| Literature DB >> 31782554 |
Liang Chen1, Lei Wang1, Yangyang Wan2, Ying Zhang1, Zeming Qi3, Xiaojun Wu2, Hangxun Xu1.
Abstract
Metal-free polymer photocatalysts have shown great promise for photocatalytic H2 O2 production via two-electron reduction of molecular O2 . The other half-reaction, which is the two-electron oxidation of water, still remains elusive toward H2 O2 production. However, enabling this water oxidation pathway is critically important to improve the yield and maximize atom utilization efficiency. It is shown that introducing acetylene (CC) or diacetylene (CCCC) moieties into covalent triazine frameworks (CTFs) can remarkably promote photocatalytic H2 O2 production. This enhancement is inherent to the incorporated carbon-carbon triple bonds which are essential in modulating the electronic structures of CTFs and suppressing charge recombinations. Furthermore, the acetylene and diacetylene moieties can significantly reduce the energy associated with OH* formation and thus enable a new two-electron oxidation pathway toward H2 O2 production. The study unveils an important reaction pathway toward photocatalytic H2 O2 production, reflecting that precise control over the chemical structures of polymer photocatalysts is vital to achieve efficient solar-to-chemical energy conversion.Entities:
Keywords: 2D polymers; covalent triazine frameworks; hydrogen peroxide; photocatalysis; two-electron process
Year: 2019 PMID: 31782554 DOI: 10.1002/adma.201904433
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849