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通过钌原子调控铂钴-铂纳米线的电子结构以促进析氢催化

Modulating Electronic Structure of PtCo-Pt Nanowires with Ru atoms for Boosted Hydrogen Evolution Catalysis.

作者信息

Cao Xianjun, Gao Li, Qu Junpeng, Li Lu, Xie Yuhan, Zhao Yufei, Wang Guoxiu, Liu Hao

机构信息

Joint International Laboratory on Environmental and Energy Frontier Materials, School of Environmental and Chemical Engineering, Shanghai University, Shanghai, 200444, P. R. China.

Centre for Clean Energy Technology, Faculty of Science, University of Technology Sydney, Broadway, Sydney, NSW, 2007, Australia.

出版信息

Small. 2023 Oct;19(41):e2302639. doi: 10.1002/smll.202302639. Epub 2023 Jun 12.

Abstract

Rational design and development of highly efficient hydrogen evolution reaction (HER) electrocatalysts is of great significance for the development of green water electrolysis hydrogen production technology. Ru-engineered 1D PtCo-Pt nanowires (Ru-Pt Co NWs) are fabricated by a facile electrodeposition method. The rich Pt surface on 1D Pt Co contributes to the fully exposed active sites and enhanced intrinsic catalytic activity (co-engineered by Ru and Co atoms) for HER. The incorporation of Ru atoms can not only accelerate the water dissociation in alkaline condition to provide sufficient H but also modulate the electronic structure of Pt to achieve optimized H adsorption energy. As a result, Ru-Pt Co NWs have exhibited ultralow HER overpotentials (η) of 8 and 112 mV to achieve current densities of 10 and 100 mA cm in 1 m KOH, respectively, which far exceed those of commercial Pt/C catalyst (η  = 29 mV, η  = 206 mV). Density functional theory (DFT) calculations further demonstrate that the incorporated Ru atoms possess strong water adsorption capacity (-0.52 vs -0.12 eV for Pt), facilitating water dissociation. The Pt atoms in the outermost Pt-rich skin of Ru-Pt Co NWs achieve optimized H adsorption free energy (ΔG ) of -0.08 eV, boosting hydrogen generation.

摘要

高效析氢反应(HER)电催化剂的合理设计与开发对于绿色水电解制氢技术的发展具有重要意义。通过简便的电沉积方法制备了钌工程化的一维铂钴-铂纳米线(Ru-Pt Co NWs)。一维铂钴上丰富的铂表面有助于活性位点的充分暴露以及增强的析氢本征催化活性(由钌和钴原子共同作用)。钌原子的引入不仅可以加速碱性条件下的水分解以提供足够的氢,还可以调节铂的电子结构以实现优化的氢吸附能。结果,Ru-Pt Co NWs在1 m KOH中分别表现出超低的析氢过电位(η),即8 mV和112 mV时分别实现电流密度为10和100 mA cm,这远远超过了商业铂碳催化剂(η = 29 mV,η = 206 mV)。密度泛函理论(DFT)计算进一步表明,引入的钌原子具有很强的水吸附能力(对于铂为-0.52 eV对-0.12 eV),有利于水的分解。Ru-Pt Co NWs最外层富铂表面的铂原子实现了-0.08 eV的优化氢吸附自由能(ΔG),促进了氢气的生成。

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