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Proximity-induced superconductivity in epitaxial topological insulator/superconductor heterostructures
The search for an unusual form of superconductivity known as topological superconductivity has attracted a great deal of attention of the quantum materials community because of its fundamental novelty and potential applications in fault-tolerant quantum computing technology.
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Discovering and Designing New Materials Using Directed Evolution
In a new seed project within the Northwestern University MRSEC, a novel approach for discovering and designing materials is being developed using directed evolution. While directed evolution approaches have been successfully applied in areas such as therapeutics or catalysis, this strategy has not been fully explored in materials science and engineering.
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Unlocking High Capacity and Fast Na+ Diffusion of HxCrS2 by Proton-Exchange Pretreatment
Princeton researchers have demonstrated that acid pre-treatment of NaCrS2 to form a new phase (named HxCrS2) results in significant improvements to the material’s performance as a sodium battery electrode.
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MEM-C IRG-1: Patterning Nanocrystals on Photonic Cavities with Electrohydrodynamic Inkjet Printing
Electrohydrodynamic ink jet printing has been used to print CsPbBr3 nanocrystals into very small features, with spot sizes down to only a few hundred nanometers across. The nanocrystals survive the printing, and even spontaneously self-organize into superlattices.
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Microfluidic Device for DNA Dynamics in Mixed Flows
Susan J. Muller, University of California Berkeley, and Eric S.G. Shaqfeh, Stanford
Highlight from Stanford MRSEC 0213618
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MEM-C IRG-2: Nematic Fluctuations in an Orbital Selective Superconductor Fe1+yTe1-xSex
Electronic nematicity is a correlated electronic state in solids that spontaneously breaks rotational symmetry. This work found that in Fe1+yTe1-xSex, one of the most strongly correlated iron-based superconductors, electronic nematicity is closely linked to magnetism, and its fluctuations may be responsible for superconducting pairing.
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Toughening Infiltrated Nanoparticle Packings: Role of Bridging and Entanglement
Researchers at UPenn investigate the fracture behavior of disordered polymer-infiltrated nanoparticle films (PINFs). Here, the extent of polymer confinement in PINFs was tuned over three orders of magnitude NPs of varying size and polymers with varying molecular weight. The results show that brittle, low molecular weight (MW) polymers can significantly toughen NP packings, and this toughening effect becomes less pronounced with increasing NP size.
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Fabricating Granular Hydrogels for 3D Printing
Granular hydrogels are jammed assemblies of hydrogel microparticles (i.e., “microgels”) widely explored in biomedical applications due to promising features such as shear-thinning to permit injectability and inherent porosity for cellular interactions. One area where this is particularly promising is in 3D printing.
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UPENN IRG2 Vimentin filaments protect cell nuclei from mechanical damage
Cells and tissues are subjected to external mechanical stresses in the body, including compressive loads, pressure gradients, and shear. This study shows that single cells become harder when compressed and that the parts inside the cells that make them strong (called the cytoskeleton) change when they are compressed. Some cells, like fibroblasts, become harder when subjected to moderate compression. However, this does not happen if a part of the cytoskeleton called vimentin is removed. This is because vimentin networks become harder when compressed or extended. This is explained using a theoretical model to based on the flexibility of vimentin filaments and their surface charge, which resists volume changes of the network under compression.
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UPENN IRG3 Shape morphing directed by spatially encoded, dually responsive liquid crystalline elastomer micro-actuators
Liquid crystal elastomers (LCEs) with intrinsic molecular anisotropy can be preprogrammed to morph shapes from 2D to 3D under external stimuli. However, it is difficult to program the positions and orientations of individual building blocks separately and locally as they are chemically linked in the polymer network.
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