Are MXenes suitable for soft multifunctional composites?

MXenes are a family of two-dimensional (2D) nanomaterials known for their high electrical and thermal conductivity, as well as high aspect ratios. Recent research has focused on dispersing MXenes within compliant polymer matrices, aiming to create flexible and stretchable composites that harness MXenes' exceptional conductivity and aspect ratios. Experimental findings demonstrate the potential of MXene polymer composites (MXPCs) as flexible electrical, thermal conductors, and high dielectric materials, with promising applications in soft matter engineered systems. However, the 2D structure of MXene inclusions and their relatively large elastic modulus can impart increased stiffness to the polymer matrix, posing limitations on the mechanical flexibility of these functional materials. Here, we introduce a modeling platform to predict the mechanics and functionality of MXene elastomer composites and assess their suitability as soft multifunctional materials. Our investigation primarily focuses on understanding the influence of MXenes' size, layered structure, and percolation arrangements on the effective properties of the resulting composites. Through our model, we successfully determined the elastic modulus, thermal conductivity, and dielectric constant of MXene elastomer composites, and our results exhibit strong agreement with those obtained through finite element analysis. By utilizing this framework, we can theoretically identify the necessary microstructures of MXenes and guide the experiments, enabling the creation of MXPCs with the desired synergistic mechanical and functional properties.

Mechanical stress-induced cell death in breast cancer cells.

Providing an external mechanical stress to cancer cells seems to be an effective approach to treat cancer locally. Numbers of reports on cancer cell death subjected to mechanical stress loading are increasing, but they are more focused on apoptosis. Inducing necrosis is also important in attracting more immune cells to the cancer site via the release of danger-associated molecular patterns from cancer cells. Here we applied dynamic compression to breast cancer cells with a low frequency (0.1-30 Hz) and for a short duration (30-300 s) and they resulted in a mixed mode of apoptosis and necrosis dominant with necrotic cell death, which we call mechanical stress-induced cell death (MSICD). The necrotic cell damage of mechanically treated breast cancer cells increased in a force-dependent and time-dependent manner while a trend of frequency-independent MSICD was observed.