电催化剂
煅烧
二硫化钼
法拉第效率
硫黄
电化学
材料科学
催化作用
钒
氮气
过渡金属
氧化还原
化学工程
可逆氢电极
纳米技术
化学
无机化学
电极
冶金
物理化学
有机化学
参比电极
工程类
作者
Liang Zhao,Yi Xiong,Xiaoxuan Wang,Rui Zhao,Xinyue Chi,Yunshan Zhou,Huaizhi Wang,Zhiyu Yang,Yi‐Ming Yan
出处
期刊:Small
[Wiley]
日期:2022-01-09
卷期号:18 (11)
被引量:17
标识
DOI:10.1002/smll.202106939
摘要
Electrochemical N2 fixation requires effective electrocatalysts to expedite the nitrogen reduction reaction (NRR) kinetics and suppress the concomitant hydrogen evolution reaction (HER). Although transition metal sulfides have been deemed as efficient NRR electrocatalysts, it remains a great challenge to suppress the serious HER to achieve high Faradaic efficiency (FE). Herein, vanadium disulfide (VS2 ) is deliberately designed by partially shearing its sulfur (S) edges through a simple calcination treatment at 350 °C. The as-prepared VS2 -350 electrocatalyst exhibits a highest NH3 yield of 20.29 µg h-1 mgcat-1 with a promising FE of 3.86%, which is significantly higher than the counterpart of untreated VS2 (VNH3 : 15.92 µg h-1 mgcat-1 , FE: 1.69%). Experimental and computational results reveal that shearing the S edges can substantially inhibit the HER and expose more V atoms as active sites. Meanwhile, the mechanistic analysis shows that the N2 activation at V active sites follows an "acceptance-donation" mechanism, while the N2 conversion to NH3 follows a hybrid 2 pathway at the VS2 -350 electrocatalyst. This work provides a simple strategy of designing high-performance NRR electrocatalysts based on a deep understanding of the atomic sites dependent catalytical activity.
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