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PtIr/Ti4O7 as a bifunctional electrocatalyst for improved oxygen reduction and oxygen evolution reactions
被引:66
|作者:
Won, Ji-Eun
[1
]
Kwak, Da-Hee
[1
]
Han, Sang-Beom
[1
]
Park, Hyun-Suk
[1
]
Park, Jin-Young
[1
]
Ma, Kyeng-Bae
[1
]
Kim, Do-Hyoung
[1
]
Park, Kyung-Won
[1
]
机构:
[1] Soongsil Univ, Dept Chem Engn, Seoul 156743, South Korea
关键词:
URFC;
Ti4O7;
Oxygen reduction;
Oxygen evolution;
Round-trip efficiency;
REGENERATIVE FUEL-CELL;
CATALYST SUPPORT;
HIGH-PERFORMANCE;
MESOPOROUS CARBON;
PEMFC CATALYSTS;
IR;
STABILITY;
CORROSION;
ELECTRODES;
OXIDES;
D O I:
10.1016/j.jcat.2017.12.013
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:
A unitized regenerative fuel cell (URFC) that combines a fuel cell with a water electrolyzer is attractive as a portable power source. To enhance the efficiency of the URFC, a bifunctional oxygen catalyst for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) needs to be developed. In this study, Ti4O7 supported Pt-based catalysts were prepared for a bifunctional oxygen catalyst (BOC) in URFC. Ti4O7 support was prepared using a low-temperature process with TiO2 and cobalt chloride hexahydrate at 950 degrees C under an H-2 atmosphere. The metal catalysts (60 wt%) were deposited on a Ti4O7 support using a borohydride reduction method. The catalysts were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Compared to Pt/C and Pt/Ti4O7, PdriTi(4)O(2) exhibited enhanced activity and stability in ORR and OER. The improved electrocatalytic performance of Rlr alloy supported by Ti4O7 might be attributed to the PtIr alloy phase, the highly stable Ti4O7 support in an acid medium, and the interaction between catalyst and support. (C) 2017 Elsevier Inc. All rights reserved.
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页码:287 / 294
页数:8
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