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用于氧还原反应的应变调制铂钯纳米线

Strain-Modulated Platinum-Palladium Nanowires for Oxygen Reduction Reaction.

作者信息

Chang Fangfang, Bai Zhengyu, Li Matthew, Ren Mengyun, Liu Tongchao, Yang Lin, Zhong Chuan-Jian, Lu Jun

机构信息

Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Henan Key Laboratory of Boron Chemistry and Advanced Energy Materials, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, China.

Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.

出版信息

Nano Lett. 2020 Apr 8;20(4):2416-2422. doi: 10.1021/acs.nanolett.9b05123. Epub 2020 Mar 5.

Abstract

Electrocatalytic activity of alloy nanocatalytsts can be manipulated effectively by tuning their physical properties (ensemble, geometric, and ligand effects) to afford optimal surface structure and compositions for proton exchange membrane fuel cell (PEMFC) application. Herein, highly catalytic platinum-palladium nanowires (PtPd NWs) with a subtle lattice strain and Boerdijk-Coxeter helix type morphology are synthesized through a surfactant-free, thermal single phase solvent method. X-ray diffraction results show that PtPd NWs are exposed through the (111) facets and their shrinking or expanding lattice parameters can be modulated by the alloy compositions. Electrochemical results reveal that their high catalytic activity correlates with the lattice shrinking, facets, and bimetallic compositions, showing higher activity when the ratio of Pt and Pd is ∼78:22, which is further supported by DFT results. Compared to the nanoparticle type platinum-palladium alloyed catalysts with similar metal compositions (PtPd NPs), the PtPd NWs exhibit significantly improved electrocatalytic activity and stability for the oxygen reduction reaction. These findings open new strategies to design the highly active and stable alloy nanocatalysts with controllable compositions.

摘要

通过调整合金纳米催化剂的物理性质(整体效应、几何效应和配体效应),可以有效地调控其电催化活性,从而为质子交换膜燃料电池(PEMFC)应用提供最佳的表面结构和组成。在此,通过无表面活性剂的热单相溶剂法合成了具有细微晶格应变和伯迪克-考克斯特螺旋型形态的高催化活性铂钯纳米线(PtPd NWs)。X射线衍射结果表明,PtPd NWs通过(111)晶面暴露,其晶格参数的收缩或扩张可通过合金组成进行调节。电化学结果表明,它们的高催化活性与晶格收缩、晶面和双金属组成相关,当Pt和Pd的比例约为78:22时活性更高,这得到了密度泛函理论(DFT)结果的进一步支持。与具有相似金属组成的纳米颗粒型铂钯合金催化剂(PtPd NPs)相比,PtPd NWs对氧还原反应表现出显著提高的电催化活性和稳定性。这些发现为设计具有可控组成的高活性和稳定合金纳米催化剂开辟了新策略。

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