Nothing Special   »   [go: up one dir, main page]

Lee et al., 2011 - Google Patents

Effect of main ligands on organic photovoltaic performance of Ir (III) complexes

Lee et al., 2011

View PDF
Document ID
2345880305253027341
Author
Lee W
Kwon T
Kwon J
Kim J
Lee C
Hong J
Publication year
Publication venue
New Journal of Chemistry

External Links

Snippet

The photovoltaic performance of devices fabricated using three iridium complexes (1, 2, and 3) containing different main ligands (1-phenylisoquinoline,(4-isoquinolin-1-yl-phenyl) diphenylamine, and 1-pyren-1-yl-isoquinoline for 1, 2, and 3, respectively) was investigated …
Continue reading at hosting01.snu.ac.kr (PDF) (other versions)

Classifications

    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0084Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • H01L51/0085Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0084Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • H01L51/0087Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising platinum
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/50Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];
    • H01L51/5012Electroluminescent [EL] layer
    • H01L51/5016Triplet emission
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • 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
    • H01L51/0071Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0079Metal complexes comprising a IIIB-metal (B, Al, Ga, In or TI), e.g. Tris (8-hydroxyquinoline) gallium (Gaq3)
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/549Material technologies organic PV cells
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1044Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
    • C07F15/0033Iridium compounds

Similar Documents

Publication Publication Date Title
Tang et al. Molecular Design of Luminescent Gold (III) Emitters as Thermally Evaporable and Solution-Processable Organic Light-Emitting Device (OLED) Materials: Focus Review
Zhao et al. EQE climbing over 6% at high brightness of 14350 cd/m2 in deep-blue OLEDs based on hybridized local and charge-transfer fluorescence
Xu et al. Recent progress in metal–organic complexes for optoelectronic applications
Ho et al. Phosphorescence Color Tuning by Ligand, and Substituent Effects of Multifunctional Iridium (III) Cyclometalates with 9‐Arylcarbazole Moieties
Fan et al. Phosphoryl/sulfonyl-substituted iridium complexes as blue phosphorescent emitters for single-layer blue and white organic light-emitting diodes by solution process
US8258297B2 (en) Transition metal complexes with bridged carbene ligands and use thereof in OLEDs
Sun et al. Highly efficient deep-red organic light-emitting devices based on asymmetric iridium (iii) complexes with the thianthrene 5, 5, 10, 10-tetraoxide moiety
Cao et al. Iridium (III) complexes adopting 1, 2-diphenyl-1 H-benzoimidazole ligands for highly efficient organic light-emitting diodes with low efficiency roll-off and non-doped feature
He et al. Nonconjugated carbazoles: a series of novel host materials for highly efficient blue electrophosphorescent OLEDs
Lai et al. Gold (III) corroles for high performance organic solar cells
Beucher et al. Highly efficient green solution processable organic light-emitting diodes based on a phosphorescent κ3-(N^ C^ C) gold (iii)-alkynyl complex
Au Organic light-emitting diodes based on luminescent self-assembled materials of copper (I)
Wang et al. Self-host blue-emitting iridium dendrimer containing bipolar dendrons for nondoped electrophosphorescent devices with superior high-brightness performance
CN1973386A (en) Heavy metal complexes for organic photosensitive devices
Park et al. Synthesis, characterization of the phenylquinoline-based on iridium (III) complexes for solution processable phosphorescent organic light-emitting diodes
Ku et al. Spiro‐Configured Bipolar Host Materials for Highly Efficient Electrophosphorescent Devices
Jou et al. Solution-process-feasible deep-red phosphorescent emitter
Ren et al. A yellow-emitting homoleptic iridium (III) complex constructed from a multifunctional spiro ligand for highly efficient phosphorescent organic light-emitting diodes
Mao et al. Achieving high performances of nondoped OLEDs using carbazole and diphenylphosphoryl-functionalized Ir (III) complexes as active components
You et al. Rigid phenanthro [4, 5-abc] phenazine-cored iridium (III) complexes for high-performance near-infrared emission at about 800 nm in solution-processed OLEDs
Li et al. Phosphorescent tetradentate platinum (II) complexes containing fused 6/5/5 or 6/5/6 metallocycles
Lee et al. Effect of main ligands on organic photovoltaic performance of Ir (III) complexes
Cui et al. A rational molecular design on choosing suitable spacer for better host materials in highly efficient blue and white phosphorescent organic light-emitting diodes
Huh et al. Control of the horizontal dipole ratio and emission color of deep blue tetradentate Pt (II) complexes using aliphatic spacer groups
Ding et al. Saturated red phosphorescent Iridium (III) complexes containing phenylquinoline ligands for efficient organic light-emitting diodes