4.8 Article

Self-Assembled Au/CdSe Nanocrystal Clusters for Plasmon-Mediated Photocatalytic Hydrogen Evolution

Journal

ADVANCED MATERIALS
Volume 29, Issue 27, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201700803

Keywords

CdSe QDs; nanocrystal clusters; photocatalytic H-2 evolution; self-assembly; surface plasmon resonance

Funding

  1. Ministry of Science and Technology of China [2014CB239402, 2013CB834505, 2015CB932403]
  2. National Key Projects for Fundamental Research and Development of China [2016YFB0600900]
  3. National Natural Science Foundation of China [U1662118, 51572270, 51322213, 21401206, 21401207, 21301183]
  4. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17030300]
  5. Beijing Natural Science Foundation [2152033, 2154058]
  6. Youth Innovation Promotion Association
  7. National Program for Support of Top-notch Young Professionals

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Plasmon-mediated photocatalytic systems generally suffer from poor efficiency due to weak absorption overlap and thus limited energy transfer between the plasmonic metal and the semiconductor. Herein, a near-ideal plasmon-mediated photocatalyst system is developed. Au/CdSe nanocrystal clusters (NCs) are successfully fabricated through a facile emulsion-based self-assembly approach, containing Au nanoparticles (NPs) of size 2.8, 4.6, 7.2, or 9.0 nm and CdSe quantum dots (QDs) of size approximate to 3.3 nm. Under visible-light irradiation, the Au/CdSe NCs with 7.2 nm Au NPs afford very stable operation and a remarkable H-2-evolution rate of 73 mmol g(CdSe)(-1)h(-1) (10x higher than bare CdSe NCs). Plasmon resonance energy transfer from the Au NPs to the CdSe QDs, which enhances charge-carrier generation in the semiconductor and suppresses bulk recombination, is responsible for the outstanding photocatalytic performance. The approach used here to fabricate the Au/CdSe NCs is suitable for the construction of other plasmon-mediated photocatalysts.

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