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Preparation of surface-tethered polymer layer on inorganic substrates by photoreactive self-assembled monolayer

Identifieur interne : 000053 ( Main/Repository ); précédent : 000052; suivant : 000054

Preparation of surface-tethered polymer layer on inorganic substrates by photoreactive self-assembled monolayer

Auteurs : RBID : Pascal:14-0091084

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English descriptors

Abstract

A self-assembled monolayer (SAM) that has benzophenone (BP) terminal group was prepared on Si and indium-tin oxide (ITO) substrates, on which poly(9-vinyl carbazol) (PVK) was spin-coated and then irradiated with ultraviolet (UV) light. Upon UV irradiation, the BP unit reacted with the PVK backbone, yielding a crosslinked PVK layer that was covalently tethered to the substrate surface. Using this procedure, a patterned thin film of PVK was obtained by irradiating UV light through a photomask and then rinsing in chloroform. When polystylene (PSt) was spin-coated on the BP-SAM, only a thin interfacial layer was tethered by UV irradiation because PSt does not crosslink upon UV irradiation. The BP-SAM improved the adhesion strength between the PVK layer and ITO substrate without reducing the carrier injection from ITO to PVK. The photoreactive BP-SAM appeared to be an effective method to improve the interface between an inorganic electrode and a polymer layer deposited on its surface.

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Pascal:14-0091084

Le document en format XML

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<name sortKey="Usui, Hiroaki" uniqKey="Usui H">Hiroaki Usui</name>
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<term>Indium oxide</term>
<term>Interfaces</term>
<term>Mechanical properties</term>
<term>Patterning</term>
<term>Polymers</term>
<term>Radiation effects</term>
<term>Self-assembled layers</term>
<term>Spin-on coating</term>
<term>Surface treatments</term>
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<term>Tribology</term>
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<term>Traitement surface</term>
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<term>Oxyde d'étain</term>
<term>Dépôt centrifugation</term>
<term>Effet rayonnement</term>
<term>Couche mince</term>
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<term>Adhérence</term>
<term>Tribologie</term>
<term>Propriété mécanique</term>
<term>Interface</term>
<term>Polymère</term>
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<term>Substrat polymère</term>
<term>Substrat silicium</term>
<term>Substrat indium</term>
<term>Substrat InSnO</term>
<term>Substrat oxyde d'indium et de zinc</term>
<term>6180</term>
<term>6860B</term>
<term>8116R</term>
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<div type="abstract" xml:lang="en">A self-assembled monolayer (SAM) that has benzophenone (BP) terminal group was prepared on Si and indium-tin oxide (ITO) substrates, on which poly(9-vinyl carbazol) (PVK) was spin-coated and then irradiated with ultraviolet (UV) light. Upon UV irradiation, the BP unit reacted with the PVK backbone, yielding a crosslinked PVK layer that was covalently tethered to the substrate surface. Using this procedure, a patterned thin film of PVK was obtained by irradiating UV light through a photomask and then rinsing in chloroform. When polystylene (PSt) was spin-coated on the BP-SAM, only a thin interfacial layer was tethered by UV irradiation because PSt does not crosslink upon UV irradiation. The BP-SAM improved the adhesion strength between the PVK layer and ITO substrate without reducing the carrier injection from ITO to PVK. The photoreactive BP-SAM appeared to be an effective method to improve the interface between an inorganic electrode and a polymer layer deposited on its surface.</div>
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<s0>A self-assembled monolayer (SAM) that has benzophenone (BP) terminal group was prepared on Si and indium-tin oxide (ITO) substrates, on which poly(9-vinyl carbazol) (PVK) was spin-coated and then irradiated with ultraviolet (UV) light. Upon UV irradiation, the BP unit reacted with the PVK backbone, yielding a crosslinked PVK layer that was covalently tethered to the substrate surface. Using this procedure, a patterned thin film of PVK was obtained by irradiating UV light through a photomask and then rinsing in chloroform. When polystylene (PSt) was spin-coated on the BP-SAM, only a thin interfacial layer was tethered by UV irradiation because PSt does not crosslink upon UV irradiation. The BP-SAM improved the adhesion strength between the PVK layer and ITO substrate without reducing the carrier injection from ITO to PVK. The photoreactive BP-SAM appeared to be an effective method to improve the interface between an inorganic electrode and a polymer layer deposited on its surface.</s0>
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