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Electro-Oxidation of Borohydride on Rhodium, Iridium, and Rhodium-Iridium Bimetallic Nanoparticles with Implications to Direct Borohydride Fuel Cells
被引:36
作者:
Kiran, V.
[1
]
Ravikumar, T.
[1
]
Kalyanasundaram, N. T.
[1
]
Krishnamurty, S.
[3
]
Shukla, A. K.
[2
]
Sampath, S.
[1
]
机构:
[1] Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India
[2] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
[3] Cent Electrochem Res Inst, Karaikkudi 630006, Tamil Nadu, India
关键词:
OXYGEN REDUCTION;
ELECTRON LOCALIZATION;
ULTRASOFT PSEUDOPOTENTIALS;
SODIUM-BOROHYDRIDE;
BINARY CLUSTERS;
PT-AU;
GOLD;
OXIDATION;
PLATINUM;
HYDROGEN;
D O I:
10.1149/1.3442372
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
Electrochemical oxidation of borohydride is studied on nanosized rhodium, iridium, and bimetallic rhodium-iridium catalysts supported onto Vulcan XC72R carbon. The catalysts are characterized by X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy in conjunction with cyclic voltammetry and polarization studies. The studies reveal that a 20 wt % bimetallic Rh-Ir catalyst supported onto carbon (Rh-Ir/C) is quite effective for the oxidation of borohydride. Direct borohydride fuel cell with Rh-Ir/C as the anode catalyst and Pt/C as the cathode catalyst exhibits a peak power density of 270 mW/cm(2) at a load current density of 290 mA/cm(2) as against 200 mW/cm(2) at 225 mA/cm(2) for Rh/C and 140 mW/cm(2) at 165 mA/cm(2) for Ir/C while operating at 80 degrees C. The synergistic catalytic activity for the bimetallic Rh-Ir nanoparticles toward borohydride oxidation is corroborated by density-functional theory calculations using electron-localization function. (C) 2010 The Electrochemical Society. [DOI:10.1149/1.3442372] All rights reserved.
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页码:B1201 / B1208
页数:8
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