In materials science, there is an intrinsic conflict between high strength and high toughness, which can be resolved for different materials only through the use of innovative design principles. Advanced materials must be highly resistant to both deformation and fracture. We overcome this conflict in man-made polymer fibers and show multifibrillar polyacrylonitrile yarn with a toughness of 137 ± 21 joules per gram in combination with a tensile strength of 1236 ± 40 megapascals. The nearly perfect uniaxial orientation of the fibrils, annealing under tension in the presence of linking molecules, is essential for the yarn’s notable mechanical properties. This underlying principle can be used to create similar strong and tough fibers from other commodity polymers in the future and can be used in a variety of applications in areas such as biomedicine, satellite technology, textiles, aircrafts, and automobiles.

Though beam-based lattices have dominated mechanical metamaterials for the past two decades, low structural efficiency limits their performance to fractions of the Hashin-Shtrikman and Suquet upper bounds, i.e. the theoretical stiffness and strength limits of any isotropic cellular topology, respectively. While plate-based designs are predicted to reach the upper bounds, experimental verification has remained elusive due to significant manufacturing challenges. Here, we present a new class of nanolattices, constructed from closedcell plate-architectures. Carbon plate-nanolattices are fabricated via two-photon lithography and pyrolysis and shown to reach the Hashin-Shtrikman and Suquet upper bounds, via in situ mechanical compression, nano-computed tomography and micro-Raman spectroscopy. Demonstrating specific strengths surpassing those of bulk diamond and average performance improvements up to 639% over the best beam-nanolattices, this study provides detailed experimental evidence of plate architectures as a superior mechanical metamaterial topology.

Vaccines and therapies are not available for several diseases caused by viruses, thus viral infections result in morbidity and mortality of millions of people every year. Nanoparticles are considered to be potentially effective in inhibiting viral infections. However, critical issues related to their use include their toxicity and their mechanisms of antiviral action, which are not yet completely elucidated. To tackle these problems, we synthesized silica nanoparticles with distinct surface properties and evaluated their biocompatibility and antiviral efficacy. We show that nanoparticles exhibited no significant toxicity to mammalian cells, while declines up to 50% in the viral transduction ability of two distinct recombinant viruses were observed. We designed experiments to address the mechanism of antiviral action of our nanoparticles and found that their hydrophobic/hydrophilic characters play a crucial role. Our results reveal that the use of functionalized silica particles is a promising approach for controlling viral infection and offer promising strategies for viral control.

No abstract