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東海大學奈米科技研究中心-中心成員-中心成員-張源杰 副教授

張源杰 副教授

信箱:jaychang@thu.edu.tw
個人網站:https://sites.google.com/site/2015jaysama/home
分機:32224
 

學歷

Ph.D., National Taiwan University

經歷

Associate Professor, Tunghai University, Taiwan(2016-)
Assistant Professor, Tunghai University, Taiwan(2012-2016)
Postdoctoral Fellow, Institute of Chemistry, Academia Sinica, Taiwan(2010-2012)
Senior Engineer, AU Optronics Corporation (AUO) (Large Size OLED Technology Dept.(2009-10)
Postdoctoral Fellow, Institute of Chemistry, Academia Sinica, Taiwan(2009)
Visiting Scholar, Institute for Materials Chemistry and Engineering (IMCE) and Department of Molecular Chemistry, Kyushu University, Japan(2008-2009)
Research Assistant, Military service at Academia Sinica, Taiwan(2003-04)

專長

有機染料敏化太陽能電池(DSSCs)、鈣鈦礦太陽能電池(Perovskites)、有機發光二極體(TADF-OLEDs)、液晶材料(LCs)

計畫

106學年度
有機化學以Carbazole衍生物及[3.3]Paracyclophane為核心分子架構新穎電洞傳輸材料於鈣鈦礦太陽能電池(一般型研究計畫)
有機化學以奈米能源點亮綠色東海--高效能太陽能轉化與儲存(提升私校研發能量專案計畫)
105學年度
貴儀總計畫東海大學自有貴重儀器共同使用服務計畫(附屬/支援單位補助計畫)
有機化學新穎電洞傳輸材料應用於鈣鈦礦太陽能電池及D-A-π-A系列於有機染敏太陽能電池(中型儀器補助計畫)
有機化學新穎電洞傳輸材料應用於鈣鈦礦太陽能電池及D-A-π-A系列於有機染敏太陽能電池(新進人員研究計畫)
103學年度
有機化學發展新型架橋基團與多電子予體應用於有機染敏太陽能電池材料(新進人員研究計畫)
有機化學發展新型架橋基團與多電子予體應用於有機染敏太陽能電池材料(中型儀器補助計畫)
有機材料新型有機染敏太陽能電池材料及小分子薄膜太陽能電池材料之合成與元件特性(新進人員研究計畫)

期刊

(37). Weng, Y.-L.; Li, T.-C.; Chen, C.-P.*; Chang, Y. J.* “Effect of intermolecular interaction with phenothiazine core on inverted organic photovoltaics by using different acceptor moiety” Dyes and Pigments, 2017146, 374-385.
(36). Huang, R.-Y.; Chiu, Y.-H.; Chang, Y.-H.; Chen, K.-Y.; Huang, P.-T.; Chiang, T.-H.; Chang, Y. J.* “Influence of D–π–A System Through Linked Unit of Double and Triple Bonds in Triarylene Bridge for Dye-Sensitised Solar Cells” New J. Chem., 201741, 8016.
(35). Chang, Y. J.*, Hsu, J.-L.; Li, Y.-H.; Biring, S.; Yeh, T.-H.; Guo, J.-Y.;  Liu, S.-W.* “Carbazole-based small molecules for vacuum-deposited organic photovoltaic devices with open-circuit voltage exceeding 1 VOrganic Electronics201747, 162-173.
(34). Tsai, H.-Y.; Chang, Y. J.; Hu, J.-W.; Chen, K.-Y. Chen* “Synthesis, Crystal Structure, Spectroscopic Properties, and DFT Studies of 7,9-Dibromobenzo[h]quinolin-10-ol” Crystals2017, 7, 60.
(33).  Chen, Y.-C.; Watatnabe*, M.; Wen, Y.-S.; Chang, Y. J.* “Crystal structure of racemic 2,7-dibromo-10'H-spiro[fluorene-9,9'-phenanthren]-10'-one” IUCrData, 20172, x170301.
(32). Chiu, Y.-H.; Shibahara, M.; Huang, R.-Y.; Watanabe, M.;  Wang, Z.-S.; Hsiao, Y.-J.; Chang, B.-F.; Chiang,T.-H.; Chang, Y. J.* “Triphenylamine Derivatives and the Lithium-Ion Capture of [3.3]Cyclophane Used in Organic Dye-Sensitized Solar Cells” Dyes and Pigments2017136, 761-772.
(31). Lin, Y.-D.;Ke, B.-Y.; Lee, K.-M.; Chang, S. H.; Wang, K.-H.; Huang, S.-H.; Wu, C.-G.; Chou, P. –T.; Jhulki, S.; Moorthy, J. N.;  Chang, Y. J.; Liau, K.-L.; Chung, H.-C.; Liu, C.-Y.; Sun, S.-S.; Chow, T. J.* “Hole-transporting materials based on twisted bimesitylenes for high performance perovskite solar cellChemSusChem, 2016, DOI: 10.1002/cssc.201501392R1.
(30).  Fan, S.; Lu, Sun, H.; Zhou, G.; Chang, Y. J.; Wang, Z.-S.* “Co-Sensitization of TiO2 Films with a Porphyrin Dye and an Organic Dye for Quasi-Solid-State Dye-Sensitized Solar Cells” Phys. Chem. Chem. Phys.2016, 18.932.
(29). Chen, Y.-C.; Lin, Y.-Z.; Cheng, Y.-T.; Chang, Y. J.* “Use of Isophorone-based Linker for Fabricating Dye-Sensitised Solar Cells” RSC Advances20155, 96428-96436
(28). Watanabe, M.*; Hagiwara, H.; Ogata, Y.; Staykov, A.; Bishopa, S. R.; Perrya, N. H.; Chang, Y. J.; Ida, S.; Tanaka, K.; Ishihara, T.* “Impact of Alkoxy Chain Length on Hydrogen Production via Carbazole-based, Visible-lightdriven Dye-sensitized Water SplittingJ. Mater. Chem. A, 2015, 3, 21713-21721.
(27). Lin, Y.-D.;Ke, B.-Y.; Chang, Y. J.; Chou, P. –T.; Liau, K.-L.; Liu, C.-Y.; Chow, T. J.* “Pyridomethene-BF2 complex/phenothiazine-hybrid sensitizer with high molar extinction coefficient for efficient sensitized solar cells J. Mater. Chem. A, 2015, 3, 16831.
(26). Watanabe, M.*; Chang, Y. J.; Chou, P. –T.; Staykov, A.; Shibahara, M.; Sako, K.; Ishihara, T.; Chow, T. J.* “Synthesis, spectra, and electrochemical properties of ferrocene-thiophene-cyanoacrylic acid dyadsTetrahedron Lett.2015, 56, 1548.
(25). Su, W.-T.; Watanabe, M.*; Chang, Y. J.; Chow, T. J.* “Cycloaddition of hexacene and fullerene[60]Tetrahedron Lett.2015 , 56, 1092.
(24). Huang, C. H.; Chang, Y. J.* “Dyes for sensitized solar cells using [2.2]Paracyclophane as a bridging unitTetrahedron Lett.201455, 4938.
(23). Lin, Y.-Z.; Yeh, C.-W.; Chou, P.-T.; Watanabe, M.; Chang, Y.-H.; Chang, Y. J.*; Chow, T. J.* “Benzo[1,2-b:4,5-b’]dithiophene and Benzo[1,2-b:4,5-b’]difuran Based Organic Dipolar Compounds for Sensitized Solar Cells” Dyes and Pigments2014109, 81-89. 
(22). Chang, Y. J.*; Chou, P. –T.; Watanabe, M.; Chow, T. J.* “Triarylene linked spacer effect for dye sensitized solar cellsThin Solid Films, 2014, 558, 330.
(21). Watanabe, M.*;  Chien, C.-T.;  Lin, Y.-D, Chang, Y. J.; Wen, Y.-S.; Goto, K.; Shibahara, M.; Shinmyozu, T.; Chow, T. J.* “Synthesis, physical properties, and structure of TIPS-difuranoacenes” TetrahedronLett.201455, 1424.
(20). Lin, Y.-Z.; Huang, C. H.; Chang, Y. J.*; Yeh, C.-W.; Chin, T.-M.; Chi, K.-M.; Chou, P.-T.; Watanabe, M.; Chow, T. J.* “Anthracene Based Organic Dipolar Compounds for Sensitized Solar CellsTetrahedron, 2014, 70, 262.
(19). Watanabe, M.; Chen, K.-Y.; Chang, Y. J.; Chow, T. J.* “Generation of Acene from Precursors and ApplicationAcc. Chem. Res., 2013, 46, 1606.
(18). Watanabe, M.; Su, W.-T.; Chen, K.-Y.*; Chien, C.-T.; Chao, T.-H.; Chang, Y. J.; Liu, S.-W.; Chow, T. J.* “Soluble Precursor of Hexacene and its Application on Thin Film TransistorChem.Comm., 2013, 49, 2240.
(17). Chiang, T.-C.; Chien, C.-T.; Watanabe, M.; Chao, T.-H, Chang, Y. J.; Lin, Y.-D.; Lee, H.-K.; Liu, C.-Y.; Tu, C.-H.; Sun, C.-H.; Chow, T. J.* “The synthesis and ambipolar charge transport properties of 1,2,3,4-tetrafluoropentaceneTetrahedronLett., 2013, 54, 903.
(16). Watanabe, M.; Su, W.-T.; Chang, Y. J.*; Chao, T. –H.; Wen, Y. S.; Chow, T. J.* “Solution-processed Opto-electronics Properties by Functionalized AnthradifuranChem. Asian J., 2013, 8, 60.
(15). Chang, Y. J.; Chen, K. Y.* “7-Methoxyindan-1-oneActa Cryst.,2012, E68, o3063.
(14). Chang, Y. J.*; Chou, P. –T.; Lin, Y. –Z.; Watanabe, M.; Yang, C. –J.; Chin, T. –M.; Chow, T. J.* “Organic Dyads Containing Oligo-Phenothiazine for Dye-Sensitized Soalr CellsJ. Mater. Chem., 2012, 22, 21704.
(13). Chao, T. –H.; Chang, M. –J.; Watanabe, M.; Luo, M. –H.; Chang, Y. J.; Fang, T. –C.; Chen, K. –Y.; Chow, T. J.* “Organic thin-film transistors based on a highly soluble pentacene precursor Chem. Comm.201248, 6148.
(12). Watanabe, M.; Chang, Y. J.; Liu, S. –W.; Chao, T. –H.; Goto, K.; Islam, M. M.; Yuan. C. –H.; Tao. Y. –T.; Shinmyozu, T.; Chow, T. J.* “Hexacene: synthesis, crystal structure and charge transporting property” Nature Chemistry2012, 574. [SCI] (Impact Factor: 20.5). (citation:22)
(11). Yang, C. –J.; Chang, Y. J.; Watanabe, M.; Hon, Y. –S.; Chow, T. J.* “Highly efficient D-π-A system with phenothiazine for Dye-Sensitized Solar Cells” J. Mater. Chem.201222, 4040. [SCI] (Impact Factor: 5.968). (citation:23)
(10). Watanabe, M.; Chao, T. H.; Chien, C. T.; Liu, S. W.; Chang, Y. J.; Chen, K. –Y.; Chow, T. J.* “2-Helo-subsituted tetracenes: their generation and single crystal OFET characteristics”  Tetrahedron Lett.2012, 53, 2284-2287. [SCI] (Impact Factor: 2.618)
(9). Chang, Y. J.; Watanabe, M; Chou, P. –T.; Chow, T. J.* “[2.2]Paracyclophane as a bridging unit in the design of organic dyes for sensitized solar cells” Chem. Commun.201248, 726. [SCI] (Impact Factor: 6.169). (citation:6)
(8). Chang, Y. J.; Chou, P. –T.; Lin, S. –Y.; Watanabe, M.; Liu, Z. –Q.; Lin, J. –L.; Chen, K. –Y.; Sun, S. –S.; Liu, C. –T.; Chow, T. J.* “High Performance Organic Materials for Dye-Sensitized Solar Cell: Triarylene-Linked Dyads with a 4-tert-Butylphenylamine Donor” Chem. Asian J.20127, 572. [SCI] (Impact Factor: 4.50). (citation:8)
(7). Watanabe, M.; Chao, T. –H.; Liu, S. W.; Chien, C. T.; Chang, Y. J.; Yuan, C. –H.; Shinmyozu, T.; Chow, T. J.*  “Solution-processed Organic Micro-crystalline Transistors Based on Tetraceno [2,3-b]thiophene from Monoketone Precursors” J. Mater. Chem.201121, 11317-11322. [SCI] (Impact Factor: 5.968).
(6). Chen, K. Y.*; Wen, Y. S.; Fang, T. C.; Chang, Y. J.; Chang, M. J.  “7-hydroxy-1-indanone” Acta Cryst.2011E67, o927. [SCI] (Impact Factor: 0.413).
(5). Chang, Y. J.; Chow, T. J.* “Highly Efficient Triarylene Conjugated Dyes for Sensitized Soalr Cells” J. Mater. Chem.201121, 9523-9532. [SCI] (Impact Factor: 6.101). (citation:24)
(4). Chang, Y. J.; Chow, T. J.* “Highly Efficient Fluorescent Red Dyes for Organic Light Emitting Diodes” J. Mater. Chem.201121, 3091-3099. [SCI] (Impact Factor: 5.968). (citation:11)
(3). Chang, Y. J.; Chow, T. J.* “Hole-Transporting Materials Bridged by Triaryl Linkages for Dye-Sensitized Solar Cells” Tetrahedron200965, 9626-9632. [SCI] (Impact Factor: 3.219). (citation:30)
(2). Chang, Y. J.; Chow, T. J.* “Dye-Sensitized Solar Cell Utilizing Organic Dyads Containing Triarylene Conjugates” Tetrahedron200965, 4726-4734. [SCI] (Impact Factor: 3.219). (citation:45)
(1). Lin, Y. -C.; Lai, C. K.*; Chang, Y. -C.; Liu, K. -T.* “Formation of hexagonal columnar phases by heterocyclic pyrimidine derivatives” Liquid Crystal200229, 237-242. [SCI] (Impact Factor: 1.597).

 

學歷

Ph.D., National Taiwan University

經歷

Associate Professor, Tunghai University, Taiwan(2016-)
Assistant Professor, Tunghai University, Taiwan(2012-2016)
Postdoctoral Fellow, Institute of Chemistry, Academia Sinica, Taiwan(2010-2012)
Senior Engineer, AU Optronics Corporation (AUO) (Large Size OLED Technology Dept.(2009-10)
Postdoctoral Fellow, Institute of Chemistry, Academia Sinica, Taiwan(2009)
Visiting Scholar, Institute for Materials Chemistry and Engineering (IMCE) and Department of Molecular Chemistry, Kyushu University, Japan(2008-2009)
Research Assistant, Military service at Academia Sinica, Taiwan(2003-04)

專長

有機染料敏化太陽能電池(DSSCs)、鈣鈦礦太陽能電池(Perovskites)、有機發光二極體(TADF-OLEDs)、液晶材料(LCs)

計畫

106學年度
有機化學以Carbazole衍生物及[3.3]Paracyclophane為核心分子架構新穎電洞傳輸材料於鈣鈦礦太陽能電池(一般型研究計畫)
有機化學以奈米能源點亮綠色東海--高效能太陽能轉化與儲存(提升私校研發能量專案計畫)
105學年度
貴儀總計畫東海大學自有貴重儀器共同使用服務計畫(附屬/支援單位補助計畫)
有機化學新穎電洞傳輸材料應用於鈣鈦礦太陽能電池及D-A-π-A系列於有機染敏太陽能電池(中型儀器補助計畫)
有機化學新穎電洞傳輸材料應用於鈣鈦礦太陽能電池及D-A-π-A系列於有機染敏太陽能電池(新進人員研究計畫)
103學年度
有機化學發展新型架橋基團與多電子予體應用於有機染敏太陽能電池材料(新進人員研究計畫)
有機化學發展新型架橋基團與多電子予體應用於有機染敏太陽能電池材料(中型儀器補助計畫)
有機材料新型有機染敏太陽能電池材料及小分子薄膜太陽能電池材料之合成與元件特性(新進人員研究計畫)

期刊

(37). Weng, Y.-L.; Li, T.-C.; Chen, C.-P.*; Chang, Y. J.* “Effect of intermolecular interaction with phenothiazine core on inverted organic photovoltaics by using different acceptor moiety” Dyes and Pigments, 2017146, 374-385.
(36). Huang, R.-Y.; Chiu, Y.-H.; Chang, Y.-H.; Chen, K.-Y.; Huang, P.-T.; Chiang, T.-H.; Chang, Y. J.* “Influence of D–π–A System Through Linked Unit of Double and Triple Bonds in Triarylene Bridge for Dye-Sensitised Solar Cells” New J. Chem., 201741, 8016.
(35). Chang, Y. J.*, Hsu, J.-L.; Li, Y.-H.; Biring, S.; Yeh, T.-H.; Guo, J.-Y.;  Liu, S.-W.* “Carbazole-based small molecules for vacuum-deposited organic photovoltaic devices with open-circuit voltage exceeding 1 VOrganic Electronics201747, 162-173.
(34). Tsai, H.-Y.; Chang, Y. J.; Hu, J.-W.; Chen, K.-Y. Chen* “Synthesis, Crystal Structure, Spectroscopic Properties, and DFT Studies of 7,9-Dibromobenzo[h]quinolin-10-ol” Crystals2017, 7, 60.
(33).  Chen, Y.-C.; Watatnabe*, M.; Wen, Y.-S.; Chang, Y. J.* “Crystal structure of racemic 2,7-dibromo-10'H-spiro[fluorene-9,9'-phenanthren]-10'-one” IUCrData, 20172, x170301.
(32). Chiu, Y.-H.; Shibahara, M.; Huang, R.-Y.; Watanabe, M.;  Wang, Z.-S.; Hsiao, Y.-J.; Chang, B.-F.; Chiang,T.-H.; Chang, Y. J.* “Triphenylamine Derivatives and the Lithium-Ion Capture of [3.3]Cyclophane Used in Organic Dye-Sensitized Solar Cells” Dyes and Pigments2017136, 761-772.
(31). Lin, Y.-D.;Ke, B.-Y.; Lee, K.-M.; Chang, S. H.; Wang, K.-H.; Huang, S.-H.; Wu, C.-G.; Chou, P. –T.; Jhulki, S.; Moorthy, J. N.;  Chang, Y. J.; Liau, K.-L.; Chung, H.-C.; Liu, C.-Y.; Sun, S.-S.; Chow, T. J.* “Hole-transporting materials based on twisted bimesitylenes for high performance perovskite solar cellChemSusChem, 2016, DOI: 10.1002/cssc.201501392R1.
(30).  Fan, S.; Lu, Sun, H.; Zhou, G.; Chang, Y. J.; Wang, Z.-S.* “Co-Sensitization of TiO2 Films with a Porphyrin Dye and an Organic Dye for Quasi-Solid-State Dye-Sensitized Solar Cells” Phys. Chem. Chem. Phys.2016, 18.932.
(29). Chen, Y.-C.; Lin, Y.-Z.; Cheng, Y.-T.; Chang, Y. J.* “Use of Isophorone-based Linker for Fabricating Dye-Sensitised Solar Cells” RSC Advances20155, 96428-96436
(28). Watanabe, M.*; Hagiwara, H.; Ogata, Y.; Staykov, A.; Bishopa, S. R.; Perrya, N. H.; Chang, Y. J.; Ida, S.; Tanaka, K.; Ishihara, T.* “Impact of Alkoxy Chain Length on Hydrogen Production via Carbazole-based, Visible-lightdriven Dye-sensitized Water SplittingJ. Mater. Chem. A, 2015, 3, 21713-21721.
(27). Lin, Y.-D.;Ke, B.-Y.; Chang, Y. J.; Chou, P. –T.; Liau, K.-L.; Liu, C.-Y.; Chow, T. J.* “Pyridomethene-BF2 complex/phenothiazine-hybrid sensitizer with high molar extinction coefficient for efficient sensitized solar cells J. Mater. Chem. A, 2015, 3, 16831.
(26). Watanabe, M.*; Chang, Y. J.; Chou, P. –T.; Staykov, A.; Shibahara, M.; Sako, K.; Ishihara, T.; Chow, T. J.* “Synthesis, spectra, and electrochemical properties of ferrocene-thiophene-cyanoacrylic acid dyadsTetrahedron Lett.2015, 56, 1548.
(25). Su, W.-T.; Watanabe, M.*; Chang, Y. J.; Chow, T. J.* “Cycloaddition of hexacene and fullerene[60]Tetrahedron Lett.2015 , 56, 1092.
(24). Huang, C. H.; Chang, Y. J.* “Dyes for sensitized solar cells using [2.2]Paracyclophane as a bridging unitTetrahedron Lett.201455, 4938.
(23). Lin, Y.-Z.; Yeh, C.-W.; Chou, P.-T.; Watanabe, M.; Chang, Y.-H.; Chang, Y. J.*; Chow, T. J.* “Benzo[1,2-b:4,5-b’]dithiophene and Benzo[1,2-b:4,5-b’]difuran Based Organic Dipolar Compounds for Sensitized Solar Cells” Dyes and Pigments2014109, 81-89. 
(22). Chang, Y. J.*; Chou, P. –T.; Watanabe, M.; Chow, T. J.* “Triarylene linked spacer effect for dye sensitized solar cellsThin Solid Films, 2014, 558, 330.
(21). Watanabe, M.*;  Chien, C.-T.;  Lin, Y.-D, Chang, Y. J.; Wen, Y.-S.; Goto, K.; Shibahara, M.; Shinmyozu, T.; Chow, T. J.* “Synthesis, physical properties, and structure of TIPS-difuranoacenes” TetrahedronLett.201455, 1424.
(20). Lin, Y.-Z.; Huang, C. H.; Chang, Y. J.*; Yeh, C.-W.; Chin, T.-M.; Chi, K.-M.; Chou, P.-T.; Watanabe, M.; Chow, T. J.* “Anthracene Based Organic Dipolar Compounds for Sensitized Solar CellsTetrahedron, 2014, 70, 262.
(19). Watanabe, M.; Chen, K.-Y.; Chang, Y. J.; Chow, T. J.* “Generation of Acene from Precursors and ApplicationAcc. Chem. Res., 2013, 46, 1606.
(18). Watanabe, M.; Su, W.-T.; Chen, K.-Y.*; Chien, C.-T.; Chao, T.-H.; Chang, Y. J.; Liu, S.-W.; Chow, T. J.* “Soluble Precursor of Hexacene and its Application on Thin Film TransistorChem.Comm., 2013, 49, 2240.
(17). Chiang, T.-C.; Chien, C.-T.; Watanabe, M.; Chao, T.-H, Chang, Y. J.; Lin, Y.-D.; Lee, H.-K.; Liu, C.-Y.; Tu, C.-H.; Sun, C.-H.; Chow, T. J.* “The synthesis and ambipolar charge transport properties of 1,2,3,4-tetrafluoropentaceneTetrahedronLett., 2013, 54, 903.
(16). Watanabe, M.; Su, W.-T.; Chang, Y. J.*; Chao, T. –H.; Wen, Y. S.; Chow, T. J.* “Solution-processed Opto-electronics Properties by Functionalized AnthradifuranChem. Asian J., 2013, 8, 60.
(15). Chang, Y. J.; Chen, K. Y.* “7-Methoxyindan-1-oneActa Cryst.,2012, E68, o3063.
(14). Chang, Y. J.*; Chou, P. –T.; Lin, Y. –Z.; Watanabe, M.; Yang, C. –J.; Chin, T. –M.; Chow, T. J.* “Organic Dyads Containing Oligo-Phenothiazine for Dye-Sensitized Soalr CellsJ. Mater. Chem., 2012, 22, 21704.
(13). Chao, T. –H.; Chang, M. –J.; Watanabe, M.; Luo, M. –H.; Chang, Y. J.; Fang, T. –C.; Chen, K. –Y.; Chow, T. J.* “Organic thin-film transistors based on a highly soluble pentacene precursor Chem. Comm.201248, 6148.
(12). Watanabe, M.; Chang, Y. J.; Liu, S. –W.; Chao, T. –H.; Goto, K.; Islam, M. M.; Yuan. C. –H.; Tao. Y. –T.; Shinmyozu, T.; Chow, T. J.* “Hexacene: synthesis, crystal structure and charge transporting property” Nature Chemistry2012, 574. [SCI] (Impact Factor: 20.5). (citation:22)
(11). Yang, C. –J.; Chang, Y. J.; Watanabe, M.; Hon, Y. –S.; Chow, T. J.* “Highly efficient D-π-A system with phenothiazine for Dye-Sensitized Solar Cells” J. Mater. Chem.201222, 4040. [SCI] (Impact Factor: 5.968). (citation:23)
(10). Watanabe, M.; Chao, T. H.; Chien, C. T.; Liu, S. W.; Chang, Y. J.; Chen, K. –Y.; Chow, T. J.* “2-Helo-subsituted tetracenes: their generation and single crystal OFET characteristics”  Tetrahedron Lett.2012, 53, 2284-2287. [SCI] (Impact Factor: 2.618)
(9). Chang, Y. J.; Watanabe, M; Chou, P. –T.; Chow, T. J.* “[2.2]Paracyclophane as a bridging unit in the design of organic dyes for sensitized solar cells” Chem. Commun.201248, 726. [SCI] (Impact Factor: 6.169). (citation:6)
(8). Chang, Y. J.; Chou, P. –T.; Lin, S. –Y.; Watanabe, M.; Liu, Z. –Q.; Lin, J. –L.; Chen, K. –Y.; Sun, S. –S.; Liu, C. –T.; Chow, T. J.* “High Performance Organic Materials for Dye-Sensitized Solar Cell: Triarylene-Linked Dyads with a 4-tert-Butylphenylamine Donor” Chem. Asian J.20127, 572. [SCI] (Impact Factor: 4.50). (citation:8)
(7). Watanabe, M.; Chao, T. –H.; Liu, S. W.; Chien, C. T.; Chang, Y. J.; Yuan, C. –H.; Shinmyozu, T.; Chow, T. J.*  “Solution-processed Organic Micro-crystalline Transistors Based on Tetraceno [2,3-b]thiophene from Monoketone Precursors” J. Mater. Chem.201121, 11317-11322. [SCI] (Impact Factor: 5.968).
(6). Chen, K. Y.*; Wen, Y. S.; Fang, T. C.; Chang, Y. J.; Chang, M. J.  “7-hydroxy-1-indanone” Acta Cryst.2011E67, o927. [SCI] (Impact Factor: 0.413).
(5). Chang, Y. J.; Chow, T. J.* “Highly Efficient Triarylene Conjugated Dyes for Sensitized Soalr Cells” J. Mater. Chem.201121, 9523-9532. [SCI] (Impact Factor: 6.101). (citation:24)
(4). Chang, Y. J.; Chow, T. J.* “Highly Efficient Fluorescent Red Dyes for Organic Light Emitting Diodes” J. Mater. Chem.201121, 3091-3099. [SCI] (Impact Factor: 5.968). (citation:11)
(3). Chang, Y. J.; Chow, T. J.* “Hole-Transporting Materials Bridged by Triaryl Linkages for Dye-Sensitized Solar Cells” Tetrahedron200965, 9626-9632. [SCI] (Impact Factor: 3.219). (citation:30)
(2). Chang, Y. J.; Chow, T. J.* “Dye-Sensitized Solar Cell Utilizing Organic Dyads Containing Triarylene Conjugates” Tetrahedron200965, 4726-4734. [SCI] (Impact Factor: 3.219). (citation:45)
(1). Lin, Y. -C.; Lai, C. K.*; Chang, Y. -C.; Liu, K. -T.* “Formation of hexagonal columnar phases by heterocyclic pyrimidine derivatives” Liquid Crystal200229, 237-242. [SCI] (Impact Factor: 1.597).