The need for mechanical manipulation during the curing of conventional liquid crystal elastomers diminishes their applicability in the field of shape-programmable soft materials and future applications in additive manufacturing. Here we report on polymer-dispersed liquid crystal elastomers, novel composite materials that eliminate this difficulty. Their thermal shape memory anisotropy is imprinted by curing in external magnetic field, providing for conventional moulding of macroscopically sized soft, thermomechanically active elastic objects of general shapes. The binary soft-soft composition of isotropic elastomer matrix, filled with freeze-fracture-fabricated, oriented liquid crystal elastomer microparticles as colloidal inclusions, allows for fine-tuning of thermal morphing behaviour. This is accomplished by adjusting the concentration, spatial distribution and orientation of microparticles or using blends of microparticles with different thermomechanical characteristics. We demonstrate that any Gaussian thermomechanical deformation mode (bend, cup, saddle, left and right twist) of a planar sample, as well as beat-like actuation, is attainable with bilayer microparticle configurations.
The widespread use of polymers and elastomers in modern technologies strongly relies on the fact that they are relatively undemanding for moulding, reshaping and machining. In most applications, these materials are used as passive mechanical components. Only recently, smart soft materials with external stimuli-induced mechanical responsiveness have been developed. Among them, electroactive polymers1, have been employed most extensively. Nevertheless, liquid crystal elastomers (LCEs) are becoming an increasingly strong competitor in the development of a new generation of actuator and transducer elements2, both for macroscopic devices, for example, artificial muscles, and micro- and nano-sized devices, for example, microelectromechanical systems (MEMS) and nanoelectromechanical systems (NEMS)3,4. In these smart polymer materials, changes in the molecular orientational order, equivalently nematic order, are manifested macroscopically as deformation of specimen geometry5. The control of nematic order and the consecutive morphing can be achieved by varying the temperature, either by contact heat conduction6,7, indirect heating via electromagnetic radiation-absorbing nanoparticle inclusions8,9,10, or by photoisomerization11.
Among the more exciting prototype devices12 exploiting shape memory behaviour of LCEs are microfluidic valves, Braille readers, holographic gratings and artificial cilia13,14,15,16. However, current LCE synthesis methods still lack easy implementation into larger scale production environment. The major obstacle is the microscopic size of LCE domains: although individual LCE domains possess shape memory, the sample as a whole is inert since conventional polymerization methods yield isotropic distribution of domain orientations. A crucial step of imprinting shape memory into a macroscopically-sized LCE specimen is, therefore, to instil permanent orientational alignment of domains, that is, an effectively ‘monodomain’ state with anisotropic physical properties on the macroscopic scale. Currently, the most efficient way to achieve this is thermal polymerization of a mechanically stressed, partially crosslinked network6. Unfortunately, this procedure allows neither for preparation of samples of arbitrary shapes, nor for the miniaturization and templating of the geometry17,18. An alternative method that omits partial crosslinking has recently been invented19, but the alignment of domains still needs to be performed mechanically. Mouldable LCE materials for production of macroscopically sized monodomain parts of arbitrary shapes, that is, bulk parts with anisotropic thermomechanical properties, thus remain rather elusive. The availability of such materials could considerably expand the application scope of three-dimensional (3D) printing technologies16,20, which currently rely almost exclusively on isotropic raw materials. Moreover, shape-programmable21,22 3D soft objects could be fabricated through imprinting spatially inhomogeneous thermomechanical or photomechanical anisotropy via curing in the presence of gradiented or voxelized (individually adjusted to small volume elements) non-mechanical external orienting field, using conventional fused deposition modelling and stereolithography additive technologies20,23. For two-dimensional (2D) elastic objects, the concept of programmable shape-changes has been demonstrated experimentally in thin elastic gel sheets with non-uniform shrinkage properties24 and in LCE films with voxelized nematic director field25, as well as explained theoretically in terms of non-Euclidean metrics-driven out-of-plane curving of planar sheets exposed to external stimuli26,27,28. Poor choice of suitable materials has so far impeded the extension of this concept to 3D.
In this paper, we present a new composite material, polymer-dispersed liquid crystal elastomer (PDLCE) that overcomes the above restrictions: it provides for moulding of soft elastomeric bulk or miniature, thermally morphable parts of any given shape. The main idea is to dope a conventional elastomer like polydimethylsiloxane (PDMS) with LCE microparticles (μLCEs) (Fig. 1a). Used as fillers or inclusions in a soft polymer matrix, μLCEs render the composite material effectively thermomechanically active, provided that their axes of anisotropy are at least partially aligned. The latter is accomplished by curing the mixture of polymer resin and μLCE in external magnetic field, exploiting the diamagnetic anisotropy of the μLCEs29. Since these are small with respect to the size of the composite specimen, inhomogeneities in local stress and strain can be disregarded, and the composite’s effective elastic and thermomechanical properties resemble those of a conventional bulk, oriented LCE material. Unlike in competing approaches6,19, macroscopic thermomechanical anisotropy is imprinted into PDLCEs without mechanical stressing, using external orienting magnetic field, which imposes no restrictions on the shape and size of the specimen. In contrast to currently prevailing efforts of designing LCE composites where LCE is used as the matrix, functionalized with micro- or nanoparticles8,10,30, in PDLCEs it is μLCEs themselves that have the role of the colloid. We demonstrate that this paves the path towards designing thermomechanically functionalized conventional elastomers with tailorable shape memory and thermal expansion behaviour.
Thermomechanical functionalizing with oriented μLCEs
The availability of nematic monodomain μLCEs is mandatory for the design of PDLCEs. In view of the target application domain of PDLCEs, that is, moulding of macroscopically sized, thermomechanically functionalized soft objects that require abundant quantities of microparticles, recent breakthroughs in the synthesis of anisotropic colloidal μLCEs using templating18 or microfluidics31,32 approach offer a straightforward choice of particle production, but are technologically rather demanding as far as rapid, high-volume production is concerned. We propose a much simpler approach of low-temperature milling to freeze-fracture bulk LCE samples into micropowder with particle sizes in the 1–150 μm range (step 1 of Fig. 1a). It is assumed that μLCEs retain the thermomechanical behaviour of their bulk LCE parent, that is, λμLCE(T)=λLCE(T) ≡ LLCE(T)/LLCE(Tref), with the strain (λLCE(T)−1)∝S(T) reflecting temperature dependence of the nematic order parameter S(T) associated with spontaneous orientational ordering of the mesogenic LCE network components5. In contrast to pure bulk liquid crystals, which typically exhibit sharp, weakly first order type S(T) anomaly at the clearing temperature TNI, in LCEs, where the mesogens are embedded into the network, the S(T) anomaly and hence the λLCE(T) anomaly is smeared about the nominal thermomechanical transition temperature Tλ (ref. 33). The degree of smearing and the shift of Tλ with respect to TNI depend on structural parameters like, for example, concentration of crosslinkers34. The reference specimen length LLCE(Tref) is measured in the isotropic phase at Tref≫Tλ where λLCE(S→0)→1.
Individual PDLCE specimens discussed here are labelled sequentially as PDLCE-β. The hyphenated sequential suffix β=A, Ap, B, B1/B2, C, or Cp is associated with the type of embedded μLCE particles. These are labelled as μLCE-α, with α=A, Ap, B1, B2, C, or Cp denoting chemical composition and fabrication parameters of their respective bulk LCE-α parents (see Methods for details on the fabrication procedure and Table 1 for parameters associated with the α suffix). All investigated PDLCEs contain a single type of μLCE particles, equivalently β=α, except for PDLCE-B composed with a mix of μLCE-B1 and μLCE-B2, and PDLCE-B1/B2 composed of fused μLCE-B1 and μLCE-B2 layers. Secondary index p in Ap and Cp is used to mark polydomain bulk LCE material.
Although monodomain bulk LCE pieces (LCE-A, LCE-B1, LCE-B2, LCE-C) represent the optimal choice that guarantees individual grains of the powderized material to retain nematic monodomain state (Supplementary Fig. 1 and Supplementary Note 1), polydomain bulk LCE starting material (LCE-Ap, LCE-Cp) can be used as well, since the specimens are crushed into microparticles of the size of nematic domains, typically several μm (ref. 5). Subsequently, microparticles are dispersed into conventional liquid elastomer resin, favourably in a 1:1 particle/matrix weight ratio (step 2 of Fig. 1a). A specific selection of thermally curable PDMS as the matrix material provides for chemically inert, appropriately viscous environment for efficient mixing and negligible particle aggregation on the timescale of the curing process.
Macroscopic shape memory is rendered into the composite material by orienting the prepolymer dispersion of μLCEs in the external magnetic field of magnitude B=|B| and subsequently locking the orientations by thermal curing of the matrix at elevated temperature T0 (steps 3 to 5, respectively, of Fig. 1a). The degree of diamagnetic anisotropy-driven μLCE alignment35 is quantified by the orientational order parameter (ref. 36), which is rather independent of temperature since μLCE orientational distribution is locked during the setting of the resin. is to be distinguished from the nematic order parameter S(T) measuring molecular orientational order within a nematic domain and exhibiting strong temperature dependence (see above). At moderate magnetic fields (B≈1 T), saturation of occurs within several minutes, whereas at higher, nevertheless readily available fields of several T, it only takes a few seconds with our particular choice of materials37 (for details on magnetic alignment dynamics see Supplementary Fig. 2 and Supplementary Note 2). Moreover, the aligning efficiency depends very little on the shape of microparticles38. Such a rapid magnetic manipulation of bulk quantity PDLCE material thus offers a competitive advantage over existing techniques that rely on mechanical manipulation. The effective thermomechanical response λ(T)=L(T)/L(Tref) of the resulting cured PDLCE, depicted schematically in Fig. 1c, is shown in Fig. 2 for a selection of specimens. λ(T0) performance figures of all investigated PDLCEs are given in Table 2. The observed response, typically λ(Troom)≈λ(T0)≈1.12 for PDLCE-A and PDLCE-C, is reduced with respect to the response of bulk monodomain LCE where λLCE(Troom)≈1.45, due to the presence of thermomechanically inactive PDMS matrix (see the modelling of effective response in Supplementary Note 3).
Structurally, the obtained composites are analogous to polymer-dispersed liquid crystals where the nematic director of liquid-crystalline microdroplets, embedded in a polymer matrix, is manipulated by external fields or temperature to control the optical anisotropy of the system39. In PDLCEs presented here, μLCEs, embedded in an elastomer matrix, can be manipulated in a similar fashion to control the elastic anisotropy and mechanical dimensions of the sample. These can be fine-tuned by using μLCEs composed of different monomer species40, like for example, M4 and M11 in the present study (Fig. 1d).
The main characteristics of PDLCE structure can easily be observed under polarizing optical microscope. Depending whether crossed polarizers are used or not, the particles are seen as dark (Fig. 3a) or bright spots (Fig. 3b), respectively. In spite of a relatively wide distribution of particles’ size, their dispersion inside the matrix is rather homogeneous. The alignment of particles was verified by reorienting the sample with respect to the polarizers. Specifically, the magnified view of Fig. 3c reveals synchronous changes in the brightnesses of an arbitrary pair of particles on changing the orientation angle ϕ, indicating that nematic directors are well aligned on the microscopic scale. Macroscopic alignment uniformity of field-aligned μLCE is demonstrated in Fig. 3d via anisotropic (ϕ−dependent) overall light transmittivity; the latter is isotropic in PDLCE with disordered μLCE.
Shape-change programming of PDLCEs
Probably the most applicable feature of PDLCEs is the ability to program their shape memory behaviour, beyond the currently prevalent contraction/dilatation and bending-style reshaping2. In the simplest case, this can be achieved by controlling the orientation of μLCE during the curing phase. In order to demonstrate this, we manufactured two identically shaped PDLCE-A disks with different orientation of nematic director n with respect to disk symmetry axis Z, one with an ‘out-of-plane’ and the other with an ‘in-plane’ orientation (Fig. 4a). On actuating the particles by raising T above Tλ, an isovolumetric shape change thins the n||Z disk and increases its diameter, whereas it thickens the n⊥Z disk and makes it elliptically shaped (Fig. 4b,c).
It is also straightforward to imagine morphable objects of higher complexity, produced in a similar way by spatially modulating the direction and/or the magnitude of B, for example, by additive layer manufacturing of partially polymerized layers41. In general, by controlling the spatial profile of the μLCE director field, the final, thermomechanically inhomogeneous sample could exhibit arbitrary deformations on temperature changes. We demonstrated this functionality by fabricating bilayer discs of various director configurations, resulting in, on external heat stimuli, curved shapes with all possible combinations of principal curvatures, that is, with positive and negative values of respective Gaussian curvatures22 at disc centres (Fig. 5, animated version in Supplementary Movie 2). The observed shapes are reminiscent of the ones recently predicted for thin nematic elastomer sheets with inhomogeneous director field26, realized by surface-aligning the voxels of inherently 2D specimen25. In our case, however, we address the programming of thermomechanical response of 3D objects since our fabrication approach imposes little restrictions on the shape and size of the sample and on the spatial configuration of nematic director. Moreover, our approach of creating such objects by fused deposition modelling of multilayer PDLCEs with compositionally identical matrix/μLCE layers may prove advantageous over fabricating hybrid structures with laminated substrate/LCE layers42, as well as over gel lithography where the programming of buckling behaviour is achieved by voxelizing swelling response43. Also notable is that in our simple scenario of a bilayer structure, any desired Gaussian curvature of the surface of the object can be established with a rather trivial nematic director configuration, in contrast to 2D case where relatively complex patterns of n (ref. 26) are required. We achieved this by programming distinct values of n and in each layer while keeping these values homogeneous within a layer (Fig. 5). Another intriguing feature, pertaining to 3D-character of n, is that the handedness of thermomechanically deformed object can be controlled by the handedness of chiral thermomechanical anisotropy field (Fig. 5d,e). Contrary to recent applications where this field is homogeneous across the sample and where morphing is controlled by spatially inhomogeneous external fields44, PDLCEs allow for homogeneous external stimuli since shape-change response is intrinsic to the specimen owing to spatially inhomogeneous thermomechanical anisotropy field.
Designing bimodal shape-change behaviour
Since PDLCEs are effectively binary soft-soft composites, they exhibit elastic behaviour intermediate between the rubber elasticity of the cured matrix and soft/semi soft elasticity5 of μLCE. Properties of the final composite can thus be tailored by varying the concentration of particles, particle size and the type of particles or matrix material. More than one LCE type can be used to prepare composites with advanced features. In multicomponent PDLCE composites, the elastic and thermomechanical properties are determined by the relative concentrations and the individual properties of the constituting species. Qualitatively, the effective response of the composite should behave as a superposition of responses of individual components. Specifically, in PDLCEs made of two-component μLCE blend, the overall thermomechanical response should amount to λ(T)=k1λ1(T)+k2λ2(T). k1 and k2 are the weights of respective individual LCE species. We have experimentally verified this assumption by preparing PDLCE-B, comprising of blended μLCE-B1 and μLCE-B2, in 1:1 wt ratio. Their respective bulk LCE parents, LCE-B1 and LCE-B2, exhibit well-separated temperatures of thermomechanical anomalies, with Tλ,2−Tλ,1≈25 °C (Fig. 6a). Individual Tλ can be fine-tuned by adjusting the ratio of the M4 to the M11 mesogen (Fig. 1d), with the limiting values Tλ,min≈80 °C for 100% M4-based bulk LCE (LCE-A) and Tλ,max≈120 °C for M11-only bulk LCE (not used in this study)40. The λ(T) profile of PDLCE-B clearly exhibits bimodal behaviour (Fig. 6b), with two anomalies arising from the two distinct phase transitions associated with the two microparticle species. The optimal fit is obtained with k1=0.1 and k2=0.18. We attribute the stronger impact of the μLCE-B2 component (k2>k1) to its much higher Young’s modulus (E2=3.2 MPa as compared with E1=230 kPa of the μLCE-B1). This is so, since, in addition to orientational ordering of mesogenic molecules (nematic phase) below Tλ,1 in the M4-rich LCE-B1, molecular layers perpendicular to nematic director (smectic A phase) are formed below Tλ,2 in the M11-rich LCE-B2, and these are less prone to mechanical deformation5.
The potential of PDLCEs for programming non-monotonous thermomechanical response, more intricate than conventional smeared step-like one, is further demonstrated using bilayer sample geometry, discussed above. Specifically, the specimen PDLCE-B1/B2 comprising of fused PDLCE-B1 and PDLCE-B2 layers is planar at high and low temperatures, but exhibits cup-shaped out-of-plane deformation in a beat-like fashion on low–high temperature stepping (Fig. 7 and Supplementary Movie 3).
Controlling effective thermomechanical and elastic response
A simple quantitative analysis of PDLCE behaviour can be made by considering combined elasticity models (Supplementary Fig. 3 and Supplementary Note 3), providing for an estimate of the upper and lower limits of composite’s effective Young’s modulus E and thermomechanical response λ in terms of ‘series’ scenario (alternating matrix and filler layers orthogonal to n) and ‘parallel’ scenario (layers parallel to n)45. The ‘parallel’ model predictions, calculated by solely considering the individual properties of the matrix and filler materials, not by fitting, are in particularly good agreement with the experimental results of the measurements of PDLCE’s E and λ as a function of composition parameters, specifically the LCE material fraction ν and relative elastic modulus y=ELCE/EPDMS (Fig. 8a–d). This can be efficiently utilized for tailoring elastic and thermomechanical properties of PDLCEs. The optimal region for maximizing the strain response of the composite is 40–60 wt% filler (ν within 0.4 and 0.6, that is, about 1:1 μLCEs versus PDMS ratio), as determined experimentally from the saturation of the strain in Fig. 8c. The deviation of experimental points from the prediction in the strain versus LCE fraction plot for ν>0.6 can be attributed to percolation of μLCEs, which prevents the alignment in the external field. We note that μLCEs, produced by freeze-fracturing, do not have controlled shapes and are not homogeneously sized, so that using smooth-surfaced32, optimally spherical31, particles might result in increased thermomechanical performance, with the theoretical limit of 18% maximal effective strain for ν=0.74 that corresponds to close-packed equal spheres.
The highest achieved strain at Troom is about 12% in the 50% LCE fraction PDLCE-A, at E≈100 kPa modulus. This may seem as a rather modest performance, particularly in view of targeting the performance of pure materials, that is, the 45% (λLCE(Troom)≈1.45) typical strain of LCE-A and EPDMS≈1 MPa typical modulus of PDMS. However, strains below 10% are quite adequate for many shape-programming applications46 and lead to substantial buckling, provided that material’s internal strain matrix is properly programmed, as evidently demonstrated with bilayer PDLCEs (Fig. 5). Moreover, the proposed methodology for preparing PDLCEs imposes practically no restrictions on the choice of matrix and filler materials. Selection e.g., of a main-chain μLCE as a thermomechanical filler, with λLCE(Troom)≈2 and ELCE≈1 MPa (ref. 47), should result in an excellent thermomechanical and elastic performance, λ(Troom)>1.5 and E>1 MPa, as inferred by relations for E and λ(T) for the ‘parallel’ model.
Comparing performance of PDLCEs to conventional LCEs
Strain versus temperature curves, presented in Fig. 2, reveal that thermomechanical response in the form of λ(T) anomaly, although in general somewhat suppressed with respect to PDLCE-A where monodomain LCE bulk material is used, is even observed in PDLCEs with magnetic field-aligned μLCEs made either of conventionally two-step crosslinked6 polydomain bulk LCE (for example, PDLCE-Ap containing μLCE-Ap), or of one-step crosslinked polydomain bulk LCE (for example, PDLCE-Cp containing μLCE-Cp). Obviously, the freeze-fracturing approach is sufficiently effective in generating μLCEs small enough to possess diamagnetic anisotropy and thus to become field-reorientable as a whole (see Supplementary Note 1). Even more notably, when μLCEs are fabricated from bulk LCE that is one-step crosslinked in high magnetic field (LCE-C, cured in 12 T magnet), the resulting composite material (PDLCE-C) performs thermomechanically on par with PDLCE-A. Evidently, μLCE-C particles are nematic monodomains and can be successfully used in place of μLCE-A particles, with the advantage of eliminating the second crosslinking step, that is, external mechanical straining, from the fabrication process of their bulk LCE parent. Availability of one-step crosslinked bulk parent materials like LCE-C further enhances the mass-production potential of μLCEs.
No attempt at quantifying the residual soft elasticity5 of PDLCEs has been made, but the opportunity of investigating this phenomenon should not be ignored, particularly in view of multitude of possible geometries, that is, easily accessible extension, compression and shear deformation modes. As also evident from Figs 1b, 4c, 5a–e and 7a, filling an intrinsically transparent PDMS with μLCE, made of transparent bulk monodomain LCE, results in an opaque PDLCE specimen. To diminish this light-scattering-inflicted disadvantage, μLCE material of either nanometric dimensions or a composite with refractive index of thermomechanically active microparticles matched with the index of the matrix should be used48. Although the potential of freeze-fracturing and microfluidics techniques for high-throughput production of nano-LCEs is yet to be investigated, we find these approaches more promising than index matching, since the latter imposes serious restrictions on the choice of matrix and filler materials. We conjecture that microsized and thin film PDLCE objects, composed of nano-LCEs as thermomechanical fillers and photodefinable matrix49, could readily be prepared by employing the already existing arsenal of polymer micromoulding technologies50.
Here we demonstrate that the common and prevailing, nevertheless rather tedious approach of inventing new chemistry, in order to marry, within a single material, thermomechanical responsiveness of LCEs with manufacturing advantages of conventional thermosetting or photosetting polymers, can be overcome with PDLCEs. These novel composite soft materials exploit an idea of thermomechanical doping, that is, the fact that a fair degree of thermomechanical activity of the embedded microparticles can be propagated into the effective response of the elastomer matrix, provided that microparticles are aligned. Our specific choice of PDMS matrix and μLCE dopant could be replaced with any choice of compatible soft materials, an inert isotropic elastomer as the matrix and thermomechanically or photomechanically responsive microparticles as fillers. Very importantly, functionalization, for example, with electrically conductive, thermally conductive, electromagnetic radiation-absorbing, ferroelectric and ferromagnetic particles can be performed on the matrix material rather than on the LCE material. The new concept of simple thermomechanical activation of conventional isotropic elastomers, introduced in this study by developing PDLCEs, opens up exciting new possibilities for future additive manufacturing technologies targeted towards 3D printing of thermally- or photomorphable artefacts.
Fabricating bulk LCE materials
Bulk LCE materials were polymerized by employing the standard two-step crosslinking approach6, consisting of partial crosslinking of prepolymer resin in thermally stabilized centrifuge and subsequent crosslinking of the sample exposed to mechanical stress, typically σ≈100 kPa (LCE-A, LCE-B1, LCE-B2), in the oven. LCE-C bulk material was one-step polymerized in the cryostat of a B=12 T superconducting magnet. Polydomain bulk material LCE-Ap was obtained by omitting external mechanical stress in the second crosslinking step. Similarly, the absence of external magnetic field gave rise to polydomain bulk LCE-Cp. Networks were crosslinked with 15 mole % of V1 (percentage with respect to M4, M11 and V1 monomer total). LCE-A and LCE-C exhibiting nematic phase below Tλ≈80 °C were prepared with nematogenic M4, whereas LCE-B1 with nematic phase below Tλ,1≈87 °C and LCE-B2 with smectic A phase below Tλ,2≈112 °C were prepared with M40.6M110.4 and M40.2M110.8 respective compositions of M4 and smectogenic M11 (ref. 40).
Fabricating PDLCE composites
Bulk materials were first cut into smaller pieces (1 mm3) to prepare for freeze-milling in a mortar. The milling process was performed with a mix of LCE pieces and with liquid PDMS base (Sylgard 184 silicon elastomer kit) in 3:1 weight ratio. The LCE/PDMS mixture was frozen by repeatedly pouring liquid nitrogen over it. A pestle was used to crush the LCE/PDMS mixture into smaller size pieces for as long as the mixture remained frozen. This process was repeated until the emerging paste became homogeneous, containing small enough μLCEs. Water condensate was removed by drying at Troom. Subsequently, PDMS resin of appropriate weight and base/hardener ratio was added in order to obtain the μLCE/PDMS prepolymer mixture of a desirable μLCE mass weight ν and cured PDMS Young’s modulus EPDMS. After being evacuated to get rid of entrapped air, the final mix of uncured PDMS and μLCE, typically 80 mg in mass, was introduced, using a spatula, into a glass tube (50 mm length, 3 mm inner diameter). The inner surface of the tube was covered with a thin Teflon sleeve to prevent PDMS adhesion to the glass. The partially filled tube, sealed with Teflon tape on both sides, containing cylindrically-shaped, uncured and non-aligned PDLCE specimen, was finally put in a B=9 T superconducting magnet, with the tube oriented in parallel with the magnetic field and left 2 h at Troom for the μLCEs to get aligned so that the nematic director pointed along the field, equivalently along the long axis of the sample. The superconducting magnet was used for efficiency reasons, since it provided for almost instant alignment, within several seconds, and for convenient and fast temperature control with its liquid nitrogen-operated continuous flow cryostat. The magnetic field-driven alignment has also been successfully tested in a B=1.2 T permanent magnet, however, with longer alignment times of several 10 min. Once aligned, the sample was left curing at T0≈50 °C<Tλ for about 12 h (see Supplementary Note 3 and Supplementary Fig. 4 for justification on the choice of T0). The resulting cured PDLCE specimens were cylindrical rods, 15 to 25 mm in length and 2.8 mm in diameter, with the look and feel of conventional PDMS (Fig. 1b). Disk-shaped samples were prepared in a similar way, using a sealed Teflon mould with a ϕ18, 2 mm high cylindrical cavity. Bilayer samples were made in two steps, by first setting the bottom layer and subsequently by fuse-depositing and setting the second layer on top of it. The orientation of thermomechanical anisotropy axis, equivalently of nematic director of oriented μLCEs, was controlled by individually orienting the mould with respect to external magnetic field for each layer.
λ(T) was measured in a home-built, step motor-driven and strain gauge-equipped thermomechanical analyser in a constant mechanical stress regime, σ≈0.2 kPa. A specimen was typically heated from Troom to 100 °C>Tλ(μLCE-A) in the case of thermomechanically unimodal PDLCE-A and to 120°C>Tλ(μLCE-B2) in the case of thermomechanically bimodal PDLCE-B. Measurements were then taken on cooling with a rate of about −10 °C per h down to Troom. Young’s modulus E of PDLCEs was determined from the tilt of the stress versus strain curve in the 0.2 to 5 kPa stress range. Partial moduli EPDMS and ELCE of the PDMS matrix and μLCEs were determined on bulk monodomain LCE stripes (typically 15 mm long, 5 mm wide, and 0.3 mm thick) and cured pure PDMS samples of the same geometry as PDLCEs (ϕ2.8 × 25 mm), respectively.
Optimization of elastic properties
By systematically varying the base/hardener composition of the uncured PDMS resin, its relation with EPDMS of the cured pure PDMS was determined and taken into account in fine-tuning the EPDMS of the PDMS matrix component of PDLCEs. In particular, EPDMS was found to decrease exponentially from 800 to 80 kPa on increasing the base share from 20:1 to 35:1. In order to maximize λ(T), all PDLCE composites, except for the ones used to investigate the dependence of λ and E on y=ELCE/EPDMS (Fig. 8b,d), were prepared with 35:1 base/hardener composition of the PDMS matrix that exhibited a correspondingly low elastic modulus (EPDMS≈180 kPa). For compositions higher than 40:1, curing did not result in an elastically stable samples.
The data that support the findings of this study are available from the corresponding author upon request.
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This work was supported by the Slovenian Research Agency (ARRS), contracts P1-0125 and J1-4307.
The authors declare no competing financial interests.
Supplementary Figures 1-4, Supplementary Notes 1-3 and Supplementary References (PDF 1512 kb)
Animated simulation of fabrication and thermal actuation of PDLCEs with oriented L CE microparticles (MOV 5417 kb)
Thermal actuation of differently shape-change-programmed bilayer PDLCE-A specimens (MOV 1882 kb)
Beat-like thermal response of PDLCE - B1/B2 specimen (MOV 1439 kb)
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Rešetič, A., Milavec, J., Zupančič, B. et al. Polymer-dispersed liquid crystal elastomers. Nat Commun 7, 13140 (2016). https://doi.org/10.1038/ncomms13140
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