Manganese Oxide as an Inorganic Catalyst for the Oxygen Evolution Reaction Studied by X-Ray Photoelectron and Operando Raman Spectroscopy

被引:51
|
作者
Radinger, Hannes [1 ,2 ]
Connor, Paula [1 ]
Stark, Robert [3 ]
Jaegermann, Wolfram [1 ]
Kaiser, Bernhard [1 ]
机构
[1] Tech Univ Darmstadt, Inst Mat Sci, Surface Sci Lab, D-64287 Darmstadt, Germany
[2] Karlsruhe Inst Technol, Inst Appl Mat, D-76344 Eggenstein Leopoldshafen, Germany
[3] Tech Univ Darmstadt, Inst Mat Sci, Phys Surfaces, D-64287 Darmstadt, Germany
关键词
operando Raman spectroscopy; X-ray photoelectron spectroscopy; manganese oxide; oxygen evolution reaction; electrocatalysis; IN-SITU; WATER OXIDATION; HYDROGEN; ELECTROCATALYSTS; SPECTRA; XPS; NANOPARTICLES; BIRNESSITE; REDUCTION; MECHANISM;
D O I
10.1002/cctc.202001756
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
Manganese oxide (MnOx) is considered a promising material for the oxygen evolution reaction (OER) to replace noble metal catalysts in water splitting. The improvement of MnOx requires mechanistic and kinetic knowledge of the four-electron transfer steps of the OER. X-ray photoelectron spectroscopy, a widely used tool to characterize the electronic structure of thin films, is used in combination with surface-enhanced Raman spectroscopy to gain a deeper knowledge of the different mixed MnOx types and their respective change in chemical composition. Using Raman spectroscopy during electrochemical measurements, all samples were found to reveal Birnessite-type MnO2 motifs in alkaline media at an applied potential. Their activity correlates with two shifting Raman active modes, one of them being assigned to the formation of Mn-III species, and one to the expansion of layers of MnO6 octahedra. A special activation treatment leads independent of the starting material to a highly amorphous mixed-valence oxide, which shows the highest OER activity.
引用
收藏
页码:1175 / 1185
页数:11
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