Transition-Metal Doping of Oxide Nanocrystals for Enhanced Catalytic Oxygen Evolution

被引:95
|
作者
Jang, Dong Myung [1 ]
Kwak, In Hye [1 ]
Kwon, El Lim [1 ]
Jung, Chan Su [1 ]
Im, Hyung Soon [1 ]
Park, Kidong [1 ]
Park, Jeunghee [1 ]
机构
[1] Korea Univ, Dept Chem, Jochiwon 339700, South Korea
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2015年 / 119卷 / 04期
关键词
ELECTROCHEMICAL WATER OXIDATION; RAY-ABSORPTION SPECTROSCOPY; BIFUNCTIONAL ELECTROCATALYST; HIGHLY EFFICIENT; REDUCTION; STATE; PHOSPHATE; GRAPHENE; TIO2; IRON;
D O I
10.1021/jp511561k
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
Catalysts for the oxygen reduction and evolution reactions are central to key renewable-energy technologies including fuel cells and water splitting. Despite tremendous effort, the development of oxygen electrode catalysts with high activity at low cost remains a great challenge. In this study, we report a generalized sol-gel method for the synthesis of various oxide nanocrystals (TiO2, ZnO, Nb2O5, In2O3, SnO2, and Ta2O5) with appropriate transition metal dopants for an efficient electrocatalytic oxygen evolution reaction (OER). Although TiO2 and ZnO nanocrystals alone have little activity, all the Mn-, Fe-, Co-, and Ni-doped nanocrystals exhibit greatly enhanced OER activity. A remarkable finding is that Co dopant produces higher OER activity than the other doped metals. X-ray photoelectron and X-ray absorption spectroscopies revealed the highly oxidized metal ions that are responsible for the enhanced catalytic reactivity. The excellent OER activity of the Co-doped nanocrystals was explained by a synergistic effect in which the oxide matrix effectively guards the most active Co dopants at higher oxidation states by withdrawing the electrons from the metal dopants. The metal-doped NCs exhibit enhanced catalytic activity under visible light irradiation, suggesting their potential as efficient solar-driven OER photoelectrocatalysts.
引用
收藏
页码:1921 / 1927
页数:7
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