过电位
材料科学
电催化剂
单层
化学物理
氢
肖特基势垒
范德瓦尔斯力
动力学
纳米技术
异质结
兴奋剂
费米能级
催化作用
光电子学
肖特基二极管
结合能
载流子
工作(物理)
氢燃料
活化能
化学工程
化学动力学
接触电阻
带隙
电子能带结构
紧密结合
分子物理学
工作职能
作者
Shen'ao Xue,Lan Luo,Hao Huang,Tao Xu,Sicheng Tao,Yuzhou Cao,Qinghao Meng,Yali Lan,Junjie Jiang,Yijia Wang,Quanlong Yang,Fangping Ouyang,Junwei Fu
摘要
ABSTRACT On‐chip electrocatalytic microdevices (OCEMs) are versatile platforms for probing the intrinsic kinetics of individual nanomaterials. However, their applications in evaluating 2D van der Waals materials often suffer from substantial interfacial contact resistance at the electrode/catalyst junction and sluggish catalytic reaction kinetics at the catalyst/electrolyte interface. Herein, we develop an yttrium‐doping strategy for monolayer MoS 2 (Y‐MoS 2 ) that simultaneously optimizes charge injection across the solid–solid (electrode/catalyst) interface and hydrogen binding on the basal plane of MoS 2 . The Y doping downshifts the conduction band minimum of MoS 2 , lowering the Schottky barrier from 0.47 to 0.23 eV and enhancing electron injection across the electrode/catalyst interface. The matching spatial orbital symmetry of Y and Mo 4 d xz/yz induces strong d‐d electronic coupling, driving the formation of a favorable bridge hydrogen intermediate () with an optimized binding energy of 0.36 eV for hydrogen evolution reaction (HER) at the catalyst/electrolyte interface. Benefiting from this synergistic optimization of band alignment and hydrogen binding, Y‐MoS 2 exhibits superior HER performance, delivering an overpotential of 187 mV at 10 mA cm −2 , competitive with recent 2D MoS 2 ‐based electrocatalysts. This work establishes an optimized OCEM platform for decoupled mechanistic analysis and an orbital‐level tuning strategy for efficient electrocatalyst design.
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