Active and Stable Ir@Pt Core-Shell Catalysts for Electrochemical Oxygen Reduction

被引:76
作者
Strickler, Alaina L. [1 ]
Jackson, Ariel [1 ]
Jaramillo, Thomas F. [1 ,2 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, Menlo Pk, CA 94025 USA
基金
美国国家科学基金会;
关键词
PLATINUM-MONOLAYER ELECTROCATALYSTS; DENSITY-FUNCTIONAL THEORY; SURFACE SEGREGATION; HIGH-PERFORMANCE; ALLOY; NANOPARTICLES; RU; DEGRADATION; STABILITY; OXIDATION;
D O I
10.1021/acsenergylett.6b00585
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
Electrochemical oxygen reduction is an important reaction for many sustainable energy technologies, such as fuel cells and metal-air batteries. Kinetic limitations of this reaction, expensive electrocatalysts, and catalyst instability, however, limit the commercial viability of such devices. Herein, we report an active Ir@Pt core-shell catalyst that combines platinum overlayers with nanostructure effects to tune the oxygen binding to the Pt surface, thereby achieving enhanced activity and stability for the oxygen reduction reaction. Ir@ Pt nanoparticles with several shell thicknesses were synthesized in a scalable, inexpensive, one-pot polyol method. Electrochemical analysis demonstrates the activity and stability of the Ir@Pt catalyst, with specific and mass activities increasing to 2.6 and 1.8 times that of commercial Pt/C (TKK), respectively, after 10 000 stability cycles. Activity enhancement of the Ir@Pt catalyst is attributed to weakening of the oxygen binding to the Pt surface induced by the Ir core.
引用
收藏
页码:244 / 249
页数:6
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