Classical photopolymerization kinetics, exceptional gelation, and improved diffraction efficiency and driving voltage in scaffolding morphological H-PDLCs afforded using a photoinitibitor | |
Peng, Haiyan; Chen, Guannan; Ni, Mingli; Yan, Yan; Zhuang, Jiaqing; Roy, V. A. L.; Li, Robert K. Y.; Xie, Xiaolin | |
刊名 | Polymer Chemistry |
2015 | |
英文摘要 | Holographic polymer dispersed liquid crystals (H-PDLCs) pertain to one type of intriguing switchable electro-optical device, and there is a constant need to quantitatively understand the photopolymerization kinetics and gelation process during the formation of H-PDLCs for the purpose of improving the diffraction efficiency and driving voltage. Herein, we quantitatively investigate the effect of the photoinitibitor composed of 3,3'-carbonylbis(7-diethylaminocoumarin) (KCD) and N-phenylglycine (NPG), with initiation and inhibition functions simultaneously generated under monochromatic illumination, on the formation of H-PDLCs. The outcomes reveal that an augmentation of KCD loading from 0.3 x 10(-3) to 1.4 x 10(-3) mol L-1 dramatically promotes the photopolymerization rate and monomer conversion. Reversely, a further increase in KCD content drastically depressesphotopolymerization. The numerical deduction shows that the kinetics complies with the classical photopolymerization kinetics characteristics in the full range of the KCD content. Counterintuitively, the gelation time almost keeps constant when the KCD content is less than 1.8 x 10(-3) mol L-1, and then is able to grow by more than 4 times when the KCD loading further increases. Ketyl radical inhibition, which subsequently results in shortened weight-average chain lengths and increased gel point conversions, is believed to account for the kinetics and exceptional gelation behaviors. H-PDLCs with a scaffolding morphology are formed, and with an augmentation of the KCD content, the segregation degree and diffraction efficiency significantly improve from zero to 64% and 78 +/- 11%, respectively, and then level off, allowing for the facile fabrication of glass-free colored 3D images; while the critical driving voltage gradually decreases from 8.9 +/- 1.0 to 4.6 +/- 0.7 V mu m(-1). |
收录类别 | SCI |
原文出处 | http://pubs.rsc.org/en/Content/ArticleLanding/2015/PY/C5PY01414J#!divAbstract |
语种 | 英语 |
内容类型 | 期刊论文 |
源URL | [http://ir.siat.ac.cn:8080/handle/172644/9170] |
专题 | 深圳先进技术研究院_其他 |
作者单位 | Polymer Chemistry |
推荐引用方式 GB/T 7714 | Peng, Haiyan,Chen, Guannan,Ni, Mingli,et al. Classical photopolymerization kinetics, exceptional gelation, and improved diffraction efficiency and driving voltage in scaffolding morphological H-PDLCs afforded using a photoinitibitor[J]. Polymer Chemistry,2015. |
APA | Peng, Haiyan.,Chen, Guannan.,Ni, Mingli.,Yan, Yan.,Zhuang, Jiaqing.,...&Xie, Xiaolin.(2015).Classical photopolymerization kinetics, exceptional gelation, and improved diffraction efficiency and driving voltage in scaffolding morphological H-PDLCs afforded using a photoinitibitor.Polymer Chemistry. |
MLA | Peng, Haiyan,et al."Classical photopolymerization kinetics, exceptional gelation, and improved diffraction efficiency and driving voltage in scaffolding morphological H-PDLCs afforded using a photoinitibitor".Polymer Chemistry (2015). |
个性服务 |
查看访问统计 |
相关权益政策 |
暂无数据 |
收藏/分享 |
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。
修改评论