about
Axle length effect on photoinduced electron transfer in triad rotaxane with porphyrin, [60]fullerene, and triphenylamine.2-Phenylpyrimidine skeleton-based electron-transport materials for extremely efficient green organic light-emitting devices.Unique Solid-State Emission Behavior of Aromatic Difluoroboronated β-Diketones as an Emitter in Organic Light-Emitting Devices.A Novel Sterically Bulky Hole Transporter to Remarkably Improve the Lifetime of Thermally Activated Delayed Fluorescent OLEDs at High Brightness.High Power Efficiency Blue-to-Green Organic Light-Emitting Diodes Using Isonicotinonitrile-Based Fluorescent Emitters.Highly Luminescent π-Conjugated Terpyridine Derivatives Exhibiting Thermally Activated Delayed Fluorescence.Manipulating the Electronic Excited State Energies of Pyrimidine-Based Thermally Activated Delayed Fluorescence Emitters To Realize Efficient Deep-Blue Emission.A Series of Lithium Pyridyl Phenolate Complexes with a Pendant Pyridyl Group for Electron-Injection Layers in Organic Light-Emitting Devices.Blue thermally activated delayed fluorescence materials based on bis(phenylsulfonyl)benzene derivatives.Solution-processed multilayer small-molecule light-emitting devices with high-efficiency white-light emission.Instant low-temperature cross-linking of poly(N-vinylcarbazole) for solution-processed multilayer blue phosphorescent organic light-emitting devices.High-performance blue phosphorescent OLEDs using energy transfer from exciplex.High-Performance Green OLEDs Using Thermally Activated Delayed Fluorescence with a Power Efficiency of over 100 lm W(-1).3,3'-Bicarbazole-based host materials for high-efficiency blue phosphorescent OLEDs with extremely low driving voltage.Optimizing the charge balance of fluorescent organic light-emitting devices to achieve high external quantum efficiency beyond the conventional upper limit.Asymmetrical Squaraines Bearing Fluorine-Substituted Indoline Moieties for High-Performance Solution-Processed Small-Molecule Organic Solar Cells.Low-driving-voltage blue phosphorescent organic light-emitting devices with external quantum efficiency of 30%.High-efficiency blue and white organic light-emitting devices incorporating a blue iridium carbene complex.A single-molecule excimer-emitting compound for highly efficient fluorescent organic light-emitting devices.Novel four-pyridylbenzene-armed biphenyls as electron-transport materials for phosphorescent OLEDs.End-capping of a pseudorotaxane via Diels-Alder reaction for the construction of C60-terminated [2]rotaxanes.Chloroboron (III) subnaphthalocyanine as an electron donor in bulk heterojunction photovoltaic cells.A minimal non-radiative recombination loss for efficient non-fullerene all-small-molecule organic solar cells with a low energy loss of 0.54 eV and high open-circuit voltage of 1.15 VCo-evaporated bulk heterojunction solar cells with >6.0% efficiencyTuning energy levels of electron-transport materials by nitrogen orientation for electrophosphorescent devices with an 'ideal' operating voltageAxle charge effects on photoinduced electron transfer processes in rotaxanes containing porphyrin and [60]fullereneSolution-processed inorganic-organic hybrid electron injection layer for polymer light-emitting devicesSolution-processed organic photovoltaic cells based on a squaraine dyeRoom-Temperature Phosphorescence from a Series of 3-Pyridylcarbazole DerivativesColorful Squaraines Dyes for Efficient Solution-Processed All Small-Molecule Semitransparent Organic Solar CellsControl of Molecular Orientation in Organic Semiconductor Films using Weak Hydrogen Bonds
P50
Q43143245-73F795F8-16CA-43DA-ACF5-7A4BE025B544Q46246770-1CBC980E-3F04-4B1C-AF2A-C4F2646B138FQ47929210-385C26EF-F249-4D72-8352-89C70F80901AQ48047582-90E6BAE8-69D1-4A3B-BC1D-E1CEFB314925Q48112513-789237F4-1B3E-4BCD-90F0-96AA07171A23Q48249161-F8C20484-D5CD-495B-BD86-3140188C8317Q48313818-5CB828A9-F772-497B-B69C-A47FEC437007Q48352013-EDD1FE1A-9AD3-4141-8D6F-DC4EBFD8F85FQ50209341-C5F61DD1-6C37-4FEF-922F-6E81FB3D9544Q50219224-00C430B4-EE7D-446A-8D47-A66EDEABCACFQ50221782-CC80180D-9C05-48DA-AFFC-DE7136C9B4B1Q50226013-45521317-02CD-45B6-9E8E-DCDF1BB9AADEQ50232382-6C51E76E-2FA3-4C22-A880-1783F80CD614Q50246346-487DFC4C-18A9-45BE-A268-4F3661C14B52Q50250336-E51873B9-8101-4F6E-9819-A996196A45FFQ50271594-6F6F05AC-E821-43F8-854E-1EC17F3B530DQ50426520-CA199FD5-53FF-4649-866C-B22CCEC8D7CFQ50442267-173926DE-D90F-4D18-9C6E-B3C7C820E684Q50493592-61AB0067-D2B1-4AD4-AC91-AD7F8A94B948Q50648123-173A9E47-F871-49DF-AFEE-34E8896BD331Q51596285-A52FCBF6-D328-43A9-8FC9-658A0078D5A3Q53676535-616D4089-A9E4-46B2-9744-41F2406BF9B5Q57967760-4998A152-21CF-4254-B4D3-473AD3852FF4Q83924200-5E6AF92B-E586-4383-B803-C96501700455Q84417826-E51BDEE6-FDFD-4C36-93ED-C513F3433FB4Q84927318-08521A2A-5897-463E-A235-88C4A82E7619Q85248586-CB45812B-6B24-4A47-AD5A-5AA7A3BB7D98Q87405652-2CFBFC01-8F06-4AD9-8942-FE88BE10B571Q90406877-7D56A6D0-F1EF-4975-8F14-ED517EE790A2Q90438039-9C76B8CA-711A-4F46-9956-490B108BEDF8Q92216361-16DD3FDD-FB5A-4DB6-B987-8D7F66A7D489
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Hisahiro Sasabe
@ast
Hisahiro Sasabe
@en
Hisahiro Sasabe
@es
Hisahiro Sasabe
@nl
Hisahiro Sasabe
@sl
type
label
Hisahiro Sasabe
@ast
Hisahiro Sasabe
@en
Hisahiro Sasabe
@es
Hisahiro Sasabe
@nl
Hisahiro Sasabe
@sl
prefLabel
Hisahiro Sasabe
@ast
Hisahiro Sasabe
@en
Hisahiro Sasabe
@es
Hisahiro Sasabe
@nl
Hisahiro Sasabe
@sl
P1053
E-4306-2010
P106
P1153
7101795026
P31
P3829
P3835
hisahiro-sasabe
P496
0000-0002-1312-0111