Shearing Sulfur Edges of VS<sub>2</sub> Electrocatalyst Enhances its Nitrogen Reduction Performance
Liang Zhao, Yuanyuan Xiong, Xiaoxuan Wang, Rui Zhao, Xinyue Chi, Yixiang Zhou, Huaizhi Wang, Zhiyu Yang, Yi‐Ming Yan
Abstract
Abstract Electrochemical N 2 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 (VS 2 ) is deliberately designed by partially shearing its sulfur (S) edges through a simple calcination treatment at 350 °C. The as‐prepared VS 2 ‐350 electrocatalyst exhibits a highest NH 3 yield of 20.29 µg h −1 mg cat −1 with a promising FE of 3.86%, which is significantly higher than the counterpart of untreated VS 2 ( V NH3 : 15.92 µg h −1 mg cat −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 N 2 activation at V active sites follows an “acceptance‐donation” mechanism, while the N 2 conversion to NH 3 follows a hybrid 2 pathway at the VS 2 ‐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.