Abstract
Controlling the thermal expansion of materials is of great technological importance. Uncontrolled thermal expansion can lead to failure or irreversible destruction of structures and devices. In ordinary crystals, thermal expansion is governed by the asymmetry of the microscopic binding potential, which cannot be adjusted easily. In artificial crystals called metamaterials, thermal expansion can be controlled by structure. Here, following previous theoretical work, we fabricate threedimensional (3D) twocomponent polymer microlattices by using graytone laser lithography. We perform crosscorrelation analysis of optical microscopy images taken at different sample temperatures. The derived displacementvector field reveals that the thermal expansion and resulting bending of the bimaterial beams leads to a rotation of the 3D chiral crosses arranged onto a 3D checkerboard pattern within one metamaterial unit cell. These rotations can compensate the expansion of the all positive constituents, leading to an effectively nearzero thermal lengthexpansion coefficient, or overcompensate the expansion, leading to an effectively negative thermal lengthexpansion coefficient. This evidences a striking level of thermalexpansion control.
Introduction
Threedimensional (3D) printing of materials is a huge trend. It allows for individualizing products and for fabricating architectures that are very difficult if not impossible to make otherwise. Ultimately, one would like to 3D print any functional structure or device at the push of a button. Apart from boosting spatial resolution and printing speed, achieving this goal requires the ability to obtain hundreds or thousands of different material properties with one 3D printer. Today’s 2D graphical printers realize thousands of colors from only three cartridges (cyan, magenta, yellow). By analogy, future 3D material printers might be able to print thousands of different effective materials from only a few constituentmaterial “cartridges”.
Physics is on our side: Upon 3D printing two constituent materials A and B to obtain a composite or metamaterial, one might naively think that its effective properties will always be in between those of A and B. Fortunately, this is not the case^{1,2,3,4}. In some cases, the behavior is even conceptually unbounded, i.e., an effective material parameter can assume any value from minus infinity to plus infinity even if those of the constituents are all finite and, e.g., positive. Examples are the electric permittivity and the magnetic permeability in electromagnetism or the compressibility and the mass density in mechanics^{5,6,7,8,9,10,11,12,13}. However, for the mentioned examples, sign reversal and unbounded effective parameters are only possible near resonances at finite frequency and not in the truly static regime for reasons of stability in mechanics and nonnegative energy density in electromagnetism^{5,13}.
Static examples are rare. Theoretically, the thermal lengthexpansion coefficient and the Hall coefficient have been discussed^{1,2,3,14,15,16,17,18,19,20,21}. Regarding the Hall coefficient, even one constituent material A and voids within suffice^{20}. The situation is distinct for the thermal lengthexpansion coefficient. Within the range of validity of the continuum approximation, any connected structure composed of one constituent material A and voids within will show exactly the same thermal lengthexpansion coefficient as the bulk constituent material A. In contrast, the work of Lakes and others has shown that the behavior of composites containing two components A and B plus voids within is principally unbounded^{1}. These twodimensional structures were reviewed in Milton’s textbook^{2}. Concrete blueprints for threedimensional structures showing isotropic behavior were suggested later^{14}. Refinements and twodimensional macroscopic model structures composed of bimetallic beams were published as well^{15,16,17,18,22}. Discussed theoretically a related twodimensional structure composed of bimetallic strips showing a negative effective compressibility (at fixed temperature).
In regard to applications, thermal lengthexpansion is a small effect with huge consequences. A relative thermal lengthexpansion around 10^{−4} to 10^{−3} can lead to severe misalignment, failure, or cracks. Atomicscale composites can provide nearzero or negative thermallength expansion by changing the microscopic binding potential^{23,24,25}. More macroscopic composites with nearzero length expansion are based on one constituent material with positive and another one with negative thermal expansion. For example, CERAN® glass cooking fields are made like that and have led to considerable markets.
Results
In this work, by using 3D graytone twophoton laser lithography, we fabricate microstructured twocomponent metamaterials using a single photoresist, leading to an effectively negative thermal lengthexpansion coefficient from allpositive constituents. Applying image crosscorrelation analysis, we directly measure the temperatureinduced displacementvector field in different layers of the microlattice with subpixel precision and thereby visualize the underlying microscopic mechanism.
We have considered different blueprints from the literature^{14,16}. For implementation using 3D laser printing, it is of utmost importance that the structure is robust against variations of structural and material parameters. Based on this consideration and on preliminary tests, we have focused our experimental work on one approach^{16}. Figure 1a exhibits a single lattice constant of the microlattice blueprint we start from. This unit cell is placed onto a threedimensional simplecubic translational lattice. Apart from minor modifications, this blueprint has been taken from the literature^{16}. The two components A and B shown in different colors have different positive thermal lengthexpansion coefficients. A mathematical discussion closely following ref. 1 is given in Supplementary Fig. S1. Intuitively, the operation principle is as follows (see Fig. 1b): The bimaterial beams expand and bend upon heating. The bending leads to a rotation of the 3D crosses, the arms of which make them chiral. The chirality and hence the sense of rotation alternates between clockwise and counterclockwise from one 3D cross to its neighbors, forming a 3D checkerboard pattern. The rotations counteract the length expansion of the beams. The amplitude of the rotations can be adjusted by the ratio of the thermal lengthexpansion coefficients of the constituent materials A and B. On this basis, one can tune the effective metamaterial thermal lengthexpansion coefficient (see Supplementary Figs S1 and S3). For the geometrical parameters used, the sign of the effective metamaterial thermal lengthexpansion coefficient changes sign at around . The absolute values of the Young’s moduli of A and B do not influence the effective metamaterial thermal lengthexpansion coefficient at all. The ratio of the Young’s moduli, i.e., E_{A}/E_{B}, does have an influence. However, even when changing this ratio by factors, the overall qualitative behavior remains the same (see Supplementary Figs S1 and S3). If component B is left away, i.e., replaced by vacuum, the effective thermal lengthexpansion coefficient of the microlattice is identical to that of bulk A. The same is true if B equals A.
We mention in passing that the structure shown in Fig. 1a has an effective Poisson’s ratio of v = −0.41. However, in general, the sign of the thermallength expansion coefficient is not necessarily the same as the sign of the Poisson’s ratio^{15}.
3D laser printing
How can we fabricate such complex 3D twocomponent metamaterials? Threedimensional twophoton laser printing of a single polymer component is a wellestablished technology. Here, we use a commercial instrument (Photonics Professional, Nanoscribe GmbH). While characterizing the thermal lengthexpansion coefficients of various polymers in bulk cuboid form, we noticed that the thermal lengthexpansion coefficient does not only depend on the type of monomer we start from. For a given monomer (we use IPDip, Nanoscribe GmbH), it also depends on the light exposure dose during photopolymerization. For example, when writing a bulk cube at a power scaling factor (see Methods) of 65% at a scan speed of 2 cm/s, we find a thermal lengthexpansion coefficient of α_{L} = (+5 ± 0.5) × 10^{−5} K^{−1}. At a power scaling factor of 35% and the same speed, this value increases to α_{L} = (+8 ± 0.5) × 10^{−5} K^{−1}. In between, the behavior is approximately linear (see Fig. S2). The measurement procedure shall be described below. We interpret this behavior in that the exposure dose influences the polymer crosslinking density. A correlation between crosslinking density and thermal expansion has been established previously^{26}. The bottom line of this finding is that we can realize two different components A and B plus voids within by using only a single photoresist and graytone optical lithography.
For the temperaturedependent measurements, the samples are fixed to a Peltierelement heater within a small encapsulated chamber. In this fashion, the air within the chamber is heated as well, such that, after a certain waiting time (we chose several hours here), we can safely assume that the polymer microlattice temperature is actually equal to the temperature measured by a calibrated thermoresistor at the Peltierelement location (as well as by a second one at the upper end of the cell). The chamber has a glass window to allow for optical access via a homebuilt widefield optical microscope. It is based on a single microscope lens (Zeiss LD Achroplan 20× with a numerical aperture NA = 0.4) which images a sample plane directly onto the chip of a siliconbased chargecoupleddevice (CCD) camera. We illuminate the sample by diffuse white light, for which we obtain the best image contrast for our microlattices. The entire chamber can be moved with respect to the microscope by using a 3D piezoelectric translation stage (Piezosystem Jena 1469), which is controlled by a computer.
Crosscorrelation analysis
How can we directly characterize the thermal lengthexpansion and the operation principle underlying the microlattices? For example, for temperature differences on the order of ΔT = 20 K, we expect relative length changes of the samples on the order of ΔL/L = 10^{−3}. If one images the entire sample onto a camera chip with 1000 pixels in one direction, this relative change corresponds to a movement of merely 1 pixel. Obviously, the measurement accuracy must be yet better than that. Image crosscorrelation analysis can provide such subpixel sensitivity^{27}. Our analysis, which is illustrated in Fig. S4a, starts from two optical images of a sample taken at two different temperatures. The images can refer to the sample’s surface. For transparent samples, they can alternatively correspond to a plane below the surface within the volume of the sample (e.g., plane P_{1} or P_{2} in Fig. 1c). We take a first image, the reference I_{ref}(x, y), at room temperature. A second image is taken at a temperature elevated by ΔT with respect to room temperature. In this image, regions of interest (ROI) are defined. These small regions (we choose 33 × 33 pixels) can be centered around characteristic points (x, y) of the sample, e.g., onto the lattice points of a microlattice (compare Fig. 1c). Outside of the ROI, the image points are set to zero, leading to the function I_{ROI}(x, y). Next, the twodimensional crosscorrelation function C(Δx, Δy) of the reference image and the ROI is computed, i.e.,
we normalize according to C(x, y) → C(x, y)/C(0, 0). If both images are identical, the cross correlation peaks at displacement vector (0, 0); if they are shifted with respect to each other, it peaks at the corresponding displacement vector . Thus, by identifying the position of the maximum of the crosscorrelation function in two dimensions, the local displacement vector can be identified. We average over the results obtained from ten different images at the elevated temperature. By repeating the procedure for many ROI at different coordinates (x, y) in the image, we obtain the displacementvector field . Figure S4b shows the result for a copper surface. The derived average lengthexpansion coefficient of α_{L} = (+1.6 ± 0.1) × 10^{−5} K^{−1} is consistent with the literature value of α_{L} = +1.65 × 10^{−5} K^{−1} within the error bars. Generally, upon changing the temperature of the sample and its holder, the sample as a whole can also move or drift across the image and/or through the focal plane of the microscope. The former effect can be eliminated by subtracting the average displacement vector of all ROI, i.e., → . This subtraction is unproblematic if the camera chip is perfectly homogeneous. To avoid possible artifacts from inhomogeneities, we rather compensate most of this average displacement by the piezoelectric translation stage, such that the sample’s image on the camera chip does not change with respect to the camera chip. Remaining small average shifts are subtracted in the processing of the images. Likewise, we compensate a possible thermally induced defocus (i.e., movement in zdirection) by an autofocus function. It is based on acquiring images while moving the sample along the zaxis using the piezoelectric translation stage. The sharpest image is selected in the postprocessing.
Electron micrographs of selected fabricated samples on glass substrates are shown in Fig. 2. The structure in Fig. 2b is composed of two different components, corresponding to different exposure doses during the printing process (see above). Note that the beams are bent, whereas they are straight for the control sample (depicted in Fig. 2a), in which exclusively the first component has been written. The bending originates from the different crosslinking densities resulting from different exposure doses, leading to different levels of volume shrinkage of the constituents during development. Notably, this shrinkage leads to an overall expansion of the metamaterial sample – in agreement with the operation principle^{28}. This prebending also directly evidences that the two components actually have different properties. Within the linear regime, the prebending does not change the operation principle compared to that of the blueprint (compare Fig. 1b). The samples shown in Fig. 2 contain 4 × 4 × 2 = 32 complex threedimensional unit cells following the blueprint shown in Fig. 1a.
Figure 3 summarizes measurements of the displacementvector field induced by a temperature rise of ΔT = 20 K with respect to room temperature. The background shows the roomtemperature optical image as recorded by the CCD camera, corresponding to plane P_{1} in Fig. 1c. The yellow arrows are the displacement vectors at the 3D crossing points. To make them visible, the length of the arrows has been multiplied by a common factor with respect to the optical image as indicated. Obviously, all yellow arrows in Fig. 3c roughly point towards the center of the sample. Furthermore, the length of the arrows roughly increases linearly from the center to the sides. These two observations indicate a nearly homogeneous and isotropic behavior of the 3D crossing points. It is thus meaningful to describe the metamaterial by an effective thermal lengthexpansion coefficient. Upon reducing the temperature difference to ΔT = 10 K, we find essentially the same behavior as for ΔT = 20 K, albeit with worse signaltonoise ratio (not depicted). From these data at ΔT = 20 K, we extract an average effective metamaterial thermal lengthexpansion coefficient of α_{L} = (−5 ± 0.5) × 10^{−5} K^{−1}. The value of α_{L} = (−5 ± 0.5) × 10^{−5} K^{−1} for ΔT = 10 K is the same. When imaging the next lower plane of crossing points (compare P_{2} in Fig. 1c), we again find essentially the same behavior (average α_{L} = (−5 ± 0.5) × 10^{−5} K^{−1}). In contrast, the singlecomponent control sample depicted in Fig. 3a and b exhibits a positive value of α_{L} = (+4 ± 0.5) × 10^{−5} K^{−1}. All of the described aspects are reversible, i.e., we have observed them more than three times on a given sample. We have also seen them on more than five sets of samples. Our analysis also allows for quantifying deviations from ideal isotropy. We find that the modulus of the expansion coefficient is 25% larger along the ydirection as compared to the xdirection for the twocomponent sample. This anisotropy is assigned to remaining fabrication imperfections. In particular, due to drift during writing, some beam connections in the microlattice may actually be missing.
To further investigate whether the samples actually follow the behavior anticipated by the design as discussed above, we also track other points within the unit cell (compare plane P_{1} in Fig. 1c). The blue arrows in Fig. 3d show that the connecting beams actually expand upon heating. Here, for clarity, their average displacement vector has been subtracted. A similar behavior is found for all other beams as well (not depicted). The red arrows reveal the anticipated rotation of the crosses, with alternating clockwise and counterclockwise sense of rotation. Again, for clarity, the average displacement vector for each cross has been subtracted from the corresponding set of four arrows. Note that the red rotation vectors are generally longer than the blue ones. As explained above, this behavior leads to the negative thermal lengthexpansion: The shrinkage induced by the rotations overcompensates the expansions of the individual beams. For the control sample in Fig. 3b, no significant rotations are found within the noise (hence the red arrows are not depicted here) and the thermal expansion is positive – as for the bulk polymer constituents discussed above. The measured behavior in Fig. 3 is in good overall agreement with the calculated one shown in Fig. 4. Finally, Fig. 5 shows results for closer to , for which the rotations merely compensate the expansion of the beams, leading to effectively nearzero thermal lengthexpansion coefficient. Again, experiment and theory agree.
In summary, we have fabricated and characterized micrometerscale twocomponent polymerbased metamaterials exhibiting an effectively negative thermal lengthexpansion coefficient from positive constituents. The necessary two components plus voids have been realized by 3D graytone laser lithography using only a single photoresist.
Methods
Sample design
For the metamaterial design, a simple cubic unit cell was analyzed by a finiteelement approach using the commercially available software package COMSOL Multiphysics and the MUMPS solver within. For the mechanical part of the problem, the thermal expansion was introduced as a volumetric stress. The constituent materials A and B were modeled with a Young’s modulus of E_{A} = 4 GPa and E_{B} = 3 GPa (actually only the ratio E_{A}/E_{B} enters into the effective thermal expansion/contraction, see Supplementary Figs S1 and S3), a Poisson’s ratio of v_{A} = 0.4 (and v_{B} = 0.4), and a thermal lengthexpansion coefficient of throughout this manuscript. For the negative effective thermal lengthexpansion metamaterials shown in Figs 1 and 4 we used . For the nearzero effective thermal lengthexpansion metamaterial shown in Fig. 5 we used . For the calculations shown in Figs 1b and S3, we used periodic boundary conditions^{29}. To assess the influence of finite sample size, we also performed calculations for samples containing 4 × 4 × 2 unit cells fixed to a rigid substrate (Figs 4 and 5). Based on the two mirror planes cutting the structure through the middle, one parallel to the xz and one parallel to the yzplane, we reduced the computational domain to 2 × 2 × 2 unit cells fixed to a rigid substrate. The other sides are left free to move (stressfree boundary conditions). The derived effective thermal lengthexpansion coefficients were different from those for the periodic boundary conditions by only a few percent. Typically, each unit cell (compare Fig. 1a) was discretized into 5 × 10^{5} tetrahedral elements.
Sample fabrication
The structures composed of 4 × 4 × 2 unit cells were written using a liquid photoresist (IPDip, Nanoscribe GmbH, Germany) and a commercial threedimensional laser lithography system (Photonics Professional, Nanoscribe GmbH). The objective lens (63×, NA = 1.4, Carl Zeiss) was dipped directly into the photoresist. An average power of 50 mW measured at the backfocal aperture of the objective lens with a diameter of 7.3 mm was defined as the reference power. The actual power was given by this reference power times the power scaling factor, which was varied locally in the spirit of graytone lithography. The component with low (high) thermal lengthexpansion coefficient was written with a power scaling factor of 65% (38%). The line spacing in the x and ydirection was 200 mm, that in the zdirection was 500 nm. Small parts were written in the galvoscanning mode with a scan speed of 2 cm/s and stitched by using micropositioning stages^{29}. The exposed samples were developed in mrDev 600 for 60 minutes, transferred to acetone, followed by supercriticalpointdrying in acetone.
Additional Information
How to cite this article: Qu, J. et al. MicroStructured TwoComponent 3D Metamaterials with Negative ThermalExpansion Coefficient from Positive Constituents. Sci. Rep. 7, 40643; doi: 10.1038/srep40643 (2017).
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Acknowledgements
We acknowledge discussions with Claudio Findeisen and Peter Gumbsch (KIT). We are grateful to Martin Schumann (KIT) for help regarding the electron micrographs. We thank the Hector Fellow Academy, the Helmholtz program Science and Technology of Nanosystems (STN), and the Karlsruhe School of Optics & Photonics (KSOP) for support. We acknowledge support by Deutsche Forschungsgemeinschaft and Open Access Publishing Fund of Karlsruhe Institute of Technology.
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J.Q. has fabricated the samples and has performed the measurements and the data processing. M.K. has helped in the simulations and discussions. A.N. has helped in the discussions. M.W. has led the effort and has written the first draft of the paper. All authors have contributed to the final version of the manuscript.
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Qu, J., Kadic, M., Naber, A. et al. MicroStructured TwoComponent 3D Metamaterials with Negative ThermalExpansion Coefficient from Positive Constituents. Sci Rep 7, 40643 (2017). https://doi.org/10.1038/srep40643
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