TY - JOUR
T1 - Tunable White-Light Emission from Conjugated Polymer-Di-Ureasil Materials
AU - Willis-Fox, N.
AU - Kraft, Mario
AU - Arlt, Jochen
AU - Scherf, Ullrich
A2 - Evans, Rachel C.
PY - 2016/1/26
Y1 - 2016/1/26
N2 - 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 °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.
AB - 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 °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.
UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-84981287462&partnerID=MN8TOARS
U2 - 10.1002/adfm.201504017
DO - 10.1002/adfm.201504017
M3 - Article
SN - 1616-3028
VL - 26
SP - 532
EP - 542
JO - Advanced Functional Materials
JF - Advanced Functional Materials
ER -