Construction of Highly-efficient Photon Upconversion System Utilizing Precise Control of Configuration of Dyads
Project/Area Number |
18K14202
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Research Category |
Grant-in-Aid for Early-Career Scientists
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Allocation Type | Multi-year Fund |
Review Section |
Basic Section 33010:Structural organic chemistry and physical organic chemistry-related
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Research Institution | Osaka Prefecture University |
Principal Investigator |
Matsui Yasunori 大阪府立大学, 工学(系)研究科(研究院), 助教 (90709586)
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Project Period (FY) |
2018-04-01 – 2020-03-31
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Project Status |
Completed (Fiscal Year 2019)
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Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
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Keywords | アップコンバージョン / エネルギー移動 / 三重項-三重項消滅 / 一重項分裂 / フォトンアップコンバージョン / 三重項ー三重項消滅 / 光波長変換 |
Outline of Final Research Achievements |
During the study period, dyads of diphenylanthracene linked by various linkers were synthesized and their TTA-UC behavior was evaluated. We have constructed a new optical system using a continuous-wave laser and studied the effect of the excitation light intensity on TTA-UC. The threshold intensity was a little higher than the corresponding monomer. The major factor is that the construction of dyads reduced the selectivity of the singlet in TTA. However, the results also support the progression of intramolecular TTAs proposed in this study, and it will be a breakthrough if we can synthesize dyads possessing a high selectivity of singlet excited state. We also synthesized an adamantane-linked tetracene dyed, and confirmed the progress of intramolecular singlet fission, which is the reverse process of TTA.
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Academic Significance and Societal Importance of the Research Achievements |
本研究では,非共役リンカーで連結したダイアドを合成し,それを用いたフォトンアップコンバージョンの検討を行った.その結果,多重励起子に関する様々な知見が得られ,将来的には光触媒や太陽光発電の高効率化につながる知見が得られた.
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Report
(3 results)
Research Products
(117 results)
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[Presentation] Microflow Photochemical Synthesis and Organic Semiconductor Characteristics of Tetrathienonaphthalene2019
Author(s)
K. Taniguchi, Y. Matsui, T. Asada, M. Kumeda, A. Yamamoto, K. Takagi, Y. Suenaga, K. Nagae, E. Ohta, S. Koseki, H. Naito, H. Ikeda
Organizer
The 18th International Symposium on Novel Aromatic Compounds (ISNA-18) (Sapporo, Japan, July 2019)
Related Report
Int'l Joint Research
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[Presentation] Induction of Helical Chirality of Foldamer Possessing Triethylene Glygol Chains2019
Author(s)
T. Tsuno, S. Koga, E. Ohta, S. Tani, T. Ogaki, Y. Matsui, H. Ikeda
Organizer
The 7th HCMUT-TKU-OPU-KMITL-DLU-TNU Joint Symposium on Chemistry, Environment, Natural Sciences and Technologies (JSCENS-7) (Ho Chi Minh City, Vietnam, November 2019)
Related Report
Int'l Joint Research
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[Presentation] Microflow Photosynthesis and Organic Semiconductor Characteristics of Tetrathienonaphthalene2018
Author(s)
K. Taniguchi, Y. Matsui, T. Asada, M. Kumeda, A. Yamamoto, K. Takagi, Y. Suenaga, K. Nagae, E. Ohta, S. Koseki, H. Naito, H. Ikeda
Organizer
14th Korea-Japan Symposium on Frontier Photoscience (KJFP2018)
Related Report
Int'l Joint Research
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[Presentation] Microflow Synthesis and Organic Semiconductor Characteristics of Tetrathienonaphthalene2018
Author(s)
K. Taniguchi, Y. Matsui, T. Asada, M. Kumeda, A. Yamamoto, K. Takagi, Y. Suenaga, K. Nagae, E. Ohta, S. Koseki, H. Naito, H. Ikeda
Organizer
The 7th ECUST-TKU-KIST-OPU on Advanced Materials and Their Applications
Related Report
Int'l Joint Research
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[Presentation] Microflow Synthesis and Organic Semiconductor Characteristics of Alkylated Tetrathienonaphthalenes2018
Author(s)
Y. Matsui, K. Taniguchi, T. Asada, M. Kumeda, A. Yamamoto, K. Takagi, Y. Suenaga, K. Nagae, E. Ohta, S. Koseki, H. Naito, H. Ikeda
Organizer
The 13th International Symposium on Organic Reactions (ISOR-13)(2018年11月,新竹,台湾)
Related Report
Int'l Joint Research
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