异构化
均分解
光催化
原子层沉积
催化作用
纳米技术
材料科学
分解水
氢化物
共价键
密度泛函理论
化学
光化学
金属
图层(电子)
计算化学
激进的
生物化学
有机化学
冶金
作者
Yuanjie Cao,Si Chen,Qiquan Luo,Huan Yan,Yue Lin,Wei Liu,Linlin Cao,Junling Lu,Jinlong Yang,Tao Yao,Shiqiang Wei
标识
DOI:10.1002/ange.201706467
摘要
Abstract Knowledge of the photocatalytic H 2 evolution mechanism is of great importance for designing active catalysts toward a sustainable energy supply. An atomic‐level insight, design, and fabrication of single‐site Co 1 ‐N 4 composite as a prototypical photocatalyst for efficient H 2 production is reported. Correlated atomic characterizations verify that atomically dispersed Co atoms are successfully grafted by covalently forming a Co 1 ‐N 4 structure on g‐C 3 N 4 nanosheets by atomic layer deposition. Different from the conventional homolytic or heterolytic pathway, theoretical investigations reveal that the coordinated donor nitrogen increases the electron density and lowers the formation barrier of key Co hydride intermediate, thereby accelerating H–H coupling to facilitate H 2 generation. As a result, the composite photocatalyst exhibits a robust H 2 production activity up to 10.8 μmol h −1 , 11 times higher than that of pristine counterpart.
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