Effect of the type of Pt precursor on Pt-Ni nanostructures for electro-oxidation of ammonia

被引:7
|
作者
Kim, Haengsoo [1 ]
Won, Dongsin [1 ]
Lee, Hong-Ki [3 ]
Yoo, Sung Jong [4 ]
Nahm, Kee Suk [1 ,2 ]
Kim, Pil [1 ,2 ]
机构
[1] Chonbuk Natl Univ, Ctr Nanomat & Proc, Dept Energy Storage Convers Engn, Jeonju, Jeonbuk, South Korea
[2] Chonbuk Natl Univ, Sch Semicond & Chem Engn, Jeonju, Jeonbuk, South Korea
[3] Hydrogen Fuel Cell Parts & Appl Technol Reg Innov, Jeonju, Jeonbuk, South Korea
[4] Korea Inst Sci & Technol, Fuel Cell Res Ctr, Seoul 136791, South Korea
基金
新加坡国家研究基金会;
关键词
Nanostructures; Composite materials; Electrochemical techniques; Electrochemical properties; HOLLOW NANOPARTICLES; METHANOL OXIDATION; OXYGEN-REDUCTION; PLATINUM; NANOCRYSTALS; NANOSPHERES; ELECTROCATALYSTS; FABRICATION; NANOTUBES; NANOCUBES;
D O I
10.1016/j.matchemphys.2014.06.012
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The properties of Pt-Ni nanostructures were successfully controlled by employing different Pt precursors in the preparation of Pt-Ni nanocomposites, which were synthesized by a co-reducing Pt and Ni precursors. Pt-Ni nanostructures were obtained by leaching Ni species from the Pt-Ni nanocomposite. The use of H2PtCl6 as a precursor yielded aggregated small Pt particles, while [Pt(NH3)(4)]Cl-2 yielded large hollow Pt nanostructures. A possible mechanism leading to the morphological difference between the two structures was suggested. Owing to a higher electrochemically active surface area and a favorable surface structure, hollow Pt nanostructures from the [Pt(NH3)(4)]Cl-2 precursor showed significantly better performance in ammonia oxidation than the aggregated Pt particles resulting from the H2PtCl6 precursor. (C) 2014 Elsevier B.V. All rights reserved.
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页码:722 / 727
页数:6
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