催化作用
氧还原反应
氧还原
合金
纳米颗粒
材料科学
纳米技术
外延
单晶
氧气
化学工程
比表面积
化学
结晶学
冶金
物理化学
电化学
电极
有机化学
图层(电子)
工程类
作者
Shuyan Gong,Mingze Sun,Yiyang Lee,Nigel Becknell,Jiangwei Zhang,Zhongqi Wang,Liang Zhang,Zhiqiang Niu
标识
DOI:10.1002/anie.202214516
摘要
Single crystal surfaces with highly coordinated sites very often hold high specific activities toward oxygen reduction reaction (ORR) and others. Transposing their high specific activity to practical high-surface-area electrocatalysts remains challenging. Here, ultrathin Pt(100) alloy surface is constructed via epitaxial growth. The surface shows 3.1-6.9 % compressive strain and bulk-like characteristics as demonstrated by site-probe reactions and different spectroscopies. Its ORR activity exceeds that of bulk Pt3 Ni(100) and Pt(111) and presents a 19-fold increase in specific activity and a 13-fold increase in mass activity relative to commercial Pt/C. Moreover, the electrochemically active surface area (ECSA) is increased by 4-fold compared to traditional thin films (e.g. NSTF), which makes the catalyst more tolerant to voltage loss at high current densities under fuel cell operation. This work broadens the family of extended surface catalysts and highlights the knowledge-driven approach in the development of advanced electrocatalysts.
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