Construction of dendritic Pt–Pd bimetallic nanotubular heterostructure for advanced oxygen reduction

IF 24.5 Q1 CHEMISTRY, PHYSICAL Interdisciplinary Materials Pub Date : 2024-08-23 DOI:10.1002/idm2.12212
Mingwei Wang, Zhiyi Hu, Jieheng Lv, Zhiwen Yin, Zhewei Xu, Jingfeng Liu, Shihao Feng, Xiaoqian Wang, Jiazhen He, Sicheng Luo, Dafu Zhao, Hang Li, Xuemin Luo, Qi Liu, Damin Liu, Baolian Su, Dongyuan Zhao, Yong Liu
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Abstract

Compositions and morphologies of Pt-based electrocatalysts have great impact on the electrocatalytic activity and stability of oxygen reduction reaction (ORR). Herein, we report a novel design of one-dimensional (1D) Pt–Pd dendritic nanotubular heterostructures (DTHs) by controlling the degree of Pt2+-Pt reduction reaction and Pd-Pt galvanic replacement reaction with uniform Pd nanowires as sacrificial templates. The obtained Pt–Pd bimetallic DTHs catalyst exhibited uniform and dense Pt dendritic nanobranches on the surface of 1D hollow Pt–Pd alloy nanotubes, possessing superior catalytic activity for ORR compared to state-of-the-art commercial Pt/C catalysts. Typically, the Pt4Pd DTHs catalyst showed efficient mass activity (MA, 1.05 A mgPt−1) and specific activity (SA, 1.25 mA cmPt−2) at 0.9 V (vs. RHE), and the catalyst exhibited high stability with 90.4% MA retention after 20 000 potential cycles. The Pt–Pd bimetallic DTHs configuration combines the advantages of 1D hollow nanostructures and dense Pt dendritic nanobranches, which results in rich electrochemical active surface sites, fast charge transport, and multiple dendritic anchoring points contact on carbon support, thus boosting its catalytic activity and stability towards electrocatalysis.

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构建用于高级氧还原的树枝状铂钯双金属纳米管异质结构
铂基电催化剂的组成和形态对氧还原反应(ORR)的电催化活性和稳定性有很大影响。在此,我们以均匀的钯纳米线为牺牲模板,通过控制铂2+-铂还原反应和钯-铂电化学置换反应的程度,设计出了一种新型的一维(1D)铂钯树枝状纳米管异质结构(DTHs)。获得的铂钯双金属 DTHs 催化剂在一维空心铂钯合金纳米管表面呈现出均匀致密的铂树枝状纳米条纹,与最先进的商用 Pt/C 催化剂相比,具有更高的 ORR 催化活性。通常情况下,Pt4Pd DTHs 催化剂在 0.9 V(相对于 RHE)电压下表现出高效的质量活性(MA,1.05 A mgPt-1)和比活性(SA,1.25 mA cmPt-2),并且催化剂表现出很高的稳定性,在 20 000 个电位循环后,MA 保留率达到 90.4%。铂钯双金属 DTHs 构型结合了一维中空纳米结构和致密铂树枝状纳米分枝的优点,从而在碳载体上形成了丰富的电化学活性表面位点、快速的电荷传输和多个树枝状锚点接触,从而提高了其催化活性和电催化稳定性。
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