上海交通大学材料学院材料人才创新基地韩礼元

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韩礼元，日本国立物质材料研究所研究员，上海交通大学讲席教授。1988年博士毕业于日本大阪府立大学应用化学专业；1990-1993年，日本Dainippon Ink & Chemicals Inc公司助理研究员；1993—2008年，夏普公司研究所负责染料敏化太阳能电池的研究开发；2008年—至今，日本物材研究所下一代太阳能电池中心主任。


姓名：         韩礼元
职称：         教授
博导/硕导：         博导
所属二级机构：          人才创新基地
通讯地址：         上海市闵行区东川路800号上海交通大学材料D楼505室
邮编：         200240
E-mail：         Han.liyuan@sjtu.edu.cn
联系电话：         021-54742414
从事专业：        染料敏化太阳能电池
学习与工作简历：            1988年毕业于日本大阪府立大学应用化学专业。1990 – 1993工作于日本Dainippon Ink & Chemicals Inc. 之后在夏普公司研究所工作15年,主要负责染料敏化太阳能电池的研究开发。在提高太阳能电池的转换效率和模块技术创新上有很高的造诣。深入、系统地研究了染料敏化太阳能电池的电子传运机理，率先提出了电池的等效回路模型,为系统地提高转换效率和长期稳定性做出了贡献。本人所领导的团队，在此模型的基础上，成功地提高了电池的光电流和降低了电池的内电阻，创造了单片电池最高光电转换效率的世界纪录。该成果于2006年在日本物理学会杂志(Japanese Journal of Applied Physics Express Letter)上刊登，4年来被引用了500次以上。基于本人卓越的研究成果,在2008年被聘请到日本物材研究机构,担任下一代太阳能电池中心主任,负责5个研究方向(染料敏化,有机薄膜,量子点,薄膜硅,化合物太阳能电池),领导40名研究者。2011年6月, 本人领导的团队再次创造染料敏化太阳能电池单片电池公认最高光电转换效率的世界纪录11.4%。此外,本人还对在氧化钛上的染料吸附状态、从染料到氧化钛的电子转移等基础研究，以及在新染料的开发上做出了很多贡献。同时在有机薄膜太阳能电池、有机半导体材料上也有着深厚的造诣。基于这些贡献，本人在国际期刊上发表了近80篇学术论文，同时本人申请了90多项日本专利和40多项国际专利(美国、欧洲、中国、澳大利亚)，在染料敏化太阳能电池领域，按发明者计算的专利申请件数也被列为世界第一(根据2005年度日本专利局调查)。现阶段本人的研究方向主要集中在染料敏化太阳能电池基础研究，有机薄膜太阳能电池和量子点太阳能电池。
研究方向一        染料敏化太阳能电池, 有机薄膜太阳能电池和量子点太阳能电池。
研究方向二        
研究情况        
讲授主要课程        
教学研究        
代表性论文、论著        
1. “Bulk-heterojunction organic photovoltaic cells fabricated using a high viscosity solution of poly (3-hexylthiophene) with extreme” Polym. J. 45[2] (2013) 129-132
2. “Structure of electron collection electrode in dye-sensitized nanocrystalline TiO2” Electrochim. Acta 87 (2013) 309-316 “Improving the Spectral Response of Black Dye by Cosensitization with a Simple Indoline Based Dye in Dye-Sensitized Solar Cell” J. Mater. Chem. 2013 (2013) 910527-1
3. “Functional 2-benzyl-12-dihydro[60]fullerenes as acceptors for organic photovoltaics: facile synthesis and high photovoltaic per” Tetrahedron 69[4] (2013) 1302-1306
4. “Multiwall Carbon Nanotube Coated with Conducting Polyaniline Nanocomposites for Quasi-Solid-State Dye-Sensitized Solar Cells” JOURNAL OF CHEMISTRY 2013 (2013) 962387-1
5. “Improved power conversion efficiency of bulk-heterojunction organic solar cells using a benzothiadiazole-triphenylamine polymer” J. Mater. Chem. 22[6] (2012) 2539-2544
6. “Synthesis Characterizarion and Self-assembly of Colloidal Quantum Dots” Intelligent Nanomaterials (2012) 3-38
7. “Surface Treatment for Effective Dye Adsorption on Nanocrystalline TiO2” Jpn. J. Appl. Phys 51[10] (2012) 10NE16-1
8. “Fast Carrier Formation from Acceptor Exciton in Low-Gap Organic Photovotalic” Appl. Phys. Express 5[4] (2012) 042302-1
9. “Carrier Formation Dynamics of Organic Photovoltaics as Investigated by Time-Resolved Spectroscopy” ADVANCES IN OPTICAL TECHNOLOGIES 2012 (2012) 316045-1
10. “Use of benzothiadiazole–triphenylamine amorphous polymer for reproducible performance of polymer–fullerene bulk-heterojunction solar cells” Org. Electron. 13 (2012) 1802-1808
11. “Template method for fabricating interdigitate p-n heterojunction for organic solar cell” Nanoscale Res. Lett. 7 (2012) 469-1
12. “Aggregation-free branch-type organic dye with a twisted molecular architecture for dye-sensitized solar cells” ENERGY & ENVIRONMENTAL SCIENCE 5[9] (2012) 8548-8552
13. “ A New Factor Affecting the Performance of Dye-Sensitized Solar Cells in the Presence of 4- tert -Butylpyridine ” APPLIED PHYSICS EXPRESS 5 (2012) 042303-1
14. “Effect of Cerium Doping in the TiO2 Photoanode on the Electron Transport of Dye-Sensitized Solar Cells” J. Phys. Chem. C 116 (2012) 19182-19190
15. “Tuning the Electrical and Optical Properties of Diketopyrrolopyrrole Complexes for Panchromatic Dye-Sensitized Solar Cells” Chem.-Asian J. 7[12] (2012) 2895-2903
16. “Evaluation of carrier transport and recombinations in cadmium selenide quantum-dot-sensitized solar cells” Sol. Energy Mater. Sol. Cells 101[6] (2012) 5-10
17. “High-Efficiency Dye-Sensitized Solar Cell with a Novel Co-Adsorbent” ENERGY & ENVIRONMENTAL SCIENCE 3 (2012) 6057-6060
18. “Cascade cyclization of aryldiynes using iodine: synthesis of iodo-substituted benzonaphtho[2 1-d]thiophene derivatives for dye-sensitized solar cells” Tetrahedron Lett 53 (2012) 1946-1950
19. “Donor–acceptor dyes incorporating a stable dibenzosilole π-conjugated spacer for dye-sensitized solar cells” J. Mater. Chem. 22 (2012) 10771-10778
20. “Metal-Free and Fluorescent Diketopyrrolopyrrole Fluorophores for Dye-Sensitized Solar Cells” CHEM PLUS CHEM 77[6] (2012) 462-469
21. “Efficient thiocyanate-free sensitizer: a viable alternative to N719 dye for dye-sensitized solar cells” Dalton Trans 41 (2012) 7604-7608
22. “Highly efficient nanoporous graphitic carbon with tunable textural properties for dye-sensitized solar cells” J. Mater. Chem. 22 (2012) 20866-20869
23. “One bipyridine and triple advantages: tailoring ancillary ligands in ruthenium complexes for efficient sensitization in dye solar cells” J. Mater. Chem. 22 (2012) 18757-18760
24. “Functionalized styryl bipyridine as a superior chelate for a ruthenium sensitizer in dye sensitized solar cells” Dalton Trans 41 (2012) 8770-8772
25. “Structure–property relationship of naphthalene based donor–π–acceptor organic dyes for dye-sensitized solar cells: remarkable improvement of open-circuit photovoltage” J. Mater. Chem. 22 (2012) 22550-22557
26. “A novel carbazole-based dye outperformed the benchmark dye N719 for high efficiency dye-sensitized solar cells (DSSCs)” J. Mater. Chem. 22 (2012) 24048-24056
27. “Directly Determine an Additive-Induced Shift in Quasi-Fermi Level of TiO$_{2}$ Films in Dye-Sensitized Solar Cells” Jpn. J. Appl. Phys 51[10NE15] (2012) 10NE15-1
28. “Ellipsoidal TiO2 Hierarchitectures with Enhanced Photovoltaic Performance” Chem.-Eur. J. 18[17] (2012) 5269-5274
29. “Reliable evaluation of dye-sensitized solar cells” ENERGY & ENVIRONMENTAL SCIENCE 6[1] (2012) 54-66