Abstract
Methods to synthesize crystalline covalent triazine frameworks (CTFs) are limited and little attention has been paid to development of hydrophilic CTFs and photocatalytic overall water splitting. A route to synthesize crystalline and hydrophilic CTF-HUST-A1 with a benzylamine-functionalized monomer is presented. The base reagent used plays an important role in the enhancement of crystallinity and hydrophilicity. CTF-HUST-A1 exhibits good crystallinity, excellent hydrophilicity, and excellent photocatalytic activity in sacrificial photocatalytic hydrogen evolution (hydrogen evolution rate up to 9200 μmol g-1 h-1 ). Photocatalytic overall water splitting is achieved by depositing dual co-catalysts in CTF-HUST-A1, with H2 evolution and O2 evolution rates of 25.4 μmol g-1 h-1 and 12.9 μmol g-1 h-1 in pure water without using sacrificial agent.
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