In situ investigations of electrogenerated polybithiophene film growth on indium tin oxide substrate using optical fixed-angle reflectometry
Identifieur interne : 001A23 ( Main/Repository ); précédent : 001A22; suivant : 001A24In situ investigations of electrogenerated polybithiophene film growth on indium tin oxide substrate using optical fixed-angle reflectometry
Auteurs : RBID : Pascal:13-0160954Descripteurs français
- Pascal (Inist)
- Wicri :
- geographic : Valence (Drôme).
- concept : Dopage.
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Abstract
Electrochemical synthesis of polybithiophene films onto indium tin oxide was monitored by optical fixed-angle reflectometry in situ. Deposition was done in acetonitrile with NBu4PF6 as the supporting electrolyte at a scan rate of 100 mV.s-1 using cyclic voltammetry. A correlation between the reflectometric output and the current density was observed. A mechanism to explain the shape of the reflectometric signal was proposed, based on ionic species motion (doping/undoping) and the state of oxidation of the film. The effects of several physico-chemical parameters were recorded. A low adsorbed amount of film was obtained when the monomer solution was injected when compared with electropolymerization in static conditions. Conversely, an increase in bithiophene concentration or a reduction in scan rate at 50 mV.s-1 leads to thicker film. Finally a special reflectometric output was monitored when LiClO4 was employed as supporting electrolyte.
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Pascal:13-0160954Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">In situ investigations of electrogenerated polybithiophene film growth on indium tin oxide substrate using optical fixed-angle reflectometry</title>
<author><name sortKey="Monnin, Alexandra F" uniqKey="Monnin A">Alexandra F. Monnin</name>
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<author><name sortKey="Buron, Cedric C" uniqKey="Buron C">Cedric C. Buron</name>
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<author><name sortKey="Guyard, Laurent" uniqKey="Guyard L">Laurent Guyard</name>
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<author><name sortKey="Filiatre, Claudine" uniqKey="Filiatre C">Claudine Filiatre</name>
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<s2>25030 Besançon</s2>
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<term>Cyclic voltammetry</term>
<term>Doping</term>
<term>Electrochemical method</term>
<term>Electrodeposition</term>
<term>Electrolytes</term>
<term>Film growth</term>
<term>Indium oxide</term>
<term>Monomers</term>
<term>Reflectometry</term>
<term>Thin films</term>
<term>Tin oxide</term>
<term>Valence</term>
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<term>Réflectométrie</term>
<term>Couche mince</term>
<term>Acétonitrile</term>
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<term>Voltammétrie cyclique</term>
<term>Densité courant</term>
<term>Dopage</term>
<term>Valence</term>
<term>Monomère</term>
<term>Méthode électrochimique</term>
<term>Dépôt électrolytique</term>
<term>Oxyde d'indium</term>
<term>Oxyde d'étain</term>
<term>Substrat oxyde d'indium et de zinc</term>
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<front><div type="abstract" xml:lang="en">Electrochemical synthesis of polybithiophene films onto indium tin oxide was monitored by optical fixed-angle reflectometry in situ. Deposition was done in acetonitrile with NBu<sub>4</sub>
PF<sub>6</sub>
as the supporting electrolyte at a scan rate of 100 mV.s<sup>-1</sup>
using cyclic voltammetry. A correlation between the reflectometric output and the current density was observed. A mechanism to explain the shape of the reflectometric signal was proposed, based on ionic species motion (doping/undoping) and the state of oxidation of the film. The effects of several physico-chemical parameters were recorded. A low adsorbed amount of film was obtained when the monomer solution was injected when compared with electropolymerization in static conditions. Conversely, an increase in bithiophene concentration or a reduction in scan rate at 50 mV.s<sup>-1</sup>
leads to thicker film. Finally a special reflectometric output was monitored when LiClO<sub>4</sub>
was employed as supporting electrolyte.</div>
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<fA11 i1="01" i2="1"><s1>MONNIN (Alexandra F.)</s1>
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<fA11 i1="02" i2="1"><s1>BURON (Cedric C.)</s1>
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<fA14 i1="01"><s1>Institut UTINAM, UMR CNRS 6213, Université de Franche-Comté, 16, Route de Gray</s1>
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<sZ>1 aut.</sZ>
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PF<sub>6</sub>
as the supporting electrolyte at a scan rate of 100 mV.s<sup>-1</sup>
using cyclic voltammetry. A correlation between the reflectometric output and the current density was observed. A mechanism to explain the shape of the reflectometric signal was proposed, based on ionic species motion (doping/undoping) and the state of oxidation of the film. The effects of several physico-chemical parameters were recorded. A low adsorbed amount of film was obtained when the monomer solution was injected when compared with electropolymerization in static conditions. Conversely, an increase in bithiophene concentration or a reduction in scan rate at 50 mV.s<sup>-1</sup>
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<s5>16</s5>
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<fC03 i1="15" i2="3" l="FRE"><s0>Substrat oxyde d'indium et de zinc</s0>
<s4>INC</s4>
<s5>46</s5>
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<fC03 i1="16" i2="3" l="FRE"><s0>LiClO4</s0>
<s4>INC</s4>
<s5>47</s5>
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<fC03 i1="17" i2="3" l="FRE"><s0>6855J</s0>
<s4>INC</s4>
<s5>65</s5>
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<s4>INC</s4>
<s5>71</s5>
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