Optimizing Electrocatalytic Nitrogen Reduction via Interfacial Electric Field Modulation: Elevating d‐Band Center in WS2‐WO3 for Enhanced Intermediate Adsorption

质子化 催化作用 吸附 化学 反应中间体 电场 光化学 电化学 选择性催化还原 氮气 费米能级 无机化学 材料科学 电极 物理化学 有机化学 电子 离子 物理 量子力学
作者
Xiaoxuan Wang,Shuyuan Li,Zhi Hao Yuan,Yanfei Sun,Zheng Tang,Xueying Gao,Huiying Zhang,Jingxian Li,Shiyu Wang,Deguo Yang,Jiangzhou Xie,Zhiyu Yang,Yi‐Ming Yan
出处
期刊:Angewandte Chemie [Wiley]
卷期号:62 (29) 被引量:27
标识
DOI:10.1002/anie.202303794
摘要

Electrocatalytic nitrogen reduction reaction (ENRR) has emerged as a promising approach to synthesizing green ammonia under ambient conditions. Tungsten (W) is one of the most effective ENRR catalysts. In this reaction, the protonation of intermediates is the rate-determining step (RDS). Enhancing the adsorption of intermediates is crucial to increase the protonation of intermediates, which can lead to improved catalytic performance. Herein, we constructed a strong interfacial electric field in WS2 -WO3 to elevate the d-band center of W, thereby strengthening the adsorption of intermediates. Experimental results demonstrated that this approach led to a significantly improved ENRR performance. Specifically, WS2 -WO3 exhibited a high NH3 yield of 62.38 μg h-1 mgcat-1 and a promoted faraday efficiency (FE) of 24.24 %. Furthermore, in situ characterizations and theoretical calculations showed that the strong interfacial electric field in WS2 -WO3 upshifted the d-band center of W towards the Fermi level, leading to enhanced adsorption of -NH2 and -NH intermediates on the catalyst surface. This resulted in a significantly promoted reaction rate of the RDS. Overall, our study offers new insights into the relationship between interfacial electric field and d-band center and provides a promising strategy to enhance the intermediates adsorption during the ENRR process.
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