Polymer-stabilized fast-relaxation dye-doped cholesteric liquid crystals with a wide temperature range by thiol-Michael addition polymerization

被引:3
|
作者
Zhu, Mengmeng [1 ,2 ]
Cao, Ying [1 ,2 ]
Liang, Yuge [1 ,2 ]
Ma, Chao [1 ,3 ]
Lu, Hongbo [1 ,2 ]
Xu, Miao [1 ]
Qiu, Longzhen [1 ,3 ]
Zhu, Jun [1 ,2 ]
机构
[1] Hefei Univ Technol, Acad Optoelect Technol, Special Display & Imaging Technol Innovat Ctr Anhu, Natl Engn Lab Special Display Technol,State Key La, Hefei 230009, Peoples R China
[2] Hefei Univ Technol, Sch Chem & Chem Engn, Anhui Prov Key Lab Adv Funct Mat & Devices, Hefei 230009, Peoples R China
[3] Sch Instrument Sci & Optoelect Engn, Anhui Prov Key Lab Measuring Theory & Precis Instr, Hefei 230009, Peoples R China
关键词
Dye-doped cholesteric liquid crystals; Fast-relaxation; Thiol-Michael addition polymerization; Wide temperature range; LIGHT;
D O I
10.1016/j.dyepig.2023.111628
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The transient planar (TP) state during the relaxation process, from homeotropic (H) to planar (P) state, of dyedoped cholesteric liquid crystals (DDCLCs) can be eliminated by adjusting the elastic constants, reducing the time and haze of the relaxation process. However, the elastic constants are easily influenced by temperature. Therefore, the operating temperature range for fast-relaxation DDCLCs is relatively narrow. This work demonstrates that a polymer helical template can be formed in the P state of DDCLCs by thiol-Michael addition polymerization. It can significantly expand the temperature range from 20 degrees C to 60 degrees C for fast-relaxation DDCLCs. More importantly, polymer-stabilized dye-doped cholesteric liquid crystals (PS-DDCLCs) did not show any reduction in the absorption of the dye or discoloration after polymerization. PS-DDCLCs could still achieve tri-state switching and could be used for fast-relaxation smart windows capable of adapting to increasing environmental temperatures. The proposed smart window can be used in vehicles and aircraft to prevent glare and protect privacy.
引用
收藏
页数:7
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