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Liquid crystal polymers (LCPs) are polymers with the property of liquid crystal, usually containing aromatic rings as mesogens. Despite uncrosslinked LCPs, polymeric materials like LCEs (liquid crystal elastomers) and LCNs (liquid crystal networks) can exhibit liquid crystallinity as well. They are both crosslinked LCPs but have different cross link density.[1] They are already widely used in the display market.[2] In addition, LCPs have unique properties like thermal actuation, anisotropic swelling, and soft elasticity. Therefore, they can be good actuators and sensors.[3] One of the most famous and classical applications for LCPs is Kevlar, a strong but light fiber with wide applications like a bulletproof vest.
Mesophases edit
Same as the small molecular liquid crystal, liquid crystal polymers also have different mesophases. The mesogen cores of the polymers will aggregate into different mesophases: Nematics (N), Cholesterics (Ch), Smectics (S), compounds with highly plar end groups. [4]More information about the mesophases can be found on liquid crystal page.
Classification edit
LCPs are categorized by the location of liquid crystal cores. Main chain liquid crystal polymers (MCLCPs), as the name indicates, have liquid crystal cores in the main chain. To contrast, side chain liquid crystal polymers (SCLCPs) have pedant side chains containing the liquid crystal cores. The basic structures for these two kinds of LCPs are shown in the figure.[4]
Main chain LCP edit
Main chain LCPs have rigid, rod-like mesogens in the polymer backbones, which indirectly leads to the high melting temperature of this kind of LCPs. To make this kind of polymer easy to process, different methods are applied to lower the transition temperature: (1) Introducing flexible sequences; (2) Introducing bends or kinks; (3) Adding substituent groups to the aromatic mesogens...
Side Chain LCP[5] edit
In side chain LCPs, the mesogens are in the polymer side chains. The mesogens usually are linked to the backbones through flexible spacers (Although for a few LCPs, the side chains directly link to the backbones). If the mesogens are directly linked to the backbones, the coil-like conformation of the backbones will impede the mesogens from forming an orientational structure. However, by introducing flexible spacers between the backbones and the mesogens, the ordering of mesogens can be decoupled from the conformation of the backbones.
Becasause of the researcher's effort, more and more LCPs of different structures are synthesized. Therefore, latin letters are used to help the classification of LCPs.[4]
Mechanism edit
Mesogens in LCPs can self-organize to form liquid crystal regions in different conditions. Based on the mechanism of aggregation and ordering, LCPs can be roughly divided into two subcategories as shown below. However, the distinction is not rigidly defined. LCPs can be transformed into liquid crystals with more than one method.[4]
Lyotropic systems[6] edit
Lyotropic main chain LCPs have rigid mesogen cores (like aromatic rings) in the backbones. This kind of LCPs forms liquid crystals due to their rigid chain conformation but not only the aggregation of mesogen cores. Because of the rigid structure, strong solvent is needed to dissolve the lyotropic main chain polymers. When the concentration of the polymers reaches critical concentration, the mesophases begin to form and the viscosity of the polymer solution begins to decrease. Lyotropic main chain LCPs have been mainly used to generate high-strength fibers such as Kevlar.
Side chain LCPs usually consist of both photophobic and photophilic segments. Usually, the side chain ends are hydrophilic. When they are dissolved in water, micelles will form due to hydrophobic force. If the volume fraction of the polymers exceeds the critical volume fraction, the micellar segregates will be packed to form a liquid crystal structure. As the concentration varies above the critical volume fraction, the liquid crystal generated may have different packing ways. Temperature, the stiffness of the polymers, molecular weight of the polymers can affect the liquid crystal transformation. Lyotropic side chain LCPs like alkyl polyoxyethylene surfactants attached to polysiloxane polymers may be applied to personal care products like liquid soap etc.
Thermotropic systems[7] edit
The study of thermotropic LCPs is inspired by the success of the lyotropic LCPs. This kind of LCPs can only be processable when the melting temperature is far below the decomposition temperature. Above the melting temperature and glass transition temperature and below the clearing point, the thermotropic LCPs will form liquid crystals. After the clearing point, the melt will be isotropic and clear again. What is different from the small molecular liquid crystals is that we can get frozen liquid crystals by quenching the liquid crystal polymers below the glass transition temperature. Moreover, we can use copolymerization to justify the melting temperature and mesophase temperature.
There are other systems like phototropic systems.
Liquid crystal elastomers (LCEs)[3] edit
LCEs is first proposed in 1981 by Finkelmann. After that, LCEs have attracted a lot of attention from researches and industry. LCEs can be synthesized both from the polymeric precursors and from exclusively monomers. LCEs can show special properties when responding to heat, light, and magnetic fields.[1] Furthermore, Different nanomaterials can be introduced into the LCE matrix (LCE-based composites) to provide LCEs with different properties and tailor LCEs' ability to respond to different stimuli.[3] LCEs have many applications. For example, the LCE films can be used as opticle retarders due to their anisotropic structure. Because they can control the polarization state of the transmitted light, they are commonly used in 3D glasses, patterned retarders for transflective displays, the flat panel LC television. If the LCE is modified with azobenzen, it can show light response properties and thus can be applied for controlled wettability, autonomous lenses, and haptic surfaces. [2] Besides the display application which has already been commoditized, now researches have focused on other interesting properties of the LCEs like its special thermally and photogenerated macroscale mechanical responses, which means they can be good actuators. A recent paper systematically reviewed the programmable and adaptive mechanics with liquid crystal polymer networks and elastomers.[1]
There are different synthetic routes to get LCEs.[3]
LCEs synthesized from the polymeric precursors edit
LCEs synthesized from the polymeric precursors can be divided into two subcategories:
LCEs can be synthesized from poly(hydrosiloxane). A two-step crosslinking technique is applied to get LCEs from poly(hydrosiloxane). Poly(dydrosiloxane) is mixed with a monovinyl-functionalized liquid crystalline monomer, a multifunctional vinyl crosslinker, and catalyst. This mixture is used to generate a weakly crosslinked gel, in which the monomers are linked to the poly(dydrosiloxane) backbones. During the first crosslinking step or shortly after that, orientation is introduced into the mesogen cores of the gel with mechanical alignment methods. After that, the gel is dehydrated and the crosslinking reaction is completed. Therefore, the orientation is kept in the elastomer by crosslinking. In this way, we can get highly ordered side chain LCEs, which are also called single-crystal or monodomain LCEs.
LCEs can be synthesized from LCPs. With LCPs as precursors, we can use the two-step method shown in the previous subcategory. Also, we can use aligned LCPs mixed with multifunctional crosslinkers to directly generate LCEs. The mixture is first heated to isotopic. Fibers are drawn from the mixture and then crosslinked, thus the orientation can be trapped in the LCE. This method is widely used to generate a lot of LCEs. However, it is limited by the difficulty of processing caused by the high viscosity of the starting material.
LCEs synthesized from low molar mass monomers edit
Liquid crystal low molar mass monomers are mixed with crosslinkers and catalysts. The monomers can be aligned and then polymerized to keep the orientation. One advantage of this method is that the low molar mass monomers can be aligned by not only mechanical alignment, but also diamagnetic, dielectric, surface alignment. In recent years, methods to get a well-defined structure in LCEs have attracted a lot of attention. For example, thiol-ene radical step-growth polymerization and Michael addition are used to get well-ordered LCEs.[8] This is also a good way to synthesize moderately to densely crosslinked glassy LCNs.
The main difference between LCEs and LCNs is the cross link density. LCNs are primarily synthesized from (meth)acrylate-based multifunctional monomers while LCEs usually come from crosslinked polysiloxanes. More information about the synthesis, properties and applications of LCNs and LCEs can be found in this book published in 2011.[9]
References edit
- ^ a b c White, Timothy J.; Broer, Dirk J. (2015). "Programmable and adaptive mechanics with liquid crystal polymer networks and elastomers". Nature Materials. 14 (11): 1087–1098. doi:10.1038/nmat4433. ISSN 1476-4660.
- ^ a b Liu, Danqing; Broer, Dirk J. (2014-04-22). "Liquid Crystal Polymer Networks: Preparation, Properties, and Applications of Films with Patterned Molecular Alignment". Langmuir. 30 (45): 13499–13509. doi:10.1021/la500454d. ISSN 0743-7463.
- ^ a b c d Kularatne, Ruvini S.; Kim, Hyun; Boothby, Jennifer M.; Ware, Taylor H. (2017). "Liquid crystal elastomer actuators: Synthesis, alignment, and applications". Journal of Polymer Science Part B: Polymer Physics. 55 (5): 395–411. doi:10.1002/polb.24287. ISSN 1099-0488.
- ^ a b c d Collyer, A. A (1992). Liquid crystal polymers: from structures to applications. London; New York: Elsevier Applied Science. ISBN 978-1-85166-797-0. OCLC 25409693.
- ^ Ganicz, Tomasz; Stańczyk, Włodzimierz (2009). "Side-chain Liquid Crystal Polymers (SCLCP): Methods and Materials. An Overview". Materials. 2 (1): 95–128. doi:10.3390/ma2010095.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ "Liquid crystal polymers". Progress in Polymer Science. 16 (1): 55–110. 1991-01-01. doi:10.1016/0079-6700(91)90007-8. ISSN 0079-6700.
- ^ Shibaev, Valery P.; Platé, Nicolai A. (1984), "Thermotropic liquid-crystalline polymers with mesogenic side groups", Liquid Crystal Polymers II/III, Berlin, Heidelberg: Springer Berlin Heidelberg, pp. 173–252, ISBN 978-3-540-12994-3, retrieved 2021-05-08
- ^ Ware, Taylor H.; Biggins, John S.; Shick, Andreas F.; Warner, Mark; White, Timothy J. (2016-02-23). "Localized soft elasticity in liquid crystal elastomers". Nature Communications. 7 (1). doi:10.1038/ncomms10781. ISSN 2041-1723.
- ^ Cross-Linked Liquid Crystalline Systems : From Rigid Polymer Networks to Elastomers. CRC Press. 2011-01-24. doi:10.1201/b10525. ISBN 978-0-429-14395-3.