催化作用
材料科学
单体
光催化
聚合
多孔性
产量(工程)
金属有机骨架
Atom(片上系统)
化学工程
氢
纳米技术
聚合物
光化学
物理化学
有机化学
复合材料
化学
工程类
吸附
计算机科学
嵌入式系统
作者
Yuting Yang,Jing Wang,Jiang Li,Jiahui Li,Jialu Li,Jiangtao Jia,Cafer T. Yavuz,Fengchao Cui,Xiaofei Jing,Guangshan Zhu
标识
DOI:10.1002/adma.202404791
摘要
Abstract Supported single‐atom catalysts (SACs) are promising in heterogeneous catalysis because of their atom economy, unusual transformations, and mechanistic clarity. The metal SAs loading, however, limits the catalytic efficiency. Herein, an in situ pre‐metallated monomer‐based preparation strategy is shown to achieve ultrahigh Au SAs loading in catalyst formations. The polymerization of single‐atom loaded monomers yield a new porous aromatic framework (PAF‐164) with Au SAs loading up to a record high 45.3 wt.%. SACs of Au‐PAFs exhibit excellent photocatalytic activity in hydrogen (H 2 ) evolution, and the H 2 evolution rate of Au 100% ‐SAs‐PAF‐164 can reach 4.82 mmol g −1 h −1 with great recyclability.
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