogenides such as MoS2 and WS2 have been promising as good H2 evolution electrocatalysts when they are engineered into the structures with active sites. In this work, we have performed systematic studies on the catalytic reactivity of both MoS2 and WS2 materials produced by one-step and scalable thermolysis from (NH4)2WS4 and (NH4)2MoS4 precursors respectively. Structural analysis shows that these materials prepared at a higher thermolysis temperature exhibit higher crystallinity. The H2 evolution electrocatalysts efficiency for the MoS2 prepared at a lower temperature is higher than those at higher temperatures, where amorphous MoS2 or S 2 2 − species instead of crystalline MoS2 is the main active site. By contrast, crystalline WS2 prepared at high temperature is identified to be the key reaction site. Both catalysts display excellent efficiency and durability as an electrocatalyst operating in acidic electrolytes. This work provides fundamental insights for further design and preparation of emergent metal dichalcogenide catalysts, beneficial for the development in clean energy.
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