Tunable White-Light Emission from Conjugated Polymer-Di-Ureasil Materials

被引:35
作者
Willis-Fox, Niamh [1 ,2 ]
Kraft, Mario [3 ]
Arlt, Jochen [4 ,5 ]
Scherf, Ullrich [3 ]
Evans, Rachel C. [1 ,2 ]
机构
[1] Univ Dublin Trinity Coll, Sch Chem, Dublin 2, Ireland
[2] Univ Dublin Trinity Coll, CRANN, Dublin 2, Ireland
[3] Berg Univ Wuppertal, Makromol Chem, D-42097 Wuppertal, Germany
[4] Univ Edinburgh, Sch Phys & Astron, Collaborat Opt Spect Micromanipulat & Imaging Ctr, Kings Bldg, Edinburgh EH9 3JZ, Midlothian, Scotland
[5] Univ Edinburgh, Sch Phys & Astron, SUPA, Kings Bldg, Edinburgh EH9 3JZ, Midlothian, Scotland
基金
爱尔兰科学基金会;
关键词
composites; conjugated polymers; hybrid materials; optically active materials; photoluminescence; ORGANIC-INORGANIC HYBRIDS; CARBOXYLIC-ACID SOLVOLYSIS; RESONANCE ENERGY-TRANSFER; EMITTING-DIODES; SOLAR-CELLS; ORGANIC/INORGANIC HYBRIDS; CATIONIC POLYTHIOPHENE; RECENT PROGRESS; QUANTUM YIELDS; OXYGEN SENSORS;
D O I
10.1002/adfm.201504017
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Conjugated polymer (CP)-di-ureasil composite materials displaying a tunable emission color from blue to yellow through white have been prepared using a simple sol-gel processing method. The tunability of the emission color arises from a combination of energy transfer between the di-ureasil and the CP dopant and the excitation wavelength dependence of the di-ureasil emission. Incorporation of the CP does not adversely affect the bulk or local structure of the di-ureasil, enabling retention of the structural and mechanical properties of the host. Furthermore, CP-di-ureasils display superior thermal and photostability compared to the parent CPs. Thermogravimetric analysis shows that the onset of thermal decomposition can be increased by up to 130 degrees C for CP-di-ureasils, while photostability studies reveal a significant decrease in the extent of photodegradation. Steady-state photoluminescence spectroscopy and picosecond time-resolved emission studies indicate that the observed tunable emission arises as a consequence of incomplete energy transfer between the di-ureasil and the CP dopant, resulting in emission from both species on direct excitation of the di-ureasil matrix. The facile synthetic approach and tunable emission demonstrate that CP-di-ureasils are a highly promising route to white-light-emitters that simultaneously improve the stability and reduce the complexity of CP-based multilayer device architectures.
引用
收藏
页码:532 / 542
页数:11
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