Oxygen electrocatalysis on (001)-oriented manganese perovskite films: Mn valency and charge transfer at the nanoscale

被引:140
作者
Stoerzinger, Kelsey A. [1 ,2 ]
Risch, Marcel [2 ]
Suntivich, Jin [3 ]
Lue, W. M. [4 ,5 ]
Zhou, Jigang [6 ]
Biegalski, Michael D. [7 ]
Christen, Hans M. [7 ]
Ariando [5 ,8 ]
Venkatesan, T. [4 ,5 ,8 ]
Shao-Horn, Yang [1 ,2 ,9 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] MIT, Electrochem Energy Lab, Cambridge, MA 02139 USA
[3] Harvard Univ, Ctr Environm, Cambridge, MA 02138 USA
[4] Natl Univ Singapore, Dept Elect & Comp Engn, Singapore 117583, Singapore
[5] Natl Univ Singapore, NUSNNI NanoCore, Singapore 117411, Singapore
[6] Canadian Light Source, Saskatoon, SK S7N 2V3, Canada
[7] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[8] Natl Univ Singapore, Dept Phys, Singapore 117542, Singapore
[9] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
REDUCTION REACTION; OXIDE CATALYSTS; CARBON; NANOWIRES; EVOLUTION; ELECTRODE; WATER;
D O I
10.1039/c3ee40321a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report that the oxygen reduction reaction (ORR) activities of (001)-oriented manganese perovskite films decrease from 10 to 1 nm by more than an order of magnitude, which can be attributed to the barrier associated with interfacial band bending that impedes electron transfer to the electrolyte, and reduction of Mn3+ due to charge transfer from the Nb:SrTiO3 substrate. Furthermore, we show by substitution in La1-x(Ca,Sr)(x)MnO3 that Mn3+, not Mn4+, is the active valence state for ORR.
引用
收藏
页码:1582 / 1588
页数:7
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