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共价有机框架的氟化增强钯纳米团簇的限域作用可提高过氧化氢光合作用。

Fluorination of Covalent Organic Framework Reinforcing the Confinement of Pd Nanoclusters Enhances Hydrogen Peroxide Photosynthesis.

作者信息

Liu Youxing, Li Lu, Tan Hao, Ye Na, Gu Yu, Zhao Shuoqing, Zhang Shipeng, Luo Mingchuan, Guo Shaojun

机构信息

School of Materials Science and Engineering, Peking University, Beijing 100871, China.

Beijing Innovation Centre for Engineering Science and Advanced Technology, Peking University, Beijing 100871, China.

出版信息

J Am Chem Soc. 2023 Sep 13;145(36):19877-19884. doi: 10.1021/jacs.3c05914. Epub 2023 Aug 16.

Abstract

Metal-isolated clusters (MICs) physically confined on photoactive materials are of great interest in the field of photosynthesis of hydrogen peroxide (HO). Despite recent important endeavors, weak confinement of MICs in the reported photocatalytic systems leads to their low catalytic activity and stability. Herein, we report a new strategy of fluorinated covalent organic frameworks (COFs) to strongly confine Pd ICs for greatly boosting the photocatalytic activity and stability of HO photosynthesis. Both experimental and theoretical results reveal that strong electronegative fluorine can increase the metal-support interaction and optimize the d-band center of Pd ICs, thus significantly enhancing the stability and activity of photocatalytic HO. An optimal TAPT-TFPA COFs@Pd ICs photocatalyst delivers a stable HO yield rate of 2143 μmol h g. Most importantly, the as-made TAPT-TFPA COFs@Pd ICs exhibit high catalytic stability over 100 h, which is the best among the reported materials.

摘要

物理限制在光活性材料上的金属隔离簇(MICs)在过氧化氢(HO)光合作用领域具有极大的研究价值。尽管近期已做出重要努力,但在已报道的光催化体系中,MICs的弱限制导致其催化活性和稳定性较低。在此,我们报道一种新策略,即通过氟化共价有机框架(COFs)来强力限制钯隔离簇(Pd ICs),以大幅提高HO光合作用的光催化活性和稳定性。实验和理论结果均表明,强电负性的氟可增强金属 - 载体相互作用并优化Pd ICs的d带中心,从而显著提高光催化HO的稳定性和活性。一种优化的TAPT - TFPA COFs@Pd ICs光催化剂的HO产率稳定在2143 μmol h g。最重要的是,所制备的TAPT - TFPA COFs@Pd ICs在100小时以上表现出高催化稳定性,这在已报道的材料中是最佳的。

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