催化作用
氧化还原
电催化剂
电化学
材料科学
氨生产
纳米
氨
氮气
电子转移
化学工程
碳纤维
纳米技术
无机化学
金属
光化学
化学
电极
物理化学
有机化学
工程类
复合材料
复合数
冶金
作者
Xiaowei Wang,Siyao Qiu,Jianmin Feng,Yueyu Tong,Fengling Zhou,Qinye Li,Li Song,Shuangming Chen,Kuang‐Hsu Wu,Panpan Su,Sheng Ye,Feng Hou,Shi Xue Dou,Huan Liu,Gao Qing Lu,Chenghua Sun,Jian Liu,Ji Liang
标识
DOI:10.1002/adma.202004382
摘要
Electrochemical nitrogen reduction reaction (NRR) over nonprecious-metal and single-atom catalysts has received increasing attention as a sustainable strategy to synthesize ammonia. However, the atomic-scale regulation of such active sites for NRR catalysis remains challenging because of the large distance between them, which significantly weakens their cooperation. Herein, the utilization of regular surface cavities with unique microenvironment on graphitic carbon nitride as "subnano reactors" to precisely confine multiple Fe and Cu atoms for NRR electrocatalysis is reported. The synergy of Fe and Cu atoms in such confined subnano space provides significantly enhanced NRR performance, with nearly doubles ammonia yield and 54%-increased Faradic efficiency up to 34%, comparing with the single-metal counterparts. First principle simulation reveals this synergistic effect originates from the unique Fe-Cu coordination, which effectively modifies the N2 absorption, improves electron transfer, and offers extra redox couples for NRR. This work thus provides new strategies of manipulating catalysts active centers at the sub-nanometer scale.
科研通智能强力驱动
Strongly Powered by AbleSci AI