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- W3183241518 abstract "The first‐principles calculation within the density functional theory (DFT) is used to study the hydrogen evolution reaction (HER) activity and related electronic properties of monolayer black phosphorus under the uniaxial strains. Herein, it is found that different compressive and tensile strains would modulate the Gibbs free energy (Δ G H* ), partial charge density of the lowest unoccupied state ( ε LUS ), and band structure of black phosphorene. Specifically, as the Δ G H* decreases, the HER activity of phosphorene system with uniaxial strain is improved except for the +3% strain case. Importantly, the HER catalytic performance of phosphorene can be reduced by 0.4 eV and the bandgap decreased to 0.23 eV by applying the −10% strain. Comparing with strained‐free case, the larger partial charge density of ε LUS on the surface of black phosphorene shows more H adsorption sites for electrocatalysis. Moreover, the HER activity is related to the partial charge density of ε LUS rather than the value of ε LUS site. These results reveal that strain could effectively modulate the HER performance for electrocatalysis. And it is expected to provide further understanding in practical applications." @default.
- W3183241518 created "2021-08-02" @default.
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- W3183241518 date "2021-08-08" @default.
- W3183241518 modified "2023-10-17" @default.
- W3183241518 title "Strain Modulation of Black Phosphorene for the Hydrogen Evolution Reaction Activity" @default.
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- W3183241518 doi "https://doi.org/10.1002/pssb.202100195" @default.
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