4.8 Article

Visible-Light-Driven Hydrogen Evolution Using Planarized Conjugated Polymer Photocatalysts

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 5, 页码 1824-1828

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201510542

关键词

conjugated polymer; extended conjugation; photocatalysis; planarization; water splitting

资金

  1. EPSRC [EP/C511794/1, EP/N004884/1, EP/I004424/1, EP/L021978/1, EP/L000202/1]
  2. DTA
  3. EPSRC National Service for Computational Chemistry Software
  4. European Research Council under the European Unions/ERC [321156]
  5. EPSRC [EP/N004884/1, EP/L021978/1, EP/K039687/1, EP/I004424/1, EP/J003921/1, EP/L000202/1] Funding Source: UKRI
  6. Engineering and Physical Sciences Research Council [EP/K039687/1, EP/C511794/1, EP/L021978/1, EP/J003921/1, 1510930, EP/I004424/1, EP/L000202/1, EP/N004884/1] Funding Source: researchfish
  7. European Research Council (ERC) [321156] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Linear poly(p-phenylene)s are modestly active UV photocatalysts for hydrogen production in the presence of a sacrificial electron donor. Introduction of planarized fluorene, carbazole, dibenzo[b,d]thiophene or dibenzo[b, d]thiophene sulfone units greatly enhances the H-2 evolution rate. The most active dibenzo[b, d] thiophene sulfone copolymer has a UV photocatalytic activity that rivals TiO2, but is much more active under visible light. The dibenzo[b, d]thiophene sulfone co-polymer has an apparent quantum yield of 2.3% at 420 nm, as compared to 0.1% for platinized commercial pristine carbon nitride.

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