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Building Asymmetric Zn-N Bridge between 2D Photocatalyst and Co-catalyst for Directed Charge Transfer toward Efficient HO Synthesis. | LitMetric

Building Asymmetric Zn-N Bridge between 2D Photocatalyst and Co-catalyst for Directed Charge Transfer toward Efficient HO Synthesis.

Angew Chem Int Ed Engl

Anhui Engineering Research Center of Carbon Neutrality, The Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials, Anhui Normal University, Wuhu, Anhui, 241002, P. R. China.

Published: October 2024

AI Article Synopsis

  • Two-dimensional polymeric semiconductors hold potential as photocatalysts, but efficient charge transfer between their layers is still a major challenge.
  • The introduction of asymmetric Zn-N3 units helps bridge the gap between nitrogen-doped carbon layers and polymeric carbon nitride nanosheets, promoting directed charge transfer.
  • This novel approach significantly improves charge separation and boosts the performance of the C3N4-Zn-N(C) catalyst, enhancing its hydrogen peroxide production compared to other C3N4-based catalysts.

Article Abstract

Two-dimensional (2D) polymeric semiconductors are a class of promising photocatalysts; however, it remains challenging to facilitate their interlayer charge transfer for suppressed in-plane charge recombination and thus improved quantum efficiency. Although some strategies, such as π-π stacking and van der Waals interaction, have been developed so far, directed interlayer charge transfer still cannot be achieved. Herein, we report a strategy of forming asymmetric Zn-N units that can bridge nitrogen (N)-doped carbon layers with polymeric carbon nitride nanosheets (CN-Zn-N(C)) to address this challenge. The symmetry-breaking Zn-N moiety, which has an asymmetric local charge distribution, enables directed interfacial charge transfer between the CN photocatalyst and the N-doped carbon co-catalyst. As evidenced by femtosecond transient absorption spectroscopy, charge separation can be significantly enhanced by the interfacial asymmetric Zn-N bonding bridges. As a result, the designed CN-Zn-N(C) catalyst exhibits dramatically enhanced HO photosynthesis activity, outperforming most of the reported CN-based catalysts. This work highlights the importance of tailoring interfacial chemical bonding channels in polymeric photocatalysts at the molecular level to achieve effective spatial charge separation.

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Source
http://dx.doi.org/10.1002/anie.202415800DOI Listing

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