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Cobalt Oxide Electrode Doped with Iridium Oxide as Highly Efficient Water Oxidation Electrode
被引:33
|作者:
Tae, Eunju Lee
[1
]
Song, Jihye
[1
]
Lee, A. Reum
[1
]
Kim, Caroline Hewon
[1
]
Yoon, Seokjun
[1
]
Hwang, In Chul
[1
]
Kim, Min Gyu
[2
]
Yoon, Kyung Byung
[1
]
机构:
[1] Sogang Univ, Dept Chem, Seoul 04107, South Korea
[2] Pohang Univ Sci & Technol, PAL, Pohang 790784, Gyeongbuk, South Korea
来源:
ACS CATALYSIS
|
2015年
/
5卷
/
09期
基金:
新加坡国家研究基金会;
关键词:
water oxidation;
crystalline cobalt oxide;
crystalline iridium oxide;
Tafel plot;
XAS;
EXAFS;
oxygen vacancy;
OXYGEN EVOLUTION REACTION;
X-RAY-ABSORPTION;
NEUTRAL PH;
CATALYST;
ELECTROCATALYSTS;
NANOPARTICLES;
PHOSPHATE;
FILM;
SPECTROSCOPY;
MECHANISM;
D O I:
10.1021/acscatal.5b00979
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:
Crystalline cobalt oxide nanoparticles (nc-CoOx) supported on ITO glass or Ni foam doped with 5 mol % crystalline iridium oxide nanoparticles (nc-IrOx) showed performances which are higher than those of nc-CoOx on ITO or Ni foam and nc-IrOx on a rotating glassy carbon disc electrode or Ni foam. The initial Co-III and Ir-IV become Co-IV and Ir-VI upon applying positive potentials. The nc-CoOx particles intrinsically carry (CoO5)-O-III centers which become (CoO6)-O-IV centers upon application of positive potentials. The O vacancy in (CoO5)-O-III is transferred to (IrO6)-O-VI upon application of positive potentials, giving rise to the formation of (IrO5)-O-VI centers, which are proposed to be the highly active catalytic centers for water oxidation.
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收藏
页码:5525 / 5529
页数:5
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