Details

Autor(en) / Beteiligte

• Shu, Chang
• Yang, Xiaoju
• Liu, Lunjie
• Hu, Xunliang
• Sun, Ruixue
• Yang, Xuan
• Cooper, Andrew I.
• Tan, Bien
• Wang, Xiaoyan

Titel

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

Ist Teil von

• Angewandte Chemie International Edition, 2024-05, Vol.63 (22), p.e202403926-n/a

Auflage

International ed. in English

Ort / Verlag

Germany: Wiley Subscription Services, Inc

Erscheinungsjahr

2024

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• The solar‐driven photocatalytic production of hydrogen peroxide (H2O2) from water and oxygen using semiconductor catalysts offers a promising approach for converting solar energy into storable chemical energy. However, the efficiency of photocatalytic H2O2 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 H2O2 production (up to 1.0 mM h−1) with an H2O2 output of 19 mM after 72 hours of irradiation. Furthermore, the catalyst demonstrates high stability, which sustained activity over 192 hours of photocatalytic experiment. Sulfone‐containing D–A–A covalent organic framework photocatalyst was synthesized via a mixed‐linker strategy to facilitate charge transport and surface reactions with water. High photocatalytic H2O2 production activity was achieved to create solutions that can be used directly for the degradation of organic pollutants.