Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence

The nature of chain aggregation in solution always results in variable spin-coated film mesoscale morphology and uncontrollable device performance. The abundant variety and increasing chemical complexity of conjugated polymers induced additional diverse electrostatic and dispersion interactions (non...

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Κύριοι συγγραφείς: Lin, J, Liu, B, Yu, M, Wang, X, Bai, L, Han, Y, Ou, C, Xie, L, Liu, F, Zhu, W, Zhang, X, Ling, H, Stavrinou, P, Wang, J, Bradley, D, Huang, W
Μορφή: Journal article
Έκδοση: Royal Society of Chemistry 2018
_version_ 1826270808525242368
author Lin, J
Liu, B
Yu, M
Wang, X
Bai, L
Han, Y
Ou, C
Xie, L
Liu, F
Zhu, W
Zhang, X
Ling, H
Stavrinou, P
Wang, J
Bradley, D
Huang, W
author_facet Lin, J
Liu, B
Yu, M
Wang, X
Bai, L
Han, Y
Ou, C
Xie, L
Liu, F
Zhu, W
Zhang, X
Ling, H
Stavrinou, P
Wang, J
Bradley, D
Huang, W
author_sort Lin, J
collection OXFORD
description The nature of chain aggregation in solution always results in variable spin-coated film mesoscale morphology and uncontrollable device performance. The abundant variety and increasing chemical complexity of conjugated polymers induced additional diverse electrostatic and dispersion interactions (non-covalent interactions), although it is not fully understood how the interplay of these forces results in the observed conformational order, chain aggregates and film morphologies. Herein, we present a precise study on the role of non-covalent interaction in the self-organization behavior, conformational order and optoelectrical properties of polyfluorene (PPFOH) toward tuning its electroluminescence (EL). The supramolecular PPFOH system consisted of an intrinsically doped hydrogen-bond-assisted microstructure as a "guest" and a blue light-emitting backbone chain as a "host", which show a special binary emissive property of solution-induced self-dopant formation in the amorphous films. As a result of a strong non-covalent interaction between polymer chains and solvent molecules (type II solvent), a likely distorted or fold chain in rod-coil or branch cluster shows a narrow and strong aggregation emission at 525-540 nm. Low-polar solvents (called type I) can also induce a shoulder low-energy emission at 550-580 nm in the films, attributed to the extended and stretched chain complex for the tendency of interchain hydrogen-bonding interaction. Further evidence from nanoscale infrared (AFM-IR) analysis confirmed the stronger hydrogen-bonding interaction in the type II films than those in the type I films. Finally, supramolecular PPFOH electroluminescence colours can be tuned from blue to sky blue, green, white, yellow and orange.
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spelling oxford-uuid:49d22cc3-3ca8-4b51-a297-b8091e0b4ac82022-03-26T15:33:59ZSystematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescenceJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:49d22cc3-3ca8-4b51-a297-b8091e0b4ac8Symplectic Elements at OxfordRoyal Society of Chemistry2018Lin, JLiu, BYu, MWang, XBai, LHan, YOu, CXie, LLiu, FZhu, WZhang, XLing, HStavrinou, PWang, JBradley, DHuang, WThe nature of chain aggregation in solution always results in variable spin-coated film mesoscale morphology and uncontrollable device performance. The abundant variety and increasing chemical complexity of conjugated polymers induced additional diverse electrostatic and dispersion interactions (non-covalent interactions), although it is not fully understood how the interplay of these forces results in the observed conformational order, chain aggregates and film morphologies. Herein, we present a precise study on the role of non-covalent interaction in the self-organization behavior, conformational order and optoelectrical properties of polyfluorene (PPFOH) toward tuning its electroluminescence (EL). The supramolecular PPFOH system consisted of an intrinsically doped hydrogen-bond-assisted microstructure as a "guest" and a blue light-emitting backbone chain as a "host", which show a special binary emissive property of solution-induced self-dopant formation in the amorphous films. As a result of a strong non-covalent interaction between polymer chains and solvent molecules (type II solvent), a likely distorted or fold chain in rod-coil or branch cluster shows a narrow and strong aggregation emission at 525-540 nm. Low-polar solvents (called type I) can also induce a shoulder low-energy emission at 550-580 nm in the films, attributed to the extended and stretched chain complex for the tendency of interchain hydrogen-bonding interaction. Further evidence from nanoscale infrared (AFM-IR) analysis confirmed the stronger hydrogen-bonding interaction in the type II films than those in the type I films. Finally, supramolecular PPFOH electroluminescence colours can be tuned from blue to sky blue, green, white, yellow and orange.
spellingShingle Lin, J
Liu, B
Yu, M
Wang, X
Bai, L
Han, Y
Ou, C
Xie, L
Liu, F
Zhu, W
Zhang, X
Ling, H
Stavrinou, P
Wang, J
Bradley, D
Huang, W
Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence
title Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence
title_full Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence
title_fullStr Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence
title_full_unstemmed Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence
title_short Systematic investigation of self-organization behavior in supramolecular π-conjugated polymer for multi-color electroluminescence
title_sort systematic investigation of self organization behavior in supramolecular π conjugated polymer for multi color electroluminescence
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