sameAs
P184
Identification of a quenching species in ruthenium tris-bipyridine electroluminescent devices.Tuning the electronic coupling in a low-bandgap donor-acceptor copolymer via the placement of side-chains.An Efficient, "Burn in" Free Organic Solar Cell Employing a Nonfullerene Electron Acceptor.High-Performance Flexible Bottom-Gate Organic Field-Effect Transistors with Gravure Printed Thin Organic Dielectric.Comparing blends and blocks: Synthesis of partially fluorinated diblock polythiophene copolymers to investigate the thermal stability of optical and morphological propertiesSpectroscopic properties of poly(9,9-dioctylfluorene) thin films possessing varied fractions of β-phase chain segments: enhanced photoluminescence efficiency via conformation structuringA characterization of the Raman modes in a J-aggregate-forming dye: a comparison between theory and experiment.Work function engineering of ZnO electrodes by using p-type and n-type doped carbon nanotubes.Controlling microstructure of pentacene derivatives by solution processing: impact of structural anisotropy on optoelectronic properties.Highly efficient red-emitting hybrid polymer light-emitting diodes via Förster resonance energy transfer based on homogeneous polymer blends with the same polyfluorene backbone.Charge-transfer character of excitons in poly[2,7-(9,9-di-n-octylfluorene)(1-x)-co-4,7-(2,1,3-benzothiadiazole)(x)].Influence of Backbone Fluorination in Regioregular Poly(3-alkyl-4-fluoro)thiophenes.Exciplex emission from electroluminescent ladder-type pentaphenylene oligomers bearing both electron- and hole-accepting substituents.Optoelectronic and charge transport properties at organic-organic semiconductor interfaces: comparison between polyfluorene-based polymer blend and copolymer.High-Efficiency Polymer LEDs with Fast Response Times Fabricated via Selection of Electron-Injecting Conjugated Polyelectrolyte Backbone Structure.Highly efficient inverted polymer light-emitting diodes using surface modifications of ZnO layer.Uniaxial alignment of liquid-crystalline conjugated polymers by nanoconfinement.Interfacial Chemical Composition and Molecular Order in Organic Photovoltaic Blend Thin Films Probed by Surface-Enhanced Raman Spectroscopy.Quantitative bioluminescence imaging of transgene expression in vivo.Effects of packing structure on the optoelectronic and charge transport properties in poly(9,9-di-n-octylfluorene-alt-benzothiadiazole).Performance enhancement of fullerene-based solar cells by light processing.Controlling Molecular Conformation for Highly Efficient and Stable Deep-Blue Copolymer Light-Emitting Diodes.In situ formation of organic-inorganic hybrid nanostructures for photovoltaic applications.Operational electrochemical stability of thiophene-thiazole copolymers probed by resonant Raman spectroscopy.Spectroscopy and single-molecule emission of a fluorene-terthiophene oligomer.High-crystalline medium-band-gap polymers consisting of benzodithiophene and benzotriazole derivatives for organic photovoltaic cells.Photo-stability study of a solution-processed small molecule solar cell system: correlation between molecular conformation and degradation.Charge mobility anisotropy of functionalized pentacenes in organic field effect transistors fabricated by solution processingImpact of Fullerene Intercalation on Structural and Thermal Properties of Organic Photovoltaic BlendsPhotochemical stability of high efficiency PTB7:PC70BM solar cell blendsOptimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells1 GHz Pentacene Diode Rectifiers Enabled by Controlled Film Deposition on SAM-Treated Au AnodesPolaron stability in semiconducting polymer neat filmsNatures of optical absorption transitions and excitation energy dependent photostability of diketopyrrolopyrrole (DPP)-based photovoltaic copolymersMolecular-scale interface engineering for polymer light-emitting diodesOrganic photovoltaics and energy: general discussionThin-film morphology of inkjet-printed single-droplet organic transistors using polarized Raman spectroscopy: effect of blending TIPS-pentacene with insulating polymerUnderstanding the Influence of Morphology on Poly(3-hexylselenothiophene):PCBM Solar CellsSystematic control of heteroatoms in donor–acceptor copolymers and its effects on molecular conformation and photovoltaic performanceEffects of Fluorination and Side Chain Branching on Molecular Conformation and Photovoltaic Performance of Donor–Acceptor Copolymers
P50
Q33246658-07E4E40E-E23C-4246-83DE-7E1BCFCC582CQ33853148-90A94A5E-B6C8-4AA8-BB47-0D288D73D3FDQ38705432-2F747292-D8B3-4D9A-B677-F290F9E1D039Q41325331-D6DB581A-D904-465F-980A-2E231375C92FQ41593477-892ED0EE-8F93-4465-9B0C-D25F78433E9DQ42316783-22CD0571-5DDD-44E5-9214-8F08C7BC5C58Q42859225-9FBE4AF3-67ED-4B5E-A2E5-E242EBA81A38Q44457061-186F1364-0F10-48EB-86EC-A2F3DCC7092BQ44597100-91138A8A-166A-440F-ABC7-D6DF19A19346Q45812394-31F53994-1A02-4D87-A10E-3CC5FC76164FQ45923207-0C7DC06B-C160-4564-9D59-9DBEE14C9250Q46726120-9E14804D-F10A-4EEA-BE68-B77D689E6A25Q46773409-88428897-B330-4759-8A09-3484C5D56EBAQ47366927-7904528D-CF7F-4906-BD25-BFD6D2207119Q50239348-85351EC3-1FDF-4828-8579-E8D74F4F3149Q50449845-76029360-3DA9-4063-B9C2-07C96F64A2D9Q51054507-68436566-E769-42D6-9B8D-05E2F6F01BB0Q51108949-6EED1D16-0C9B-48CD-B0D1-F58EF4A0DC8DQ51189701-2A647ABB-DF54-4B84-BBDB-33DDE18B5D11Q51355957-47C869F5-9349-4F35-AB4D-5386D6E83D2AQ51795035-4F8B6054-D9D1-47A8-A647-EBB948567FAEQ52366055-169F4677-7888-4849-A118-FA6C15615D22Q52654001-D726D3E1-86FB-461C-9817-DFC7E7EC94A4Q52661506-F7553C11-BF72-4468-B832-A420032DF6B5Q52727475-C8FF660F-B9D5-4FCD-A018-324BCB512E62Q54407769-465004F1-1D03-4D4A-ABAA-6A891D6587ADQ55303418-3250508A-B7D1-4091-A8BC-0E9E2140DA8BQ55881023-9F2AE5DB-CC05-437F-B210-E17700CF4C3FQ55932810-F2E28F23-99E6-41C5-8C62-E9002B8117A7Q56673034-00EABCF2-F3FB-4780-8B2F-A8630BB18B21Q56673035-54E62E65-AA59-4C30-A32E-54CD7779362CQ56673037-769DDA4B-C784-4B6C-8317-859157A9FF12Q56673038-04FDA5F2-DBC8-4ECC-AA6F-94A6E832FE5DQ56673040-BED6F868-FFE2-4181-9FAF-CF3D082B9AB1Q56772402-CB6E4CD5-5E7F-4C37-AFC3-6A2831F22719Q57086033-43AF7DC9-3C47-4325-ABE0-4F74BEA2C56AQ57128453-54F4F573-C759-4E0B-B2EC-FE2ACECF32DBQ57623218-533FDA5C-6A4E-4CD5-8A63-00D55C154A66Q58009900-12E6DBA2-47A1-4113-B53B-28C01B1D5857Q58009901-7B82565E-D5D5-4D2B-B3B2-B1F4321333CC
P50
description
científica surcoreana
@ast
hulumtuese
@sq
researcher
@en
wetenschapster uit Zuid-Korea
@nl
հետազոտող
@hy
name
Ji-Seon Kim
@en
Ji-Seon Kim
@nl
Ji-Seon Kim
@sl
Kim Ji-Seon
@es
Джі-Сеон Кім
@uk
ד"ר ג'י סיאון קים
@he
type
label
Ji-Seon Kim
@en
Ji-Seon Kim
@nl
Ji-Seon Kim
@sl
Kim Ji-Seon
@es
Джі-Сеон Кім
@uk
ד"ר ג'י סיאון קים
@he
altLabel
Ji-Seon Kim
@es
prefLabel
Ji-Seon Kim
@en
Ji-Seon Kim
@nl
Ji-Seon Kim
@sl
Kim Ji-Seon
@es
Джі-Сеон Кім
@uk
ד"ר ג'י סיאון קים
@he
P106
P166
P184
P185
P21
P31
P496
0000-0003-4715-3656
P569
1950-01-01T00:00:00Z