Spatially separating redox centers on 2D carbon nitride with cobalt single atom for photocatalytic H<sub>2</sub>O<sub>2</sub> production.
basic_science · Level V
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- Record sourced from PubMed, PMID 32161133.
- Also identified by DOI 10.1073/pnas.1913403117 and PMC identifier 7104179.
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Abstract
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 (C<sub>3</sub>N<sub>4</sub>) nanosheets for photocatalytic H<sub>2</sub>O<sub>2</sub> 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 C<sub>3</sub>N<sub>4</sub> and anchoring anthraquinone at the edges of C<sub>3</sub>N<sub>4</sub> nanosheets. Such spatial separation, experimentally confirmed and computationally simulated, was found to be critical for enhancing surface charge separation and achieving efficient H<sub>2</sub>O<sub>2</sub> production. This center/edge strategy for spatial separation of cocatalysts may be applied on other 2D photocatalysts that are increasingly studied in photosynthetic reactions.