Heterogeneous Cu-Pd binary interface boosts stability and mass activity of atomic Pt clusters in the oxygen reduction reaction

被引:22
作者
Chen, Hsin-Yi Tiffany [1 ]
Chou, Jyh-Pin [2 ]
Lin, Cheng-Yang [3 ,4 ]
Hu, Chih-Wei [1 ]
Yang, Ya-Tang [3 ,4 ]
Chen, Tsan-Yao [1 ,5 ]
机构
[1] Natl Tsing Hua Univ, Dept Engn & Syst Sci, Hsinchu 30013, Taiwan
[2] Hungarian Acad Sci, Wigner Res Ctr Phys, Inst Solid State Phys & Opt, POB 49, H-1525 Budapest, Hungary
[3] Natl Tsing Hua Univ, Dept Elect Engn, Hsinchu 30013, Taiwan
[4] Natl Tsing Hua Univ, Inst Elect Engn, Hsinchu 30013, Taiwan
[5] Natl Tsing Hua Univ, Inst Nucl Engn & Sci, Hsinchu 30013, Taiwan
关键词
PLATINUM MONOLAYER; BIMETALLIC NANOPARTICLES; ELECTROCATALYSTS; SPECTROSCOPY;
D O I
10.1039/c7nr01224a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A ternary metallic CuPdPt nanocatalyst (NC) is synthesized using a wet chemical reduction method, which is sequentially designed, in the presence of acid treated carbon nanotubes. This NC is a nanocrystal with a configuration of a Cu@Pd core and atomic Pt clusters (similar to 9 wt%) on the top (Cu@Pd/Pt). A residual current of 92.6%, 5.2 times higher than that of commercial Pt catalysts (at 0.85 V vs. RHE), is retained after 40 000 cycles of an accelerated degradation test (ADT). Atomic and electronic structure analyses show that such exclusive stability mainly results from electron localization at Pt clusters in heterogeneous interfaces of the Cu-Pd core. Most importantly, we develop a robust ternary NC, which shows outstanding MA, superior chemical durability, and similar to 90 wt% lower Pt loading than commercial Pt NCs in the oxygen reduction reaction.
引用
收藏
页码:7207 / 7216
页数:10
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