期刊
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
卷 26, 期 12, 页码 2805-2815出版社
SPRINGER
DOI: 10.1007/s10008-022-05281-0
关键词
Room-temperature ionic liquid; X-ray photoelectron spectroscopy; Cyclic voltammetry; Electrochemical impedance spectroscopy; Aluminium current collector
资金
- EU through the European Regional Development Fund [2014-2020.4.01.15-0011, 2014-2020.4.01.16-0123, 3.2.0304.12-0397]
- Estonian Research Council [PRG676, IUT20-57]
- European Spallation Source: Estonian Participation in ESS Instrument design, development and building and application for scientific research [SLOKT12026T, SLTKT16432T]
- project Production of Polymer Electrolyte Membrane Fuel Cell [LLTKT20148]
- project Developing new research services and research infrastructures at MAX IV synchrotron radiation source [2014-2020.4.01.20-0278]
- Swedish Research council [2018-07152]
- Swedish Governmental Agency for Innovation Systems [2018-04969]
- Formas [2019-02496]
The in situ X-ray photoelectron spectroscopy data shows that N4111(TFSI) strongly adsorbs on the aluminum electrode within a specific potential range and undergoes electrochemical decomposition. Intensive electrochemical reduction of N4111(TFSI) occurs at lower potentials, while non-specific adsorption is observed at another potential range.
The in situ X-ray photoelectron spectroscopy data indicate that butyltrimethylammonium bis(trifluoromethylsulfonyl)imide (N4111(TFSI)) adsorbs strongly within the potential range -3.25 V < E < -2.25 V and specifically at E < -3.25 V (vs. Ag-QRE) at the Al electrode. Strong adsorption of the intermediates of N4111(TFSI) electrochemical decomposition was observed in electrochemical impedance spectroscopy and cyclic voltammetry measurements. At E < -4.25 V (vs. Ag-QRE), very intensive electrochemical reduction of N4111(TFSI) took place at the Al electrode giving gaseous products. In the potential range from - 2.25 to 0.00 V (vs. Ag-QRE), non-specific adsorption of N4111(TFSI) exists et al. surface.
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