AI Article Synopsis

  • Manipulating local coordination in photocatalysts can enhance hydrogen evolution kinetics, achieved here by constructing ZnIn S /Mo TiC Schottky junctions through interfacial coordination with an electronegative terminal group.
  • Analysis techniques show that a unidirectional electronic transport channel is established at the Schottky interface, facilitating efficient charge transfer and reducing electron backflow.
  • As a result, the ZnIn S /Mo TiC photocatalyst demonstrates a significantly improved hydrogen evolution rate of 3.12 mmol g h under visible light, indicating its potential for advancing photocatalytic applications.

Article Abstract

Regulating electronic structures of the active site by manipulating the local coordination is one of the advantageous means to improve photocatalytic hydrogen evolution (PHE) kinetics. Herein, the ZnIn S /Mo TiC Schottky junctions are designed to be constructed through the interfacial local coordination of In with the electronegative O terminal group on Mo TiC based on the different work functions. Kelvin probe force microscopy and charge density difference reveal that an electronic unidirectional transport channel across the Schottky interface from ZnIn S to Mo TiC is established by the formed local nucleophilic/electrophilic region. The increased local electron density of Mo TiC inhibits the backflow of electrons, boosts the charge transfer and separation, and optimizes the hydrogen adsorption energy. Therefore, the ZnIn S /Mo TiC photocatalyst exhibits a superior PHE rate of 3.12 mmol g h under visible light, reaching 3.03 times that of the pristine ZnIn S . This work provides some insights and inspiration for preparing MXene-based Schottky catalysts to accelerate PHE kinetics.

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Source
http://dx.doi.org/10.1002/smll.202300717DOI Listing

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