Improved ethanol electrooxidation performance by shortening Pd-Ni active site distance in Pd-Ni-P nanocatalysts

被引:528
作者
Chen, Lin [1 ]
Lu, Lilin [2 ]
Zhu, Hengli [1 ]
Chen, Yueguang [1 ,3 ]
Huang, Yu [4 ]
Li, Yadong [3 ]
Wang, Leyu [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Wuhan Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430081, Peoples R China
[3] Tsinghua Univ, Dept Chem, Beijing 100086, Peoples R China
[4] Univ Calif Los Angeles, Dept Mat Sci & Engn, Los Angeles, CA 90095 USA
基金
中国国家自然科学基金;
关键词
OXYGEN REDUCTION REACTION; ELECTROCATALYTIC ACTIVITY; FUEL-CELLS; FACILE SYNTHESIS; OXIDATION; NANOPARTICLES; CATALYSTS; NANOSTRUCTURES; NANOCRYSTALS; VOLTAMMETRY;
D O I
10.1038/ncomms14136
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Incorporating oxophilic metals into noble metal-based catalysts represents an emerging strategy to improve the catalytic performance of electrocatalysts in fuel cells. However, effects of the distance between the noble metal and oxophilic metal active sites on the catalytic performance have rarely been investigated. Herein, we report on ultrasmall (similar to 5 nm) Pd-Ni-P ternary nanoparticles for ethanol electrooxidation. The activity is improved up to 4.95A per mg(Pd), which is 6.88 times higher than commercial Pd/C (0.72A per mgPd), by shortening the distance between Pd and Ni active sites, achieved through shape transformation from Pd/Ni-P heterodimers into Pd-Ni-P nanoparticles and tuning the Ni/Pd atomic ratio to 1:1. Density functional theory calculations reveal that the improved activity and stability stems from the promoted production of free OH radicals (on Ni active sites) which facilitate the oxidative removal of carbonaceous poison and combination with CH3CO radicals on adjacent Pd active sites.
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页数:9
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