Defect Engineering Metal-Free Polymeric Carbon Nitride Electrocatalyst for Effective Nitrogen Fixation under Ambient Conditions

被引:801
作者
Lv, Chade [1 ,2 ,3 ]
Qian, Yumin [1 ,2 ]
Yan, Chunshuang [1 ,2 ,3 ]
Ding, Yu [1 ,2 ]
Liu, Yuanyue [1 ,2 ]
Chen, Gang [3 ]
Yu, Guihua [1 ,2 ]
机构
[1] Univ Texas Austin, Mat Sci & Engn Program, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Mech Engn, Austin, TX 78712 USA
[3] Harbin Inst Technol, MIIT Key Lab Crit Mat Technol New Energy Convers, Sch Chem & Chem Engn, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
defect engineering; electrocatalysis; metal-free catalysts; N-2; activation; nitrogen reduction reactions; AMMONIA-SYNTHESIS; OXYGEN VACANCIES; N-2; REDUCTION; LIGHT; DINITROGEN; CLEAVAGE; WATER; FUNCTIONALIZATION; ELECTROSYNTHESIS;
D O I
10.1002/anie.201806386
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic nitrogen reduction reaction (NRR) under ambient conditions provides an intriguing picture for the conversion of N-2 into NH3. However, electrocatalytic NRR mainly relies on metal-based catalysts, and it remains a grand challenge in enabling effective N-2 activation on metal-free catalysts. Here we report a defect engineering strategy to realize effective NRR performance (NH3 yield: 8.09gh(-1)mg(cat.)(-1), Faradaic efficiency: 11.59%) on metal-free polymeric carbon nitride (PCN) catalyst. Illustrated by density functional theory calculations, dinitrogen molecule can be chemisorbed on as-engineered nitrogen vacancies of PCN through constructing a dinuclear end-on bound structure for spatial electron transfer. Furthermore, the N-N bond length of adsorbed N-2 increases dramatically, which corresponds to strong activation system to reduce N-2 into NH3. This work also highlights the significance of defect engineering for improving electrocatalysts with weak N-2 adsorption and activation ability.
引用
收藏
页码:10246 / 10250
页数:5
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