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用于增强可见光驱动的 CO 还原的金属有机框架的光化学原位剥离

Photochemical In Situ Exfoliation of Metal-Organic Frameworks for Enhanced Visible-Light-Driven CO Reduction.

作者信息

Zheng Hui-Li, Huang Shan-Lin, Luo Ming-Bu, Wei Qin, Chen Er-Xia, He Liang, Lin Qipu

机构信息

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350002, China.

出版信息

Angew Chem Int Ed Engl. 2020 Dec 21;59(52):23588-23592. doi: 10.1002/anie.202012019. Epub 2020 Oct 19.

Abstract

Two novel two-dimensional metal-organic frameworks (2D MOFs), 2D-M TCPE (M=Co or Ni, TCPE=1,1,2,2-tetra(4-carboxylphenyl)ethylene), which are composed of staggered (4,4)-grid layers based on paddlewheel-shaped dimers, serve as heterogeneous photocatalysts for efficient reduction of CO to CO. During the visible-light-driven catalysis, these structures undergo in situ exfoliation to form nanosheets, which exhibit excellent stability and improved catalytic activity. The exfoliated 2D-M TCPE nanosheets display a high CO evolution rate of 4174 μmol g  h and high selectivity of 97.3 % for M=Co and Ni, and thus are superior to most reported MOFs. The performance differences and photocatalytic mechanisms have been studied with theoretical calculations and photoelectric experiments. This study provides new insight for the controllable synthesis of effective crystalline photocatalysts based on structural and morphological coregulation.

摘要

两种新型二维金属有机框架(2D MOF),即2D-M TCPE(M = Co或Ni,TCPE = 1,1,2,2-四(4-羧基苯基)乙烯),由基于桨轮状二聚体的交错(4,4)网格层组成,用作将CO高效还原为CO的多相光催化剂。在可见光驱动的催化过程中,这些结构会发生原位剥离形成纳米片,这些纳米片表现出优异的稳定性和提高的催化活性。对于M = Co和Ni,剥离后的2D-M TCPE纳米片显示出4174 μmol g h的高CO析出速率和97.3%的高选择性,因此优于大多数已报道的MOF。通过理论计算和光电实验研究了性能差异和光催化机理。该研究为基于结构和形态共调控的有效晶体光催化剂的可控合成提供了新的见解。

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