Enhancement of the electrocatalytic oxygen reduction reaction on Pd3Pb ordered intermetallic catalyst in alkaline aqueous solutions

被引:17
作者
Jeevagan, Arockiam John [1 ]
Gunji, Takao [1 ]
Ando, Fuma [1 ]
Tanabe, Toyokazu [1 ]
Kaneko, Shingo [2 ]
Matsumoto, Futoshi [1 ]
机构
[1] Kanagawa Univ, Dept Mat & Life Chem, Kanagawa Ku, 3-27-1 Rokkakubashi, Yokohama, Kanagawa 2218686, Japan
[2] Kanagawa Univ, Inst Engn Res, Kanagawa Ku, 3-27-1 Rokkakubashi, Yokohama, Kanagawa 2218686, Japan
关键词
Electrocatalysis; Oxygen reduction reaction; Ordered intermetallic phase; Alkaline media; FUEL-CELLS; PTPB NANOPARTICLES; FORMIC-ACID; STABILITY; OXIDATION; ELECTRODE; GRAPHENE; ELECTROOXIDATION; PALLADIUM; MEDIA;
D O I
10.1007/s10800-016-0968-7
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Enhancement of the oxygen reduction reaction (ORR) was examined with Pd3Pb ordered intermetallic nanoparticles (NPs) supported on titania (Pd3Pb/TiO2). The Pd3Pb/TiO2 catalyst was synthesized by a conventional wet chemical method with Pd and Pb ion precursors, a reducing agent and TiO2 powder under ambient temperature. X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy measurements indicated the formation of the ordered intermetallic phase of Pd3Pb in the NP form on the TiO2 surface. Electrochemical measurements showed that the Pd3Pb/TiO2 catalyst markedly enhanced the ORR in an alkaline environment due to the unique surface of Pd3Pb NPs and the strong interaction between Pd3Pb and TiO2 compared with TiO2-supported Pd, Pt, and PtPb NPs. The onset potential of Pd3Pb/TiO2 was shifted toward a higher potential by 110-150 mV compared with Pd/TiO2, PtPb/TiO2, and Pt/TiO2. [GRAPHICS] .
引用
收藏
页码:745 / 753
页数:9
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