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Shakutsui et al., 2009 - Google Patents

Improved efficiency of polymer light-emitting diodes by inserting a hole transport layer formed without thermal treatment above glass transition temperature

Shakutsui et al., 2009

Document ID
7970505338809296170
Author
Shakutsui M
Matsuura H
Fujita K
Publication year
Publication venue
Organic Electronics

External Links

Snippet

We have demonstrated a significant improvement in the performance of polymer light- emitting diodes (PLEDs) by inserting the fluorene-triatylamine copolymer as hole transport layer (HTL) without a thermal treatment above the glass transition temperature (Tg). A thin …
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    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0034Organic polymers or oligomers
    • H01L51/0035Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
    • H01L51/0039Polyeflurorene and derivatives
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    • H01L51/0034Organic polymers or oligomers
    • H01L51/0035Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
    • H01L51/0038Poly-phenylenevinylene and derivatives
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    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
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    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0059Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
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