TY - JOUR
T1 - A Modified Galvanic Cell Synthesis of Pd@Pt Core-Shell Nanowire Catalysts
T2 - Structural Insights and Enhanced ORR Performance
AU - Cao, Weijie
AU - Kumar, Mukesh
AU - Thakur, Neha
AU - Uchiyama, Tomoki
AU - Gao, Yunfei
AU - Tominaka, Satoshi
AU - Machida, Akihiko
AU - Watanabe, Toshiki
AU - Sato, Ryota
AU - Teranishi, Toshiharu
AU - Matsumoto, Masashi
AU - Imai, Hideto
AU - Sakurai, Yoshiharu
AU - Uchimoto, Yoshiharu
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/10/14
Y1 - 2024/10/14
N2 - 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.
AB - 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.
KW - Pd@Pt nanowire
KW - core−shell
KW - galvanic method
KW - nanoparticle
KW - operando X-ray absorption spectroscopy
KW - oxygen reduction reaction
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U2 - 10.1021/acsaem.4c01444
DO - 10.1021/acsaem.4c01444
M3 - Article
AN - SCOPUS:85204219518
SN - 2574-0962
VL - 7
SP - 8515
EP - 8525
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 19
ER -