Rapid Atomic Ordering Transformation toward Intermetallic Nanoparticles

被引:32
作者
Cui, Mingjin [1 ]
Yang, Chunpeng [1 ]
Hwang, Sooyeon [2 ]
Li, Boyang [3 ]
Dong, Qi [1 ]
Wu, Meiling [1 ]
Xie, Hua [1 ]
Wang, Xizheng [1 ]
Wang, Guofeng [3 ]
Hu, Liangbing [1 ,4 ]
机构
[1] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[3] Univ Pittsburgh, Dept Mech Engn & Mat Sci, Pittsburgh, PA 15261 USA
[4] Univ Maryland, Ctr Mat Innovat, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
atomic ordering; nanoparticle synthesis; intermetallic; oxygen reduction reaction; OXYGEN-REDUCTION; ACTIVATION; DIFFUSION;
D O I
10.1021/acs.nanolett.1c03714
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chemically ordered intermetallic nanoparticles are promising candidates for energy-related applications such as electrocatalysis. However, the synthesis of intermetallics generally requires long annealing (several hours) to achieve the ordered structure, which causes nanoparticles agglomeration and diminished performance, particularly for catalysis. Herein, we demonstrate a new rapid Joule heating approach that can synthesize highly ordered and well-dispersed intermetallic nanoparticles. As a proof-of-concept, we synthesized fully ordered Pd3Pb intermetallic nanoparticles that feature small size distribution (similar to 6 nm). Computational analysis of the L1(2) Pd3Pb material suggests that this rapid atomic ordering transformation can be attributed to a vacancy-mediated diffusion mechanism. Moreover, the nanoparticles demonstrate excellent electrocatalytic activity and exceptional stability for the oxygen reduction reaction (ORR), retaining >95% of the current density over 10 h of chronoamperometry test with negligible structural and compositional changes. This study demonstrates a new strategy of providing a new direction for intermetallic synthesis and catalyst discovery.
引用
收藏
页码:255 / 262
页数:8
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