Hollow Porous Carbon-Confined Atomically Ordered PtCo3 Intermetallics for an Efficient Oxygen Reduction Reaction

被引:112
作者
Hu, Yezhou [1 ]
Guo, Xuyun [1 ]
Shen, Tao [2 ]
Zhu, Ye [1 ]
Wang, Deli [2 ]
机构
[1] Hong Kong Polytech Univ, Res Inst Smart Energy, Dept Appl Phys, Hong Kong 999077, Peoples R China
[2] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Hubei Key Lab Mat Chem & Serv Failure, Sch Chem & Chem Engn,Minist Educ, Wuhan 430074, Peoples R China
关键词
fuel cells; hollow porous structure; atomically ordered structure; intermetallic electrocatalyst; carbon encapsulation; ELECTROCATALYSTS; CATALYSTS; NANOPARTICLES; PERFORMANCE; STABILITY; NANOTUBES;
D O I
10.1021/acscatal.2c01541
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
PtM3 alloys have demonstrated superior oxygen reduction reaction (ORR) activity due to the strong strain effect caused by non-noble metal cores. However, the serious corrosion of non-noble metals in acid solutions is still challenging. Herein, a hollow porous N-doped carbon sphere-encapsulated PtCo3 intermetallic electrocatalyst (O-PtCo3@pHNCS) is successfully prepared through Co pre-embedding and the subsequent impregnation-reduction method. The Co pre-embedding step is responsible for the formation of abundant mesopores, and the subsequent impregnation-reduction process leads to Pt-Co ordering and carbon encapsulation. Benefiting from the accelerated mass transfer process, enhanced metal interaction, and physical confinement effect, O-PtCo3@HNCS exhibits excellent ORR activity and durability with negligible half-wave loss after long-term stability test in acid solutions. The ordered PtCo3 nanoparticles tightly anchored in the carbon matrix without obvious aggregation, sintering, and agglomeration, responsible for the superior durability. The strategy for the carbon confinement in this work paves the way for achieving highly efficient catalysts with low Pt content, which can be used in various energy-related systems.
引用
收藏
页码:5380 / 5387
页数:8
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