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Charge Storage Properties of Nanostructured Poly (3,4–ethylenedioxythiophene) Electrodes Revealed by Advanced Electrogravimetry
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Zeitschriftentitel: | Nanomaterials |
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Personen und Körperschaften: | , , , , , , |
In: | Nanomaterials, 9, 2019, 7, S. 962 |
Format: | E-Article |
Sprache: | Englisch |
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MDPI AG
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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 |
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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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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 |