纳米团簇
合金
材料科学
卫星
纳米技术
氢
Atom(片上系统)
冶金
化学物理
化学
物理
工程类
天文
有机化学
嵌入式系统
作者
Ya‐Kun Lv,Ye Han,Kun Wang,Wenyan Sun,Chenxia Du,Ren‐Wu Huang,Peng Peng,Shuang‐Quan Zang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-11-04
标识
DOI:10.1021/acsnano.4c11554
摘要
The fabrication of hybrid active sites that synergistically contain nanoclusters and single atoms (SAs) is vital for electrocatalysts to achieve excellent activity and durability. Herein, we develop a ligand-assisted pyrolysis strategy using nanoclusters (Au4Pd2(SC2H4Ph)8) with alloy cores and protected ligands to build AuPd cluster sites embraced by satellite Pd SAs. In the thermal drive control process, different thermodynamic properties of the alloy atoms and the confinement effects of organic ligands allow for the mild spillover of the single-component metal Pd, resulting in the formation of AuPd alloy nanoclusters tightly encompassed by isolated Pd atoms. Experiments and theoretical calculations indicated that the satellite Pd atoms can optimize the electronic structure of the AuPd nanoclusters and Au sites in the alloy to facilitate the adsorption and dissociation of H2O, thus enhancing the hydrogen evolution reaction (HER) activity. The optimal AuPdNCs/PdSAs-600 exhibits outstanding electrocatalytic activity toward HER, with overpotentials of 21 and 38 mV at 10 mA cm–2 in acidic and alkaline media, respectively. Moreover, the mass activity and turnover frequency of AuPdNCs/PdSAs-600 are one order of magnitude higher than those of commercial Pd/C and Pt/C catalysts. This facile strategy for constructing hybrid catalytic centers using ligand-protected nanoclusters provides efficient insights for the further design of nanocluster-based electrocatalysts synergized by SAs.
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