| Literature DB >> 28833545 |
Lei Wang1, Yangyang Wan1, Yanjun Ding1, Sikai Wu1, Ying Zhang1, Xinlei Zhang1, Guoqing Zhang2, Yujie Xiong1,2, Xiaojun Wu1,2, Jinlong Yang1,2, Hangxun Xu1.
Abstract
Direct water splitting into H2 and O2 using photocatalysts by harnessing sunlight is very appealing to produce storable chemical fuels. Conjugated polymers, which have tunable molecular structures and optoelectronic properties, are promising alternatives to inorganic semiconductors for water splitting. Unfortunately, conjugated polymers that are able to efficiently split pure water under visible light (400 nm) via a four-electron pathway have not been previously reported. This study demonstrates that 1,3-diyne-linked conjugated microporous polymer nanosheets (CMPNs) prepared by oxidative coupling of terminal alkynes such as 1,3,5-tris-(4-ethynylphenyl)-benzene (TEPB) and 1,3,5-triethynylbenzene (TEB) can act as highly efficient photocatalysts for splitting pure water (pH ≈ 7) into stoichiometric amounts of H2 and O2 under visible light. The apparent quantum efficiencies at 420 nm are 10.3% and 7.6% for CMPNs synthesized from TEPB and TEB, respectively; the measured solar-to-hydrogen conversion efficiency using the full solar spectrum can reach 0.6%, surpassing photosynthetic plants in converting solar energy to biomass (globally average ≈0.10%). First-principles calculations reveal that photocatalytic H2 and O2 evolution reactions are energetically feasible for CMPNs under visible light irradiation. The findings suggest that organic polymers hold great potential for stable and scalable solar-fuel generation.Entities:
Keywords: conjugated microporous polymers; first-principles calculations; nanostructures; photocatalysis; water splitting
Year: 2017 PMID: 28833545 DOI: 10.1002/adma.201702428
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849