4.8 Article

A Nanocrystal Catalyst Incorporating a Surface Bound Transition Metal to Induce Photocatalytic Sequential Electron Transfer Events

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 143, 期 30, 页码 11361-11369

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c00503

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资金

  1. NSF [1851747]
  2. Center for Hybrid Organic Inorganic Semiconductors for Energy (CHOISE) an Energy Frontier Research Center - Office of Science, Office of Basic Energy Sciences within the US Department of Energy
  3. Department of Energy's Office of Energy Efficiency and Renewable Energy
  4. Facility for Electron Microscopy of Materials at the University of Colorado at Boulder (CU FEMM)
  5. Division Of Chemistry
  6. Direct For Mathematical & Physical Scien [1851747] Funding Source: National Science Foundation

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Heterogeneous photocatalysis utilizing lead-halide perovskite nanocrystals to capture photons and direct photogenerated holes to a surface bound transition metal Cu-site enables N-N heterocyclization reaction. Sequential inner sphere electron transfer events drive photogenerated holes to Cu-surface site for reaction initiation.
Heterogeneous photocatalysis is less common but can provide unique avenues for inducing novel chemical transformations and can also be utilized for energy transductions, i.e., the energy in the photons can be captured in chemical bonds. Here, we developed a novel heterogeneous photocatalytic system that employs a lead-halide perovskite nanocrystal (NC) to capture photons and direct photogenerated holes to a surface bound transition metal Cu-site, resulting in a N-N heterocyclization reaction. The reaction starts from surface coordinated diamine substrates and requires two subsequent photo-oxidation events per reaction cycle. We establish a photocatalytic pathway that incorporates sequential inner sphere electron transfer events, photons absorbed by the NC generate holes that are sequentially funneled to the Cu-surface site to perform the reaction. The photocatalyst is readily prepared via a controlled cation-exchange reaction and provides new opportunities in photodriven heterogeneous catalysis.

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