{"title":"A Modified Galvanic Cell Synthesis of Pd@Pt Core–Shell Nanowire Catalysts: Structural Insights and Enhanced ORR Performance","authors":"Weijie Cao, Mukesh Kumar, Neha Thakur, Tomoki Uchiyama, Yunfei Gao, Satoshi Tominaka, Akihiko Machida, Toshiki Watanabe, Ryota Sato, Toshiharu Teranishi, Masashi Matsumoto, Hideto Imai, Yoshiharu Sakurai, Yoshiharu Uchimoto","doi":"10.1021/acsaem.4c01444","DOIUrl":null,"url":null,"abstract":"One-dimensional nanostructures, specifically Pd@Pt core–shell nanowire catalysts, have garnered significant attention because of their potential to enhance the sluggish kinetics of the oxygen reduction reaction (ORR). However, fully realizing their potential depends on achieving consistent and uniform synthesis. In this study, we introduce an improved galvanic synthesis method for Pd@Pt core–shell nanowire catalysts (Pd-NW@Pt/C) that eliminates the need for electrochemical control or reducing agents, making it more accessible and efficient than the traditional Cu underpotential deposition (Cu-UPD) method. Our approach ensures a uniform Pt shell, resulting in superior ORR activity, with a mass activity of 1.06 A mg<sub>Pt</sub><sup>–1</sup> and a specific activity of 0.80 mA cm<sub>Pt</sub><sup>–2</sup>. Detailed <i>operando</i> X-ray absorption spectroscopy (XAS) measurements, including high-energy resolution fluorescence detection (HERFD-XAS), revealed that Pd-NW@Pt/C catalysts with a fully covered Pt shell exhibit shorter Pt–Pt bond lengths and weaker oxygen binding energies compared to partially covered Pt shell nanowire catalysts (Pd-NW@Pt/C-ref) and nanoparticle catalysts (Pd-NP@Pt/C), leading to significantly enhanced ORR activity. This study demonstrates the effectiveness of a modified galvanic cell method for producing high-performance Pd@Pt core–shell nanowire catalysts, offering insights into their structural and electronic properties.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":null,"pages":null},"PeriodicalIF":8.3000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsaem.4c01444","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
One-dimensional nanostructures, specifically Pd@Pt core–shell nanowire catalysts, have garnered significant attention because of their potential to enhance the sluggish kinetics of the oxygen reduction reaction (ORR). However, fully realizing their potential depends on achieving consistent and uniform synthesis. In this study, we introduce an improved galvanic synthesis method for Pd@Pt core–shell nanowire catalysts (Pd-NW@Pt/C) that eliminates the need for electrochemical control or reducing agents, making it more accessible and efficient than the traditional Cu underpotential deposition (Cu-UPD) method. Our approach ensures a uniform Pt shell, resulting in superior ORR activity, with a mass activity of 1.06 A mgPt–1 and a specific activity of 0.80 mA cmPt–2. Detailed operando X-ray absorption spectroscopy (XAS) measurements, including high-energy resolution fluorescence detection (HERFD-XAS), revealed that Pd-NW@Pt/C catalysts with a fully covered Pt shell exhibit shorter Pt–Pt bond lengths and weaker oxygen binding energies compared to partially covered Pt shell nanowire catalysts (Pd-NW@Pt/C-ref) and nanoparticle catalysts (Pd-NP@Pt/C), leading to significantly enhanced ORR activity. This study demonstrates the effectiveness of a modified galvanic cell method for producing high-performance Pd@Pt core–shell nanowire catalysts, offering insights into their structural and electronic properties.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.