The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents

The oxidation of hydrogen was studied at an activated platinum micro-electrode by cyclic voltammetry in the following ionic liquids: [C2mim][NTf2], [C4mim][NTf2], [N6,2,2,2][NTf2], [P14,6,6,6][NTf2], [C4mim][OTf], [C4mim][BF4], [C4mim][PF6], [C4mim][NO3], [C6mim]Cl and [C6mim][FAP] (where [Cnmim]+=...

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Main Authors: Silvester, Debbie, Ward, K., Aldous, L., Hardacre, C., Compton, R.
Format: Journal Article
Published: Elsevier 2008
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/30625
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author Silvester, Debbie
Ward, K.
Aldous, L.
Hardacre, C.
Compton, R.
author_facet Silvester, Debbie
Ward, K.
Aldous, L.
Hardacre, C.
Compton, R.
author_sort Silvester, Debbie
building Curtin Institutional Repository
collection Online Access
description The oxidation of hydrogen was studied at an activated platinum micro-electrode by cyclic voltammetry in the following ionic liquids: [C2mim][NTf2], [C4mim][NTf2], [N6,2,2,2][NTf2], [P14,6,6,6][NTf2], [C4mim][OTf], [C4mim][BF4], [C4mim][PF6], [C4mim][NO3], [C6mim]Cl and [C6mim][FAP] (where [Cnmim]+= 1-alkyl-3-methylimidazolium, [N6;2;2;2]+=n-hexyltriethylammonium, [P14;6;6;6]+= tris(n-hexyltetradecyl)phosphonium; [NTf2]-= bis(trifluoromethylsulfonyl)amide, [OTf]-= trifluoromethlysulfonate and [FAP]-= tris(perfluoroethyl)trifluorophosphate. Activation of the Pt electrode was necessary to obtain reliable and reproducible voltammetry. After activation of the electrode, the H2 oxidation waves were nearly electrochemically and chemically reversible in [Cnmim][NTf2] ionic liquids, chemically irreversible in [C6mim]Cl and [C4mim][NO3], and showed intermediate characteristics in OTf, [BF4]-, [PF6]-, [FAP]- and other [NTf2]- -based ionic liquids. These differences reflect the contrasting interactions of protons with the respective RTIL anions. The oxidation peaks are reported relative to the half-wave potential of the cobaltocenium/cobaltocene redox couple in all ionic liquids studied, giving an indication of the relative proton interactions of each ionic liquid. A preliminary temperature study (ca. 298–333 K) has also been carried out in some of the ionic liquids.Diffusion coefficients and solubilities of hydrogen at 298 K were obtained from potential-step chronoamperometry, and there was no relationship found between the diffusion coefficients and solvent viscosity. RTILs possessing [NTf2]- and [FAP]− anions showed the highest micro-electrodepeak currents for the oxidation in H2 saturated solutions, with [C4mim][NTf2] being the most sensitive. The large number of available RTIL anion/cation pairs allows scope for the possible electrochemical detection of hydrogen gas for use in gas sensor technology.
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spelling curtin-20.500.11937-306252019-02-19T04:28:02Z The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents Silvester, Debbie Ward, K. Aldous, L. Hardacre, C. Compton, R. Room temperature ionic liquids Electrochemical oxidation Hydrogen Cyclic voltammetry The oxidation of hydrogen was studied at an activated platinum micro-electrode by cyclic voltammetry in the following ionic liquids: [C2mim][NTf2], [C4mim][NTf2], [N6,2,2,2][NTf2], [P14,6,6,6][NTf2], [C4mim][OTf], [C4mim][BF4], [C4mim][PF6], [C4mim][NO3], [C6mim]Cl and [C6mim][FAP] (where [Cnmim]+= 1-alkyl-3-methylimidazolium, [N6;2;2;2]+=n-hexyltriethylammonium, [P14;6;6;6]+= tris(n-hexyltetradecyl)phosphonium; [NTf2]-= bis(trifluoromethylsulfonyl)amide, [OTf]-= trifluoromethlysulfonate and [FAP]-= tris(perfluoroethyl)trifluorophosphate. Activation of the Pt electrode was necessary to obtain reliable and reproducible voltammetry. After activation of the electrode, the H2 oxidation waves were nearly electrochemically and chemically reversible in [Cnmim][NTf2] ionic liquids, chemically irreversible in [C6mim]Cl and [C4mim][NO3], and showed intermediate characteristics in OTf, [BF4]-, [PF6]-, [FAP]- and other [NTf2]- -based ionic liquids. These differences reflect the contrasting interactions of protons with the respective RTIL anions. The oxidation peaks are reported relative to the half-wave potential of the cobaltocenium/cobaltocene redox couple in all ionic liquids studied, giving an indication of the relative proton interactions of each ionic liquid. A preliminary temperature study (ca. 298–333 K) has also been carried out in some of the ionic liquids.Diffusion coefficients and solubilities of hydrogen at 298 K were obtained from potential-step chronoamperometry, and there was no relationship found between the diffusion coefficients and solvent viscosity. RTILs possessing [NTf2]- and [FAP]− anions showed the highest micro-electrodepeak currents for the oxidation in H2 saturated solutions, with [C4mim][NTf2] being the most sensitive. The large number of available RTIL anion/cation pairs allows scope for the possible electrochemical detection of hydrogen gas for use in gas sensor technology. 2008 Journal Article http://hdl.handle.net/20.500.11937/30625 10.1016/j.jelechem.2008.02.018 Elsevier fulltext
spellingShingle Room temperature ionic liquids
Electrochemical oxidation
Hydrogen
Cyclic voltammetry
Silvester, Debbie
Ward, K.
Aldous, L.
Hardacre, C.
Compton, R.
The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
title The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
title_full The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
title_fullStr The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
title_full_unstemmed The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
title_short The electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
title_sort electrochemical oxidation of hydrogen at activated platinum electrodes in room temperature ionic liquids as solvents
topic Room temperature ionic liquids
Electrochemical oxidation
Hydrogen
Cyclic voltammetry
url http://hdl.handle.net/20.500.11937/30625