2010
DOI: 10.1002/adma.200902148
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Recent Advances in White Organic Light‐Emitting Materials and Devices (WOLEDs)

Abstract: WOLEDs offer new design opportunities in practical solid-state lighting and could play a significant role in reducing global energy consumption. Obtaining white light from organic LEDs is a considerable challenge. Alongside the development of new materials with improved color stability and balanced charge transport properties, major issues involve the fabrication of large-area devices and the development of low-cost manufacturing technology. This Review will describe the types of materials (small molecules and… Show more

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Cited by 1,005 publications
(630 citation statements)
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References 83 publications
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“…1/τ q =k r +k nr +k q (2) where, k q is the concentration quenching rate, which was evaluated by subtracting the decay rate of 0.01% complex:zeonex (eq. 1) from the decay rate of 12% complex:zeonex (eq.…”
Section: Resultsmentioning
confidence: 99%
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“…1/τ q =k r +k nr +k q (2) where, k q is the concentration quenching rate, which was evaluated by subtracting the decay rate of 0.01% complex:zeonex (eq. 1) from the decay rate of 12% complex:zeonex (eq.…”
Section: Resultsmentioning
confidence: 99%
“…2,3 Phosphorescent cyclometalated complexes provide improved electroluminescence efficiencies by utilizing both triplet and singlet electroexcitation pathways. They have the benefits of relatively short excited state lifetimes, high photoluminescence efficiency, good color tuneability and general thermal and electrochemical stability.…”
Section: Introductionmentioning
confidence: 99%
“…Interestingly, stronger absorptions of 1 and 2 were observed in the region of 1 MLCT than that of the reference FIrpic, which implies the presence of significant singlettriplet coupling due to strong spin-orbit coupling in both compounds. The emission patterns of the two compounds are very similar to each other, but the emission maximum of 2 is blue-shifted by 2-3 nm relative to that of 1.…”
Section: Mlctmentioning
confidence: 93%
“…The residue was purified by column chromatography (CH 2 Cl 2 , R f = 0.85) to give 46% yield of solid product. 1 13 Synthesis of Fac-Tris(2 0 ,6 0 -Diisopropoxy-4-tert-Butyl-2,3 0 -Bipyridinato-N,C 4 )Ir(III) (2): The product was prepared using the same procedure of 1 except that 2 0 ,6 0 -diisopropoxy-4-tert-butyl-2,3 0 -bipyridine was used instead of 2 0 ,6 0 -diisopropoxy-2,3 0 -bipyridine. Yield: 42% (CH 2 Cl 2 , …”
Section: Methodsmentioning
confidence: 99%
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