Boosting electrocatalytic ammonia production through mimicking “π back-donation”

• Main Authors: Lv, Chade, Zhong, Lixiang, Yao, Yao, Liu, Daobin, Kong, Yi, Jin, Xiaoli, Fang, Zhiwei, Xu, Wenjie, Yan, Chunshuang, Dinh, Khang Ngoc, Shao, Minhua, Song, Li, Chen, Gang, Li, Shuzhou, Yan, Qingyu, Yu, Guihua
• Other Authors: School of Materials Science and Engineering
• Format: Article
• Language: English
• Published: 2020
• Subjects: Engineering::Materials::Energy materials; Ammonia Synthesis; N2 Reduction Reaction (N2RR)
• Online Access: https://hdl.handle.net/10356/144519
• Institution: Nanyang Technological University

Electrocatalytic dinitrogen reduction reaction (N2RR) is an emerging route for ammonia synthesis at ambient conditions. Albeit the “π back-donation” process enables N2RR activity on transition metals with empty d-orbitals, given its dilemma in overcoming hydrogen evolution reaction (HER) competition, exploring p-block-element-based catalysts with relatively inferior HER activity is achievable for high selectivity. The challenge lies in designing rational structure to improve N2RR activity. Here, we synergistically integrate oxygen vacancy (VO) with hydroxyl on Bi4O5I2 (VO-Bi4O5I2-OH), which render this p-block-element-based material active to mimic “π back-donation” behavior because of sufficient vacant orbitals. In neutral media, the electrocatalytic N2RR performance of VO-Bi4O5I2-OH in terms of splendid faradic efficiency (32.4%) is superior to most of the prior reports using p-block-element-based catalysts. Our findings show a new strategy toward standout N2RR activity, which holds great potential in exploiting other p-block-element-based electrocatalysts.