Covalent organic frameworks (COFs) have unique features, including intrinsic porosity, crystallinity, and tunability, making them desirable materials for diverse applications ranging from environmental remediation to energy harvesting. Among these applications, COFs are extensively studied for their photocatalytic hydrogen evolution by converting solar energy into clean and renewable fuel via water splitting. COFs have several advantages over conventional inorganic catalysts, such as tunable band structures, high surface areas, and low cost. However, the research in this field is still in the early stages, and COFs still face some challenges, such as low charge carrier mobility, high exciton binding energy, and poor stability. To overcome these challenges, various design strategies relying on a mechanistic approach have been developed to design and modify COFs for enhanced photocatalytic performance. These include extending the p-conjugation, incorporating heteroatoms or metal complexes, and donor-acceptor (D-A) configuration, which ultimately improves the light absorption charge separation of COFs. Additionally, blending COFs with other functional materials, such as inorganic-organic semiconductors, can create synergistic effects to boost photocatalytic activity. In this review, the design aspects of the fabrication of COFs as effective photocatalysts have been reported.
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Mechanistic Approach towards Designing Covalent Organic Frameworks for Photocatalytic Hydrogen GenerationView
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Title
Mechanistic Approach towards Designing Covalent Organic Frameworks for Photocatalytic Hydrogen Generation
Publication Details
Energies (Basel), Vol.16(16), p.5888
Resource Type
Journal article
Publisher
MDPI
Format
link
Number of pages
39
Grant note
2022YFB3805801 / National key research and development program
SDHY2224 / Opening Fund of China National Textile and Apparel Council Key Laboratory of Flexible Devices for Intelligent Textile and Apparel, Soochow University