Highly Active, Nonprecious Metal Perovskite Electrocatalysts for Bifunctional Metal-Air Battery Electrodes

被引:292
作者
Hardin, William G. [4 ]
Slanac, Daniel A. [1 ]
Wang, Xiqing [5 ]
Dai, Sheng [5 ]
Johnston, Keith P. [1 ,3 ,4 ]
Stevenson, Keith J. [2 ,3 ,4 ]
机构
[1] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
[3] Univ Texas Austin, Ctr Electrochem, Austin, TX 78712 USA
[4] Univ Texas Austin, Texas Mat Inst, Austin, TX 78712 USA
[5] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2013年 / 4卷 / 08期
关键词
OXYGEN REDUCTION REACTION; REVERSE MICELLE SYNTHESIS; OXIDE CATALYSTS; EVOLUTION; WATER; UNIVERSALITY; ELECTROLYSIS; MECHANISM; OXIDATION; ENSEMBLE;
D O I
10.1021/jz400595z
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
Perovskites are of great interest as replacements for precious metals and oxides used in bifunctional air electrodes involving the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Herein, we report the synthesis and activity of a phase-pure nanocrystal perovskite catalyst that is highly active for the OER and ORR. The OER mass activity of LaNiO3, synthesized by the calcination of a rapidly dried nanoparticle dispersion and supported on nitrogen-doped carbon, is demonstrated to be nearly 3-fold that of 6 nm IrO2 and exhibits no hysteresis during oxygen evolution. Moreover, strong OER/ORR bifimctionality is shown by the low total overpotential (1.02 V) between the reactions, on par or better than that of noble metal catalysts such as Pt (1.16 V) and Ir (0.92 V). These results are examined in the context of surface hydroxylation, and a new OER cycle is proposed that unifies theory and the unique surface properties of LaNiO3.
引用
收藏
页码:1254 / 1259
页数:6
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