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用于增强析氢的卫星钯单原子包覆金钯合金纳米团簇

Satellite Pd Single-Atom Embraced AuPd Alloy Nanoclusters for Enhanced Hydrogen Evolution.

作者信息

Lv Ya-Kun, Han Ye, Wang Kun, Sun Wen-Yan, Du Chen-Xia, Huang Ren-Wu, Peng Peng, Zang Shuang-Quan

机构信息

Henan Key Laboratory of Crystalline Molecular Functional Materials and College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.

出版信息

ACS Nano. 2024 Nov 19;18(46):32186-32195. doi: 10.1021/acsnano.4c11554. Epub 2024 Nov 4.

Abstract

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 (AuPd(SCHPh)) 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 HO, thus enhancing the hydrogen evolution reaction (HER) activity. The optimal AuPd/Pd-600 exhibits outstanding electrocatalytic activity toward HER, with overpotentials of 21 and 38 mV at 10 mA cm in acidic and alkaline media, respectively. Moreover, the mass activity and turnover frequency of AuPd/Pd-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.

摘要

构建同时包含纳米团簇和单原子(SAs)的混合活性位点对于电催化剂实现优异的活性和耐久性至关重要。在此,我们开发了一种配体辅助热解策略,使用具有合金核和保护配体的纳米团簇(AuPd(SCHPh))来构建被卫星状Pd单原子包围的AuPd团簇位点。在热驱动控制过程中,合金原子的不同热力学性质和有机配体的限域效应使得单组分金属Pd能够温和溢出,从而形成被孤立的Pd原子紧密包围的AuPd合金纳米团簇。实验和理论计算表明,卫星状Pd原子可以优化合金中AuPd纳米团簇和Au位点的电子结构,以促进H₂O的吸附和解离,从而提高析氢反应(HER)活性。最优的AuPd/Pd-600对HER表现出优异的电催化活性,在酸性和碱性介质中,在10 mA cm⁻²时过电位分别为21和38 mV。此外,AuPd/Pd-600的质量活性和转换频率比商业Pd/C和Pt/C催化剂高一个数量级。这种使用配体保护纳米团簇构建混合催化中心的简便策略为进一步设计由单原子协同作用的基于纳米团簇的电催化剂提供了有效的见解。

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