光催化
催化作用
材料科学
降级(电信)
基质(水族馆)
化学工程
氮化碳
Atom(片上系统)
纳米技术
光化学
化学
有机化学
海洋学
地质学
工程类
嵌入式系统
电信
计算机科学
作者
Xiaoming Liu,Fengting He,Yang‐Ming Lu,Shuling Wang,Chaocheng Zhao,Shuaijun Wang,Xiaoguang Duan,Huayang Zhang,Xiaoli Zhao,Hongqi Sun,Jinqiang Zhang,Shaobin Wang
标识
DOI:10.1016/j.cej.2022.139833
摘要
Single atom catalysts (SACs) are suggested to be ideal materials for catalysis and will exhibit the highest performance at the maximum single atom loading. However, their influences on the intrinsic structure and properties of a photocatalytic substrate should not be neglected. Herein, we proposed a facile and green approach for large scale synthesis of Ni-SA/g-C3N4 catalysts with various contents of Ni-N4 coordination. Experimental investigations and quantum chemical calculations disclosed that the Ni-N4 and g-C3N4 host are two active sites for photocatalysis and play different roles in photocatalysis. The promoting and suppressing effects of Ni-N4 coordination on g-C3N4 matrix at Ni-N4 adjacency are also revealed. Maximum efficiency in photocatalytic water splitting and contaminant oxidation processes can only be realized at an optimized SA loading by the balance of the two effects. Extra loading of SA will make adjacent carbon nitride matrix lose semiconducting properties for generating hot carriers toward photocatalysis. This work reveals the intrinsic correlation between SAC structure and photocatalysis, shedding light on the fundamental understandings of structure-catalysis correlation and providing new insight into SACs.
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