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Abstract The spatial and temporal control of material properties at a distance has yielded many unique innovations including photo-patterning, 3D-printing, and architected material design. To date, most of these innovations have relied on light, heat, sound, or electric current as stimuli for controlling the material properties. Here, we demonstrate that an electric field can induce chemical reactions and subsequent polymerization in composites via piezoelectrically-mediated transduction. The response to an electric field rather than through direct contact with an electrode is mediated by a nanoparticle transducer, i.e., piezoelectric ZnO, which mediates reactions between thiol and alkene monomers, resulting in tunable moduli as a function of voltage, time, and the frequency of the applied AC power. The reactivity of the mixture and the modulus of a naïve material containing these elements can be programmed based on the distribution of the electric field strength. This programmability results in multi-stiffness gels. Additionally, the system can be adjusted for the formation of an electro-adhesive. This simple and generalizable design opens avenues for facile application in adaptive damping and variable-rigidity materials, adhesive, soft robotics, and potentially tissue engineering. 

A topological superconductor, characterized by either a chiral order parameter or a topological surface state in proximity to bulk superconductivity, is foundational to topological quantum computing. A key open challenge is whether electron-electron interactions can tune such topological superconducting phase. Here, we provide experimental signatures of a unique topological superconducting phase in competition with electronic correlations in 10-unit-cell thick FeTexSe1-x films grown on SrTiO3 substrates. When the Te content x exceeds 0.7, we observe a topological transition marked by the emergence of a superconducting surface state. Near the FeTe limit, the system undergoes another transition where the surface state disappears, and superconductivity is suppressed. Theory suggests that electron-electron interactions in the odd-parity xy- band drives this second topological transition. The flattening and eventual decoherence of dxy-derived bands track the superconducting dome, linking correlation effects directly to superconducting coherent transport. Our work establishes many-body electronic correlations as a sensitive knob for tuning topology and superconductivity, offering a pathway to engineer new topological phases in correlated materials. 

In situelectrochemical analysis enables access to metal aquo PCET model complexes which are synthetically elaborated and speciation was determined. 

The rising atmospheric CO₂concentration is one of the biggest challenges human civilization faces. Direct air capture (DAC) that removes CO₂from the atmosphere provides great potential in carbon neutralization. However, the massive land use and capital investment of centralized DAC plants and the energy-intensive process of adsorbent regeneration limit its wide employment. We develop a distributed carbon nanofiber (CNF)–based DAC air filter capable of adsorbing CO₂downstream in ventilation systems. The DAC air filter not only has the potential to remove 596 MtCO₂year⁻¹globally but can also decrease energy consumption in existing building systems. The CNF-based adsorbent has a capacity of 4 mmol/g and can be regenerated via solar thermal or electrothermal methods with low carbon footprints. Through life cycle assessment, the CNF air filter shows a carbon removal efficiency of 92.1% from cradle to grave. Additionally, techno-economic analysis estimates a cost of $209 to 668 in capturing and storing 1 tonne of CO₂from direct air.