4.8 Article

Conjugated Microporous Polymer Nanosheets for Overall Water Splitting Using Visible Light

期刊

ADVANCED MATERIALS
卷 29, 期 38, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201702428

关键词

conjugated microporous polymers; first-principles calculations; nanostructures; photocatalysis; water splitting

资金

  1. National Key Basic Research Program of China [2015CB351903, 2012CB922001]
  2. National Natural Science Foundation of China [51402282, 21474095, 21421063, 51172223, 21573204]
  3. MOST [2016YFA0200602, 2017YFA0207301]
  4. CAS [XDB01020300]
  5. National Program for Support of Top-notch Young Professional
  6. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

Direct water splitting into H-2 and O-2 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 approximate to 7) into stoichiometric amounts of H-2 and O-2 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 approximate to 0.10%). First-principles calculations reveal that photocatalytic H-2 and O-2 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.

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