Atomic controlled shell thickness on Pt@Pt 3 Ti core-shell nanoparticles for efficient and durable oxygen reduction

被引:1
|
作者
Jiang, Haoran [1 ]
Wang, Zichen [1 ]
Chen, Suhao [1 ]
Xiao, Yong [1 ]
Zhu, Yu [1 ]
Wu, Wei [1 ]
Chen, Runzhe [1 ]
Cheng, Niancai [1 ]
机构
[1] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350108, Peoples R China
基金
中国国家自然科学基金;
关键词
Pt-based catalysts; Core-shell structure; Atomic controllable; Compressive strain; Oxygen reduction reaction; PT3TI; ELECTROCATALYST; SELECTIVITY; CATALYSTS; SUPPORT; ALLOY;
D O I
10.1016/j.jmst.2024.03.061
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The exploitation of durable and highly active Pt-based electrocatalysts for the oxygen reduction reaction (ORR) is essential for the commercialization of proton exchange membrane fuel cells (PEMFCs). Herein, we designed Pt@Pt 3 Ti core-shell nanoparticles with atomic-controllable shells through precise thermal diffusing Ti into Pt nanoparticles for effective and durable ORR. Combining theoretical and experiment analysis, we found that the lattice strain of Pt 3 Ti shells can be tailored by precisely controlling the thickness of Pt 3 Ti shell in atomic-scale on account of the lattice constant difference between Pt and Pt 3 Ti to optimize adsorption properties of Pt 3 Ti for ORR intermediates, thus enhancing its performance. The Pt@Pt 3 Ti catalyst with one-atomic Pt 3 Ti shell (Pt@1L-Pt 3 Ti/TiO 2 -C) demonstrates excellent performance with mass activity of 592 mA mg Pt -1 and durability nearly 19.5-fold that of commercial Pt/C with negligible decay (2 %) after 30,0 0 0 potential cycles (0.6-1.0 V vs. RHE). Notably, at higher potential cycles (1.0 V-1.5 V vs. RHE), Pt@1L-Pt 3 Ti/TiO 2 -C also showed far superior durability than Pt/C (9.6 % decayed while 54.8 % for commercial Pt/C). This excellent stability is derived from the intrinsic stability of Pt 3 Ti alloy and the confinement effect of TiO 2 -C. The catalyst's enhancement was further confirmed in PEMFC configuration. (c) 2024 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:212 / 220
页数:9
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