Proton-Controlled Electron Injection in MoS<sub>2</sub> During Hydrogen Evolution Revealed by Time-Resolved Spectroelectrochemistry

Monolayer MoS<sub>2</sub> is an effective electrocatalyst for the hydrogen evolution reaction (HER). Despite significant efforts to optimize the active sites, its catalytic performance still falls short of theoretical predictions. One key factor that has often been overlooked is the electron injection from the conductive substrate into the MoS<sub>2</sub>. The charge transfer behavior at the substrate-MoS<sub>2</sub> interface is nonclassical, exhibiting a liquid-gated electron injection behavior, the underlying mechanism of which remain under debate. To investigate this, we employ nanosecond time-resolved spectroelectrochemistry to probe the electron injection dynamics into monolayer MoS<sub>2</sub> under operando HER conditions. Simultaneously, transient current measurements provide insights into the electron density at the substrate. By combining the electron density obtained from the MoS<sub>2</sub> through spectroelectrochemical analysis with the electron density at the conductive substrate derived from transient current measurements, we explore the electron injection dynamics and characterize the current density potential (J-E) behavior at the substrate-MoS<sub>2</sub> interface. Our findings show that the electron injection barrier and capability correlate strongly with proton concentration in the electrolyte. This relationship likely reflects the electron concentration-dependent conductivity of MoS<sub>2</sub>, where higher proton concentrations lead to fewer stray electrons before injection begins.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-01-22
DOI
https://doi.org/10.1021/jacs.4c16536
Citations
8
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
2.91

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article

Proton-Controlled Electron Injection in MoS2 During Hydrogen Evolution Revealed by Time-Resolved Spectroelectrochemistry

Xianchang Yan, Shengye Jin, Wenming Tian, Tao Yang et al.
8 citations
Journal of the American Chemical Society
Electrocatalysts for Energy Conversion
2.91
article

Proton-Controlled Electron Injection in MoS2 During Hydrogen Evolution Revealed by Time-Resolved Spectroelectrochemistry

Xianchang Yan, Shengye Jin, Wenming Tian, Tao Yang, Boning Wu, Chunmei Ding
article en
8 citations

Abstract

Monolayer MoS<sub>2</sub> is an effective electrocatalyst for the hydrogen evolution reaction (HER). Despite significant efforts to optimize the active sites, its catalytic performance still falls short of theoretical predictions. One key factor that has often been overlooked is the electron injection from the conductive substrate into the MoS<sub>2</sub>. The charge transfer behavior at the substrate-MoS<sub>2</sub> interface is nonclassical, exhibiting a liquid-gated electron injection behavior, the underlying mechanism of which remain under debate. To investigate this, we employ nanosecond time-resolved spectroelectrochemistry to probe the electron injection dynamics into monolayer MoS<sub>2</sub> under operando HER conditions. Simultaneously, transient current measurements provide insights into the electron density at the substrate. By combining the electron density obtained from the MoS<sub>2</sub> through spectroelectrochemical analysis with the electron density at the conductive substrate derived from transient current measurements, we explore the electron injection dynamics and characterize the current density potential (J-E) behavior at the substrate-MoS<sub>2</sub> interface. Our findings show that the electron injection barrier and capability correlate strongly with proton concentration in the electrolyte. This relationship likely reflects the electron concentration-dependent conductivity of MoS<sub>2</sub>, where higher proton concentrations lead to fewer stray electrons before injection begins.

Journal of the American Chemical SocietyVol. 147(5)
University of Science and Technology of China (CN), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Liaoning Revitalization Talents Program, National Key Research and Development Program of China
Openalex Percentile: Top 10%
Electrocatalysts for Energy Conversion
2.91
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