Chen Liangjun, Chen Guinan, Gong Chengtao, Zhang Yifei, Xing Zhihao, Li Jiahao, Xu Guodong, Li Gao, Peng Yongwu
College of Materials Science and Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang, China.
Institute of Catalysis for Energy and Environment, College of Chemistry and Chemical Engineering, Shenyang Normal University, Shenyang, Liaoning, China.
Nat Commun. 2024 Dec 3;15(1):10501. doi: 10.1038/s41467-024-54959-8.
This study focuses on optimizing catalytic activity in photocatalytic hydrogen evolution reaction by precisely designing and modulating the electronic structure of metal single atoms. The catalyst, denoted as PtSA@S-TFPT, integrates low-valence platinum single atoms into sulfur-containing covalent organic frameworks. The robust asymmetric four-coordination between sulfur and platinum within the framework enables a high platinum loading of 12.1 wt%, resulting in efficient photocatalytic hydrogen production activity of 11.4 mmol g h and stable performance under visible light. These outcomes are attributed to a reduced hydrogen desorption barrier and enhanced photogenerated charge separation, as indicated by density functional theory calculations and dynamic carrier analysis. This work challenges traditional notions and opens an avenue for developing low-valence metal single atom-loaded covalent organic framework catalysts to advance photocatalytic hydrogen evolution.
本研究聚焦于通过精确设计和调控金属单原子的电子结构来优化光催化析氢反应中的催化活性。该催化剂被标记为PtSA@S-TFPT,它将低价态铂单原子整合到含硫共价有机框架中。框架内硫与铂之间强大的不对称四配位使得铂负载量高达12.1 wt%,从而在可见光下产生了11.4 mmol g h的高效光催化产氢活性以及稳定的性能。密度泛函理论计算和动态载流子分析表明,这些结果归因于氢脱附势垒的降低和光生电荷分离的增强。这项工作挑战了传统观念,并为开发低价态金属单原子负载的共价有机框架催化剂以推动光催化析氢开辟了一条途径。