Efficient oxygen reduction catalysis by subnanometer Pt alloy nanowires

双金属片 纳米线 催化作用 合金 纳米颗粒 纳米结构 化学工程 氧还原反应 纳米技术 材料科学 密度泛函理论 铂金 化学 电化学 冶金 计算化学 物理化学 有机化学 工程类 电极
作者
Kezhu Jiang,Dandan Zhao,Shaojun Guo,Xu Zhang,Xing Zhu,Jun Guo,Gang Lü,Xiaoqing Huang
出处
期刊:Science Advances [American Association for the Advancement of Science]
卷期号:3 (2): e1601705-e1601705 被引量:419
标识
DOI:10.1126/sciadv.1601705
摘要

The common knowledge is that Pt and Pt alloy nanoparticles (NPs) less than 2 nm are not desirable for oxygen reduction reaction (ORR). However, whether the same trend is expected in Pt-based nanowires (NWs) and nanoplates remains questionable because there is no scalable approach to make such Pt nanostructures. We report a general approach for preparing subnanometer Pt alloy NWs with a diameter of only 4 to 5 atomic layer thickness, ranging from monometallic Pt NWs to bimetallic PtNi and PtCo NWs and to trimetallic PtNiCo NWs. In a sharp contrast to Pt alloy NPs, the subnanometer Pt alloy NWs demonstrate exceptional mass and specific activities of 4.20 A/mg and 5.11 mA/cm2 at 0.9 V versus reversible hydrogen electrode (RHE), respectively, 32.3 and 26.9 times higher than those of the commercial Pt/C. Density functional theory simulations reveal that the enhanced ORR activities are attributed to the catalytically active sites on high-density (111) facets in the subnanometer Pt alloy NWs. They are also very stable under the ORR condition with negligible activity decay over the course of 30,000 cycles. Our work presents a new approach to maximize Pt catalytic efficiency with atomic level utilization for efficient heterogeneous catalysis and beyond.
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