电化学
电催化剂
电场
拉曼光谱
催化作用
氨
法拉第效率
材料科学
傅里叶变换红外光谱
氨生产
分子
化学
化学工程
纳米技术
电极
物理化学
有机化学
物理
量子力学
光学
工程类
作者
Xiaoxuan Wang,Xinyue Chi,Zhenzhen Fu,Yuanyuan Xiong,Shuyuan Li,Yebo Yao,Qian Zhang,Yongjia Li,Shiyu Wang,Rui Zhao,Zhiyu Yang,Yi‐Ming Yan
标识
DOI:10.1016/j.apcatb.2022.122130
摘要
Electrochemical nitrogen reduction reaction (ENRR) is a sustainable approach to producing carbon-free ammonia under ambient conditions, while its performance has been severely limited by the poor activity of electrocatalysts. Here, we report the deliberate modulation of interfacial electric field at the CoO-Co3O4 interface as an effective strategy for boosting ENRR performance. The prepared CoO-Co3O4 showed a promising NH3 yield of 59.96 µg h−1 mgcat−1 and high Faradaic efficiency (FE) of 22.37 % in 0.1 M Li2SO4. In situ Raman spectroscopy, in situ Fourier transform infrared (FTIR) spectra and theoretical calculations demonstrated that the engineered strong interfacial electric field in CoO-Co3O4 electrocatalyst act synergistically to capture inert N2 by forming strong Co-N bonds. Subsequently, the interfacial electric field enhanced σ-d orbital hybridization between N2 molecule and Co site of CoO-Co3O4, achieving highly efficient N2 molecule activation. This work provides a deep understanding of electric field effect on the performance of ENRR catalysts.
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