author_facet Lé, Tao
Aradilla, David
Bidan, Gérard
Billon, Florence
Debiemme-Chouvy, Catherine
Perrot, Hubert
Sel, Ozlem
Lé, Tao
Aradilla, David
Bidan, Gérard
Billon, Florence
Debiemme-Chouvy, Catherine
Perrot, Hubert
Sel, Ozlem
author Lé, Tao
Aradilla, David
Bidan, Gérard
Billon, Florence
Debiemme-Chouvy, Catherine
Perrot, Hubert
Sel, Ozlem
spellingShingle Lé, Tao
Aradilla, David
Bidan, Gérard
Billon, Florence
Debiemme-Chouvy, Catherine
Perrot, Hubert
Sel, Ozlem
Nanomaterials
Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
General Materials Science
General Chemical Engineering
author_sort lé, tao
spelling Lé, Tao Aradilla, David Bidan, Gérard Billon, Florence Debiemme-Chouvy, Catherine Perrot, Hubert Sel, Ozlem 2079-4991 MDPI AG General Materials Science General Chemical Engineering http://dx.doi.org/10.3390/nano9070962 <jats:p>PEDOT nanowires (NWs) directly grown on the conducting electrode of quartz resonators enable an advanced electrogravimetric analysis of their charge storage behavior. Electrochemical quartz crystal microbalance (EQCM) and its coupling with electrochemical impedance spectroscopy (ac–electrogravimetry or AC–EG) were used complementarily and reveal that TBA+, BF4− and ACN participate in the charge compensation process with different kinetics and quantity. BF4− anions were dominant in terms of concentration over TBA+ cations and the anion transfer results in the exclusion of the solvent molecules. TBA+ concentration variation in the electrode was small compared to that of the BF4− counterpart. However, Mw of TBA+ is much higher than BF4− (242.3 vs. 86.6 g·mol−1). Thus, TBA+ cations’ gravimetric contribution to the EQCM response was more significant than that of BF4−. Additional contribution of ACN with an opposite flux direction compared with BF4−, led to a net mass gain/lost during a negative/positive potential scan, masking partially the anion response. Such subtleties of the interfacial ion transfer processes were disentangled due to the complementarity of the EQCM and AC–EG methodologies, which were applied here for the characterization of electrochemical processes at the PEDOT NW electrode/organic electrolyte interface.</jats:p> Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry Nanomaterials
doi_str_mv 10.3390/nano9070962
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source_id 49
title Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_unstemmed Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_full Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_fullStr Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_full_unstemmed Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_short Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_sort charge storage properties of nanostructured poly (3,4–ethylenedioxythiophene) electrodes revealed by advanced electrogravimetry
topic General Materials Science
General Chemical Engineering
url http://dx.doi.org/10.3390/nano9070962
publishDate 2019
physical 962
description <jats:p>PEDOT nanowires (NWs) directly grown on the conducting electrode of quartz resonators enable an advanced electrogravimetric analysis of their charge storage behavior. Electrochemical quartz crystal microbalance (EQCM) and its coupling with electrochemical impedance spectroscopy (ac–electrogravimetry or AC–EG) were used complementarily and reveal that TBA+, BF4− and ACN participate in the charge compensation process with different kinetics and quantity. BF4− anions were dominant in terms of concentration over TBA+ cations and the anion transfer results in the exclusion of the solvent molecules. TBA+ concentration variation in the electrode was small compared to that of the BF4− counterpart. However, Mw of TBA+ is much higher than BF4− (242.3 vs. 86.6 g·mol−1). Thus, TBA+ cations’ gravimetric contribution to the EQCM response was more significant than that of BF4−. Additional contribution of ACN with an opposite flux direction compared with BF4−, led to a net mass gain/lost during a negative/positive potential scan, masking partially the anion response. Such subtleties of the interfacial ion transfer processes were disentangled due to the complementarity of the EQCM and AC–EG methodologies, which were applied here for the characterization of electrochemical processes at the PEDOT NW electrode/organic electrolyte interface.</jats:p>
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author Lé, Tao, Aradilla, David, Bidan, Gérard, Billon, Florence, Debiemme-Chouvy, Catherine, Perrot, Hubert, Sel, Ozlem
author_facet Lé, Tao, Aradilla, David, Bidan, Gérard, Billon, Florence, Debiemme-Chouvy, Catherine, Perrot, Hubert, Sel, Ozlem, Lé, Tao, Aradilla, David, Bidan, Gérard, Billon, Florence, Debiemme-Chouvy, Catherine, Perrot, Hubert, Sel, Ozlem
author_sort lé, tao
container_issue 7
container_start_page 0
container_title Nanomaterials
container_volume 9
description <jats:p>PEDOT nanowires (NWs) directly grown on the conducting electrode of quartz resonators enable an advanced electrogravimetric analysis of their charge storage behavior. Electrochemical quartz crystal microbalance (EQCM) and its coupling with electrochemical impedance spectroscopy (ac–electrogravimetry or AC–EG) were used complementarily and reveal that TBA+, BF4− and ACN participate in the charge compensation process with different kinetics and quantity. BF4− anions were dominant in terms of concentration over TBA+ cations and the anion transfer results in the exclusion of the solvent molecules. TBA+ concentration variation in the electrode was small compared to that of the BF4− counterpart. However, Mw of TBA+ is much higher than BF4− (242.3 vs. 86.6 g·mol−1). Thus, TBA+ cations’ gravimetric contribution to the EQCM response was more significant than that of BF4−. Additional contribution of ACN with an opposite flux direction compared with BF4−, led to a net mass gain/lost during a negative/positive potential scan, masking partially the anion response. Such subtleties of the interfacial ion transfer processes were disentangled due to the complementarity of the EQCM and AC–EG methodologies, which were applied here for the characterization of electrochemical processes at the PEDOT NW electrode/organic electrolyte interface.</jats:p>
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spelling Lé, Tao Aradilla, David Bidan, Gérard Billon, Florence Debiemme-Chouvy, Catherine Perrot, Hubert Sel, Ozlem 2079-4991 MDPI AG General Materials Science General Chemical Engineering http://dx.doi.org/10.3390/nano9070962 <jats:p>PEDOT nanowires (NWs) directly grown on the conducting electrode of quartz resonators enable an advanced electrogravimetric analysis of their charge storage behavior. Electrochemical quartz crystal microbalance (EQCM) and its coupling with electrochemical impedance spectroscopy (ac–electrogravimetry or AC–EG) were used complementarily and reveal that TBA+, BF4− and ACN participate in the charge compensation process with different kinetics and quantity. BF4− anions were dominant in terms of concentration over TBA+ cations and the anion transfer results in the exclusion of the solvent molecules. TBA+ concentration variation in the electrode was small compared to that of the BF4− counterpart. However, Mw of TBA+ is much higher than BF4− (242.3 vs. 86.6 g·mol−1). Thus, TBA+ cations’ gravimetric contribution to the EQCM response was more significant than that of BF4−. Additional contribution of ACN with an opposite flux direction compared with BF4−, led to a net mass gain/lost during a negative/positive potential scan, masking partially the anion response. Such subtleties of the interfacial ion transfer processes were disentangled due to the complementarity of the EQCM and AC–EG methodologies, which were applied here for the characterization of electrochemical processes at the PEDOT NW electrode/organic electrolyte interface.</jats:p> Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry Nanomaterials
spellingShingle Lé, Tao, Aradilla, David, Bidan, Gérard, Billon, Florence, Debiemme-Chouvy, Catherine, Perrot, Hubert, Sel, Ozlem, Nanomaterials, Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry, General Materials Science, General Chemical Engineering
title Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_full Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_fullStr Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_full_unstemmed Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_short Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
title_sort charge storage properties of nanostructured poly (3,4–ethylenedioxythiophene) electrodes revealed by advanced electrogravimetry
title_unstemmed Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
topic General Materials Science, General Chemical Engineering
url http://dx.doi.org/10.3390/nano9070962