Uniform size and composition tuning of PtNi octahedra for systematic studies of oxygen reduction reactions

被引:38
|
作者
Chou, Shang-Wei [1 ,2 ]
Lai, Ying-Ren [1 ,3 ]
Yang, Ya Yun [4 ]
Tang, Chih-Yuan [4 ]
Hayashi, Michitoshi [3 ]
Chen, Hsieh-Chih [1 ,2 ]
Chen, Hui-Lung [5 ,6 ]
Chou, Pi-Tai [1 ,2 ]
机构
[1] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Ctr Emerging Mat & Adv Devices, Taipei 10617, Taiwan
[3] Natl Taiwan Univ, Ctr Condensed Matter Sci, Taipei 10617, Taiwan
[4] Natl Taiwan Univ, Instrumentat Ctr, Taipei 10617, Taiwan
[5] Chinese Culture Univ, Dept Chem, Taipei 111, Taiwan
[6] Chinese Culture Univ, Inst Appl Chem, Taipei 111, Taiwan
关键词
PtNi octahedra; Shape control; Oxygen reduction reaction; Volcano-shaped plot; DFT calculations; Surface energy; Adsorption energy; ALLOY NANOPARTICLES; ELECTROCATALYSIS; CATALYSTS; PT3NI; NI; SURFACES; PERFORMANCE; NETWORKS; FE; CO;
D O I
10.1016/j.jcat.2013.09.008
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
Uniform size and composition tuning of PtNi octahedra enclosed by 8 (11 1) facets were achieved by the control of specific crystal facet surfactant bindings. In this chemical method, the optimal ratio of dioctyl amine to oleic acid is a key factor in the formation of PtNi octahedra with different alloying compositions, Pt:Ni = 18:6, 12:12, and 10:14. Careful electrochemical examinations show that the oxygen reduction reaction (ORR) mass activity and specific area activity of all PtNi octahedra outperform those of commercial Pt/C catalyst. The volcano-shaped trend of ORR enhancement proves that Pt12Ni12 octahedra have superior ORR activities. Further firm support is provided by the theoretical approach, which concludes that the adsorption energies of the H, 0, 02, and OH species on a surface of Pt12Ni12(111) are much higher than those for Pt18Ni6(111) and Pt10Ni14(1 1 1) counterparts, whereas the molecularly adsorbed H2O product is calculated to be the lowest in adsorption energy on the Pt12Ni12(111) surface. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:343 / 350
页数:8
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