Lin, Tzu-Chau
Position Professor and Director
Name Lin, Tzu-Chau
Email tclin@ncu.edu.tw
Office Tel No. (03) 4227151 ext. 65925
website http://tclinlab.wix.com/lin-tc-lab
professional field Organic Chemistry, Organic Spectroscopy, Materials Chemistry
研究專長 Development of novel optoelectronic materials, Two-photon materials: Synthesis and characterization, Molecular design for strong fluorescent materials
Diploma
Country School Name Department Degree Duration
U.S.A. State University of New York at Buffalo Department of Chemistry Ph.D. 1998.08 ~ 2002.10
Taiwan Tamkang University Department of Chemistry B.S 1990.09 ~ 1994.06
Experience
Duration
2019.08 ~ 2021.07
2015.08 ~ Up to today
2010.08 ~ 2015.07
2005.08 ~ 2010.07
2004.02 ~ 2005.07
2002.10 ~ 2004.01
Personal Book
譯著
原著: D. L. Pavia, G. M. Lampman, G. S. Kriz, and James R. Vyvyan: Introduction to Spectroscopy (有機光譜學) 5th Ed.; 編譯: 林子超 (Annotated by Tzu-Chau Lin);    新加坡商聖智學習亞洲私人有限公司台灣分公司 (Cengage Learning Asian Pte Ltd.) 2015 年1月出版。
Personal Honor
Honor Category Year Award Name Awarding Unit
Inside School Honor 2018
Inside School Honor 2018
Inside School Honor 2015
Inside School Honor 2015
Inside School Honor 2014
Inside School Honor 2013
Inside School Honor 2013
Inside School Honor 2007
Personal Research
 

歡迎參觀林子超老師的有機光子材料實驗室!

 

我們的核心研究方向:多功能有機螢光材料的開發與合成


本實驗室目前致力於開發及合成在溶液態、固態與膜態皆具有強吸光及螢光特性之有機共軛分子,此類分子乃是具有極高經濟價值的特用化學品,可作為許多有機光電元件的核心與關鍵材料,諸如有機發光二極體(OLED)、有機太陽能電池(OSC)、有機固態染料雷射(Organic solid-state lasers)、生醫顯像劑 (bio-imaging agents)與化學感測器(chemosensors)等。


單層有機發光二極體雛型元件
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另一方面,我們也長期致力於雙光子吸收材料的研發並探索分子結構與雙光子吸收行為間的細微關聯。此類材料在有機3D光學記憶體(3D-Optical Data Storage Device)及光功率限幅器深具應用潛力。


雙光子激發螢光發射
This is an image

因此,我們的研究不僅體現了化學與材料、電子及光學等學科的結合,更可與主動式全彩顯示器、光通訊、全光開關及光信息儲存等相關的材料和元件的應用研究接軌,可謂跨領域的研究。元件的靈魂乃是材料,而材料的物理及化學特性乃掌控於分子結構。唯有材料化學家才可以大展身手並巧妙地調整分子的結構以控制其巨觀材料所展現出來的物化特性使其具有應用價值。本實驗室專注於材料的分子設計與合成,本身就是一種藝術,也是材料化學家可以實現「運籌帷幄,致勝千里」的地方!


本實驗室歡迎有興趣從事 “有機材料合成”的新血加入!!

Personal Journal
Tzu-Chau Lin, Wei Chien, Shu-Wen Dai, Hao-Wu Lin, Yueh-Ching Liu "Multi-photon properties in various condensed phases of dendritic chromophores derived from carbazole and indenoquioxaline units: Synthesis and characterization. " Dyes and Pigments2019, 168, 140-150.

Man Ling Jiang, JunJie Wen, ZiMing Chen, WenHsuan Tsai,TzuChau Lin, Tahsin J. Chow, Yuan Jay Chang "HighPerformance Organic Dyes with ElectronDeficient Quinoxalinoid Heterocycles for DyeSensitized Solar Cells under One Sun and Indoor Light." ChemSusChem, 2019, 12(15), 3654-3665.

Youhei Chitose, Manabu Abe, Ko Furukawa, Jhe-Yi Lin,Tzu-Chau Lin, Claudine Katan, "Design and Synthesis of a Caged Carboxylic Acid with a Donor−π−Donor Coumarin Structure: One-photon and Two-photon Uncaging Reactions Using Visible and Near-Infrared Lights." Organic Letters, 2017, 19, 2622-2625.

Tzu-Chau Lin, Wei Chien, Leszek Mateusz Mazur, Yi-You Liu, Konrad Jakubowski, Katarzyna Matczyszyn, Marek Samoc, Rekfa Wika Amini, "Two- and three-photon absorption properties of fan-shaped dendrons derived from 2,3,8-trifunctionalized indenoquinoxaline units: synthesis and characterization. " Journal of Materials Chemistry C, 2017, 5, 8219-8232.

Tzu-Chau Lin, Ying-Hsuan Lee, Bor-Rong Huang, Ming-Yu Tsai, Jhe-Yi Lin. "Functionalized tetrafluorenylethylene-type chromophores: Synthesis, two-photon absorption and effective optical power-limiting properties in the visible-to-near IR region." Dyes and Pigments2016, 134, 325-333.

Pragya Priyanka, Sureshraju Vegiraju, Jhe-Yi Lin, Jen-Shyang Ni, Hsun-Ying Huang, Rachmawati Dwi Agustin, Shueh Lin Yau,Tzu-Chau Lin, Ming-Chou Chen. "Synthesis and characterization of two-photon active chromophores based on asymmetrically substituted tetrathienoacene scaffolds." Dyes and Pigments2016, 133, 65-72.

Tzu-Chau Lin, Jhe-Yi Lin, Bo-Kai Tsai, Nai-Yi Liang, Wei Chien. "Synthesis and multi-photon absorption properties of symmetric bisarylacetylene chromophores using functionalized isomeric pyrazinoindenocarbazole units as the rigid aryl substituents." Dyes and Pigments2016, 132, 347-359.
  1. T.-C. Lin,* B.-K. Tsai, T.-Y. Huang, W. Chien, Y.-Y. Liu, M.-H. Li, M.-Y. Tsai, Dyes and Pigments 2015120, 99-111.

     

  2. P. Kumaresan, Y.-Y. Liu, S. Vegiraju, Y. Ezhumalai, H.-C. Yu, S. L. Yau, M.-C. Chen,* T.-C. Lin,* Chem. Asian J. 201510, 1640-1646.

     

  3. S. Vegiraju, Y.-Y. Liu, K. Prabakaran, J.-S. Ni, Y. Ezhumalai, H.-C. Yu, S. L. Yau, J. T. Lin, M.-C. Chen,* T.-C. Lin,* RSC Adv. 2015, 54003-54010.

     

  4. T.-C. Lin,* B.-K. Tsai, Y.-Y. Liu, M.-Y. Tsai, Eur. J. Org. Chem. 2014, 6163-6174.

     

  5. T.-C. Lin,* Y.-Y. Liu, M.-H. Li, C.-Y. Liu, S.-Y. Tseng, Y.-T. Wang, Y.-H. Tseng, H.-H. Chu, C.-W. Luo, Chem. Asian J. 20149, 1601-1610.

     

  6. T.-C. Lin,* Y.-Y. Liu, M.-H. Li, Y.-H. Lee, Dyes and Pigments 2014109, 72-80.

     

  7. T.-C. Lin,* C.-Y. Liu, M.-H. Li, Y.-Y. Liu, S.-Y. Tseng, Y.-T. Wang, Y.-H. Tseng, H.-H. Chu, C.-W. Luo, J. Mater. Chem. C 20142, 821-828.

     

  8. T.-C. Lin,* M.-L. Li, C.-Y. Liu, M.-Y. Tsai, Y.-H. Lee, Y. Febriani, J.-H. Lin, Y.-K. Shen, Eur. J. Org. Chem. 2014, 1615-1621.

     

  9. T.-C. Lin,* C. Y. Liu, B.-R. Huang, J.-H. Lin, Y.-K. Shen, C.-Y. Wu, Eur. J. Org. Chem. 2013, 498-508.

     

  10. T.-C. Lin,* Y.-H. Lee, C.-Y. Liu, B.-R. Huang, M.-Y. Tsai, Y.-J. Huang, J.-H. Lin,* Y.-K. Shen, C.-Y. Wu, Chem. Eur. J. 201319, 749-760.

     

  11. T.-C. Lin,* M.-H. Li, C.-Y. Liu, J.-H. Lin, Y.-K. Shen, Y.-H. Lee, J. Mater. Chem. C 20131, 2764-2772.

     

  12. T.-C. Lin,* F.-L. Guo, M.-H. Li, C.-Y. Liu, Chem. Asian J. 20138, 2102-2110.

     

  13. T.-C. Lin,* W. Chien, C.-Y. Liu, M.-Y. Tsai, Y.-J. Huang, Eur. J. Org. Chem. 2013, 4262-4269.

     

  14. T.-C. Lin,* Y.-H. Lee, C.-L. Hu, Y.-K. Li, Y.-J. Huang, Eur. J. Org. Chem. 2012, 1737-1745.

     

  15. T.-C. Lin,* Y.-H. Lee, B.-R. Huang, C.-L. Hu, Y.-K. Li, Tetrahedron 201268, 4935-4949.

     

  16. T.-C. Lin,* W.-L. Lin, C.-M. Wang, C.-W. Fu, Eur. J. Org. Chem. 2011, 912-921.

     

  17. T.-C. Lin,* Y.-J. Huang, B.-R. Huang, Y.-H. Lee, Tetrahedron Lett. 201152, 6748-6753.

     

  18. T.-C. Lin,* Y.-J. Huang, Y.-F. Chen, C.-L. Hu, Tetrahedron 201066, 1375-1382.

     

  19. T.-C. Lin,* C.-Y. Liu, M.-H. Li, Y.-Y. Liu, S.-Y. Tseng, Y.-T. Wang, Y.-H. Tseng, H.-H. Chu, C.-W. Luo, J. Mater. Chem. 200919, 7075-7080.

     

  20. T.-C. Lin,* C.-S. Hsu, C.-L. Hu, Y.-F. Chen, W.-J. Huang, Tetrahedron Lett. 200950, 182-185.

     

  21. T.-C. Lin,* Q. Zheng, C.-Y. Chen, G. S. He, W.-J. Huang, A. I. Ryasnyanskiy, P. N. Prasad, Chem. Commun. 2008, 389-391.

     

  22. T.-C. Lin,* G. S. He, Q. Zheng, P. N. Prasad, J. Mater. Chem. 200616, 2490-2498.
Personal Conference
  1. T.-C. Lin,* C.-Y. Liu, M.-H. Li, Y.-Y. Liu, S.-Y. Tseng, Y.-T. Wang, Y.-H. Tseng, H.-H. Chu, C.-W. Luo, "Two-Photon and Optical Power-limiting Properties of A Dendrimer Derived from Functionalized Indenoquinoxaline Units" in the 7th International Congress on Laser Advanced Materials Processing (LAMP 2015) May 26th to May 29th, Kitakyushu, Fukuoka, Japan, 2015.

     

  2. T.-C. Lin,* C.-Y. Liu, M.-H. Li, Y.-Y. Liu, S.-Y. Tseng, Y.-T. Wang, Y.-H. Tseng, H.-H. Chu, C.-W. Luo, "A Highly Two-photon Active Dendrimer Derived from 2,3,8-Trifunctionalized Indenoquinoxaline Units" in the 15th International Union of Materials Research Societies, International Conference in Asia (IUMRS-ICA, 2014) Aug. 24 to Aug. 30, Fukuoka, Japan, 2014.

     

  3. T.-C. Lin,* Y.-H. Lee, C.-Y. Liu, J.-H. Lin, Y.-K. Shen, "Synthesis and Two-photon-related Properties of Small Dendritic Chromophores Derived from Functionalized Quinoxalinoids" in the 8th International Symposium on Organic Molecular Electronics (ISOME 2014) May 15 to May 16, Tokyo, Japan, 2014.

     

  4. T.-C. Lin,* Y.-H. Lee, C.-Y. Liu, J.-H. Lin, Y.-K. Shen, "Synthesis and Two-photon Properties of Small Dendritic Chromophores Containing Functionalized Quinoxalinoid Heterocycles" in the 18th OptoElectronics and Communications Conference / Photonics in Switching 2013 (CLEO-PR&OECC/PS 2013), June 30 to July 4, Kyoto, Japan, 2013.

     

  5. T.-C. Lin,* Y.-H. Lee, C.-L. Hu, Y.-K. Li, Y.-J. Huang, "Synthesis and Two-Photon Properties of Small Dendritic Chromophores with Symmetrical and Unsymmetrical Substituted Skeletons" in the 5th International Conference on Optical and Optoelectronic Properties of Materials and Applications (ICOOPMA 2012), June 3 to June 7, Nara, Japan, 2012.