نتایج جستجو برای: carbon ionic liquid electrode
تعداد نتایج: 574837 فیلتر نتایج به سال:
A thermally chargeable capacitor containing a binary solution of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)-imide in acetonitrile is electrically charged by applying a temperature gradient to two ideally polarisable electrodes. The corresponding thermoelectric coefficient is -1.7 mV/K for platinum foil electrodes and -0.3 mV/K for nanoporous carbon electrodes. Stored electrical en...
Ionic actuators have attracted attention due to their remarkably large strain under low-voltage stimulation. Because actuation performance is mainly dominated by the electrochemical and electromechanical processes of the electrode layer, the electrode material and structure are crucial. Here, we report a graphitic carbon nitride nanosheet electrode-based ionic actuator that displays high electr...
A novel carbon paste electrode modified with ionic liquid (n-hexyl-3-methylimidazolium hexafluoro phosphate) and magnetic core-shell manganese ferrite nanoparticles (MCSILCPE) was fabricated. The electrochemical study of the modified electrode, as well as its efficiency for electro-oxidation of tryptophan, is described. Cyclic voltammetry (CV), choronoamperometry (CHA) and square wave voltammet...
A novel glassy carbon electrode modified by a gel containing multi-walled carbon nanotubes (MWNTs) and ionic liquid of 1-butyl-3-methylimidazolium hexafluorophosphate (BMIPF6) is reported. The gel is formed by grinding of MWNTs and BMIPF6. Such gel is then coated on the surface of a glassy carbon electrode. We have employed scanning electron microscopy, Fourier transform infrared spectrometry (...
Ionic liquids exhibit a remarkably diverse interfacial chemistry. Recent theoretical and experimental results show that conventional double layers do not form on metal electrodes in ionic liquid systems, rather a multilayer morphology is present. The number of layers and the strength of adsorption are strongly dependent on ionic liquid chemical species, solutes and applied electrode potential. ...
Ionic liquids exhibit a remarkably diverse interfacial chemistry. Recent theoretical and experimental results show that conventional double layers do not form on metal electrodes in ionic liquid systems, rather a multilayer morphology is present. The number of layers and the strength of adsorption are strongly dependent on ionic liquid chemical species, solutes and applied electrode potential. ...
Ionic liquids exhibit a remarkably diverse interfacial chemistry. Recent theoretical and experimental results show that conventional double layers do not form on metal electrodes in ionic liquid systems, rather a multilayer morphology is present. The number of layers and the strength of adsorption are strongly dependent on ionic liquid chemical species, solutes and applied electrode potential. ...
in this work, reactive absorption of gases in aqueous electrolyte solutions has been investigated resulting in the development of a procedure in order to calculate the concentrations of ionic and molecular species in the liquid phase. two duplicate experiments were conducted to investigate simultaneous reactive absorption of ammonia and carbon dioxide in partially carbonated ammonia solutions. ...
A long cycle-life, high-voltage supercapacitor featuring an activated carbon//poly(3methylthiophene) hybrid configuration with N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide ionic liquid, a solvent-free green electrolyte, was developed. The cyclability of a laboratory scale cell with electrode mass loading sized for practical uses was tested at 60 °C over 16,000 galvanostatic ...
The ionic liquid trihexyltetradecylphosphonium 1,2,4-triazolide, [P66614][124Triz], has been shown to chemisorb CO2 through equimolar binding of the carbon dioxide with the 1,2,4-triazolide anion. This leads to a possible new, low energy pathway for the electrochemical reduction of carbon dioxide to formate and syngas at low overpotentials, utilizing this reactive ionic liquid media. Herein, an...
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