Mixed-Linker Strategy for the Construction of Sulfone-Containing D-A-A Covalent Organic Frameworks for Efficient Photocatalytic Hydrogen Peroxide Production.

Angew Chem Int Ed Engl

Key Laboratory of Material Chemistry for Energy Conversion and Storage Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Luoyu Road No. 1037, 430074, Wuhan, China.

Published: May 2024

AI Article Synopsis

  • The text discusses the development of a new photocatalyst, FS-OHOMe-COF, for producing hydrogen peroxide from water and oxygen using solar energy, addressing common efficiency issues like poor charge separation and stability.
  • This new approach employs a mixed-linker strategy that enhances charge mobility and promotes surface reactions due to special sulfone units, resulting in better performance.
  • The FS-OHOMe-COF catalyst shows high efficiency, achieving a hydrogen peroxide output of 19 mM after 72 hours and maintaining activity over 192 hours of use.

Article Abstract

The solar-driven photocatalytic production of hydrogen peroxide (HO) from water and oxygen using semiconductor catalysts offers a promising approach for converting solar energy into storable chemical energy. However, the efficiency of photocatalytic HO production is often restricted by the low photo-generated charge separation, slow surface reactions and inadequate stability. Here, we developed a mixed-linker strategy to build a donor-acceptor-acceptor (D-A-A) type covalent organic framework (COF) photocatalyst, FS-OHOMe-COF. The FS-OHOMe-COF structure features extended π-π conjugation that improves charge mobility, while the introduction of sulfone units not only as active sites facilitates surface reactions with water but also bolsters stability through increased interlayer forces. The resulting FS-OHOMe-COF has a low exciton binding energy, long excited-state lifetime and high photo-stability that leads to high performance for photocatalytic HO production (up to 1.0 mM h) with an HO output of 19 mM after 72 hours of irradiation. Furthermore, the catalyst demonstrates high stability, which sustained activity over 192 hours of photocatalytic experiment.

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Source
http://dx.doi.org/10.1002/anie.202403926DOI Listing

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