材料科学
过电位
催化作用
单层
贵金属
密度泛函理论
吉布斯自由能
电化学
Atom(片上系统)
微观结构
化学物理
电子转移
微型反应器
金属
纳米技术
化学工程
物理化学
计算化学
热力学
冶金
计算机科学
电极
物理
化学
生物化学
工程类
嵌入式系统
作者
Wenxiu Yan,Zhitao Zhao,Zeqin Xin,Jingyi Hu,Jing Xia,Liang Zhou,Yingying Xu,Yanfeng Zhang,Kai Liu,Rongming Wang,Yinghui Sun
标识
DOI:10.1002/adfm.202423262
摘要
Abstract Maintaining high catalytic performance while maximizing metal atom utilization requires atomic‐level modulation of catalyst microstructure in noble‐metal catalyst design. On‐chip microreactors enable precise measurements of catalytic activity in specific regions, advancing the understanding of structure‐property relationships. Here, Pt single atoms (SAs), clusters, and sub‐2.5 nm nanoparticles (NPs) are synthesized on monolayer MoS 2 via defect‐anchoring. On‐chip electrochemical measurements during hydrogen evolution reaction (HER) demonstrated that Pt clusters‐MoS 2 exhibited superior activity, achieving a 94 mV overpotential at 10 mA cm −2 , much lower than that of Pt SAs‐MoS 2 (202 mV) and Pt NPs‐MoS 2 (259 mV). Density functional theory calculations revealed that the electron transfer from MoS 2 to Pt clusters altered H* adsorption site, yielding a near‐zero Gibbs free energy for enhanced HER activity. The work reveals the structure‐property relationships in Pt‐modified MoS 2 catalysts, guiding atom‐efficient noble metal catalyst development for HER and emphasizing precise mapping between preparation, microstructure, and performance.
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