Nano-engineered intrapores in nanoparticles of PtNi networks for increased oxygen reduction reaction activity

被引:46
作者
Ding, Jieting [1 ,4 ]
Ji, Shan [2 ]
Wang, Hui [1 ]
Key, Julian [1 ]
Brett, Dan J. L. [3 ]
Wang, Rongfang [1 ,4 ]
机构
[1] Qingdao Univ Sci & Technol, Inst Chem Engn, Qingdao 266042, Peoples R China
[2] Jinxing Univ, Coll Biol Chem Sci & Chem Engn, Jinxing 314001, Peoples R China
[3] UCL, Electrochem Innovat Lab, Dept Chem Engn, London WC1E 7JE, England
[4] Northwest Normal Univ, Coll Chem & Chem Engn, Lanzhou 730070, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrocatalyst; Metallic alloys; Nanopores; Network; Oxygen reduction reaction; ROOM-TEMPERATURE SYNTHESIS; ASTERISK-MESSMETHODEN; FACILE SYNTHESIS; ONE-STEP; CARBON; ELECTROCATALYSTS; CATALYSTS; NANOSTRUCTURES; PERFORMANCE; SIZE;
D O I
10.1016/j.jpowsour.2017.11.002
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
Network-like metallic alloys of solid nanoparticles have been frequently reported as promising electrocatalysts for fuel cells. The three-dimensional structure of such networks is rich in pores in the form of voids between nanoparticles, which collectively expose a large surface area for catalytic activity. Herein, we present a novel solution to this problem using a precursor comprising a flocculent core-shell PtNi@Ni to produce PtNi network catalysts with nanoparticle intraporosity after carefully controlled electrochemical dealloying. Physical characterization shows a hierarchical level of nanoporosity (intrapores within nanoparticles and pores between them) evolves during the controlled electrochemical dealloying, and that a Pt-rich surface also forms after 22 cycles of Ni leaching. In ORR cycling, the PtNi networks gain 4-fold activity in both j(ECSA) and j(mass) over a state of the art Pt/C electrocatalyst, and also significantly exceed previously reported PtNi networks. In ORR degradation tests, the PtNi networks also proved stable, dropping by 30.4% and 62.6% in j(ECSA) and j(mass) respectively. The enhanced performance of the catalyst is evident, and we also propose that the presented synthesis procedure can be generally applied to developing other metallic networks.
引用
收藏
页码:48 / 54
页数:7
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