Light-Driven Hydrogen Evolution Assisted by Covalent Organic Frameworks

• Published in: Catalysts Vol. 11; no. 6; p. 754
• Main Authors: Nuria Romero, Roger Bofill, Laia Francàs, Jordi García-Antón, Xavier Sala
• Format: Journal Article
• Language: English
• Published: MDPI AG 01-06-2021
• Subjects: co-catalyst; covalent organic framework; covalent triazine framework; hydrogen evolution; metal nanoparticle; photocatalysis
• ISSN: 2073-4344
• DOI: 10.3390/catal11060754

Covalent organic frameworks (COFs) are crystalline porous organic polymers built from covalent organic blocks that can be photochemically active when incorporating organic semiconducting units, such as triazine rings or diacetylene bridges. The bandgap, charge separation capacity, porosity, wettability, and chemical stability of COFs can be tuned by properly choosing their constitutive building blocks, by extension of conjugation, by adjustment of the size and crystallinity of the pores, and by synthetic post-functionalization. This review focuses on the recent uses of COFs as photoactive platforms for the hydrogen evolution reaction (HER), in which usually metal nanoparticles (NPs) or metallic compounds (generally Pt-based) act as co-catalysts. The most promising COF-based photocatalytic HER systems will be discussed, and special emphasis will be placed on rationalizing their structure and light-harvesting properties in relation to their catalytic activity and stability under turnover conditions. Finally, the aspects that need to be improved in the coming years will be discussed, such as the degree of dispersibility in water, the global photocatalytic efficiency, and the robustness and stability of the hybrid systems, putting emphasis on both the COF and the metal co-catalyst.