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新型可溶性酞菁的合成和光致发光及电致发光性质
引用本文:白青龙,张春花,程传辉,李万程,申人升,杜国同.新型可溶性酞菁的合成和光致发光及电致发光性质[J].物理化学学报,2011,27(5):1195-1200.
作者姓名:白青龙  张春花  程传辉  李万程  申人升  杜国同
作者单位:1. School of Physics and Optoelectronic Technology, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China; 2. College of Chemistry and Chemical Engineering, Inner Mongglia University for Nationalities, Tongliao 028043, Inner Mongglia, P. R. China; 3. State Key Laboratory of Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun 130021, P. R. China
基金项目:国家自然科学基金,中央高校基本科研业务费专项资金和高等学校博士学科点专项科研基金
摘    要:以3(4)-硝基邻苯二腈和对甲氧基苯酚为原料, 经过两步反应合成了α(β)-四(4-甲氧基苯氧基)酞菁锌, 通过谱学方法和元素分析表征了其结构. 比较研究其溶液和旋涂膜的紫外可见光谱、光致发光光谱和固体薄片的光致发光光谱. 并以其旋涂膜为发光层制备了电致发光器件, 研究其电致发光性质. 结果表明, 固态酞菁材料与其溶液的荧光发射波长相比均向长波方向移动了145 nm以上, 而且都有不同程度的宽展. 在固态下β-位取代酞菁荧光发射波长红移的程度比α-位取代酞菁大. 电致发光光谱的发射波长和其旋涂膜的光致发光光谱的发射波长基本一致, 大约在856和862 nm左右. 在固态下酞菁分子排列紧密, 分子间相互作用增强导致了荧光发射波长的巨大红移.

关 键 词:可溶性酞菁  合成  光致发光  电致发光  红移  
收稿时间:2010-11-02
修稿时间:2011-03-11

Photoluminescence and Electroluminescence of the Novel Soluble Zinc Phthalocyanine
BAI Qing-Long,ZHANG Chun-Hua,CHENG Chuan-Hui,LI Wan-Cheng,SHEN Ren-Sheng,DU Guo-Tong.Photoluminescence and Electroluminescence of the Novel Soluble Zinc Phthalocyanine[J].Acta Physico-Chimica Sinica,2011,27(5):1195-1200.
Authors:BAI Qing-Long  ZHANG Chun-Hua  CHENG Chuan-Hui  LI Wan-Cheng  SHEN Ren-Sheng  DU Guo-Tong
Institution:1. School of Physics and Optoelectronic Technology, Dalian University of Technology, Dalian 116024, Liaoning Province, P. R. China; 2. College of Chemistry and Chemical Engineering, Inner Mongglia University for Nationalities, Tongliao 028043, Inner Mongglia, P. R. China; 3. State Key Laboratory of Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun 130021, P. R. China
Abstract:α(β)-tetra-(methoxy-phenoxy)-zinc phthalocyanine are synthesized by employing 3(4)- nitrobenzene-1,2-dicarbonitrile as precursors. They are characterized by spectrum methods and elemental analysis. The UV-Vis spectrum, photoluminescence spectra of spin-coated film and solid pellet are compared. The electroluminescent devices are fabricated by using spin coating. The results indicate that the fluorescence of solid phthalocyanine has a red-shift of more than 145 nm compared to that in solution. The fluorescences are broader in solid state than that in solution. The fluorescence of β-substituted phthalcyanines has a more red-shift than α-substituted phthalcyanines. The electroluminescent spectra around 856 and 862 nm are consisted with the photoluminescence spectra of spin-coated film. The shorter inter-molecule space leads to the large red-shift of the fluorescence.
Keywords:Soluble phthalocyanine  Synthesis  Photoluminescence  Electroluminescence  Red-shift  
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