材料科学
离解(化学)
共价键
氨生产
氨
接受者
光化学
法拉第效率
放热反应
纳米技术
阳极
有机化学
化学
物理化学
凝聚态物理
物理
电极
作者
Yanzheng He,Mengfan Wang,Lifang Zhang,Qiyang Cheng,Sisi Liu,Xing Sun,Yuzhuo Jiang,Tao Qian,Chenglin Yan
标识
DOI:10.1002/adfm.202315548
摘要
Abstract Photoelectrochemical (PEC) technology offers new opportunities for pushing the renewable energy‐driven ammonia synthesis toward a practical level, while still facing unsatisfactory efficiency due to the obstacle of dissociating inert nitrogen triple‐bonds. Herein, a novel donor‐site‐acceptor system is constructed in covalent organic frameworks to tackle this challenge for highly efficient PEC ammonia synthesis. Highly active boron site is elaborately embedded between the donor and acceptor units, which can be effectively activated with continuous electron flow upon photoexcitation. With the assistance of solar irradiation, the stubborn nitrogen dissociation is successfully changed from a passive endothermic reaction to a spontaneous exothermic process, completely eliminating the energy barrier of the rate‐determining step and facilitating the overall reaction kinetics. The proof‐of‐concept system achieved an excellent PEC NRR performance with a remarkable Faradaic efficiency of 91.6%, reaching the target set by the U.S. Department of Energy (90%).
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