材料科学
过氧化氢
氮化碳
氧气
分解水
氮化物
碳纤维
人工光合作用
析氧
接口(物质)
氢
化学工程
光合作用
光化学
纳米技术
催化作用
电化学
光催化
有机化学
复合材料
电极
物理化学
化学
接触角
图层(电子)
生物化学
坐滴法
复合数
工程类
作者
Zhenchun Yang,Kunlong Liu,Hangyu Zhuzhang,Wandong Xing,Masakazu Anpo,Guigang Zhang
标识
DOI:10.1002/adfm.202510267
摘要
Abstract Photosynthesis of H 2 O 2 from O 2 and H 2 O with inexhaustible sunlight as an energy source is a promising approach. However, the photocatalytic performance of pristine polymeric carbon nitride (PCN) is extremely restrained due to the rapid recombination of photo‐generated electrons and holes, and slow surface reaction processes. Herein, a new strategy is developed to rationally integrate N, S‐co‐doped carbon (C NS ), and CoS 2 on cyano‐rich PCN (PCN‐Cy) for photosynthesis of H 2 O 2 under ambient conditions. The engineering with cyano groups (electron‐withdrawing groups) promotes the bulk charge separation of PCN. Experimental results reveal that the CoS 2 co‐catalyst not only serves as an electron acceptor to extract charges from the bulk but also functions as an active site to promote the 2‐e − ORR process. Besides, the N, S‐co‐doped carbon performs as an electron channel to promote migration of charges at the interface of PCN‐Cy and CoS 2 . Accordingly, the as‐synthesized cyano‐rich PCN photocatalyst integrated with N, S‐co‐doped carbon and CoS 2 exhibits a remarkable activity of 321.9 µ m h −1 for photocatalytic production of H 2 O 2 , which is 44.9 times higher than that of the pristine PCN.
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