略歴
2005年	東京工業大学 大学院総合理工学研究科 博士課程修了
2005年~	東京大学 大学院理学系研究科 COE特任研究員
2006年~	日本学術振興会特別研究員(PD) (東京大学 工学系研究科)
2008年~	東京大学 大学院工学系研究科 化学生命工学専攻 助教
2010年~	九州大学 大学院工学研究院 応用化学部門 准教授 (2011年~　JSTさきがけ研究員 兼任)
学位
博士(工学) （東京工業大学、2005年）
所属学会
日本化学会、高分子学会、日本液晶学会、有機合成化学協会、米国化学会、米国MRS
研究分野
機能性有機材料化学
趣味
スポーツ (野球、バレー、スキー、ジム通い)、食べ歩き 😆
Profile
Takuma YASUDA was born in 1977 in Aichi, Japan. He received his PhD in 2005 from Tokyo Institute of Technology under the supervision of Prof. Takakazu Yamamoto. He then began postdoctoral research focusing on functional liquid-crystalline materials with Prof. Takashi Kato at the University of Tokyo. In 2008, he was appointed to an Assistant Professor at the University of Tokyo. Currently, he is an Associate Professor, working in the group of Prof. Chihaya Adachi at Kyushu University. He is also a concurrent researcher of PRESTO, Japan Science and Technology Agency (JST). His research is directed towards the design, synthesis, and functionalization of π-conjugated molecular materials. Current topics of research include their applications to organic electronics devices. He received the Chemical Society of Japan Award for Young Chemists (2014), the Hitachi Chemical Award from the Society of Polymer Science, Japan (2013), and the Award for Young Researchers from the Japanese Liquid Crystal Society (2010).

研究業績 (Achievements)

原著論文 (Original Papers with Peer Review)

[58]

W. Shin, T. Yasuda,* Y. Hidaka, G. Watanabe, R. Arai, K. Nasu, T. Yamaguchi, W. Murakami, K. Makita, and C. Adachi,*
“π-Extended Narrow-Bandgap Diketopyrrolopyrrole-Based Oligomers for Solution-Processed Inverted Organic Solar Cells”
Adv. Energy Mater. 2014, 4, in press. 

[57]

C. Mayr, S. Y. Lee, T. D. Schmidt, T. Yasuda, C. Adachi, and W. Brütting,*
“Efficiency Enhancement of Organic Light-Emitting Diodes Incorporating a Highly Oriented Thermally Activated Delayed Fluorescence Emitter”
Adv. Funct. Mater. 2014, 24, in press. 

[56]

H. Nakanotani, T. Higuchi, T. Furukawa, K. Masui, K. Morimoto, M. Numata, H. Tanaka, Y. Sagara, T. Yasuda, and C. Adachi,*
“High Efficiency Light-Emitting Diodes with Fluorescent Emitters”
Nature Commun. 2014, 5, 4016. 

[55]

S. Y. Lee, T. Yasuda,* Y. S. Yang, Q. Zhang, and C. Adachi,*
“Luminous Butterflies: Efficient Exciton Harvesting by Benzophenone Derivatives for Full-Color Delayed Fluorescence OLEDs”
Angew. Chem. Int. Ed. 2014, 53, 6520-6524. 

[54]

H. Ohkuma, T. Nakagawa, K. Shizu, T. Yasuda,* and C. Adachi,*
“Thermally Activated Delayed Fluorescence from a Spiro-Diazafluorene Derivative”
Chem. Lett. 2014, 43, 1017-1019. (Selected as an Editor’s Choice) 

[53]

T. Takahashi, K. Shizu, T. Yasuda,* K. Togashi, and C. Adachi,*
“Donor–Acceptor Structured 1,4-Diazatriphenylene Derivatives Exhibiting Thermally Activated Delayed Fluorescence: Design and Synthesis, Photophysical Properties and OLED Characteristics”
Sci. Technol. Adv. Mater. 2014, 15, 034202. 

[52]

T. Komori, H. Nakanotani, T. Yasuda,* and C. Adachi,*
“Light-Emitting Organic Field-Effect Transistors Based on Highly Luminescent Single Crystals of Thiophene/Phenylene Co-Oligomers”
J. Mater. Chem. C 2014, 2, 4918-4921. 

[51]

J. Y. Kim, T. Yasuda,* Y. S. Yang, N. Matsumto, and C. Adachi,*
“Polymorphism in 9,9-Diarylfluorene-Based Organic Semiconductors: Influence on Optoelectronic Functions”
Chem. Commun. 2014, 50, 1523-1526. (Highlighted as an Inside Front Cover) 

[50]

H. Mieno, T. Yasuda,* Y. S. Yang, and C. Adachi,*
“Self-Assembly, Physicochemical, and Field-Effect Transistor Properties of Solution-Crystallized Organic Semiconductors Based on π-Extended Dithieno[3,2-b:2′,3′-d]thiophenes”
Chem. Lett. 2014, 43, 293-295.

[49]

T. Nishimoto, T. Yasuda,* Y. S. Yang, R. Kondo, and C. Adachi,*
“A Six-Carbazole-Decorated Cyclophosphazene as a Host with High Triplet Energy Host to Realize Efficient Delayed-Fluorescence OLEDs”
Mater. Horiz. 2014, 1, 264-269. 

[48]

K. Nasu, T. Nakagawa, H. Nomura, C.-J. Lin, C.-H. Cheng, M.-R. Tseng, T. Yasuda, and C. Adachi,*
“A Highly Luminescent Spiro-Anthracenone-Based Organic Light-Emitting Diode through Thermally Activated Delayed Fluorescence”
Chem. Commun. 2013, 49, 10385–10387. 

[47]

Y. S. Yang, T. Yasuda,* H. Kakizoe, H. Mieno, H. Kino, Y. Tateyama, and C. Adachi,*
“High Performance Organic Field-Effect Transistors Based on Single-Crystal Microribbons and Microsheets of Solution-Processed Dithieno[3,2-b:2′,3′-d]thiophene Derivatives”
Chem. Commun. 2013, 49, 6483–6485. (Highlighted as an Inside Back Cover) 

[46]

W. Shin, T. Yasuda,* G. Watanabe, Y. S. Yang, and C. Adachi,*
“Self-Organizing Mesomorphic Diketopyrrolopyrrole Derivatives for Efficient Solution-Processed Organic Solar Cells”
Chem. Mater. 2013, 25, 2549–2556. 

[45]

J. Lee, K. Shizu, H. Tanaka, H. Nomura, T. Yasuda, and C. Adachi,*
“Oxadiazole- and Triazole-Based Highly-Efficient Thermally-Activated Delayed Fluorescence Emitters for Organic Light-Emitting Diodes”
J. Mater. Chem. C 2013, 1, 4599-4604. 

[44]

K. Togashi, Y. Sagara, T. Yasuda, and C. Adachi,*
“Molecular Design of High-Molecular-Orientation Electron-Transport Materials and Application to Organic Light-Emitting Diodes”
Chem. Lett. 2013, 42, 651–653. 

[43]

A. Wada, T. Yasuda,* Q. Zhang, Y. S. Yang, I. Takasu, S. Enomoto, and C. Adachi,*
“A Host Material Consisting of a Phosphinic Amide Directly Linked Donor–Acceptor Structure for Efficient Blue Phosphorescent Organic Light-Emitting Diodes”
J. Mater. Chem. C 2013, 1, 2404-2407. (Selected as Top 10 most-read Journal of
Materials Chemistry C articles in February and March 2013) 

[42]

M. Hirade, T. Yasuda, and C. Adachi,*
“Effects of Intramolecular Donor–Acceptor Interactions on Bimolecular Recombination in Small-Molecule Organic Photovoltaic Cells”
J. Phys. Chem. C 2013, 117, 4986–4991. 

[41]

K. Togashi, T. Yasuda, and C. Adachi,*
“Triphenylene-Based Host Materials for Low-Voltage and Highly Efficient Red Phosphorescent Organic Light-Emitting Diodes”
Chem. Lett. 2013, 42, 383–385. 

[40]

J. Y. Kim, T. Yasuda,* Y. S. Yang, and C. Adachi,*
“Bifunctional Star-Burst Amorphous Molecular Materials for OLEDs: Achieving Highly Efficient Solid-State Luminescence and Carrier Transport Induced by Spontaneous Molecular Orientation”
Adv. Mater. 2013, 25, 2666–2671. (Highlighted as an Inside Front Cover) 

[39]

Y. S. Yang, T. Yasuda,* and C. Adachi,*
“Organic Single-Crystal Transistors Based on π-Extended Heteroheptacene Microribbons”
Bull. Chem. Soc. Jpn. 2012, 85, 1186-1191. (Selected as a BCSJ Award Article and highlighted as a Cover) 

[38]

K. Togashi, S. Nomura, N. Yokoyama, T. Yasuda, and C. Adachi,*
“Low Driving Voltage Characteristics of Triphenylene Derivatives as Electron Transport Materials in Organic Light-Emitting Diodes”
J. Mater. Chem. 2012, 22, 20689-20695. 

[37]

S. Y. Lee, T. Yasuda, H. Nomura, and C. Adachi,*
“High-Performance Organic Light-Emitting Diodes Utilizing Efficient Thermally Activated Delayed Fluorescence from Triazine-Based Donor-Acceptor Hybrid Molecules”
Appl. Phys. Lett. 2012, 101, 093306. (Ranked in Top 20 Most Read Articles) 

[36]

R. Kondo, T. Yasuda,* Y. S. Yang, J. Y. Kim, and C. Adachi,*
“Highly Luminescent π-Conjugated Dithienometalloles: Photophysical Properties and Their Application in Organic Light-Emitting Diodes”
J. Mater. Chem. 2012, 22, 16810-16816. (Selected as Top 10 most-read JMC articles, and highlighted in Noteworthy Chemistry by the American Chemical Society) 

[35]

A. Wada, Q. Zhang, T. Yasuda, I. Takasu, S. Enomoto, and C. Adachi,*
“Efficient Luminescence from a Copper(I) Complex Doped in Organic Light-Emitting Diodes by Suppressing C-H Vibrational Quenching”
Chem. Commun. 2012, 48, 5340-5342. 

[34]

T. Yasuda,* T. Shimizu, F. Liu, G. Ungar, and T. Kato,*
“Electro-Functional Octupolar π-Conjugated Liquid Crystals”
J. Am. Chem. Soc. 2011, 133, 13437-13444. 

[33]

M. Taneda, T. Yasuda, and C. Adachi,*
“Horizontal Orientation of a Linear-Shaped Platinum(II) Complex in Organic Light-Emitting Diodes with a High Light Out-Coupling Efficiency”
Appl. Phys. Exp. 2011, 4, 071602. 

[32]

T. Yasuda, K. Tanabe, T. Tsuji, K. K. Coti, I. Aprahamian, J. F. Stoddart,* and T. Kato,*
“A Redox-Switchable [2]Rotaxane in a Liquid-Crystalline State”
Chem. Commun. 2010, 46, 1224-1226. (Selected as a Hot Article, and highlighted in NPG Asia Materials) 

[31]

Y. Shoji, M. Yoshio, T. Yasuda, M. Funahashi, and T. Kato,
“Alignment of Photoconductive Self-Assembled Fibers Composed of π-Conjugated Molecules under Electric Fields”
J. Mater. Chem. 2010, 20, 173-179. 

[30]

Y. Hirai, S. S. Babu, V. K. Praveen, T. Yasuda, A. Ajayaghosh, and T. Kato,
“Anisotropic Self-Assembly of Photoluminescent Oligo(p-phenylenevinylene) Derivatives in Liquid Crystals: An Effective Strategy for the Macroscopic Alignment of π-Gels”
Adv. Mater. 2009, 21, 4029-4033. (Highlighted as an Inside Front Cover) 

[29]

K. Isoda, T. Yasuda, and T. Kato,
“Truxene-Based Columnar Liquid Crystals: Self-Assembled Structures and Electro-Active Properties”
Chem. Asian J. 2009, 4, 1619-1625. (Selected as a VIP paper and highlighted as a Cover Picture) 

[28]

E. D. Baranoff, J. Voignier, T. Yasuda, V. Heitz, J.-P. Sauvage, and T. Kato,
“Macrocycle-Based Liquid Crystals: A Study of Topological Effects on Mesomorphism”
Mol. Cryst. Liq. Cryst. 2009, 509, 165-172. 

[27]

M. Kimura, T. Hatano, T. Yasuda, J. Morita, Y. Akama, K. Minoura, T. Shimomura, and T. Kato,
“Photoluminescent Liquid Crystals Based on Trithienylphosphine Oxides”
Chem. Lett. 2009, 38, 800-801. 

[26]

K. Minoura, Y. Akama, J. Morita, T. Yasuda, T. Kato, and T. Shimomura,
“Supramolecular Structure of Columnar Liquid Crystalline π-Conjugated Oligothiophenes with Highly Polarized Photoluminescent Properties”
J. Appl. Phys. 2009, 105, 113513-6. 

[25]

Y.-L. Zhao, N. Erina, T. Yasuda, T. Kato, and J. F. Stoddart,
“A Layered Liquid Crystalline Droplet”
J. Mater. Chem. 2009, 19, 3469-3474. 

[24]

T. Yasuda, H. Ooi, J. Morita, Y. Akama, K. Minoura, M. Funahashi, T. Shimomura, and T. Kato,
“π-Conjugated Oligothiophene-Based Polycatenar Liquid Crystals: Self-Organization and Photoconductive, Luminescent, and Redox Properties”
Adv. Funct. Mater. 2009, 19, 411-419. (Highlighted as an Inside Front Cover, and selected as a Fast Breaking Paper in Materials Science by Thomson Reuters)

[23]

K. Tanabe, T. Yasuda, and T. Kato,
“Luminescent Ionic Liquid Crystals Based on Tripodal Pyridinium Salts”
Chem. Lett. 2008, 37, 1208-1209. 

[22]

K. Isoda, T. Yasuda, and T. Kato,
“Dipole-Driven Self-Assembly of Redox-Active Mesogenic Tetracyanoanthraquinodimethanes”
J. Mater. Chem. 2008, 18, 4522-4528. 

[21]

T. Morikita, T. Yasuda, and T. Yamamoto,
“Luminescent π-Conjugated Poly(aryleneethynylene)s Consisting of Plural Aromatic Units: Preparation and Systematic Studies on Their Optical Properties”
React. Funct. Polym. 2008, 68, 1483-1491. 

[20]

K. Tanabe, T. Yasuda, M. Yoshio, and T. Kato,
“Viologen-Based Redox-Active Ionic Liquid Crystals Forming Columnar Phases”
Org. Lett. 2007, 9, 4271-4274. 

[19]

T. Yasuda, K. Namekawa, T. Iijima, and T. Yamamoto,
“New Luminescent 1,2,4-Triazole/Thiophene Alternating Copolymers: Synthesis, Characterization, and Optical Properties”
Polymer 2007, 48, 4375-4384. 

[18]

E. D. Baranoff, J. Voignier, T. Yasuda, V. Heitz, J.-P. Sauvage, and T. Kato,
“A Liquid-Crystalline [2]Catenane and Its Copper(I) Complex”
Angew. Chem. Int. Ed. 2007, 46, 4680-4683. 

[17]

I. Aprahamian, T. Yasuda, T. Ikeda, S. Saha, W. R. Dichtel, K. Isoda, T. Kato, and J. F. Stoddart,
“A Liquid-Crystalline Bistable [2]Rotaxane”
Angew. Chem. Int. Ed. 2007, 46, 4675-4679. 

[16]

M. Kimura, T. Yasuda, K. Kishimoto, G. Gotz, P. Bauerle, and T. Kato,
“Oligothiophene-Based Liquid Crystals Exhibiting Smectic A Phases in Wider Temperature Ranges”
Chem. Lett. 2006, 35, 1150-1151. 

[15]

T. Yasuda, K. Kishimoto, and T. Kato,
“Columnar Liquid Crystalline π-Conjugated Oligothiophenes”
Chem. Commun. 2006, 3399-3401. 

[14]

T. Yamamoto, T. Yasuda, K. Kobayashi, I. Yamaguchi, T. Koizumi, D. Ishii, M. Nakagawa, Y. Mashiko, and N. Shimizu,
“Utilization of Industrially Available 2,3-Dichloro-1,3-butadiene for Direct Synthesis of 2,3-Diaryl-1,3-butadienes”
Bull. Chem. Soc. Jpn. 2006, 79, 498-500. 

[13]

T. Yasuda, Y. Sakai, S. Aramaki, and T. Yamamoto,
“New Coplanar (ABA)n-Type Donor-Acceptor π-Conjugated Copolymers Constituted of Alkylthiophene and Pyridazine: Synthesis Using Hexamethylditin, Self-Organized Solid Structure, and Optical and Electrochemical Properties of the Copolymers”
Chem. Mater. 2005, 17, 6060-6068. 

[12]

T. Yasuda, T. Imase, and T. Yamamoto,
“Synthesis, Characterization, and Optical and Electrochemical Properties of New 2,1,3-Benzoselenadiazole-Based CT-Type Copolymers”
Macromolecules 2005, 38, 7378-7385. 

[11]

T. Yamamoto, T. Yasuda, Y. Sakai, and S. Aramaki,
“Ambipolar Field-Effect Transistor (FET) and Redox Characteristics of a π-Conjugated Thiophene/1,3,4-Thiadiazole CT-Type Copolymer”
Macromol. Rapid Commun. 2005, 26, 1214-1217. (Highlighted as a Back Cover) 

[10]

T. Yamamoto, B.-L. Lee, I. Nurulla, T. Yasuda, I. Yamaguchi, A. Wada, C. Hirose, M. Tasumi, A. Sakamoto, and E. Kobayashi,
“Transfer of Photoenergy in π-Conjugated Polymers. Two Types of Photoluminescence that Involve Energy Transfer along a Polymer Chain”
J. Phys. Chem. B 2005, 109, 10605-10610. 

[9]

T. Yasuda, T. Imase, Y. Nakamura, and T. Yamamoto,
“New Alternative Donor-Acceptor Arranged Poly(Aryleneethynylene)s and Their Related Compounds Composed of Five-Membered Electron-Accepting 1,3,4-Thiadiazole, 1,2,4-Triazole, or ,4-Dinitrothiophene Units: Synthesis, Packing Structure, and Optical Properties”
Macromolecules 2005, 38, 4687-4697. 

[8]

T. Yasuda, T. Imase, S. Sasaki, and T. Yamamoto, “Synthesis,
Solid Structure, and Optical Properties of New Thiophene-Based Alternating π-Conjugated Copolymers Containing 4-Alkyl-1,2,4-triazole or 1,3,4-Thiadiazole Unit as the Partner Unit”
Macromolecules 2005, 38, 1500-1503. 

[7]

T. Yamamoto, K. Kobayashi, T. Yasuda, Z.-H. Zhou, I. Yamaguchi, T. Ishikawa, and S. Koshihara,
“Preparation of Polyacetylenes via Organometallic C-C Coupling Reactions”
Polym. Bull. 2004, 52, 315-319. 

[6]

T. Yasuda, I. Yamaguchi, and T. Yamamoto,
“Preparation of N-Grafted Polyanilines with Oligoether Side Chains by Using Ring-Opening Graft Copolymerization of Epoxide, and Their Optical, Electrochemical and Thermal Properties and Ionic Conductivity”
J. Mater. Chem. 2003, 13, 2138-2144. 

[5]

T. Yasuda and T. Yamamoto,
“Synthesis and Characterization of New Luminescent 1,10-Phenanthroline- and Pyridine-Containing π-Conjugated Polymers. Their Optical Response to Protic Acid, Mⁿ⁺, and Solvents”
Macromolecules 2003, 36, 7513-7519. 

[4]

T. Yamamoto, Y. Saitoh, K. Anzai, H. Fukumoto, T. Yasuda, Y. Fujiwara, B.-K. Choi, K. Kuboto, and T. Miyamae,
“Poly(1,10-phenanthroline-3,8-diyl) and Its Derivatives. Preparation, Optical and Electrochemical Properties, Solid Structure, and Their Metal Complexes”
Macromolecules 2003, 36, 6722-6729. 

[3]

T. Yasuda, I. Yamaguchi, and T. Yamamoto,
“Preparation of N-Grafted Polyanilines Utilizing Ring-Opening Copolymerization of Epoxide. Tuning of Solubility and Optical and Electrochemical Properties of Polyaniline”
Synth. Met. 2003, 139, 35-38. 

[2]

T. Yasuda, I. Yamaguchi, and T. Yamamoto,
“A New Soluble 1,10-Phenanthroline-Containing π-Conjugated Polymer: Synthesis and Effect of Metal Complexation on Optical Properties”
Adv. Mater. 2003, 15, 293-296. 

[1]

I. Yamaguchi, T. Yasuda, and T. Yamamoto,
“Ring-Opening Graft Copolymerization of Epoxide with Polyaniline: Chemical Properties and Lithium Ionic Conductivity of the Copolymer”
J. Polym. Sci., Part A: Polym. Chem. 2001, 39, 3137-3142. 

総説・解説 (Review Papers)

[6]

J. Sakuda, T. Yasuda, and T. Kato,
“Liquid-Crystalline Catenanes and Rotaxanes”
Isr. J. Chem. 2012, 52, 854-862. 

[5]

安田 琢麿・加藤 隆史,
“電子活性π共役液晶の新材料設計と機能化”
液晶 2011, 15, 132-137. 

[4]

T. Kato, Y. Shoji, M. Yoshio, S. Yamane, and T. Yasuda,
“Functional Soft Materials: Nanostructured Liquid crystals and Self-Assembled Fibrous Aggregates”
J. Synth. Org. Chem. Jpn. 2010, 68, 1169-1174. 

[3]

T. Kato, T. Yasuda, Y. Kamikawa, and M. Yoshio,
“Self-Assembly of Functional Columnar Liquid Crystals”
Chem. Commun. 2009, 729-739. (Ranked as a ChemComm Most Cited Feature Article 2009) 

[2]

I. Aprahamian, O. S. Miljanic, W. R. Dichtel, K. Isoda, T. Yasuda, T. Kato, and J. F. Stoddart,
“Clicked Interlocked Molecules”
Bull. Chem. Soc. Jpn. 2007, 80, 1856-1869. 

[1]

T. Yamamoto, I. Yamaguchi, and T. Yasuda,
“PAEs with Heteroaromatic Rings”
Adv. Polym. Sci. 2005, 177, 181-208. 

著書 (Book Chapters)

[7]

K. Isoda, T. Yasuda, M. Funahashi, and T. Kato,
“Redox-Active (Electrochromic) Liquid Crystals”
Handbook of Liquid Crystals, 2nd edition (Ed. J. W. Goodby et al.), Chapter 24, in press, Wiley-VCH, Germany (2014) 

[6]

M. Funahashi, T. Yasuda, and T. Kato,
“Liquid Crystal Semiconductors: Oligothiophene and Related Materials”
Handbook of Liquid Crystals, 2nd edition (Ed. J. W. Goodby et al.), Chapter 23, in press, Wiley-VCH, Germany (2014) 

[5]

安田 琢麿,
最先端材料システムOne Point（第3巻）：自己組織化と機能材料（高分子学会 編, 分担執筆）
pp. 78-88, 共立出版 (2012) 

[4]

T. Yasuda and T. Kato,
“Advanced Systems of Supramolecular Liquid Crystals”
Supramolecular Soft Matter: Applications in Materials and Organic Electronics
(Ed: T. Nakanishi), Chapter 14, pp. 283-299, Wiley, Germany (2011) 

[3]

安田 琢麿・加藤 隆史,
“機能性ナノ構造液晶の新展開”
月刊ファインケミカル　2011年3月号 (Vol. 40, No. 3)
pp. 36-41, シーエムシー出版 (2011) 

[2]

舟橋 正浩・安田 琢麿・加藤 隆史,
“液晶性有機半導体のナノ構造化”
液晶―構造制御と機能化の最前線（加藤隆史 監修, 分担執筆）
pp. 151-158, シーエムシー出版 (2010) 

[1]

安田 琢麿・加藤 隆史,
“電子共役系の自己組織化と機能”
電子共役系有機材料の創製・機能開発・応用 （檜山爲次郎 監修, 分担執筆）
pp. 254-264, シーエムシー出版 (2008) 

受賞 (Awards)

2014年3月

日本化学会 進歩賞
(The Chemical Society of Japan Award for Young Chemists) 

2013年9月

高分子学会 日立化成賞
(SPSJ Hitachi Chemical Award) 

2013年6月

有機合成化学協会九州山口支部 奨励賞
(Award for a Creative Young Chemist, Kyushu-Yamaguchi Branch, The Society of Synthetic Organic Chemistry, Japan) 

2012年11月

日本化学会 BCSJ論文賞
(BCSJ Award from the Chemical Society of Japan) 

2012年4月

日本化学会 優秀講演賞(学術)
(CSJ Presentation Award 2012 from the Chemical Society of Japan) 

2011年2月

有機合成化学協会 富士フィルム研究企画賞
(Fujifilm Award in Synthetic Organic Chemistry, Japan) 

2010年9月

日本液晶学会賞 奨励賞
(Award for Young Researchers from the Japanese Liquid Crystal Society) 

2009年4月

日本化学会 優秀講演賞(学術)
(CSJ Presentation Award 2009 from the Chemical Society of Japan) 

2007年1月

日本MRS学術シンポジウム 奨励賞
(Award for Encouragement of Research in Materials Science from the Materials Research Society of Japan) 

2006年9月

日本液晶学会 虹彩賞
(Kosai Award from Japanese Liquid CrystalSociety) 

2006年2月

手島記念研究賞 博士論文賞
(Tejima Doctoral Dissertation Award)