The effect of alloying on the oxygen reduction reaction activity of carbon-supported PtCu and PtPd nanorods

被引:39
作者
Tseng, Yi-Chia [1 ]
Chen, Hong-Shuo [1 ]
Liu, Chen-Wei [2 ]
Yeh, Tzu-Hau [1 ]
Wang, Kuan-Wen [1 ]
机构
[1] Natl Cent Univ, Inst Mat Sci & Engn, Tao Yuan 32001, Taiwan
[2] Ind Technol Res Inst, Green Energy & Environm Res Labs, Hsinchu 31040, Taiwan
关键词
PEMFC SCIENCE; QUANTUM JUMPS; PART II; ELECTROCATALYSTS; PD; FABRICATION; TECHNOLOGY; CATALYSTS; ELECTRODE; METHANOL;
D O I
10.1039/c3ta14705c
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
In this study, we have investigated the effect of alloying on the modification of the d-band vacancies and oxygen reduction reaction (ORR) activity of PtPd and PtCu nanorods (NRs). PtCu and PtPd NRs with various ratios can be prepared successfully by a facile formic acid reduction method. The number of unfilled d-states (H-Ts) value of Pt nanoparticles is decreased due to the formation of NRs, and further decreased due to the alloying with different metals. For the Pt3Pd NRs, the H-Ts value is as low as 0.3056, suggesting that they have lower unfilled Pt d-states, and more d-band electrons transfer from Pd to Pt, leading to higher ORR activities than Pt/C. Besides, the electron transfer number (n) of Pt3Pd NRs towards the ORR is 3.7, meaning that they complete the O-2 reduction to water and exhibit low hydrogen peroxide production during the ORR. As a result, the correlation between the H-Ts and ORR performance of PtPd and PtCu NRs highlights that the one-dimensional (1-D) structure and the electronic modification effect from Pd to Pt result in the excellent ORR activity and durability of Pt3Pd NRs synergistically.
引用
收藏
页码:4270 / 4275
页数:6
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