The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI)
In this study, we used the in situ X-ray photoelectron spectroscopy (XPS), in situ mass spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy methods, for the first time, in a detailed exploration of the electrochemical behaviour of a quaternary amine cation-based room-temperat...
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2021
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oai:doaj.org-article:f3867e6d6a114e49b83b89bc196c66df2021-11-25T17:05:48ZThe Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI)10.3390/catal111113152073-4344https://doaj.org/article/f3867e6d6a114e49b83b89bc196c66df2021-10-01T00:00:00Zhttps://www.mdpi.com/2073-4344/11/11/1315https://doaj.org/toc/2073-4344In this study, we used the in situ X-ray photoelectron spectroscopy (XPS), in situ mass spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy methods, for the first time, in a detailed exploration of the electrochemical behaviour of a quaternary amine cation-based room-temperature ionic liquid, butyl-trimethyl-ammonium bis(trifluoromethylsulfonyl)imide (N4111(TFSI)), at the negatively and positively polarised molybdenum carbide-derived micro-mesoporous carbon (mmp-C(Mo<sub>2</sub>C)) electrodes that can be used as high surface area supporting material for electrocatalysts. The shapes of the C 1s, N 1s, O 1s, F 1s and S 2p XPS spectra were stable for N4111(TFSI) within a very wide potential range. The XPS data indicated the non-specific adsorption character of the cations and anions in the potential range from −2.00 V to 0.00 V. Thus, this region can be used for the detailed analysis of catalytic reaction mechanisms. We observed strong adsorption from 0.00 V to 1.80 V, and at <i>E</i> > 1.80 V, very strong adsorption of the N4111(TFSI) at the mmp-C(Mo<sub>2</sub>C) took place. At more negative potentials than −2.00 V, the formation of a surface layer containing both N4111<sup>+</sup> cations and TFSI<sup>−</sup> anions was established with the formation of various gaseous compounds. Collected data indicated the electrochemical instability of the N4111<sup>+</sup> cation at <i>E</i> < −2.00 V.Jaanus KruusmaArvo TõnisooRainer PärnaThomas ThombergMati KookTavo RomannVambola KisandEnn LustMDPI AGarticleroom-temperature ionic liquidmicro-mesoporous carbon electrodein situ X-ray photoelectron spectroscopyin situ mass spectroscopyelectrochemical impedance spectroscopycyclic voltammetryChemical technologyTP1-1185ChemistryQD1-999ENCatalysts, Vol 11, Iss 1315, p 1315 (2021) |
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room-temperature ionic liquid micro-mesoporous carbon electrode in situ X-ray photoelectron spectroscopy in situ mass spectroscopy electrochemical impedance spectroscopy cyclic voltammetry Chemical technology TP1-1185 Chemistry QD1-999 |
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room-temperature ionic liquid micro-mesoporous carbon electrode in situ X-ray photoelectron spectroscopy in situ mass spectroscopy electrochemical impedance spectroscopy cyclic voltammetry Chemical technology TP1-1185 Chemistry QD1-999 Jaanus Kruusma Arvo Tõnisoo Rainer Pärna Thomas Thomberg Mati Kook Tavo Romann Vambola Kisand Enn Lust The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI) |
description |
In this study, we used the in situ X-ray photoelectron spectroscopy (XPS), in situ mass spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy methods, for the first time, in a detailed exploration of the electrochemical behaviour of a quaternary amine cation-based room-temperature ionic liquid, butyl-trimethyl-ammonium bis(trifluoromethylsulfonyl)imide (N4111(TFSI)), at the negatively and positively polarised molybdenum carbide-derived micro-mesoporous carbon (mmp-C(Mo<sub>2</sub>C)) electrodes that can be used as high surface area supporting material for electrocatalysts. The shapes of the C 1s, N 1s, O 1s, F 1s and S 2p XPS spectra were stable for N4111(TFSI) within a very wide potential range. The XPS data indicated the non-specific adsorption character of the cations and anions in the potential range from −2.00 V to 0.00 V. Thus, this region can be used for the detailed analysis of catalytic reaction mechanisms. We observed strong adsorption from 0.00 V to 1.80 V, and at <i>E</i> > 1.80 V, very strong adsorption of the N4111(TFSI) at the mmp-C(Mo<sub>2</sub>C) took place. At more negative potentials than −2.00 V, the formation of a surface layer containing both N4111<sup>+</sup> cations and TFSI<sup>−</sup> anions was established with the formation of various gaseous compounds. Collected data indicated the electrochemical instability of the N4111<sup>+</sup> cation at <i>E</i> < −2.00 V. |
format |
article |
author |
Jaanus Kruusma Arvo Tõnisoo Rainer Pärna Thomas Thomberg Mati Kook Tavo Romann Vambola Kisand Enn Lust |
author_facet |
Jaanus Kruusma Arvo Tõnisoo Rainer Pärna Thomas Thomberg Mati Kook Tavo Romann Vambola Kisand Enn Lust |
author_sort |
Jaanus Kruusma |
title |
The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI) |
title_short |
The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI) |
title_full |
The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI) |
title_fullStr |
The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI) |
title_full_unstemmed |
The Electrochemical Behaviour of Quaternary Amine-Based Room-Temperature Ionic Liquid N4111(TFSI) |
title_sort |
electrochemical behaviour of quaternary amine-based room-temperature ionic liquid n4111(tfsi) |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/f3867e6d6a114e49b83b89bc196c66df |
work_keys_str_mv |
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