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Elastomers often exhibit large stretchability but are not typically designed with robust energy dissipating mechanisms. As such, many elastomers are sensitive to the presence of flaws: cracks, notches, or any other features that cause inhomogeneous deformation significantly decrease the effective stretchability. To address this issue, we have dispersed voids into a silicone elastomer matrix, thereby creating a “negative” composite that provides increased fracture resistance and stretchability in pre-cut specimens while simultaneously decreasing the weight. Experiments and simulations show that the voids locally weaken the specimen, guiding the crack along a tortuous path that ultimately dissipates more energy. We investigate two geometries in pre-cut specimens (interconnected patterns of voids and randomly distributed discrete voids), each of which more than double the energy dissipated prior to complete rupture, as compared to that of the pristine elastomer. We also demonstrate that the energy dissipated during fracture increases with the volume fraction of the voids. Overall, this work demonstrates that voids can impart increased resistance to rupture in elastomers with flaws. Since additive manufacturing processes can readily introduce/pattern voids, we expect that applications of these elastomer–void​ “composites” will only increase going forward, as will the need to understand their mechanics. 

We have devised an approach to fabricate dense textured V 2 O 5 thin films, which allows us to scrutinize the root cause of capacity fade in V 2 O 5 cathodes of Li-ion batteries. Specifically, we performed in situ measurements of stress of V 2 O 5 thin films during 50 electrochemical cycles. Surprisingly, electrochemical cycling appears to induce elastic and rate-independent deformation over a voltage range relevant to battery operation (4–2.8 V). However, the compressive stresses gradually increase with cycle number during the first few cycles, likely due to side reactions and/or residual Li left in the V 2 O 5 , even after delithiation (to 4 V). Further cycling leads to accumulated mechanical damage ( e.g. , fracture, delamination) and structural damage ( e.g. , amorphization), which ultimately result in severe capacity fade. 

The utilization of metallic anodes holds promise for unlocking high gravimetric and volumetric energy densities and is pivotal to the adoption of ‘beyond Li’ battery chemistries. Much of the promise of magnesium batteries stems from claims regarding their lower predilection for dendrite growth. Whilst considerable effort has been invested in the design of novel electrolytes and cathodes, detailed studies of Mg plating are scarce. Using galvanostatic electrodeposition of metallic Mg from Grignard reagents in symmetric Mg–Mg cells, we establish a phase map characterized by disparate morphologies spanning the range from fractal aggregates of 2D nanoplatelets to highly anisotropic dendrites with singular growth fronts and nanowires entangled in the form of mats. The effects of electrolyte concentration, applied current density, and coordinating ligands have been explored. The study demonstrates a complex range of electrodeposited morphologies including canonical dendrites with shear moduli conducive to penetration through typical polymeric separators. We further demonstrate a strategy for mitigating Mg dendrite formation based on the addition of molecular Lewis bases that promote nanowire growth through selective surface coordination.