Thermally cross-linkable hyperbranched polymers containing triphenylamine moieties: Synthesis, curing and application in light-emitting diodes

This paper demonstrates synthesis of hyperbranched polymers ( HTP and HTPOCH 3 ), containing triphenylamine moieties in main chain and thermally cross-linkable periphery or terminal vinyl groups, and application as hole-transporting layer (HTL) in multilayer light-emitting diodes. Absorption and pho...

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Published inPolymer (Guilford) Vol. 51; no. 20; pp. 4484 - 4492
Main Authors Yu, Juin-Meng, Chen, Yun
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 17.09.2010
Elsevier
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Summary:This paper demonstrates synthesis of hyperbranched polymers ( HTP and HTPOCH 3 ), containing triphenylamine moieties in main chain and thermally cross-linkable periphery or terminal vinyl groups, and application as hole-transporting layer (HTL) in multilayer light-emitting diodes. Absorption and photoluminescence (PL) spectroscopy, cyclic voltammetry (CV) and differential scanning calorimetry (DSC) were employed to investigate their photophysical, electrochemical properties and thermal curing behaviors, respectively. The hyperbranched HTP and HTPOCH 3 were readily cross-linked by heating scan, with the exothermic peaks being at 221 and 210 °C respectively. The glass-transition temperatures ( T g ) of the hyperbranched polymers were higher than 140 °C after thermal cross-linking at 210 °C for 30 min. Multilayer light-emitting diodes (ITO/PEDOT:PSS/HTL/MEH-PPV/Ca/Al), using HTP and HTPOCH 3 as HTL, were readily fabricated by successive spin-coating. The performance of MEH-PPV device (maximum luminance: 9310 cd/m 2, luminance efficiency: 0.26 cd/A) was effectively enhanced by inserting the thermally cross-linked HTP or HTPOCH 3 as HTL ( HTP: 12610 cd/m 2, 0.32 cd/A; HTPOCH 3 : 14060 cd/m 2, 0.33 cd/A). This indicates that these thermally cross-linkable hyperbranched HTP and HTPOCH 3 are very suitable for the fabrication of multilayer PLEDs using solution processes. [Display omitted]
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2010.08.001