4.8 Article

Spatially separating redox centers on 2D carbon nitride with cobalt single atom for photocatalytic H2O2 production

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1913403117

关键词

2D photocatalyst; spatially separated cocatalysts; single-atom catalyst; hydrogen peroxide

资金

  1. National Science Foundation (NSF) Nanosystems Engineering Research Center for Nanotechnology-Enabled Water Treatment [EEC-1449500]
  2. Early Postdoctoral Mobility Fellowship, Swiss National Science Foundation [P2EZP2_168796]
  3. China Scholarship Council
  4. DOE Office of Science [DESC0012704]
  5. NSF [ACI-1548562]
  6. Swiss National Science Foundation (SNF) [P2EZP2_168796] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Redox cocatalysts play crucial roles in photosynthetic reactions, yet simultaneous loading of oxidative and reductive cocatalysts often leads to enhanced charge recombination that is detrimental to photosynthesis. This study introduces an approach to simultaneously load two redox cocatalysts, atomically dispersed cobalt for improving oxidation activity and anthraquinone for improving reduction selectivity, onto graphitic carbon nitride (C3N4) nanosheets for photocatalytic H2O2 production. Spatial separation of oxidative and reductive cocatalysts was achieved on a two-dimensional (2D) photocatalyst, by coordinating cobalt single atom above the void center of C3N4 and anchoring anthraquinone at the edges of C3N4 nanosheets. Such spatial separation, experimentally confirmed and computationally simulated, was found to be critical for enhancing surface charge separation and achieving efficient H2O2 production. This center/edge strategy for spatial separation of cocatalysts may be applied on other 2D photo-catalysts that are increasingly studied in photosynthetic reactions.

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