Oxide-Carbon Nanofibrous Composite Support for a Highly Active and Stable Polymer Electrolyte Membrane Fuel-Cell Catalyst

被引:50
作者
Jeon, Yukwon [1 ,2 ]
Ji, Yunseong [1 ]
Cho, Yong Il [1 ]
Lee, Chanmin [1 ]
Park, Dae-Hwan [3 ]
Shul, Yong-Gun [1 ]
机构
[1] Yonsei Univ, Dept Chem & Biomol Engn, Yonsei Ro 50, Seoul 03722, South Korea
[2] St Andrews Univ, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[3] Kyungnam Univ, Dept Nano Mat Sci & Engn, Chang Won 51767, Gyeongsangnamdo, South Korea
基金
新加坡国家研究基金会;
关键词
PEMFC cathode catalyst; oxide-carbon composite support; nanofibrous structure; electronic configuration; electrochemical stability; OXYGEN REDUCTION REACTION; ELECTROCATALYSTS; NANOPARTICLES; DURABILITY; ANATASE; PEMFC; PERFORMANCE; CORROSION; ALIGNMENT; PLATINUM;
D O I
10.1021/acsnano.8b02040
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Well-designed electronic configurations and structural properties of electrocatalyst alter the activity, stability, and mass transport for enhanced catalytic reactions. We introduce a nanofibrous oxide-carbon composite by an in situ method of carbon nanofiber (CNF) growth by highly dispersed Ni nanoparticles that are exsoluted from a NiTiO3 surface. The nanofibrous feature has a 3D web structure with improved mass-transfer properties at the electrode. In addition, the design of the CNF/TiO2 support allows for complex properties for excellent stability and activity from the TiO2 oxide support and high electric conductivity through the connected CNF, respectively. Developed CNF/TiO2-Pt nanofibrous catalyst displays exemplary oxygen-reduction reaction (ORR) activity with significant improvement of the electrochemical surface area. Moreover, exceptional resistance to carbon corrosion and Pt dissolution is proven by durability-test protocols based on the Department of Energy. These results are well-reflected to the single-cell tests with even-better performance at the kinetic zone compared to the commercial Pt/C under different operation conditions. CNF/TiO2-Pt displays an enhanced active state due to the strong synergetic interactions, which decrease the Pt d-band vacancy by electron transfer from the oxide carbon support. A distinct reaction mechanism is also proposed and eventually demonstrates a promising example of an ORR electrocatalyst design.
引用
收藏
页码:6819 / 6829
页数:11
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