Concentration effects on spontaneous and amplified emission in benzo[c]fluorenes?
Physical Chemistry Chemical Physics Pub Date: 2015-04-09 DOI: 10.1039/C5CP01325A
Abstract
Deep-blue-emitting benzo[c]fluorene-cored compounds featuring twisted peripheral moieties for suppressed concentration quenching of emission were synthesized and investigated as potential materials for light amplification. This detailed study of the effect of concentration on the spontaneous and stimulated emission, excited-state lifetime and susceptibility to form aggregates obtained for different benzofluorenes, has enabled the understanding of the concentration dependence of the amplified spontaneous emission (ASE) threshold and revealed the optimal concentration for the lowest threshold. The weak concentration quenching accompanied by high fluorescence quantum yield (>40%) and radiative decay rate (>5 × 108 s?1) have enabled the attainment of the lowest ASE threshold in the neat amorphous film of benzofluorene bearing dihexylfluorenyl peripheral moieties. Aggregate formation was found to negligibly affect the emission efficiency of the benzofluorene films; however, it drastically increased ASE threshold via the enhanced scattering of directional stimulated emission, and thereby implied the necessity to utilize homogeneous glassy films as the lasing medium. Although the bulky dihexylfluorenyl groups at the periphery ensured the formation of glassy benzofluorene films with the ASE threshold as low as 900 W cm?2 (under nanosecond excitation), they adversely affected carrier drift mobility, which implied a tradeoff between ASE and charge transport properties for the lasing materials utilized in the neat form. Such a low ASE threshold attained in air is among the lowest reported for solution-processed neat films. The low threshold and enhanced photostability of benzofluorenes against fluorene compounds in air show great potential for benzofluorene-cored molecular glasses as active media for lasing applications.
Recommended Literature
- [1] Embedding heteroatoms: an effective approach to create porphyrin-based functional materials Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro OsukaDalton Trans., 2017,46, 13322-13341 10.1039/C7DT02815F
- [2] Esterase-responsive polymeric prodrug-based tumor targeting nanoparticles for improved anti-tumor performance against colon cancer? Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun CaoRSC Adv., 2016,6, 42109-42119 10.1039/C6RA05236C
- [3] Enabling shape memory and healable effects in a conjugated polymer by incorporating siloxane via dynamic imine bond? Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin LiuChem. Commun., 2018,54, 10092-10095 10.1039/C8CC05410J
- [4] Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra KumarRSC Adv., 2016,6, 94731-94738 10.1039/C6RA18729C
- [5] Emerging investigator series: heterogeneous reactions of sulfur dioxide on mineral dust nanoparticles: from single component to mixed components? Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin ChenEnviron. Sci.: Nano, 2018,5, 1821-1833 10.1039/C8EN00376A
- [6] Excited state potential energy surfaces and their interactions in FeIVO active sites Shaun D. Wong,Edward I. SolomonDalton Trans., 2014,43, 17567-17577 10.1039/C4DT01366B
- [7] Excellent kinetics of single-phase Gd-doped ceria fuel electrodes in solid oxide cells? Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. OpitzMater. Adv., 2021,2, 5422-5431 10.1039/D1MA00202C
- [8] Enantiocontrolled construction of sistodiolynne, an unusual polyketide from the wood-decay fungus Sistrema raduloides Chem. Commun., 1997, 767-768 10.1039/A700186J
- [9] Evolution study of photo-synthesized gold nanoparticles by spectral deconvolution model: a quantitative approach Chung-Sung Yang,Mong-Shian Shih,Fang-Yi ChangNew J. Chem., 2006,30, 729-735 10.1039/B516465F
- [10] Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis? Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-GordonPhys. Chem. Chem. Phys., 2012,14, 15328-15339 10.1039/C2CP42522J
Journal Name:Physical Chemistry Chemical Physics
research_products
-
CAS no.: 89640-58-4