In operando observation system for electrochemical reaction by soft X-ray absorption spectroscopy with potential modulation method

被引:32
作者
Nagasaka, Masanari [1 ,2 ]
Yuzawa, Hayato [1 ]
Horigome, Toshio [1 ]
Kosugi, Nobuhiro [1 ,2 ]
机构
[1] Natl Inst Nat Sci, Inst Mol Sci, Okazaki, Aichi 4448585, Japan
[2] Grad Univ Adv Studies, Okazaki, Aichi 4448585, Japan
关键词
PARTIAL FLUORESCENCE YIELD; SULFURIC-ACID-SOLUTIONS; L-EDGE; COPPER ELECTROCRYSTALLIZATION; ELECTROLYTE INTERFACE; ANION ADSORPTION; WATER-MOLECULES; LIQUID WATER; SURFACE; AU(111);
D O I
10.1063/1.4898054
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
In order to investigate local structures of electrolytes in electrochemical reactions under the same scan rate as a typical value 100 mV/s in cyclic voltammetry (CV), we have developed an in operando observation system for electrochemical reactions by soft X-ray absorption spectroscopy (XAS) with a potential modulation method. XAS spectra of electrolytes are measured by using a transmission-type liquid flow cell with built-in electrodes. The electrode potential is swept with a scan rate of 100 mV/s at a fixed photon energy, and soft X-ray absorption coefficients at different potentials are measured at the same time. By repeating the potential modulation at each fixed photon energy, it is possible to measure XAS of electrochemical reaction at the same scan rate as in CV. We have demonstrated successful measurement of the Fe L-edge XAS spectra of aqueous iron sulfate solutions and of the change in valence of Fe ions at different potentials in the Fe redox reaction. The mechanism of these Fe redox processes is discussed by correlating the XAS results with those at different scan rates. (C) 2014 AIP Publishing LLC.
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页数:7
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