Reversible Water-Induced Phase Changes of Cobalt Oxide Nanoparticles

被引:9
|
作者
Hein, Dennis [1 ,2 ]
Wartner, Garlef [1 ,2 ]
Bergmann, Arno [3 ]
Bernal, Miguel [3 ,4 ]
Roldan Cuenya, Beatriz [3 ]
Seidel, Robert [1 ,2 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie HZB, D-12489 Berlin, Germany
[2] Humboldt Univ, Inst Chem, D-12489 Berlin, Germany
[3] Fritz Haber Inst Max Planck Gesell, D-14195 Berlin, Germany
[4] Ruhr Univ Bochum, Dept Phys, D-44780 Bochum, Germany
关键词
near-ambient pressure XPS; solid-liquid interface; cobalt oxide; reversible phase change; core-shell nanoparticles; X-RAY-ABSORPTION; WURTZITE COO; L-EDGE; OXIDATION; CATALYSTS; PHOTOELECTRON; SIZE; PHOTOEMISSION; SPECTROSCOPY; IDENTIFICATION;
D O I
10.1021/acsnano.0c06066
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cobalt oxides have been identified as highly active catalysts for the electrochemical water splitting and oxygen evolution reaction. Using near-ambient pressure resonant photoelectron spectroscopy, we studied changes in the metal-oxygen coordination of size-selected core-shell CoOx nanoparticles induced by liquid water. In dry conditions, the nanoparticles exhibit an octahedrally coordinated Co2+ core and a tetrahedrally coordinated Co2+ shell. In the presence of liquid water, we observe a reversible phase change of the nanoparticle shell into octahedrally coordinated Co2+ as well as partially oxidized octahedrally coordinated Co3+. This is in contrast to previous findings, suggesting an irreversible phase change of tetrahedrally coordinated Co2+ after the oxygen evolution reaction conditioning. Our results demonstrate the appearance of water-induced structural changes different from voltage-induced changes and help us to understand the atomic scale interaction of CoOx nanoparticles with water in electrochemical processes.
引用
收藏
页码:15450 / 15457
页数:8
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