{"id":398,"date":"2012-08-31T19:08:00","date_gmt":"2012-08-31T10:08:00","guid":{"rendered":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/?page_id=398"},"modified":"2025-03-12T08:54:43","modified_gmt":"2025-03-11T23:54:43","slug":"nakanotani","status":"publish","type":"page","link":"http:\/\/www.cstf.kyushu-u.ac.jp\/~adachilab\/lab\/staff-2\/nakanotani\/","title":{"rendered":"\u4e2d\u91ce\u8c37\u3000\u4e00"},"content":{"rendered":"
\"\"<\/div>\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n\r\n
\u7565\u6b74<\/th>\r\n<\/tr>\r\n
2010<\/td>\r\n\u4e5d\u5dde\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u5e9c
\r\n\u7269\u8cea\u5275\u9020\u5de5\u5b66\u5c02\u653b \u535a\u58eb\u5f8c\u671f\u8ab2\u7a0b\u4fee\u4e86<\/td>\r\n<\/tr>\r\n
2010-2012<\/td>\r\n\uff08\u682a\uff09\u30ea\u30b3\u30fc
\r\n\u7814\u7a76\u958b\u767a\u672c\u90e8 \u7814\u7a76\u54e1<\/td>\r\n<\/tr>\r\n
2012-2014<\/td>\r\n\uff08\u8ca1\uff09\u4e5d\u5dde\u5148\u7aef\u79d1\u5b66\u6280\u8853\u7814\u7a76\u6240
\r\n\u6709\u6a5f\u5149\u30c7\u30d0\u30a4\u30b9\u7814\u7a76\u5ba4 \u7814\u7a76\u54e1
\r\n\u4e5d\u5dde\u5927\u5b66 \u672a\u6765\u5316\u5b66\u5275\u9020\u30bb\u30f3\u30bf\u30fc \u5ba2\u54e1\u52a9\u6559<\/td>\r\n<\/tr>\r\n
2014-2015<\/td>\r\n\u4e5d\u5dde\u5927\u5b66
\r\n\u6700\u5148\u7aef\u6709\u6a5f\u5149\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u7814\u7a76\u30bb\u30f3\u30bf\u30fc \u52a9\u6559<\/td>\r\n<\/tr>\r\n
2015-<\/td>\r\n\u4e5d\u5dde\u5927\u5b66
\r\n\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u9662 \u5fdc\u7528\u5316\u5b66\u90e8\u9580 \u51c6\u6559\u6388<\/td>\r\n<\/tr>\r\n
\u5b66\u4f4d<\/th>\r\n<\/tr>\r\n
\u535a\u58eb\uff08\u5de5\u5b66\uff09\uff08\u4e5d\u5dde\u5927\u5b66\u30012010\u5e74\uff09<\/td>\r\n<\/tr>\r\n
\u6240\u5c5e\u5b66\u4f1a<\/th>\r\n<\/tr>\r\n
\u5fdc\u7528\u7269\u7406\u5b66\u4f1a\u3001\u65e5\u672c\u5316\u5b66\u4f1a\u3001\u6709\u6a5fEL\u8a0e\u8ad6\u4f1a\u3001\u5149\u5316\u5b66\u8a0e\u8ad6\u4f1a<\/td>\r\n<\/tr>\r\n
\u7814\u7a76\u5206\u91ce<\/th>\r\n<\/tr>\r\n
\u6709\u6a5f\u5149\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\uff0c\u6709\u6a5f\u534a\u5c0e\u4f53\u30c7\u30d0\u30a4\u30b9\u7269\u6027\u3001\u6709\u6a5f\u5149\u5316\u5b66
\r\n\u7814\u7a76\u30c6\u30fc\u30de\uff1a\u6709\u6a5f\u767a\u5149\u5206\u5b50\u306b\u304a\u3051\u308b\u5149\u7269\u7406\u904e\u7a0b\u3001\u6709\u6a5f\u767a\u5149\u30c7\u30d0\u30a4\u30b9<\/td>\r\n<\/tr>\r\n
\u8da3\u5473<\/th>\r\n<\/tr>\r\n
\u30e1\u30c0\u30ab\u306e\u98fc\u80b2, \u6e29\u6cc9\u3081\u3050\u308a, \u8aad\u66f8, \u5b50\u4f9b\u3068\u904a\u3076\u3053\u3068, \u30b8\u30e7\u30ae\u30f3\u30b0,<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n

\u7814\u7a76\u6210\u679c<\/h3>\r\n

\u8ad6\u6587\u767a\u8868<\/h4>\r\n
\r\n
Google Scholar<\/a><\/dt>\r\n
Publons<\/a><\/dt>\r\n<\/dl>\r\n
\r\n
[2025]<\/dt>\r\n
[127]<\/dt>\r\n
Unusual anti-Stokes photoluminescence from a polymer film containing thermally activated delayed fluorescent molecules
\r\nChemical Physics Letters<\/i><\/strong>, (accepted)
\r\nDOI:10.1016\/j.cplett.2025.142017<\/a><\/strong>
\r\nM. Kaneko, S. Kohata, H. Nakanotani*<\/span><\/strong>, and C. Adachi*\r\n<\/dd>\r\n\r\n
[2024]<\/dt>\r\n
[126]<\/dt>\r\n
Anti-Stokes emission utilizing reverse intersystem crossing
\r\nAngew. Chem.,<\/i><\/strong>, (accepted)
\r\nDOI:10.1002\/anie.202419323<\/a><\/strong>
\r\nS. Kohata, H. Nakanotani*<\/span><\/strong>, T. Yasuda, T. Hosokai, Y. Tsuchiya, and C. Adachi*<\/dd>\r\n
[125]<\/dt>\r\n
Organic thermoelectric device utilizing charge transfer interface as the charge generation by harvesting thermal energy
\r\nNature Communications<\/i><\/strong>, 15, 8115 (2024)
\r\nDOI:10.1038\/s41467-024-52047-5<\/a><\/strong>
\r\nS. Kondo, M. Kameyama, K. Imaoka, Y. Shimoi, F. Mathevet, T. Fujihara, H. Goto, H. Nakanotani<\/span><\/strong>, M. Yahiro*, and C Adachi*<\/dd>\r\n
[124]<\/dt>\r\n
Simultaneous control of carrier transport and film polarization of emission layers aimed at high-performance OLEDs
\r\nNature Communications<\/i><\/strong>, 15, 5950 (2024)
\r\nDOI:10.1038\/s41467-024-50326-9<\/a><\/strong>
\r\nM. Tanaka*, C.-Y. Chan, H. Nakanotani<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[123]<\/dt>\r\n
Hexacarbazolylbenzene: An excellent host molecule causing strong guest molecular orientation and the high-performance OLEDs
\r\nAdvanced Materials<\/i><\/strong>, (in press)
\r\nDOI:10.1002\/adma.202402275<\/a><\/strong>
\r\nB. Madushani, M. Mamada*, K. Goushi, H. Katagiri, H. Nakanotani<\/span><\/strong>, T. Hatakeyama and C. Adachi*<\/dd>\r\n
[122]<\/dt>\r\n
Unexplored exciplex formation process by dual excitation of donor and acceptor layers optically and electrically
\r\nAdvanced Optical Materials<\/i><\/strong>, (in press)
\r\nDOI:10.1002\/adom.202401237<\/a><\/strong>
\r\nT. P. B. Rajakaruna1, X. Tang*, H. Nakanotani<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[121]<\/dt>\r\n
Spacer dependence of exciplex dynamics in donor\/spacer\/acceptor layers
\r\nChem. Phys. Lett.<\/i><\/strong>, 848, 141390 (2024)
\r\nDOI:10.1016\/j.cplett.2024.141390<\/a><\/strong>
\r\nT. P. B. Rajakaruna1, X. Tang, H. Nakanotani<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[120]<\/dt>\r\n
The Impact of Spontaneous Orientational Polarization on Triplet-Triplet Upconversion-Based Blue Organic Light-Emitting Diodes
\r\nACS Applied Materials & Interfaces<\/i><\/strong>, 16, 31392\u201331398 (2024)
\r\nDOI:10.1021\/acsami.4c02821<\/a><\/strong>
\r\nS. Kakumachi, H. Nakanotani*<\/span><\/strong>, Y. Nagasaki and C. Adachi*<\/dd>\r\n
[119]<\/dt>\r\n
Efficient Near-Infrared Fluorescence in Deuterated Host-Guest system for Near-Infrared Organic Light-Emitting Diodes
\r\nAdvanced Optical Materials<\/i><\/strong>, (in press)
\r\nDOI:10.1002\/adom.202400932<\/a><\/strong>
\r\nQ. Yu, Y. Tamura, H. Nakanotani*<\/span><\/strong>, M. Mamada, and C. Adachi*<\/dd>\r\n
[118]<\/dt>\r\n
Suppressed gold penetration with the molybdenum oxide interlayer to increase power conversion efficiency of perovskite solar cells
\r\nSolar RRL<\/i><\/strong>, 8, 2400029, (2024)
\r\nDOI:10.1002\/solr.202400029<\/a><\/strong>
\r\nB. Purev-Ochir, J. T. Song, P. Wang, M. Yahiro, S. Yamada, H. Nakanotani<\/span><\/strong>, T. Matsushima*, and C. Adachi*<\/dd>\r\n
[117]<\/dt>\r\n
Three-dimensional sensing of surfaces by projection of invisible electroluminescence from organic light-emitting diodes
\r\nScience Advances<\/i><\/strong>, 10, eadj6583 (2024)
\r\nDOI:10.1126\/sciadv.adj6583<\/a><\/strong>
\r\nN. Yamada, H. Nakanotani*<\/span><\/strong>, A. Takagi, M. Mamada, U. Balijapalli, T. Ichikawa, E. Hirata, S. Kaizu, A. Tanaka, K. Itonaga, and C. Adachi*<\/dd>\r\n
[2023]<\/dt>\r\n
[116]<\/dt>\r\n
The role of spontaneous orientation polarization on charge storage behavior at an interface between organic semiconductor layers
\r\nJournal of Materials Chemistry C<\/i><\/strong>, (accepted)
\r\nDOI:10.1039\/D3TC03979J<\/a><\/strong>
\r\nT. Yamanaka, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[115]<\/dt>\r\n
A polar transition of spontaneous orientation polarization in organic solid-state films
\r\nChem. Phys. Lett.<\/i><\/strong>, 833, 140915 (2023)
\r\nDOI:10.1016\/j.cplett.2023.140915<\/a><\/strong>
\r\nY. Ueda, M. Tanaka, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[114]<\/dt>\r\n
Anti-Stokes Luminescence in Thermally-Activated Delayed Fluorescence Molecules
\r\nAngew. Chem.,<\/i><\/strong>, 62, e202312326 (2023)
\r\nDOI: 10.1002\/anie.202312326<\/a><\/strong>
\r\nS. Kohata, H. Nakanotani*<\/span><\/strong>, Y. Chitose, T. Yasuda, Y. Tsuchiya and C. Adachi*<\/dd>\r\n
[113]<\/dt>\r\n
Abrupt exciton quenching in blue fluorescent organic light-emitting diodes around turn-on voltage region
\r\nChemical Engineering Journal<\/i><\/strong>, 471, 144516 (2023)
\r\nDOI:10.1016\/j.cej.2023.144516<\/a><\/strong>
\r\nS. Kakumachi, T. B. Nguyen, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[112]<\/dt>\r\n
Multiple donor-acceptor design for highly luminescent and stable thermally activated delayed fluorescence emitters
\r\nScientific Reports<\/i><\/strong>, 13, 7644 (2023)
\r\nDOI:10.1038\/s41598-023-34623-9<\/a><\/strong>
\r\nB. Madushani, M. Mamada*, K. Goushi, T.B. Nguyen, H. Nakanotani<\/span><\/strong>, H. Kaji, C. Adachi*<\/dd>\r\n
[111]<\/dt>\r\n
Enhancing triplet-triplet upconversion efficiency and operational lifetime in blue organic light-emitting diodes by utilizing thermally-activated delayed fluorescence materials
\r\nACS Applied Materials & Interfaces<\/i><\/strong>, 15, 23557 (2023)
\r\nDOI:10.1021\/acsami.3c02855<\/a><\/strong>
\r\nT. B. Nguyen, H. Nakanotani*<\/span><\/strong>, C.-Y. Chan, S. Kakumachi, and C. Adachi*<\/dd>\r\n
[110]<\/dt>\r\n
A Post-Modification of Pyrrolopyrrole aza-BODIPY toward High Near Infrared Fluorescence Brightness
\r\nOrganic Letters<\/i><\/strong>, 25, 3040 (2023)
\r\nDOI:10.1021\/acs.orglett.3c00848<\/a><\/strong>
\r\nY. Wang, S. Mori, H. Nakanotani<\/span><\/strong>, C. Adachi, and S. Shimizu*<\/dd>\r\n
[109]<\/dt>\r\n
Electron lifetime of over one month in disordered organic solid-state films
\r\nAdv. Mater.<\/i><\/strong>, 35, 2210335 (2023)
\r\nDOI:10.1002\/adma.202210335<\/a><\/strong>
\r\nT. Yamanaka, H. Nakanotani*<\/span><\/strong>, K. Nakamoto, and C. Adachi*<\/dd>\r\n
[2022]<\/dt>\r\n
[108]<\/dt>\r\n
Very low lasing threshold of DABNA derivatives with DFB structures
\r\nMater. Chem. Front.<\/i><\/strong>, 7, 259 (2022)
\r\nDOI:10.1039\/D2QM01040B <\/a><\/strong>
\r\nM. Mamada*, S. Maederaa, S. Oda, T. B. Nguyen, H. Nakanotani<\/span><\/strong>, T. Hatakeyama, and C. Adachi*<\/dd>\r\n
[107]<\/dt>\r\n
Solvent-dependent dual emission processes in charge-transfer excited states of phenothiazine-triphenyltriazine conformers
\r\nChem. Phys. Lett.<\/i><\/strong>, 809, 140155 (2022)
\r\nDOI:10.1016\/j.cplett.2022.140155<\/a><\/strong>
\r\nT. Ryu, K. Miyata, M. Saigo, Y. Shimoda, Y. Tsuchiya, H. Nakanotani<\/span><\/strong>, C. Adachi, K. Onda*<\/dd>\r\n
[106]<\/dt>\r\n
Multiple resonance type thermally activated delayed fluorescence by dibenzo[1,4]azaborine derivatives
\r\nFrontiers in Chemistry<\/i><\/strong>, 19, 990918 (2022)
\r\nDOI:10.3389\/fchem.2022.990918<\/a><\/strong>
\r\nJ. Bae, M. Sakai, Y. Tsuchiya, N. Ando, X. Chen, T. B. Nguyen, C.-Y. Chan, Y-T. Lee, M. Auffray, H. Nakanotani<\/span><\/strong>, S. Yamaguchi, C. Adachi<\/dd>\r\n
[105]<\/dt>\r\n
Modulation of intersystem crossing rate induced by singlet-triplet energy level alignment in 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene single crystal
\r\nChem. Lett.,<\/i><\/strong>, 51, 989-992, (2022)
\r\nDOI:10.1246\/cl.220304<\/a><\/strong>
\r\nS. Kohata, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[104]<\/dt>\r\n
Carbazole-2-Carbonitrile as an Acceptor in Deep-Blue Thermally Activated Delayed Fluorescence Emitters Aimed at Narrow Fluorescence-like Emission
\r\nChemical Science<\/i><\/strong>, 13, 7821 (2022)
\r\nDOI:10.1039\/D2SC02478K<\/a><\/strong>
\r\nC.-Y. Chan*, Y.-T. Lee, M. Tanaka, M. Mamada, K. Goushi, Y. Tsuchiya, H. Nakanotani<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[103]<\/dt>\r\n
An overlooked charge-transfer interaction in interfacial triplet-triplet upconversion process in blue organic light-emitting diodes
\r\nAdv. Opt. Mater.,<\/i><\/strong>, 10, 2200704 (2022)
\r\nDOI:10.1002\/adom.202200704<\/a><\/strong>
\r\nT. B. Nguyen, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[102]<\/dt>\r\n
Highly Efficient Deep-Blue Organic Light-Emitting Diodes Based on Rational Molecular Design and Device Engineering
\r\nAdv. Func. Mater.<\/i><\/strong>, 32, 2204352 (2022)
\r\nDOI:10.1002\/adfm.202204352<\/a><\/strong>
\r\nMasashi Mamada*, H. Katagiri, C.-Y. Chan, Y.-T. Lee, K. Goushi, H. Nakanotani<\/span><\/strong>, T. Hatakeyama, and C. Adachi*<\/dd>\r\n
[101]<\/dt>\r\n
Tailor-made Multi-Resonance Terminal Emitters Towards Narrowband, High-Efficiency and Stable Hyperfluorescence Organic Light-Emitting Diodes
\r\nAdv. Opt. Mater.,<\/i><\/strong>, 10, 2200682, (2022)
\r\nDOI:10.1002\/adom.202200682<\/a><\/strong>
\r\nY.-T. Lee, C.-Y. Chan*, M. Tanaka, M. Mamada, K. Goushi, X. Tang, Y. Tsuchiya, H. Nakanotani<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[100]<\/dt>\r\n
Spontaneous formation of metastable orientation with well-organized permanent dipole moment in organic glassy films
\r\nNature Materials,<\/i><\/strong>, 21, 819 (2022)
\r\nDOI:10.1038\/s41563-022-01265-7<\/a><\/strong>
\r\nM. Tanaka*, M. Auffray, H. Nakanotani*<\/span><\/strong>, and C. Adachi*
\r\n[Press Release]<\/strong><\/a>
\r\n[Media]<\/strong><\/a><\/dd>\r\n
[99]<\/dt>\r\n
Significant role of triplet spin state for exciton dissociation in organic solids
\r\nScience Advances,<\/i><\/strong>, 8, abj9188 (2022)
\r\nDOI:10.1126\/sciadv.abj9188<\/a><\/strong>
\r\nT. Yamanaka, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[2021]<\/dt>\r\n
[98]<\/dt>\r\n
Efficiency of Thermally Activated Delayed Fluorescence Sensitized Triplet Upconversion Doubled in Three-Component System
\r\nAdv. Mater.,<\/i><\/strong>, 34, 2103976 (2021)
\r\nDOI:10.1002\/adma.202103976<\/a><\/strong>
\r\nB. Yurash, A. Dixon, C. Espinoza, A. Mikhailovsky, S. Chae, H. Nakanotani, C. Adachi, T.-Q. Nguyen*<\/dd>\r\n
[97]<\/dt>\r\n
2,6-Dicarbonitrile Diphenyl-1\u03bb5-Phosphinine (DCNP)\u2014A Robust Conjugated Building Block for Multi-Functional Dyes Exhibiting Tunable Amplified Spontaneous Emission
\r\nAdv. Opt. Mater.,<\/i><\/strong>, 9, 2101122 (2021)
\r\nDOI:10.1002\/adom.202101122<\/a><\/strong>
\r\nU. Balijapalli, X. Tang, D. Okada, Y.-T. Lee, B. S. B. Karunathilaka, M. Auffray, G. Tumen-Ulzii, Y. Tsuchiya, A.S. D. Sandanayaka, T. Matsushima*, H. Nakanotani*<\/span><\/strong>, C. Adachi*<\/dd>\r\n
[96]<\/dt>\r\n
Tetrabenzo[a,c]phenazine backbone for highly efficient orange-red thermally-activated delayed fluorescence with completely horizontal molecular orientation
\r\nAngew. Chem.,<\/i><\/strong>, 60, 19364 (2021)
\r\nDOI:10.1002\/anie.202106570<\/a><\/strong>
\r\nU. Balijapalli*, Y-T. Lee, B. S. B. Karunathilaka, G. Tumen-Ulzii, M. Auffray, Y.Tsuchiya, H. Nakanotani*<\/span><\/strong>, and C.Adachi*<\/dd>\r\n
[95]<\/dt>\r\n
Direct Observation of Photoexcited Electron Dynamics in Organic Solid exhibiting Thermally-Activated Delayed Fluorescence by Time-Resolved Photoelectron Emission Microscopy
\r\nAdv. Opt. Mater.<\/i><\/strong>, 9, 2100619 (2021)
\r\nDOI:10.1002\/adom.202100619<\/a><\/strong>
\r\nY. Fukami, M. Iwasawa, M. Sasaki, T. Hosokai, H. Nakanotani<\/span><\/strong>, C. Adachi, K. Fukumoto and Y. Yamada
\r\n[Press Release]<\/strong><\/a><\/dd>\r\n
[94]<\/dt>\r\n
Amplified spontaneous emission from oligo(p-phenylenevinylene) derivatives
\r\nMater. Adv.<\/i><\/strong>, 2, 3906 (2021)
\r\nDOI:10.1039\/D0MA00756K<\/a><\/strong>
\r\nM. Mamada, H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[93]<\/dt>\r\n
Thermally Activated Delayed Fluorescence Properties of Trioxoazatriangulene Derivatives Modified with Electron Donating Groups
\r\nAdv. Opt. Mater.<\/i><\/strong>, 9, 2002174 (2021)
\r\nDOI:10.1002\/adom.202002174<\/a><\/strong>
\r\nY. Tsuchiya, Y. Ishikawa, S.-H. Lee, X.-K. Chen, J.-L. Br\u00e9das,H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[92]<\/dt>\r\n
Investigating HOMO Energy Levels of Terminal Emitters for Realizing High-Brightness and Stable TADF-Assisted Fluorescence Organic Light-Emitting Diodes
\r\nAdv. Electro. Mater.<\/i><\/strong>, 7, 2001090 (2021)
\r\nDOI:10.1002\/aelm.202001090<\/a><\/strong>
\r\nY.-T. Lee, C.-Y. Chan, M. Tanaka, M. Mamada, U. Balijapalli, Y. Tsuchiya, H. Nakanotani<\/span><\/strong>, T. Hatakeyama, C. Adachi*<\/dd>\r\n
[91]<\/dt>\r\n
Thermally-activated delayed fluorescence for light-emitting devices [Highlight Review]<\/i>
\r\nChem. Lett. <\/i><\/strong>, 50, 938 (2021)
\r\nDOI:10.1246\/cl.200915<\/a><\/strong>
\r\nH. Nakanotani*<\/span><\/strong>, Y. Tsuchiya, C. Adachi*<\/dd>\r\n
[90]<\/dt>\r\n
Isotope Effect of Host Material on Device Stability of Thermally Activated Delayed Fluorescence Organic Light-Emitting Diodes
\r\nSmall Science<\/i><\/strong>, 1, 2000057 (2021)
\r\nDOI:10.1002\/smsc.202000057<\/a><\/strong>
\r\nX. Liu, C.-Y. Chan*, F. Mathevet, M. Mamada, Y. Tsuchiya, Y.-T. Lee, H. Nakanotani<\/span><\/strong>, S. Kobayashi, M. Shiochi, C. Adachi*<\/dd>\r\n
[89]<\/dt>\r\n
Highly Efficient Near-Infrared Electrofluorescence from a Thermally-Activated Delayed Fluorescence Molecule
\r\n Angew. Chem.<\/i><\/strong>, 60, 8477 (2021)
\r\nDOI:10.1002\/anie.202016089 <\/a> <\/strong>
\r\nU. Balijapalli, R. Nagata, N. Yamada, H. Nakanotani*<\/span><\/strong>, M. Tanaka, A. D\u2019Al\u00e9o, V. Placide, M. Mamada, Y. Tsuchiya* and C. Adachi*<\/dd>\r\n
[88]<\/dt>\r\n
Stable pure-blue hyperfluorescence organic light-emitting diodes with high-efficiency and narrow emission
\r\nNature Photonics<\/i><\/strong>, 15, 203 (2021)
\r\nDOI:10.1038\/s41566-020-00745-z<\/a><\/strong>
\r\nC.-Y. Chan*, M. Tanaka, Y.-T. Lee, Y.-W. Wong, H. Nakanotani<\/span><\/strong>, T. Hatakeyama, and C. Adachi*
\r\n[Press Release]<\/strong><\/a><\/dd>\r\n
[2020]<\/dt>\r\n
[87]<\/dt>\r\n
H2<\/sub>O Induced-Crystallization of Organic Luminescent Thin Films by Direct Film Storage in High Vacuum
\r\n J. Phys. Chem. C<\/i><\/strong>, 124, 24919 (2020)
\r\nDOI:10.1021\/acs.jpcc.0c08968<\/a><\/strong>
\r\nT. Hosokai*, T. Nakanishi, A. Honda, K. Akaike, R. Tsuruta, H. Itoh, H. Nakanotani<\/span><\/strong>, and Y. Nakayama<\/dd>\r\n
[86]<\/dt>\r\n
Precise Exciton Management of Quaternary Emission Layers for Highly Stable Organic Light-Emitting Diodes Based on Thermally Activated Delayed Fluorescence
\r\nACS Appl. Mater. Interfaces<\/i><\/strong>, 12, 50668 (2020)
\r\nDOI:10.1021\/acsami.0c15208<\/a><\/strong>
\r\nM. Tanaka, R. Nagata, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[85]<\/dt>\r\n
Role of spontaneous orientational polarization in organic donor-acceptor blends for exciton binding
\r\nAdv. Opt. Mater.,<\/i><\/strong>, 8, 2000896 (2020)
\r\nDOI:10.1002\/adom.202000896<\/a><\/strong>
\r\nY. Ueda, H. Nakanotani*<\/span><\/strong>, T. Hosokai*, Y. Tanaka, H. Hamada, H. Ishii, S. Santo, and C. Adachi*<\/dd>\r\n
[84]<\/dt>\r\n
Fast Spin-Flip Enables Efficient and Stable Organic Electroluminescence from Charge-Transfer States
\r\nNature Photonics<\/i><\/strong>, 14, 636 (2020)
\r\nDOI:10.1038\/s41566-020-0668-z<\/a><\/strong>
\r\nL. Cui, A. Gillett, S.-F. Zhang, H. Ye, Y. Liu, X.-K. Chen, E. W. Evans, W. K. Myers, T. K. Ronson, Z.-S. Lin, H. Nakanotani<\/span><\/strong>, S. Reineke, J.-L. Bredas, C. Adachi, R. Friend<\/dd>\r\n
[83]<\/dt>\r\n
Molecular Design Based on Donor-Weak Donor Scaffold for Blue Thermally-Activated Delayed Fluorescence Designed by Combinatorial DFT Calculations
\r\nFront. Chem.<\/i><\/strong>, 8, 403 (2020)
\r\nDOI:10.3389\/fchem.2020.00403<\/a><\/strong>
\r\nY. Tsuchiya*, K. Tsuji, K. Inada, F. Bencheikh, Y. Geng,H. S. Kwak, T. J. L. Mustard, M. D. Halls, H. Nakanotani<\/span><\/strong> and C. Adachi<\/dd>\r\n
[82]<\/dt>\r\n
Understanding degradation of organic light-emitting diodes from magnetic field effects
\r\nCommun. Mater.<\/i><\/strong>, 1, 18, (2020)
\r\nDOI:10.1038\/s43246-020-0019-0<\/a><\/strong>
\r\nM. Tanaka, R. Nagata, H. Nakanotani*<\/span><\/strong>, C. Adachi*<\/dd>\r\n
[81]<\/dt>\r\n
Nanosecond-Time-Scale Delayed Fluorescence Molecule for Deep-Blue Organic Light-Emitting Diodes with Small Efficiency Rolloff
\r\nNature Commun.<\/i><\/strong>, 11, 1765 (2020)
\r\nDOI:10.1038\/s41467-020-15558-5<\/a><\/strong>
\r\nJ. U. Kim, I. S. Park, C.-Y. Chan, M. Tanaka, Y. Tsuchiya, H. Nakanotani<\/span><\/strong>, C. Adachi*<\/dd>\r\n
[80]<\/dt>\r\n
Utilization of multi hetero-donors in thermally activated delayed fluorescence molecules and their high performance bluish-green OLEDs
\r\nACS Appl. Mater. Interfaces<\/i><\/strong>, 12, 9498 (2020)
\r\nDOI:doi.org\/10.1021\/acsami.9b20020<\/a><\/strong>
\r\nU. Balijapalli , M. Tanaka , M. Auffray , C.-Y. Chan , Y.-T. Lee, Y. Tsuchiya, H. Nakanotani<\/span><\/strong>, C. Adachi*<\/dd>\r\n
[79]<\/dt>\r\n
Observation of Nonradiative Deactivation Behavior from Singlet and Triplet States of Thermally Activated Delayed Fluorescence Emitters in Solution
\r\nJ. Phys. Chem. Lett.<\/i><\/strong>, 11, 562-566 (2020)
\r\nDOI:10.1021\/acs.jpclett.9b03302<\/a><\/strong>
\r\nN. Notsuka, H. Nakanotani<\/span><\/strong>, H. Noda, K. Goushi, C. Adachi*<\/dd>\r\n
[78]<\/dt>\r\n
Molecular orientation of disk-shaped small molecule exhibiting thermally activated delayed fluorescence in host-guest films
\r\nAppl. Phys. Lett.<\/i><\/strong>, 116, 023302 (2020)
\r\nDOI:doi.org\/10.1063\/1.5140210<\/a><\/strong>
\r\nM. Tanaka, H. Noda, H. Nakanotani*<\/span><\/strong>, and C. Adachi*
\r\nEditor’s pick!<\/strong><\/dd>\r\n
[77]<\/dt>\r\n
Role of reverse intersystem crossing using a TADF-type acceptor molecule on the device stability of exciplex based organic-light emitting diodes
\r\nAdv. Mater.<\/i><\/strong>, 5, 1906614 (2020)
\r\nDOI:10.1002\/adma.201906614<\/a><\/strong>
\r\nT. B. Nguyen, H. Nakanotani*<\/span><\/strong>, T. Hatakeyama, and C. Adachi*<\/dd>\r\n
[2019]<\/dt>\r\n
[76]<\/dt>\r\n
Slow recombination of spontaneously dissociated organic fluorophore excitons
\r\nNature Commun.<\/i><\/strong>, 10, 5748 (2019)
\r\nDOI:10.1038\/s41467-019-13736-8 <\/a><\/strong>
\r\nT. Yamanaka*, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[75]<\/dt>\r\n
High-triplet-energy Bipolar Host Materials Based on Phosphine Oxide Derivatives for Efficient Sky-blue Thermally Activated Delayed Fluorescence Organic Light-emitting Diodes with Reduced Roll-off
\r\nChem. Lett.,<\/i><\/strong> 48, 1225-1228 (2019)
\r\nDOI:10.1246\/cl.190412<\/a><\/strong>
\r\nJ.U. Kim, M. Y. Wong, S. Kumar, O. G. Hayes, F. Duncan, C.-Y. Chan, B. Y.-W. Wong, H. Ye, L.-S. Cui, H. Nakanotani<\/span><\/strong>, E. Zysman-Colman, and C. Adachi<\/dd>\r\n
[74]<\/dt>\r\n
Critical role of intermediate electronic states for spin-flip processes in charge-transfer-type organic molecules with multiple donors and acceptors
\r\nNature Materials<\/i><\/strong> 18, 1084\u20131090 (2019)
\r\nDOI: 10.1038\/s41563-019-0465-6<\/a><\/strong>
\r\nH. Noda, X.-K. Chen, H. Nakanotani*<\/span><\/strong>, T. Hosokai, M. Miyajima, N. Noutsuka, Y. Kashima, J.-L. Br\u00e9das* and C. Adach*
\r\n[Press Release]<\/strong><\/a><\/dd>\r\n
[73]<\/dt>\r\n
Suppression of Structural Change upon S1<\/sub>-T1<\/sub> Conversion Assists Thermally Activated Delayed Fluorescence Process in Carbazole-Benzonitrile Derivatives
\r\nJ. Phys. Chem. Lett.<\/i><\/strong> 10, 2475-2480 (2019)
\r\nDOI:10.1021\/acs.jpclett.9b00810<\/a><\/strong>
\r\nM. Saigo, K. Miyata, S. Tanaka, H. Nakanotani<\/span><\/strong>, C. Adachi, K. Onda<\/dd>\r\n
[72]<\/dt>\r\n
TADF activation by solvent freezing: the role of nonradiative triplet decay and spin-orbit coupling in carbazole benzonitrile derivatives
\r\nSynthetic Metals<\/i><\/strong>252, 62-68 (2019)
\r\nDOI:10.1016\/j.synthmet.2019.04.005<\/a><\/strong>
\r\nT. Hosokai*, H. Nakanotani<\/span><\/strong>, S. Santou, H. Noda, Y. Nakayama, and C. Adachi<\/dd>\r\n
[71]<\/dt>\r\n
Photoluminescence Quenching Probes Spin Conversion and Exciton Dynamics in Thermally Activated Delayed Fluorescence Material
\r\nAdv. Mater.<\/i><\/strong>, 31, 1804490 (2019)
\r\nDOI:10.1002\/adma.201804490<\/a><\/strong>
\r\nB. Yurash, H. Nakanotani<\/span><\/strong> , Y. Olivier, D. Beljonne, C. Adachi, and T.\u2010Q. Nguyen<\/dd>\r\n
[70]<\/dt>\r\n
Photo-stable and highly emissive glassy organic dots exhibiting thermally activated delayed fluorescence
\r\nChem Commun.,<\/i><\/strong> 55, 5215-5218 (2019)
\r\nDOI:10.1039\/C9CC01420A<\/a><\/strong>
\r\nY. Tsuchiya, K. Ikesue, H. Nakanotani<\/span><\/strong> and C. Adachi<\/dd>\r\n
[69]<\/dt>\r\n
Effect of Carrier Balance on Device Degradation of Organic Light-Emitting Diodes based on Thermally Activated Delayed Fluorescence Emitters
\r\nAdv. Electron. Mater.,<\/i><\/strong> 5, 1800708 (2019)
\r\nDOI:10.1002\/aelm.201800708<\/a><\/strong>
\r\nM. Tanaka, H. Noda, H. Nakanotani<\/span><\/strong> and C. Adachi*<\/dd>\r\n
[68]<\/dt>\r\n
Highly efficient thermally activated delayed fluorescence with slow reverse intersystem crossing
\r\nChem. Lett.<\/i><\/strong> 48, 126-128 (2019)
\r\nDOI:10.1246\/cl.180813<\/a><\/strong>
\r\nH. Noda, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[2018]<\/dt>\r\n
[67]<\/dt>\r\n
Efficient and Stable Sky-Blue Delayed Fluorescence Organic Light-Emitting Diodes with CIEy < 0.4
\r\nNature Commun.<\/i><\/strong> 9, 5036 (2018)
\r\nDOI:10.1038\/s41467-018-07482-6<\/a><\/strong>
\r\nC.-Y. Chan, M. Tanaka, H. Nakanotani<\/span><\/strong>, and C. Adachi<\/dd>\r\n
[66]<\/dt>\r\n
The Importance of Excited-State Energy Alignment for Efficient Exciplex Systems Based on a Study of Phenylpyridinato Boron derivatives
\r\nAngew. Chem. Int. Ed.<\/i><\/strong>, 130, 12560-12564 (2018)
\r\nDOI:10.1002\/ange.201804218<\/a><\/strong>
\r\nM. Mamada, G. Tian, H. Nakanotani<\/span><\/strong>, J. Su, and C. Adachi<\/dd>\r\n
[65]<\/dt>\r\n
Trifluoromethane modification of thermally activated delayed fluorescence molecules for high-efficiency blue organic light-emitting diodes
\r\nChem. Commun.<\/strong>, 54, 8261-8264 (2018)
\r\nDOI:10.1039\/C8CC03425G<\/a><\/strong>
\r\nM. Yokoyama, K. Inada, Y. Tsuchiya*, H. Nakanotani*<\/span><\/strong> and C. Adachi*<\/dd>\r\n
[64]<\/dt>\r\n
Excited state engineering for efficient reverse intersystem crossing
\r\nScience Advances<\/strong>, 4, eaao6910 (2018)
\r\nDOI:10.1126\/sciadv.aao6910<\/a><\/strong>
\r\nH. Noda, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[63]<\/dt>\r\n
Exploiting singlet fission in organic light-emitting diodes
\r\nAdv. Mater.<\/strong>, 30, 1801484 (2018)
\r\nDOI:10.1002\/adma.201801484<\/a><\/strong>
\r\nR. Nagata, H. Nakanotani*<\/span><\/strong>, W. J. Potscavage Jr. and C. Adachi*
\r\n[Press Release]<\/strong><\/a>
\r\n[Media:Chem-Station]<\/strong><\/a><\/dd>\r\n
[62]<\/dt>\r\n
Well-Ordered 4CzIPN ((4s,6s)-2,4,5,6-Tetra(9-H-carbazol-9-yl)isophthalonitrile) Layers: Molecular Orientation, Electronic Structure, and Angular Distribution of Photoluminescence
\r\nJ. Phys. Chem. Lett., <\/strong>, 9, 863\u2013867 (2018)
\r\nDOI:10.1021\/acs.jpclett.7b03232<\/a><\/strong>
\r\nY. Hasegawa, Y. Yamada, M. Yamada, T. Hosokai, H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[61]<\/dt>\r\n
Well-ordered films of disk-shaped thermally activated delayed fluorescence molecules
\r\nJournal of Photonics for Energy<\/strong>, 8, 032110 (2018)
\r\nDOI:110.1117\/1.JPE.8.032110<\/a><\/strong>
\r\nY. Hasegawa, Y. Yamada, M. Yamada, T. Hosokai, H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[60]<\/dt>\r\n
Solvent-dependent investigation of carbazole benzonitrile derivatives: Does the 3LE-1CT energy gap facilitate TADF?
\r\nJournal of Photonics for Energy<\/strong>, 8, 032102 (2018)
\r\nDOI:10.1117\/1.JPE.8.032102<\/a><\/strong>
\r\nT. Hosokai*, H. Noda, H. Nakanotani<\/span><\/strong>, T. Nawata, Y. Nakayama, H. Matsuzaki, C. Adachi<\/dd>\r\n
[59]<\/dt>\r\n
Rational Molecular Design for Deep-Blue Thermally Activated Delayed Fluorescence Emitters
\r\nAdv. Func. Mater.<\/strong>, 28, 1706023 (2018)
\r\nDOI:10.1002\/adfm.201706023<\/a><\/strong>
\r\nC.-Y. Chan, L.-S. Cui, J. U. Kim, H. Nakanotani<\/span><\/strong>, and C. Adachi<\/dd>\r\n
[2017]<\/dt>\r\n
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Long-lived efficient delayed fluorescence organic light-emitting diodes using n-type hosts
\r\nNature Commun.<\/strong>, 8, 2250 (2017)
\r\nDOI:10.1038\/s41467-017-02419-x<\/a><\/strong>
\r\nL.-S. Cui, S.-B. Ruan, R. Nagata, L. Zhang, K. Inada, H. Nakanotani<\/span><\/strong>, L.-S. Liao and C. Adachi.<\/dd>\r\n
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Donor\u2010\u03c3\u2010Acceptor Motif Thermally Activated Delayed Fluorescence Emitters with Dual Upconversion
\r\nAngew. Chem. Int. Ed.<\/strong>, 129, 16763 (2017)
\r\nDOI:10.1002\/anie.201708876<\/a><\/strong>
\r\nY. Geng, A. D\u2019Aleo, K. Inada, L.-S. Cui, J. U. Kim, H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[56]<\/dt>\r\n
Molecular Design for Blue Thermal Activated Delayed Fluorescence Materials: Substitution Position Effect
\r\nChemistry Letters<\/strong>, 46, 10, 1490, (2017)
\r\nDOI:10.1246\/cl.170587<\/a><\/strong>
\r\nY. Geng, L.-S. Cui, J.U. Kim, H. Nakanotani<\/span><\/strong> and C. adachi<\/dd>\r\n
[55]<\/dt>\r\n
Highly Efficient Thermally Activated Delayed Fluorescence from an Excited-State Intramolecular Proton Transfer System
\r\nACS Central Science<\/strong>, 3, 769 (2017)
\r\nDOI:10.1021\/acscentsci.7b00183<\/a><\/strong>
\r\nM. Mamada, K. Inada, T. Komino, W. Potscavege, H. Nakanotani<\/span><\/strong>, and C. Adachi<\/dd>\r\n
[54]<\/dt>\r\n
Thermally activated delayed fluorescence of Bis(9,9-dimethyl-9,10-dihydroacridine) dibenzo[b,d]thiophene 5,5-dioxide derivatives for organic light-emitting diodes
\r\nJ. Lumines.<\/strong>, 190, 485 (2017)
\r\nDOI:10.1016\/j.jlumin.2017.06.006<\/a><\/strong>
\r\nJ.U. Kim, S.S. Reddy, L.-S. Cui, H. Nomura, S. Hwang, D.H. Kim, H. Nakanotani<\/span><\/strong>, S.-H. Jin, C. Adachi<\/dd>\r\n
[53]<\/dt>\r\n
NIR organic light-emitting diodes for bio-sensing with high operating stability
\r\nApp. Phys. Exp.<\/strong>, 10, 074101 (2017)
\r\nDOI:10.7567\/APEX.10.074101<\/a><\/strong>
\r\nT. Yamanaka, H. Nakanotani<\/span><\/strong>, S. Hara, T. Hirohara and C. Adachi<\/dd>\r\n
[52]<\/dt>\r\n
Light amplification in molecules exhibiting thermally activated delayed fluorescence
\r\nAdv. Opt. Mater.<\/strong>, (in press) (2017)
\r\nDOI:10.1002\/adom.201700051<\/a><\/strong>
\r\nH. Nakanotani*<\/span><\/strong>, T. Furukawa, T. Hosokai, T. Hatakeyama, and C. Adachi*<\/dd>\r\n
[51]<\/dt>\r\n
Evidence and Mechanism of Efficient Thermally Activated Delayed Fluorescence Promoted by Delocalized Excited States
\r\nScience Advances<\/strong>, 3, e1603282 (2017)
\r\nDOI:10.1126\/sciadv.1603282<\/a><\/strong>
\r\nT. Hosokai*, H. Matsuzaki, H. Nakanotani*<\/span><\/strong>, K. Tokumaru, T. Tsutsui, A. Furube, K. Nasu, H. Nomura, M. Yahiro, C. Adachi
\r\n[Press Release]<\/strong><\/a><\/dd>\r\n
[2016]<\/dt>\r\n
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Controlling Singlet-Triplet Energy Splitting for Deep-Blue Thermally Activated Delayed Fluorescence Emitters
\r\nAngew. Chem. Int. Ed.<\/strong>, 56, 1571-1575 (2016)
\r\nDOI:10.1002\/anie.201609459<\/a><\/strong>
\r\nL.-S. Cui, H. Nomura, Y. Geng, J. U. Kim, H. Nakanotani<\/span><\/strong>, and C. Adachi<\/dd>\r\n
[49]<\/dt>\r\n
Application of wide-energy-gap material 3,4-di(9H-carbazol-9-yl) benzonitrile in organic light-emitting diodes
\r\nThin Solid Films<\/strong>, 619, 120-124 (2016)
\r\nDOI:10.1016\/j.tsf.2016.11.016<\/a><\/strong>
\r\nY. Tanaka, T. Takahashi, J. Nishide, Y. Hiraga, H. Nakanotani<\/span><\/strong>, Chihaya Adachi<\/dd>\r\n
[48]<\/dt>\r\n
Near-Infrared Electrophosphorescence up to 1.1 \u00b5m using a Thermally Activated Delayed Fluorescence Molecule as Triplet Sensitizer
\r\nAdv. Mater.<\/strong>, 29, 1604265 (2016)
\r\nDOI:10.1002\/adma.201604265<\/a><\/strong>
\r\nR. Nagata, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
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Boron Difluoride Complexes of Expanded N-Confused Calix[n]phyrins That Demonstrate Unique Luminescent and Lasing Properties
\r\nAngew. Chem. Int. Ed.<\/strong>, 55, 12045-12049 (2016)
\r\nDOI:10.1002\/anie.201606246<\/a><\/strong>
\r\nM. Ishida, T. Omagari, R. Hirosawa, K. Jono, Y.M. Sung, Y. Yasutake, H. Uno, M. Toganoh, H. Nakanotani<\/span><\/strong>, S. Fukatsu, D. Kim, H. Furuta<\/dd>\r\n
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Color Tuning of Avobenzone Boron Difluoride as an Emitter to Achieve Full-Color Emission
\r\nAdv. Func. Mater.<\/strong>, 26, 6703-6710 (2016)
\r\nDOI:10.1002\/adfm.201601257<\/a><\/strong>
\r\nH.W. Mo, Y. Tsuchiya, Y. Geng, T. Sagawa, C. Kikuchi, H. Nakanotani<\/span><\/strong>, F. Ito, C. Adachi<\/dd>\r\n
[45]<\/dt>\r\n
Magnesium-gold binary alloy for organic light-emitting diodes with high corrosion resistance
\r\nJ. Vac.Sci.Technol.B <\/strong>, 34, 040607-040611 (2016)
\r\nDOI:10.1116\/1.4952408<\/a><\/strong>
\r\nH. Arai, H. Nakanotani*<\/span><\/strong>, and C. Adachi*<\/dd>\r\n
[44]<\/dt>\r\n
Thermally activated delayed fluorescence from pentacarbazorylbenzonitrile
\r\nChem. Lett.<\/strong>, 45, 770-772 (2016)
\r\nDOI:10.1246\/cl.160290<\/a><\/strong>
\r\nS. Tanimoto, T. Suzuki, H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[43]<\/dt>\r\n
Benzimidazobenzothiazole-Based Bipolar Hosts to Harvest Nearly All Excitons in Blue Delayed Fluorescence and Phosphorescent Organic Light-Emitting Diodes
\r\nAngew. Chem. Int. Ed.<\/strong>, 55, 6864-6868 (2016)
\r\nDOI:10.1002\/anie.201601136<\/a><\/strong>
\r\nL.-S. Cui, J. U. Kim, H. Nomura, H. Nakanotani<\/span><\/strong>, and C. Adachi<\/dd>\r\n
[42]<\/dt>\r\n
Long-range coupling of electron\u2013hole pairs in spatially separated organic donor\u2013acceptor layers
\r\nScience Advances<\/strong>, Vol. 2, no. 2, e1501470 (2016)
\r\nDOI:10.1126\/sciadv.1501470<\/a><\/strong>
\r\nH. Nakanotani*<\/span><\/strong>, T. Furukawa, K. Morimoto and C. Adachi*
\r\n[Press Release]<\/strong><\/a><\/dd>\r\n
[41]<\/dt>\r\n
Effect of Joule heating on transient current and electroluminescence in p-i-n organic light-emitting diodes under pulsed voltage operation
\r\nOrg. Electron.<\/strong>, 31, 287-294, (2016)
\r\nDOI:doi:10.1016\/j.orgel.2016.01.039<\/a><\/strong>
\r\nK. Yoshida, H. Nakanotani<\/span><\/strong>, and Chihaya Adachi<\/dd>\r\n
[40]<\/dt>\r\n
Quantification of temperature rise in unipolar organic conductors during short voltage-pulse excitation using electrical testing methods
\r\nOrg. Electron.<\/strong>, 31, 191-197, (2016)
\r\nDOI:10.1016\/j.orgel.2016.01.033<\/a><\/strong>
\r\nK. Yoshida, T. Matsushima, H. Nakanotani<\/span><\/strong>, and Chihaya Adachi<\/dd>\r\n
[39]<\/dt>\r\n
Low threshold amplified spontaneous emission and ambipolar charge transport in non-volatile liquid fluorene derivatives
\r\nChem. Commun.<\/strong>, 52, 3103-3106, (2016)
\r\nDOI:10.1039\/C5CC08331A<\/a><\/strong>
\r\nJ.-C. Ribierre, L. Zhao, M. Inoue, P.-O. schwartz, J.-H. Kim, K. Yoshida, A. Sandanayaka, H. Nakanotani<\/span><\/strong>, L. Mager, S. M\u00e9ry and Chihaya Adachi<\/dd>\r\n
[2015]<\/dt>\r\n
[38]<\/dt>\r\n
Effect of reverse intersystem crossing rate to suppress efficiency roll-off in organic light-emitting diodes with thermally activated delayed fluorescence emitters
\r\nChem. Phys. Lett.<\/strong>, 644, 62-67, (2015)
\r\nDOI:10.1016\/j.cplett.2015.11.042<\/a><\/strong>
\r\nM. Inoue, T. Serevi\u010dius, H. Nakanotani<\/span><\/strong>, K. Yoshida, T. Matsushima, S. Jur\u0161\u0117nas, and C. Adachi<\/dd>\r\n
[37]<\/dt>\r\n
High-efficiency sky-blue organic light-emitting diodes utilizing thermally-activated delayed fluorescence
\r\nIEICE Transactions<\/strong>, 98, 971-976 (2015)
\r\nDOI:1745-1353<\/a><\/strong>
\r\nY. Hiraga, J. Nishide, H. Nakanotani<\/span><\/strong>, M. Aonuma and C. Adachi<\/dd>\r\n
[36]<\/dt>\r\n
Light amplification in an organic solid-state film with the aid of triplet to singlet upconversion
\r\nAdv. Opt. Mater.<\/strong>, 3, 1381\u20131388 (2015)
\r\nDOI:10.1002\/adom.201500236<\/a><\/strong>
\r\nH. Nakanotani<\/span><\/strong>, T. Furukawa and C. Adachi
\r\n[Top 5 Most Downloaded Articles: Sep. 2015!]<\/span><\/strong><\/a>
\r\n[Top 5 Most Downloaded Articles: Oct. 2015!]<\/span><\/strong><\/a>
\r\n[selected as the Best of Advanced Optical Materials \u2013 2015 edition!]<\/span><\/a><\/strong><\/dd>\r\n
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Introduction of Oxygen into Organic Thin Films with the Aim of Suppressing Singlet-Triplet Annihilation
\r\nChem. Phys. Lett.<\/strong>, 624, 43-46 (2015)
\r\nDOI:10.1016\/j.cplett.2015.02.010<\/a><\/strong>
\r\nM. Inoue, T. Matsushima, H. Nakanotani<\/span><\/strong>, C. Adachi<\/dd>\r\n
[34]<\/dt>\r\n
Suppression of roll-off characteristics of organic light-emitting diodes by narrowing current injection\/transport area to 50 nm
\r\nAppl. Phys. Lett.<\/strong>, 106, 093301 (2015)
\r\nDOI:10.1063\/1.4913461<\/a><\/strong>
\r\nK. Hayashi, H. Nakanotani<\/span><\/strong>, M. Inoue, K. Yoshida, O. Mikhnenko, T.-Q. Nguyen and C. Adachi
\r\n[Highlighted as a Front Cover!]<\/span><\/strong><\/dd>\r\n
[33]<\/dt>\r\n
Dual Enhancement of Electroluminescence Efficiency and Operational Stability by Rapid Upconversion of Triplet Excitons in Organic Light-Emitting Diodes
\r\nSci. Rep.<\/strong>, 5, 8429 (2015)
\r\nDOI:10.1038\/srep08429<\/a><\/strong>
\r\nT. Furukawa\u2020, H. Nakanotani\u2020<\/span><\/strong>, M. Inoue, and C. Adachi<\/dd>\r\n
[32]<\/dt>\r\n
High efficiency white organic light-emitting diodes based on a blue TADF emitter combined with green and red fluorescence emitters
\r\nAdv. Mater.<\/strong>, 27, 2019\u20132023 (2015)
\r\nDOI: 10.1002\/adma.201404967<\/a><\/strong>
\r\nT. Higuchi\u2020, H. Nakanotani\u2020<\/span><\/strong>, and C. Adachi<\/dd>\r\n
[31]<\/dt>\r\n
Controlled emission color and singlet-triplet energy gap of dihydrophenazine-based thermally activated delayed fluorescence emitters
\r\nJ. Mater. Chem. C<\/strong>, 3, 2175-2181 (2015)
\r\nDOI: 10.1039\/C4TC02530J<\/a> <\/strong>
\r\nJ. Lee, K. Shizu, H. Tanaka, H. Nakanotani\u2020<\/span><\/strong>, T. Yasuda, H. Kaji and C. Adachi<\/dd>\r\n
[30]<\/dt>\r\n
Highly efficient blue electroluminescence based on thermally activated delayed fluorescence
\r\nNature Materials<\/strong>, 14, 330\u2013336 (2015)
\r\nDOI: 10.1038\/nmat4154<\/a> <\/strong>
\r\nS. Hirata, Y. Sakai, K. Masui, H. Tanaka, S. Y. Lee, H. Nomura, N. Nakamura, M. Yasumatsu, H. Nakanotani<\/span><\/strong>, Q. Zhang, K. Shizu, H. Miyazaki, C. Adachi<\/dd>\r\n
[2014]<\/dt>\r\n
[29]<\/dt>\r\n
Dual Intramolecular Charge-Transfer Fluorescence Derived from a Phenothiazine-Triphenyltriazine Derivative
\r\nJ. Phys. Chem. C.<\/strong>, 118, 15985-15994 (2014)
\r\nDOI: 10.1021\/jp501017f<\/a> <\/strong>
\r\nHiroyuki Tanaka, Katsuyuki Shizu, H. Nakanotani<\/span><\/strong>, and Chihaya Adachi<\/dd>\r\n
[28]<\/dt>\r\n
High efficiency organic light-emitting diodes with fluorescent emitters
\r\nNature Commun.<\/strong> 5, 4016 (2014)
\r\nDOI: 10.1038\/ncomms5016<\/a><\/strong>
\r\nH. Nakanotani<\/span><\/strong>, T. Higuchi, T. Furukawa, K. Masui, K. Morimoto, M. Numata, H. Tanaka, Y Sagara, T. Yasuda and C. Adachi
\r\n[Press Release]<\/strong><\/a><\/dd>\r\n
[27]<\/dt>\r\n
High-efficiency white organic light-emitting diodes using thermally activated delayed fluorescence
\r\nAppl. Phys. Lett.<\/strong>, 104, 233304-233308, (2014)
\r\nDOI: 10.1063\/1.4882456<\/a> <\/strong>
\r\nJ. Nishide\u2020, H. Nakanotani\u2020<\/span><\/strong>, Y. Hiraga, and C. Adachi<\/dd>\r\n
[26]<\/dt>\r\n
Analysis of alternative current driven electroluminescence in organic light emitting diodes: a comparative study
\r\nOrg. Electron.<\/strong>, 15, 1815-1821 (2014)
\r\nDOI: 10.1016\/j.orgel.2014.05.009<\/a> <\/strong>
\r\nL. Zhanga, H. Nakanotani<\/span><\/strong>, K. Yoshida, and C. Adachi<\/dd>\r\n
[25]<\/dt>\r\n
Light-Emitting Organic Field-Effect Transistors Based on Highly Luminescent Single Crystals of Thiophene\/Phenylene Co-Oligomers
\r\nJ. Mater. Chem. C<\/strong>, 2, 4918-4921, (2014)
\r\nDOI: 10.1039\/C4TC00164H<\/a><\/strong>
\r\nT. Komori, H. Nakanotani<\/span><\/strong>, T. Yasuda, and C. Adachi<\/dd>\r\n
[2013]<\/dt>\r\n
[24]<\/dt>\r\n
Twisted Intramolecular Charge Transfer State for Long-Wavelength Thermally Activated Delayed Fluorescence
\r\nChem. Mater.<\/strong>, 25, 3766 (2013)
\r\nDOI: 10.1021\/cm402428a<\/a><\/strong>
\r\nH. Tanaka; K. Shizu; H. Nakanotani<\/span><\/strong>; C. Adachi<\/dd>\r\n
[23]<\/dt>\r\n
Capacitance-voltage characteristics of a 4,4\u2032-bis[(N-carbazole)styryl]biphenyl based organic light-emitting diode: implications for characteristic times and their distribution
\r\nAppl. Phys. Lett.<\/strong>, 103, 093301 (2013)
\r\nDOI: 10.1063\/1.4819436<\/a><\/strong>
\r\nL. Zhang; H. Nakanotani<\/span><\/strong>; C. Adachi<\/dd>\r\n
[22]<\/dt>\r\n
Multi-color light-emitting transistors composed of organic single crystals
\r\nOrg. Electron.<\/strong>, 14, 2737?2742, (2013)
\r\nY. Yomogida; H. Sakai; K. Sawabe; S. Gocho; S. Z. Bisri; H. Nakanotani<\/span><\/strong>; C. Adachi; T. Hasobe; Y. Iwasa; T. Takenobu
\r\nDOI: 10.1016\/j.orgel.2013.07.025<\/a><\/strong><\/dd>\r\n
[21]<\/dt>\r\n
Analysis of exciton annihilation in high-effciency sky-blue organic light-emitting diodes with thermally activated delayed fluorescence
\r\nOrg. Electron.<\/strong>, 14, 2721 \u2013 2726, (2013)
\r\nK. Masui, H. Nakanotani<\/span><\/strong>, and C. Adachi
\r\nDOI: 10.1016\/j.orgel.2013.07.010<\/a><\/strong><\/dd>\r\n
[20]<\/dt>\r\n
Promising operational stability of high-efficiency organic light-emitting diodes based on thermally activated delayed fluorescence
\r\nSci. Rep.<\/strong>, 3, 2127 (2013)
\r\nH. Nakanotani<\/span><\/strong>, K. Masui, J. Nishide, T. Shibata and C. Adachi
\r\nDOI: 10.1038\/srep02127<\/a><\/strong>
\r\n[Press Release]<\/strong><\/a>
\r\n[Selected as a Focus Article by NPG Asia]<\/span><\/strong><\/a>\r\n

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[19]<\/dt>\r\n
Amplified spontaneous emission and electroluminescence from thiophene\/phenylene co-oligomer-doped p-bis(p-styrylstyryl)benzene crystals
\r\nAdv. Opt. Mater.<\/strong>, 1, 469 (2013)
\r\nH. Nakanotani<\/span><\/strong>, and C. Adachi
\r\nDOI: 10.1002\/adom.201200066<\/a><\/strong>
\r\n[High lighted as an back cover]<\/span><\/strong><\/a><\/dd>\r\n
[2011]<\/dt>\r\n
[18]<\/dt>\r\n
Photophysical characteristics of 4,4 \u2018-bis(N-carbazolyl)tolan derivatives and their application in organic light emitting diodes
\r\nJ. lumin.<\/strong> 131, 1520 (2011)
\r\nM. Ohkita, A. Endo, K. Sumiya, H. Nakanotani<\/span><\/strong>, T. Suzuki, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[17]<\/dt>\r\n
Formation of Organic Crystalline Nanopillar Arrays and Their Application to Organic Photovoltaic Cells
\r\nACS APPLIED MATERIALS<\/strong> & INTERFACES 3, 80 (2011)
\r\nH. Hirade, H. Nakanotani<\/span><\/strong>, M. Yahiro, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[16]<\/dt>\r\n
Highly conductive interface between a rubrene single crystal and a molybdenum oxide layer and its application in transistors
\r\nSolid State Commun.<\/strong> 151, 93 (2011)
\r\nH. Nakanotani<\/span><\/strong>, H. Kakizoe and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[2010]<\/dt>\r\n
[15]<\/dt>\r\n
Emission color tuning in ambipolar organic single crystal field-effect transistors by dye-doping
\r\nAdv. Funct. Mat.<\/strong> 20, 1610 (2010)
\r\nH. Nakanotani<\/span><\/strong>, M. Saito, H. Nakamura and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[14]<\/dt>\r\n
Organic light-emitting diodes containing multilayers of organic single crystals
\r\nAppl. Phys. Lett.<\/strong> 96, 053301 (2010)
\r\nH. Nakanotani<\/span><\/strong> and C. Adachi
\r\n[Top 20 Most Downloaded Articles: 11, Applied Physics Letters \u2014 February 2010]<\/span><\/strong><\/dd>\r\n<\/dl>\r\n

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\r\n
[2009]<\/dt>\r\n
[13]<\/dt>\r\n
Tuning of threshold voltage by interfacial carrier doping in organic single crystal ambipolar light-emitting transistors and their brightelectroluminescence
\r\nAppl. Phys. Lett.<\/strong> 95, 103307 (2009)
\r\nH. Nakanotani<\/span><\/strong>, M. Saito, M. Saito, H. Nakamura and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[12]<\/dt>\r\n
Highly balanced ambipolar mobilities with intense electroluminescence in field-effect transistors based on organic single crystal oligo(p- phenylenevinylene) derivatives
\r\nAppl. Phys. Lett.<\/strong> 95, 033308 (2009)
\r\nH. Nakanotani<\/span><\/strong>, M. Saito, M. Saito, H. Nakamura and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[11]<\/dt>\r\n
Effect of molecular morphology on amplified spontaneous emission of bis-styrylbenzene derivatives
\r\nAdv. Mater.<\/strong> 21, 4034 (2009)
\r\nR. Kabe, H. Nakanotani<\/span><\/strong>, T. Sakanoue, M. Yahiro, and C. Adachi\r\n\r\n\r\n\r\n

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[10]<\/dt>\r\n
Low threshold blue emission from first-order organic DFB laser using 2,7-bis[4-(N-carbazole)phenylvinyl]-9,9\u2032-spirobifluorene as active gain media
\r\nMolecular Crystal and Liquid Crystals<\/strong> 504, 1 (2009)
\r\nM. Hirade, H. Nakanotani<\/span><\/strong>, R. Hattori, A. Ikeda, M. Yahiro, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[2008]<\/dt>\r\n
[9]<\/dt>\r\n
Blue-light-emitting ambipolar field-effect transistors using an organic single crystal of 1,4-Bis(4-methylstyryl)benzene
\r\nAppl. Phys. Express<\/strong> 1 091801 (2008)
\r\nH. Nakanotani<\/span><\/strong>, R. Kabe, M. Yahiro, T. Takenobu, Y. Iwasa and C. Adachi
\r\n[Top 20 Most Downloaded Articles (September 2008)]<\/span> <\/strong><\/dd>\r\n<\/dl>\r\n

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\r\n
[2007]<\/dt>\r\n
[8]<\/dt>\r\n
Ambipolar field-effect transistor based on organic-inorganic hybrid-structure
\r\nAppl. Phys. Lett.<\/strong> 90, 262104 (2007)
\r\nH. Nakanotani<\/span><\/strong>, K. Yano, M. Yahiro and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[7]<\/dt>\r\n
Spectrally narrow emission from organic film under continuous-wave excitation
\r\nAppl. Phys. Lett.<\/strong> 90, 231109 (2007)
\r\nH. Nakanotani<\/span><\/strong>, Chihaya Adachi, Sadayuki Watanabe, and Ryuzi Katoh<\/dd>\r\n<\/dl>\r\n

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\r\n
[6]<\/dt>\r\n
Extremely low-threshold amplified spontaneous emission of 9,9\u2019-spirobifluorene derivatives and electroluminescence from field-effect transistor structure
\r\nAdv. Funct. Mater.<\/strong>, 17, 2328 (2007)
\r\nH. Nakanotani<\/span><\/strong>, S. Akiyama, D. Ohnishi, M. Moriwake, M. Yahiro, T. Yoshihara, S. Tobita, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[5]<\/dt>\r\n
Very low amplified spontaneous emission threshold and electroluminescence characteristics of 1,1\u2032-diphenyl substituted fluorene derivatives
\r\nOptical Materials,<\/strong> 30, 630 (2007)
\r\nH. Nakanotani<\/span><\/strong>, Naoki Matsumoto, Hiroyuki Uchiuzou, Masakazu Nishiyama, Masayuki Yahiro and Chihaya Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[4]<\/dt>\r\n
Spectrally Narrow Emission at Cutoff Wavelength from Edge of Electrically Pumped Organic Light-Emitting Diodes
\r\nJpn. J. Appl. Phys.<\/strong>, 46, L826 (2007)
\r\nD. Yokoyama, H. Nakanotani<\/span><\/strong>, Y. Setoguchi, M. Moriwake, D. Ohnishi, M. Yahiro, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[2006]<\/dt>\r\n
[3]<\/dt>\r\n
Optical and electrical properties of quinqueacetylphenyl derivatives and the application for organic field-effect transistors
\r\nJpn. J. Appl. Phys.<\/strong>, 45, L1331 (2006)
\r\nT. Oyamada, G. Shao, H. Uchiuzou,H. Nakanotani<\/span><\/strong>, A. Orita, J. Otera, M.Yahiro, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[2005]<\/dt>\r\n
[2]<\/dt>\r\n
Injection and transport of high current density of 1063A\/cm2 in organic light-emitting diodes under pulse excitation
\r\nJpn. J. Appl. Phys.<\/strong>, 44, 3659 (2005)
\r\nH. Nakanotani<\/span><\/strong>, T. Oyamada, Y. Kawamura, H. Sasabe, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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\r\n
[1]<\/dt>\r\n
Singlet-singlet and singlet-heat annihilations in fluorescence-based organic light-emitting diodes under steady-state high current density
\r\nAppl. Phys. Lett.<\/strong>, 86, 213506 (2005)
\r\nH. Nakanotani<\/span><\/strong>, H. Sasabe, and C. Adachi<\/dd>\r\n<\/dl>\r\n

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Proceeding<\/h4>\r\n
\r\n
<\/dt>\r\n
Low lasing threshold in organic distributed feedback solid state lasers using a Bisstyrylbenzene derivative as an active material
\r\nProc. SPIE Int. Soc. Opt. Eng. 5937, 59370W (2005)
\r\nHajime Nakanotani<\/span><\/strong>, Hiroyuki Sasabe and Chihaya Adachi<\/dd>\r\n<\/dl>\r\n

\u7dcf\u8aac,\u5358\u884c\u672c<\/h4>\r\n
\r\n
<\/dt>\r\n
\u300cLight-Emitting Organic Crystal Field-Effect Transistors for Future Organic Injection Lasers\u300d
\r\np. 603-619, Physics of Organic Semiconductors, 2nd, Completely New Revised Edition
\r\nWiley, (2012), Hajime Nakanotani and Chihaya Adachi<\/dd>\r\n
<\/dt>\r\n
\u300c\u6709\u6a5f\u8584\u819c\u592a\u967d\u96fb\u6c60\u306e\u6700\u65b0\u6280\u8853\u300d
\r\n\u30d3\u30b9\u30b9\u30c1\u30ea\u30eb\u30d9\u30f3\u30bc\u30f3\u8a98\u5c0e\u4f53\u3092\u6d3b\u6027\u5c64\u3068\u3059\u308b\u6709\u6a5fDFB\u30ec\u30fc\u30b6\u30fc\u306e\u767a\u632f\u7279\u6027\uff0c\u7b2c\uff15\u7ae0p.250-257
\r\n\u3231\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248(2005)
\r\n\u4e2d\u91ce\u8c37\u4e00\uff0c\u5b89\u9054\u5343\u6ce2\u77e2<\/dd>\r\n
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\u300c\u9032\u5316\u3059\u308b\u6709\u6a5f\u534a\u5c0e\u4f53\u300d
\r\n\u5fdc\u7528\u7de8\u7b2c\uff12\u7ae0
\r\n\u6709\u6a5f\u534a\u5c0e\u4f53\u30ec\u30fc\u30b6\u30fc\u306e\u6750\u6599\u30fb\u30c7\u30d0\u30a4\u30b9\u8a2d\u8a08
\r\n\u30a8\u30cc\u30fb\u30c6\u30a3\u30fc\u30fb\u30a8\u30b9\uff0c2006
\r\n\u5b89\u9054\u5343\u6ce2\u77e2\uff0c\u4e2d\u91ce\u8c37\u4e00<\/dd>\r\n
<\/dt>\r\n
\u300c\u6709\u6a5f\u534a\u5c0e\u4f53\u306e\u30c7\u30d0\u30a4\u30b9\u7269\u6027\u300d
\r\n\u6709\u6a5f\u767a\u5149\u30c8\u30e9\u30f3\u30b8\u30b9\u30bf\u3068\u6709\u6a5f\u534a\u5c0e\u4f53\u30ec\u30fc\u30b6\u30fc\uff089.4\u7bc0\uff09
\r\n\u8b1b\u8ac7\u793e\uff0c2012<\/dd>\r\n
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\u300c\u6709\u6a5f\u534a\u5c0e\u4f53\u754c\u9762\u306e\u5236\u5fa1\u30fb\u5206\u6790\u6280\u8853\u300d
\r\n\u60c5\u5831\u6a5f\u69cb\uff0c2012
\r\n\u52a0\u85e4\u62d3\u53f8\u3001\u4e2d\u91ce\u8c37\u4e00\u3001\u9ce5\u5c45\u660c\u53f2<\/dd>\r\n<\/dl>\r\n

\u53d7\u8cde<\/h4>\r\n
\r\n
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\u7b2c14\u56de\u5fdc\u7528\u7269\u7406\u5b66\u4f1a\u6709\u6a5f\u5206\u5b50\u30fb\u30d0\u30a4\u30aa\u30a8\u30ec\u30af\u30c8\u30ed\u30cb\u30af\u30b9\u5206\u79d1\u4f1a\u5968\u52b1\u8cde\uff082016\u5e74\uff09<\/b>
\r\n\u4e2d\u91ce\u8c37\u4e00<\/dd>\r\n
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\u7b2c9\u56de\u6709\u6a5fEL\u8a0e\u8ad6\u4f1a \u696d\u7e3e\u8cde\uff082016\u5e74\uff09<\/b>
\r\n\u984c\u76ee\u300c\u30cf\u30a4\u30d1\u30fc\u30d5\u30eb\u30aa\u30ec\u30c3\u30bb\u30f3\u30b9\u6a5f\u69cb\u306b\u3088\u308b\u9ad8\u52b9\u7387\u6709\u6a5fEL\u30c7\u30d0\u30a4\u30b9\u306e\u5b9f\u73fe\u300d
\r\n\u4e2d\u91ce\u8c37\u4e00<\/dd>\r\n
<\/dt>\r\n
\u7b2c17\u56de\u6709\u6a5fEL\u8a0e\u8ad6\u4f1a \u8b1b\u6f14\u5968\u52b1\u8cde\uff082013\u5e74\uff09<\/b>
\r\n\u984c\u76ee\u300c\u71b1\u6d3b\u6027\u5316\u9045\u5ef6\u86cd\u5149\u6709\u6a5f\uff25\uff2c\u7d20\u5b50\u306b\u304a\u3051\u308b\u7d20\u5b50\u52a3\u5316\u56e0\u5b50\u306e\u89e3\u660e\u300d
\r\n\u4e2d\u91ce\u8c37\u4e00<\/dd>\r\n
\u7b2c26\u56de\u5fdc\u7528\u7269\u7406\u5b66\u4f1a \u8b1b\u6f14\u5968\u52b1\u8cde\uff082009\u5e74\uff09<\/b>
\r\n\u984c\u76ee\u300c\u6709\u6a5f\u5358\u7d50\u6676\u8584\u819c\u3092\u7528\u3044\u305f\u6709\u6a5fEL\u7d20\u5b50\u300d
\r\n\u4e2d\u91ce\u8c37\u4e00\uff0c\u5b89\u9054\u5343\u6ce2\u77e2<\/dd>\r\n<\/dl>\r\n

\u5b66\u4f1a\u767a\u8868<\/h4>\r\n
\r\n
<\/dt>\r\n
<\/dd>\r\n<\/dl>\r\n
\r\n
\u56fd\u969b\u5b66\u4f1a (\u53e3\u982d\u767a\u8868)<\/a><\/dd>\r\n
<\/dt>\r\n
High efficiency organic light-emitting diodes with conventional fluorescent emitters
\r\nLight, Energy and the Environment Congress, OSA, Dec 3, 2014 (ANU, Canberra, Australia)
\r\nH. Nakanotani<\/span><\/strong> and C. Adachi<\/dd>\r\n
A New Route of Triplet Harvesting for High-Efficiency Fluorescence OLEDs
\r\nMRS fall, Dec 2, 2013 (Boston, USA)
\r\nH. Nakanotani<\/span><\/strong> K. Masui, H. Tanaka and C. Adachi<\/dd>\r\n
Light-emitting devices based on organic single crystals
\r\nIMID2009, 2009.10.12~10.16 (KINTEX, Seoul, Korea)
\r\nH. Nakanotani<\/span><\/strong> and C. Adachi(Invited Talk.)<\/span><\/strong><\/dd>\r\n
<\/dt>\r\n
Organic light emitting devices having multi-layer structure of thin-film organic single crystals
\r\nSPIE\u2019s International Symposium on Optics & Photonics 2009, 2009.8.2~8.6 (San Diego)
\r\nH. Nakanotani<\/span><\/strong> and C. Adachi<\/dd>\r\n
Ambipolar field-effect transistor based on organic-inorganic oxide heterostructure
\r\nE-MRS 2007 Spring Meeting Strasbourg, France \u2013 May 28th to June 1st, 2007
\r\nH. Nakanotani<\/span><\/strong>, Koki Yano and Chihaya Adachi<\/dd>\r\n
Low lasing threshold in organic distributed feedback solid state lasers using bisstyrylbenzene derivative as active material
\r\nSPIE\u2019s International Symposium on Optics & Photonics 2005, 2005.7.31~8.4 (San Diego)
\r\nH. Nakanotani<\/span><\/strong>, H. Sasabe and C. Adachi<\/dd>\r\n<\/dl>\r\n
<\/dl>\r\n

 <\/p>\r\n

<\/dl>","protected":false},"excerpt":{"rendered":"

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