Soft materials can self-assemble into highly structured phases that replicate at the mesoscopic scale the symmetry of atomic crystals. As such, they offer an unparalleled platform to design mesostructured materials for light and sound. Here, we present a bottom-up approach based on self-assembly to engineer 3D photonic and phononic crystals with topologically protected Weyl points. In addition to angular and frequency selectivity of their bulk optical response, Weyl materials are endowed with topological surface states, which allow for the existence of one-way channels, even in the presence of time-reversal invariance. Using a combination of group-theoretical methods and numerical simulations, we identify the general symmetry constraints that a self-assembled structure has to satisfy to host Weyl points and describe how to achieve such constraints using a symmetry-driven pipeline for self-assembled material design and discovery. We illustrate our general approach using block copolymer self-assembly as a model system.

We report on the synergetic effects of silicon (Si) and BaTiO3 (BTO) for applications as the anode of Li-ion batteries. The large expansion of Si during lithiation was exploited as an energy source via piezoelectric BTO nanoparticles. Si and BTO nanoparticles were dispersed in a matrix consisting of multiwalled carbon nanotubes (CNTs) using a high-energy ball-milling process. The mechanical stress resulting from the expansion of Si was transferred via the CNT matrix to the BTO, which can be poled, so that a piezoelectric potential is generated. We found that this local piezoelectric potential can improve the electrochemical performance of the Si/CNT/BTO nanocomposite anodes. Experimental measurements and simulation results support the increased mobility of Li-ions due to the local piezoelectric potential.

to external stimuli [7] are just a few examples of inspiring features that should be included within synthetic structural materials. They provide inspiration for potential solutions to address challenges associated with traditional approaches of material selection. [8] In the classical approach, a material is selected for a specific application based on the expected loading conditions, design objective and constraints, and databases of material properties with fixed values (e.g., Ashby method [9] ). This methodology does not account for unpredictable loading conditions. To address this issue, safety factors are added, which increases the associated cost and weight of the structure; thus, reduces its mechanical efficiency. A potential solution for this dichotomy is to have materials with adaptable properties responding to loading conditions. This feature can result in materials with improved mechanical efficiency and reduction in costs, resources, and environmental impact. So far, there are few synthetic materials capable of increasing stiffness in response to external stimuli. For example, some investigators have reported polymers that changed elastic moduli by changing the degree of crosslinking upon chemical, thermal, or mechanical stimuli. [10,11] In addition, a study showing an increase of the elastic modulus of liquid crystal elastomers during cyclic Natural structural materials, such as bone, can autonomously modulate their mechanical properties in response to external loading to prevent failure. These material systems smartly control the addition/removal of material in locations of high/low mechanical stress by utilizing local resources guided by biological signals. On the contrary, synthetic structural materials have unchanging mechanical properties limiting their mechanical performance and service life. Inspired by the mineralization process of bone, a material system that adapts its mechanical properties in response to external mechanical loading is reported. It is found that charges from piezoelectric scaffolds can induce mineralization from surrounding media. It is shown that the material system can adapt to external mechanical loading by inducing mineral deposition in proportion to the magnitude of the stress and the resulting piezoelectric charges. Moreover, the mineralization mechanism allows a simple one-step route for fabricating functionally graded materials by controlling the stress distribution along the scaffold. The findings can pave the way for a new class of self-regenerating materials that reinforce regions of high stress or induce deposition of minerals on the damaged areas from the increase in mechanical stress to prevent/mitigate failure. It is envisioned that the findings can contribute to addressing the current challenges of synthetic materials for load-bearing applications from self-adaptive capabilities.The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/adma.201906970.The mechanical efficiency of natural (or biological) s...

A unique rate‐dependent energy absorption behavior of liquid crystal elastomer (LCE)‐based architected materials is reported. The architected materials consist of repeating unit cells of bistable tilted LCE beams sandwiched between stiff supports. The viscoelastic behavior of the LCE causes the energy absorption to increase with strain rate according to a power‐law relationship, which can be modulated by changing the degree of mesogen alignment and the loading direction relative to the director. For a strain rate of 600 s−1, the unit cell exhibits up to a 5 MJ m−3 energy absorption density, which is two orders of magnitude higher than the same structure fabricated from poly(dimethylsiloxane) elastomer and is comparable to the dissipation from irreversible plastic deformation exhibited by denser metals. For a multilayered structure of unit cells, nonuniform buckling of the different layers produces additional viscoelastic dissipation. This synergistic interaction between viscoelastic dissipation and snap‐through buckling causes the energy absorption density to increase with the number of layers. The sequence of cell collapse can be controlled by grading the beam thickness to further promote viscous dissipation and enhance the energy absorption density. It is envisioned that the study can contribute to the development of lightweight extreme energy‐absorbing metamaterials.

Silicon/carbon (Si/C) nanocomposites have recently received much attention as Li-ion battery negative electrodes due to their mutual synergetic effects in capacity and mechanical integrity. The contribution of Si to the total capacity of the Si/C nanocomposites determines their structural efficiency. Herein, we report on a multi-layered, one-dimensional nanostructure that exhibits the theoretical specific capacity of Si in the nanocomposite. Concentrically tri-layered, compartmentalized, C-core/Si-medium/C-shell nanofibers were fabricated by triple coaxial electrospinning. The pulverization of Si was accommodated inside the C-shell, whereas the conductive pathway of the Li-ions and electrons was provided by the C-core, which was proven by ex situ Raman spectroscopy. The compartmentalized Si in between the C-core and C-shell led to excellent specific capacity at a high current rate (>820 mA h g(-1) at 12000 mA g(-1)) and the realization of the theoretical specific capacity of the Li15Si4 phase of Si nanoparticles (3627 mA h g(-1)). The electrochemical characterization and inductively coupled plasma-atomic emission spectrometry provided direct evidence of full participation of Si in the electrochemical reactions.