电催化剂
金属间化合物
催化作用
双金属片
材料科学
配体(生物化学)
密度泛函理论
化学工程
拉伤
氧气
纳米线
氧还原反应
燃料电池
氧化还原
扩散
纳米技术
化学
化学物理
氧化物
过渡金属
纳米颗粒
铂金
氧还原
无机化学
结晶学
纳米结构
电化学
物理化学
作者
Ran Zhao,Fangxu Lin,Hongyu Guo,Yi Wei,Ying Han,Menggang Li,Xiaoqing Cao,Lu Li,Changshuai Shang,C F Sun,Ruijin Zeng,Heng Luo,Mingchuan Luo,Fan Lv,Xiaoquan Lu,Shaojun Guo
摘要
ABSTRACT The integration of ligand and strain effects in core/shell architectures offers a compelling avenue for boosting the catalytic efficiency of noble metals. However, conventional thin‐Pt‐shell catalysts incorporating small‐radius transition metals suffer from an over‐compressed Pt lattice, leading to limited oxygen reduction reaction (ORR) performance toward fuel cell devices. Herein, we report a class of PdSn/PtSn/Pt sandwich‐structured nanowires based on large‐radius Sn elements, taking advantage of its diffusion inclination to Pt, to construct the sub‐nanometer PtSn interlayer so as to address this trade‐off issue. We demonstrate that the intermetallic Pt‐Sn bonds with elevated covalency downshift the d‐band center of Pt through strengthened ligand effect, and the diffusion of large‐radius Sn atoms from PdSn core to Pt shell surprisingly offsets an optimally compressive strain for surface Pt. Thanks to such two‐tier tuning from PtSn interlayer, the resulting PdSn/(PtSn/Pt) 2‐3L NWs with the thinnest Pt shell exhibit exceptional catalytic behaviors by achieving a mass activity of 4.26 A mg Pt+Pd −1 (13.91 A mg Pt −1 ) at 0.9 V RHE , with < 30% decay after 20 000 cycles, overweighing most reported Pt/Pd‐based ORR catalysts. The corresponding H 2 ‐O 2 anion‐exchange‐membrane fuel cell device delivers a very high peak power density of 1.64 W cm −2 , with an impressive Pt utilization up to 11.71 W mg Pt −1 .
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