Actuation performances of catkin fibers reinforced thiol-acrylate main-chain liquid crystalline elastomer

ABSTRACT Liquid crystalline elastomers (LCEs) have been utilized as an important class of smart actuator materials. However, the modest actuation mechanical and robustness performances remain a challenge. Inspired by the specific structures, well mechanical properties and physico-chemical characteristics of some natural plant fibers, a composite of thiol-acrylate main-chain LCE matrix incorporated with catkin fibers is designed and developed. The catkin fibers build a network as reinforcement phase, and demonstrate effective compatibility and integration property with the matrix, their high flexibility can be adapted to the large deformational performance of LCE matrix. The prepared LCE composite demonstrates strong mechanical actuation properties. The modulus and driving force triggered by the stimuli are obviously increased. The tensile strength and fatigue failure resistant property under high loadings and repeated cycles of thermal actuation or photothermal actuation are greatly enhanced. While the stimulus response deformation rate, phase transition temperature and liquid crystal phase structure of the LCE matrix, and so on, do not weaken or change. This work promotes the LCE materials’application potential and broadens the application value of natural plant fibers. Graphical abstract

The emerging application of driving LCE materials requires sufficient mechanical properties and durability. Although the LCEs may be enough robustness at room temperature, they can be seriously weakened at high temperatures, especially at the temperatures above their driving requirement, which can lead to accidental failure. Thus they are easy to break after many times actuation in the environment of high temperatures and loads. The moderate driving forces and fatigue failure resistant ability have become a arduous challenge for the industrial application development of LCE materials. One important way of improving the polymer materials'mechanical properties is preparing polymer composites by adding other reinforcing materials into the polymer matrix [44][45][46]. The rigid materials embedded in LCE matrices as continuous reinforcing phase may impede the materials' deformation performances even make the LCE materials lose their actuation capability. Though some nano fillers can improve the mechanical properties when they are added into the LCE matrices [47][48][49][50]. They belong to a separate reinforcing phase in LCE matrices, and the reinforcing effect may not be prominent relative to those continuous reinforcing phase materials. Fiber reinforcement materials have played a very important role in reinforced polymer composites due to their high freedom degree, agility and versatility [14,18,[51][52][53]. It has been reported that many natural fibers are widely used in agriculture, forestry, construction and commodity industry. They are becoming great substitutes for traditional fibers (such as glass, carbon and aramid, etc) in the research and manufacture of composites because of their light weight, carbon neutralization, recyclability, low cost, good specific strength and biodegradability [54][55][56][57][58][59][60][61][62]. Natural fibers are divided into animal fibers, plant fibers, and mineral fibers. Some of them, due to the high flexibility, enough toughness and unique structures, can be suitable for the shape change performances of smart deformable materials, including the LCEs. Our previous work revealed that the eiderdown fibers, which are a animal fibers, could effectively improve the actuation mechanical properties and durability of LCE composites [25].
In view of the more rich sources, low cost and recycling utilization requirement of some plant fibers, in this work, we study using the catkin fibers as reinforcement material to enhance the performances of LCE composites. Catkin fiber is a kind of highly flexible plant fiber with microtubule structure, low density and large surface volume ratio [63][64][65]. The characteristics of high length/diameter ratio and natural interweaving enable them to build a continuous grid network to reinforce the host materials. A classical thiol-acrylate MC-LCE is selected as the host material, for reason that the LCEs based on thiol-acrylate systems are currently widely attracted in research and application due to scalable design of matrix networks, convenient control over the processing and property tailoring, chemical and environmental stabilities, and so on [11,15,[66][67][68][69][70][71][72][73][74][75][76][77][78][79][80][81][82]. In the prepared LCE composites with the thiol-acrylate MC-LCE as the matrix and the catkin fibers as the reinforcement phase (LCE/ CFB composite), the hetero-phase structure between the catkin fibers and matrix demonstrated well compatibility and interface adhesion. The LCE/CFB composites showed strong driving mechanical properties, the driving blocking force and modulus were greatly enhanced by the reinforcing action of catkin fibers. Their tensile strength and fatigue failure resistant properties under repeated cycles of thermal actuation or photothermal actuation were significantly improved. While the stimulus response deformation rate was not attenuated by the addition of catkin fibers due to their flexible crimple and tensile properties, which could effectively comply with the large shape changing performance of LCE materials. The other properties of LCE/CFB composites, such as the LC phase structure and phase transition temperature, and so on, were also basically identical to the corresponding pure thiol-acrylate MC-LCE. Our work evidences the superiority and reliability of natural plant fibers in the development of LCE composites. It would promote the application potential of LCE materials, expand the recycling utilization of natural fibers, and be significant for the alternative solution of fossil materials and environmental conservation.
The preparation protocol of the catkin fibers incorporated thiol-acrylate MC-LCE composite (LCE/CFB) is illustrated in Scheme 1. The catkin fibers of 20 mg was evenly pre-laid at the bottom of a rectangular polytetrafluoroethylene mold, whose dimensions were 60 mm, 15 mm and 15 mm in length, width and height, respectively. The precursor reactant mixture was prepared by dissolving 1 g (1.699 mmol) RM257, 0.225 g (1.234 mmol) EDDET, 0.055 g (0.112 mmol) PETMP and 8 mg HHMP (photo-initiator) in 1 ml toluene, adding 180 µl catalyst solution. The mixture was poured into the mold. The mold was first implemented by ultrasonication for 15 seconds to eliminate micro-bubbles in the solution, then set in environment of 28°C for 10 hours to achieve the first step crosslinking. In this stage, a swollen gel elastomer containing toluene was generated. It was transferred out of the mold and dried in a vacuum drying oven at 65°C and 508 mmHg overnight to let the contained toluene evaporated, then uniaxially stretched by a 20 g load for 12 hours to be a stable length. The stretched elastomer was irradiated by the 365 nm UV light for 9 minutes to complete the second step crosslinking, and the film shaped LCE/CFB composite with 0.95 wt% of catkin fiber content was obtained. The blank thiol-acrylate MC-LCE was also prepared through the above procedure but without the addition of catkin fibers. The preparations of the dye doped LCE/CFB composite and dye doped blank thiol-acrylate MC-LCE with 0.1 wt% of dye content were consistent with those of the LCE/CFB composite and blank thiol-acrylate MC-LCE, respectively, but moderate amount of dye 'Ma001-2' was added into the above precursor reactant mixture. Scheme 1. Illustration of the experimental protocol for preparing the LCE/CFB composite.

Characterization methods
The mesomorphic properties were measured by using polarizing optical microscopy (POM) (SMZ1500, Nikon Instruments) and 2D X-ray scattering (2D-WAXS), which was a Bruker/Siemens Hi-Star 2D X-ray Diffractometer. The differential scanning calorimetry (DSC) (Q100, TA Instruments, DE) was used to investigate the phase transformation at a temperature variation rate of 5°C⋅min −1 . The scanning electron microscopy (SEM; Zeiss LEO 1530, Thornwood, NY, U.S.A) was used to observe the inner heterophase structure of LCE/CFB material. A dynamic mechanical analyzer (Q800 DMA, TA Instruments, U.S.A) was employed to measure the mechanical moduli. The contractile forces or strains performed by LCE materials upon the thermal or light stimulus were measured by using a universal material mechanical analyzer equipped with a thermostat cabinet (CMT-10, LG Company, Jinan, China). In the thermal stimulus, the examined sample was settled inside the thermostat cabinet, which regulated the heating/cooling processes. In the light stimulus, the examined sample was directly irradiated by an IR light source whose irradiation intensity could be tuned by turning the knob assembled on it. The temperature variations of material surfaces in response to light irradiation were measured in situ by using a multilogger thermometer with a detector of 2 mm in length and 100 mm in diameter. The contractile strains were measured in isoforce mode, the two ends of the sample were clamped with a constant tension load. The contractile forces were measured in isostrain mode, the two ends of the sample were clamped and elongated by a constant tension strain. The tensile strengths at different temperatures, and the fatigue failure resistant performances under passively drawing/restoring cycles of LCE materials at different temperatures were measured also by using the universal material mechanical analyzer. The examined sample was settled inside the thermostat cabinet, which regulated the temperature setting. The experiment environment temperature was about 26°C.

Results and discussion
The synthesis of matrix network of thiol-acrylate MC-LCE was via a sol-gel processed twostep Michael addition and polymerization reaction coupled with a stretching process between the two steps (TAMAP) [69,70]. As illustrated by Scheme 2, the precursor reactants included the monomers of mesogen (RM257), chain extender (EDDET), and crosslinker (PETMP). In the first step, the terminal vinyl bonds of acrylate groups in mesogenic molecules reacted with the -SH bonds of crosslinker molecules and chain extender molecules in the presence of catalyst for 'click' reaction of Michael addition to achieve polyaddition polymerization and crosslinking, and generate a polydomain network. Then an external stress was applied to establish a monodomain network with mesogen alignment along the stress direction. In the second step, the crosslinking of excess acrylate groups was completed by photo initiated polymerization to fix the alignment of mesogens and monodomain structure. The preparation protocol of our LCE/CFB composites were based on above TAMAP route of thiol-acrylate MC-LCE network synthesis, as illustrated in Scheme 1 and described in experiment section. Figure 1(a) presents a micrograph image of the catkin fibers. It shows that the catkin fibers had a circular circumferential shape with about 5 to 10 μm of diameters, and very large ratio of length to diameter, which could endow them a high ratio of surface to volume. While the catkin fibers naturally formed loose interweaving network, which could let them to easily construct continuous reinforcement phase evenly distributed in the host materials. Figure 1(b) exhibits a SEM picture of the sliced section of LCE/CFB. It shows that the catkin fibers and LCE matrix compactly bonded together, the adhesion of interface between them was tight.   matrix structure in them, and the mesogens were axially aligned along the stretch directions. 2D-WAXS measured with the normal directions of material surface being parallel to the incident beam of X-ray was implemented to further research the mesomorphic properties. The 2D-WAXS patterns of the blank LCE and LCE/CFB composite were, respectively, presented in Figure 2 (c,d). They all demonstrated the azimuthal intensity maxima at wide-angle reflection which implied the nematic LC phase structure in LCE matrices [1]. Moreover, the locations of azimuthal intensity maxima were orthogonal to the material stretch directions, thus further confirmed the axial mesogen alignment along the stretch directions, which was caused by the stress-induced orientation effect. Figure 3 (a,b), respectively, provides the DSC data curves of the blank thiol-acrylate MC-LCE and LCE/CFB composite. Each shows a distinct peak in the heating or cooling scan, corresponding to the nematic-isotropic or isotropic-nematic phase transition. The nematic-isotropic transition temperatures (T ni ) demonstrated in heating scan curves of the blank thiol-acrylate MC-LCE and LCE/CFB were, respectively, 82.71°C and 82.23°C. These results revealed that they both had enantiotropic nematic phase and that their phase transition temperatures were approximately equal to each other. The prepared blank thiol-acrylate MC-LCE and LCE/CFB composite performed thermal induced reversible deformation behavior. Figure 3 (c,d), respectively, provides the data plots of axial strain versus temperature variation of them upon the heating/cooling process, which were measured in isoforce mode with a constant axial tension of 40 kPa. Upon the heating process, their axial contraction strains increased with the increase of temperature, finally reached a stable maximum value of above sixty percent when the temperature was above T ni . During the cooling process, axial contraction strains decreased with the decrease of temperature, finally returned to initial value. This deformation was caused by the nematic order change of LCE matrices. The change of mesogen alignment degree, which was triggered by temperature variation, changed the nematic order, and hence triggered the transformation between the nematic phase and isotropic state when the LCE materials were heated above or cooled below the T ni , resulted in spontaneous contraction or elongation along alignment directions of LCE materials [3,4,6]. It is indicated by inspecting Figure 3 (c,d) that the performance of thermal driven shape changing of LCE/CFB composite was basically consistent with that of the blank thiol-acrylate MC-LCE, and almost not influenced by the incorporation of catkin fibers. This should be owed to the high flexibility of catkin fibers which derived from their microtubule structure and the high amorphous cellulose content in them [64,65]. The catkin fibers could agilely cooperated with the shape change of LCE matrix through the flexible crimple and extension behavior. The micrographs presented by Figure 3 (e,f) show the states of the catkin fibers embedded in LCE matrix at 25°C and at 90°C, respectively. The catkin fibers demonstrated a certain ordered extension pattern at 25°C, which should be caused by the external stress stretching in the preparation process of LCE/CFB composite. At 90°C which was above the T ni and the LCE/CFB composite fully contracted, the embedded catkin fibers crimped to be disordered state, and thus effectively avoided the impediment on material deformation.
The data plots of the Young modulus versus temperature variation of these two LCE materials, as given in Figure 4(a), indicated that their Young moduli gradually decreased with the increase of temperature due to the thermal softening effect of polymers, and dropped to minimal values at the temperatures around the T ni for reason of the occurrence of phase transition in matrix. But the decreasing rate of Young modulus of LCE/CFB was obviously lower than that of blank thiol-acrylate MC-LCE, and hence the LCE/CFB composite constantly kept higher Young modulus compared to the blank thiol-acrylate MC-LCE. At the temperatures around T ni , the Young modulus of the former was about 5 times as high as that of the latter, as shown in Figure 4(a). One reason of this modulus variation difference lied in the thermal stable mechanical properties of catkin fibers. The apparent Young modulus versus temperature variation of the catkin fiber bundles was measured, and the corresponding data plot is shown in Figure 4(b). It indicates that the apparent Young modulus of the catkin fiber bundles did not obviously change at the temperature range from 10°C to 110°C. The second reason lied in the large contacting interface and tight interfacial adhesion between the catkin fibers and LCE matrix. The tight interfacial adhesion could be led by the molecular attraction between the -OH groups on cellulose molecules contained in catkin fibers [64,65] and the C = O groups in LCE network. The large and tight bonding interface between the catkin fibers and LCE matrix could effectively hindered the dislocation motions in matrix and ensure a high stress transfer efficiency. These two factors made the LCE/CFB composite kept higher Young modulus compared to the blank thiol-acrylate MC-LCE at different temperatures. The higher modulus of LCE/CFB composite increased its elastic contraction capability. Under the condition of forced length fixation, the LCE materials demonstrated thermal induced reversible change of contractile actuating force. Figure 4 (c,d), respectively, show the data plots of axial contractile stresses produced by blank thiol-acrylate MC-LCE and LCE/CFB with temperature change during the heating/cooling process, which were measured in isostrain mode with a constant tension strain of 0.1%. Upon the heating process, their contractile actuation stresses gradually increased until to be maximum, which was the blocking actuation stress, when they were heated above T ni . Upon the cooling process, the contractile actuation stresses decreased and finally returned to initial value. It is indicated by inspecting Figure 4(c,d) that the blocking actuation stress of LCE/ CFB, which was about 1.35 Mpa, was obviously higher than that of blank thiol-acrylate MC-LCE, which was about 0.93 Mpa. This should be caused by the improved modulus property endued by catkin fiber reinforcement. The mechanical modulus of LCE/CFB was greatly higher than that of blank thiol-acrylate MC-LCE at T ni , at which the thermalinduced contractile actuation fully occurred, thus LCE/CFB composite demonstrated a greatly higher blocking actuation stress compared to the blank thiol-acrylate MC-LCE. Our experiment exhibited that when the catkin fiber content was below 0.8 wt%, the modulus and blocking actuation stress of LCE/CFB composites began to decrease. When the catkin fiber content was above 1.3 wt%, the maximum thermal induced contraction strain of LCE/CFB composites began to decrease. The modulus and maximum thermal induced contraction strain of LCE/CFB composites had no appreciable distinction in the catkin fiber content from 0.8 wt% to 1.2 wt%. We used 0.95 wt% of catkin fiber content as the reasonable content. Figure 5(a) shows the diagram of the measured tensile strengths at different temperatures of the blank thiol-acrylate MC-LCE and LCE/CFB. The tensile strengths decreased with temperature increasing, and decreased steeply near the T ni for reason that the LCE polymer chains lost the axial orientation, resulted in their axial strengthening effect being remarkably declined. The decreasing rate of the tensile strength of LCE/CFB composite were also obviously lower than that of the blank thiol-acrylate MC-LCE. Thus the LCE/CFB composite constantly kept higher tensile strength compared to the blank thiol-acrylate MC-LCE. At the temperatures around T ni , the tensile strength of the former was about 3 times as high as that of the latter, as shown in Figure 5(a). It is significant that the LCE materials can maintain a high tensile strength at the temperatures around the T ni because they need often undergoing such temperature environment to perform fully mechanical actuation. Experiment results indicated that the catkin fibers incorporated into LCE matrix greatly enhanced the material's tensile strength. One mechanism was that the catkin fibers effectively resisted the crack expansion. Figure 5(b), an optical micrograph of LCE/ CFB tested by tension failure, demonstrates that the catkin fibers restricted the tiny cracks and made them not further grew. The mini cracks occurred in LCE matrix inclined to propagate due to the stress action. When they encountered the catkin fibers, the crack planes had to bifurcate to bypass the catkin fibers. The crack deflection effect required much more energy dissipation, and thus the propagations of the cracks often halted [45,46]. In addition, if the crack planes bypassed the fibers, the bridging effect of catkin fibers across the tiny cracks also could retard the further growth of cracks, as shown in Figure 5(c). Another mechanism lied in the strong interfacial adhesion between the matrix and catkin fibers, as evidenced by Figure 5(d), which is an optical micrograph of LCE/CFB tested by tensile break. It indicates that there was no obvious pulling-out phenomenon of catkin fibers on the fracture plane. The strong interfacial adhesion could effectively enhance the stress transfer efficiency between the hetero phases and dissipate energy along the interface, while was beneficial for the resistance of crack propagation. For the blank thiol-acrylate MC-LCE, the mini cracks occurred at any location, such as the middle or side, could unrestrictedly grow to become large cracks, resulted in the material being easily fractured, as evidenced by Figure 5(e,f), which were the optical micrographs of the blank thiol-acrylate MC-LCE tested by tension failure.
The fatigue failure resistant performances of blank thiol-acrylate MC-LCE and LCE/ CFB upon the thermal actuation of repeated heating/cooling cycles were investigated. Figure 6 (a,b), respectively, provides the data plots of axial strains varying with time of them measured in isoforce mode under repeated temperature cycles between 45°C and 87°C. The two LCE materials all performed repeated axial strain variation of contraction/ restoration under repeated cycles of heating and cooling process. The blank thiolacrylate MC-LCE demonstrated that its repeated contraction/restoration cycle times, at which the fracture did not occurred, decreased with the increase of the constant tension load. It fractured after 20 times of repeated contraction/restoration cycle under the constant tension load of 0.36 MPa (Figure 6(a-I)). It fractured after 16 times of repeated contraction/restoration cycle under the constant tension load of 0.54 MPa ( Figure 6(a-II)). It fractured after 10 times of repeated contraction/restoration cycle under the constant tension load of 0.68 MPa (Figure 6(a-III)). However, under the same constant tension loads, the LCE/CFB composite performed stable contraction/ restoration variation without the occurring of fracture after 60 times of repeated heating and cooling process, as shown in Figure 6 (b-I), (b-II), (b-III), respectively. Figure 7 (a,b) give the measurement plots of the axial contractile stresses varying with time of the two LCE materials measured in isostrain mode under repeated temperature cycles between 45°C and 87°C. The two LCE materials all demonstrated cyclic variation of contractile stresses upon repeated cycles of heating and cooling process. The blank thiol-acrylate MC-LCE showed that its repeated cycle times of contractile stress variation without the occurring of fracture decreased with the increase of the constant pre-elongation strain. Under the constant axial pre-elongated strains of 8%, 16% or 23%, its stable cyclic variation times of contractile stress was 23 times, 17 times and 11 times, respectively, as shown in Figure 7 (a-I), (a-II) (a-III), respectively. While the LCE/CFB composite demonstrated stable cyclic variation of axial contractile stress after 60 times of repeated cycles of heating and cooling process with the same constant pre-elongated strains, as exhibited in Figure 7   that the LCE/CFB composite had a greatly better fatigue failure resistant performance under repeated thermal actuation compared to blank thiol-acrylate MC-LCE.
The fatigue failure resistant performances of blank thiol-acrylate MC-LCE and LCE/CFB upon repeated cycles of passively axial drawing/restoring at different temperature were investigated. Figure 8 (a,b), respectively, provides the measured data plots of axial strains varying with time of them which were repeatedly drawn and restored with the tension strain range being from 0 to 20%, and at 40°C, 63°C and 85°C, respectively. At 40°C, the blank thiol-acrylate MC-LCE fractured after about 35 times of repeated drawing/restoring cycles (Figure 8(a-I)). At 63°C, the blank thiol-acrylate MC-LCE fractured after about 24 times of repeated drawing/restoring cycles ( Figure 6(a-II)). At 85°C, the blank thiol-acrylate MC-LCE fractured after about 11 times of repeated drawing/restoring cycles ( Figure 6 (a-III)). However, at the same temperatures, the LCE/CFB composite did not fracture after 80 times of repeated drawing/restoring cycles, as exhibited in Figure 8  We further investigated the actuation mechanical properties and fatigue failure resistant performances of the LCE materials by using the photo stimulus. The blank thiolacrylate MC-LCE and LCE/CFB composite were doped by a little amount of IR absorption dye 'Ma001-2,' so that the dye could absorb the light irradiation and converted them into heating effect to actuate the LCE materials. Diagrams shown in Figure 9 (a,b) present the axial contraction strains and the achieved stable temperatures on materials in response to different IR irradiation intensities of the dye doped blank thiol-acrylate MC-LCE and dye doped LCE/CFB composite, respectively, which were measured in isoforce mode with a constant tension load of 60 kPa. It demonstrates that the contraction strains of the two LCE materials increased as the irradiation intensity increased for reason that a higher irradiation intensity created a higher temperature on the materials, as shown in Figure 9  (a,b). When the irradiation intensity was above 2.5 W/cm 2 , the contraction strains did not further increase because the achieved temperatures on materials in response to the IR irradiation were already above the T ni . The maximum contraction strains of the two LCE materials were above sixty percent, which was basically equal to the thermal derived maximum contraction strains, as shown in Figure 3 (c,d). The diagrams shown in Figure 9 (c,d), respectively, present the axial contractile stresses and the achieved stable temperatures of the two LCE materials in response to different IR irradiation intensities, which were measured in isostrain mode with a constant tension strain of 0.1%. It indicates that the contractile stresses increased as the irradiation intensity increased for reason that a higher irradiation intensity created a higher temperature on the materials, as shown in Figure 9 (c,d). When the irradiation intensity was above 2.5 W/cm 2 , the achieved temperatures were above the T ni , the contractile stresses arrived the blocking actuation stresses and did not continuously change. It is indicated from the showing of Figure 9 (c,d) that the blocking actuation stresses of the dye doped blank thiol-acrylate MC-LCE and dye doped LCE/CFB composite triggered by IR irradiation were about 0.94 MPa and 1.36 MPa, respectively, which were basically equal to their respective thermal triggered blocking actuation stresses, as shown in Figure 4 (a,b).   Figure 10 (a,b), respectively, exhibits the plots of axial strains varying with time of the two LCE materials measured in isoforce mode under repeated switching on/off cycles of IR with irradiation intensity of 3.5 W/cm 2 . The two LCE materials all performed repeated axial strain variation of contraction/restoration under repeated on/off IR irradiation. Under the constant tension load of 0.36 MPa, 0.54 MPa and 0.68 MPa, respectively, the dye doped blank thiol-acrylate MC-LCE fractured after 24 times (Figure 10(a-I)), 19 times (Figure 10(a-II)) and 11 times (Figure 10(a-III)) of contraction/restoration cycle, respectively. While the dye doped LCE/ CFB composite performed stable contraction/restoration variation without the occurring of fracture after 60 times of repeated on/off IR irradiation, as respectively, exhibited in Figure 10 (b-I), Figure 10 (b-II) and Figure 10 (b-III). Figure 11 (a) and Figure 11 (b) provide the measurement plots of axial contractile stresses varying with time of the two LCE materials measured in isostrain mode under repeated switching on/off cycles of IR with irradiation intensity of 3.5 W/cm 2 . They all demonstrated cyclic variation of axial contractile stresses under repeated on/off IR irradiation. It is indicated from the showing of Figure 11 (a-I), (a-II) (a-III) that under the constant axial pre-elongated strains of 8%, 16% and 23%, respectively, the stable cyclic variation times of contractile stress of the dye doped blank thiol-acrylate MC-LCE was 24 times, 20 times and 14 times, respectively. While the LCE/CFB composite demonstrated stable cyclic variation of axial contractile stress after 60 times of repeated on/off IR irradiation with the same constant preelongated strains, as exhibited in Figure 11 (b-I), (b-II) (b-III), respectively. Experiment results evidenced that the fatigue failure resistant performance upon the repeated photothermal actuation of LCE/CFB was also greatly superior to the blank thiol-acrylate MC-LCE, thus revealed a well reliability and durability of plant fibers reinforced LCE composites.

Conclusions
For several tens of years, the modest mechanical properties and robustness of LCE materials have seriously impeded their industrial applications. They are related to the using cost, using occasions, safety and service life of the materials, and thus have become a key issue of LCE research field. Some natural fibers can be used for the reinforcement of stimuli-responsive polymer deformable materials owing to their advantages, such as low weight, unique structures, high flexibility and valuable mechanical properties. Thiolacrylate LCEs are widely attracted in the application research at current. Their synthesis process can also be suitable for the convenient fabrication of large-sized LCE composites with flexile continuous fibers as reinforcement phase.
Our previous work used the eiderdown fibers to enhance the mechanical actuation performances of LCE materials [25]. But the conformation of eiderdown fibers is down cluster structure, that is the fiber clusters grow on the down stones [83]. Such structure Figure 11. Upon repeated switching on/off cycles of IR with irradiation intensity of 3.5 W/cm 2 , and in in isostrain mode, the actuation stresses versus time of dye doped blank thiol-acrylate MC-LCE (a) and dye doped LCE/CFB composite (b) with different pre-elongated strains.
may not be benefit for their even dispersity in polymer matrices, and thus limit the ultimate reinforcement effect. Moreover, in viewing that some plant fibers, such as catkin fibers, and so on, have more rich sources and and urgent recycling utilization requirement for reason they may often create environmental disturbance every year. In this work, we study using the catkin fibers as reinforcement material to enhance the performances of LCE composites.
The catkin fibers were used as the reinforcement phase to prepare LCE composite with a thiol-acrylate MC-LCE matrix. The catkin fibers built reinforcing phase network through the LCE matrix, demonstrated tight interfacial adhesion and well compatibility with the matrix, and effectively enhanced the driving mechanical properties and material robustness. The blocking actuation force and mechanical modulus were significantly increased. The tensile strength and fatigue failure resistant properties under repeated cycles of thermal actuation or photothermal actuation were also significantly improved. While the stimulus response deformation rate was not attenuated by the addition of catkin fibers due to their flexible crimple and tensile properties. The phase transition temperature and LC phase structure, and so on, were also basically not influenced by the addition of catkin fibers due to their well thermal stability and chemical stability. Our method can be expected to develop more plant fiber incorporated LCE composites with excellent driving performance, reliability and durability, and promote the application development of LCEs as artificial muscles and smart actuators, and so on. Our work is conducive to expand the recycling utilization of natural plant materials, and thus is significant for the environmental conservation and the saving of fossil materials' consumption.