Hydrogen bonds in heterojunction photocatalysts for efficient charge transfer

書誌事項

公開日
2018-10
権利情報
  • https://www.elsevier.com/tdm/userlicense/1.0/
  • https://www.elsevier.com/legal/tdmrep-license
DOI
  • 10.1016/j.apcatb.2018.04.057
公開者
Elsevier BV

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説明

Abstract A hydrogen bond-based heterojunction photocatalyst, g-C3N4/melamine-cyanurate (gMC), was synthesized by a facile alkaline hydrothermal approach. The hydrogen bonds between the two substrates (N HO C) provide not only an ultrafast pathway (hundreds of femtoseconds) but also an inner electric field for hole transfer from g-C3N4 to melamine-cyanurate. Although only the g-C3N4 moiety acts as a photocatalyst, the optimized composite presents approximately 5.4, 3 and 2.5 times higher photocatalytic activity than bulk g-C3N4 in the decomposition of acetaldehyde and 2-propanol and the generation of H2 by water splitting, respectively. In this paper, we demonstrate that hydrogen bonds can not only lower the interfacial barrier and separate redox sides but also control the direction of charge transfer, which enables the design of the photocatalytic mechanism.

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