Nagasaka Masanari, Yuzawa Hayato, Horigome Toshio, Kosugi Nobuhiro
Institute for Molecular Science, Myodaiji, Okazaki 444-8585, Japan.
Rev Sci Instrum. 2014 Oct;85(10):104105. doi: 10.1063/1.4898054.
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.
为了在循环伏安法(CV)中与典型值100 mV/s相同的扫描速率下研究电化学反应中电解质的局部结构,我们开发了一种通过软X射线吸收光谱(XAS)和电位调制方法对电化学反应进行原位观察的系统。电解质的XAS光谱通过使用带有内置电极的透射型液体流动池进行测量。在固定的光子能量下,以100 mV/s的扫描速率扫描电极电位,同时测量不同电位下的软X射线吸收系数。通过在每个固定光子能量下重复电位调制,可以在与CV相同的扫描速率下测量电化学反应的XAS。我们已经成功地测量了硫酸铁水溶液的Fe L边XAS光谱以及Fe氧化还原反应中不同电位下Fe离子的价态变化。通过将XAS结果与不同扫描速率下的结果相关联,讨论了这些Fe氧化还原过程的机制。