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Abstract Structural electromagnetic shielding materials are required to withstand high stress and electromagnetic interference in extreme environments. In this paper, a nano-magnetic Heusler phase with desired structure parameters was successfully obtained in a copper matrix by employing a multi-objective driving design strategy. The resulting copper alloy exhibits a yield strength of up to 1.5 GPa, and the attenuation degree of electromagnetic wave reaches 99.999999999% (110 dB) within the frequency range of 10 kHz to 3 GHz. The research suggests that the Ni2MnSn precipitates with optimized structure parameters (including high number density: 5 × 1023 m−3, small size: 23 nm, large aspect ratio: 4, low mismatch: 2.3%, strong bonding: -0.316 eV/atom, magnetic order: 4.05 μB/f.u.) both reinforce the matrix by strong pinning and enhance electromagnetic shielding properties through magnetic-electric coupling. This design method tailored for multiple performance requirements provides a valuable tool for the development of structure-function integrated materials.

Abstract Ionically conductive fibers have promising applications; however, complex processing techniques and poor stability limit their practicality. To overcome these challenges, we proposed a stress-induced adaptive phase transition strategy to conveniently fabricate self-encapsulated hydrogel-based ionically conductive fibers (se-HICFs). se-HICFs can be produced simply by directly stretching ionic hydrogels with ultra-stretchable networks (us-IHs) or by dip-drawing from molten us-IHs. During this process, stress facilitated the directional migration and evaporation of water molecules in us-IHs, causing a phase transition in the surface layer of ionic fibers to achieve self-encapsulation. The resulting sheath-core structure of se-HICFs enhanced mechanical strength and stability while endowing se-HICFs with powerful non-contact electrostatic induction capabilities. Mimicking nature, se-HICFs were woven into spider web structures and camouflaged in wild environments to achieve high spatiotemporal resolution 3D depth-of-field sensing for different moving media. This work opens up a convenient route to fabricate stable functionalized ionic fibers.

Abstract Harvesting biomechanical energy from cardiac motion is an attractive power source for implantable bioelectronic devices. Here, we report a battery-free, transcatheter, self-powered intracardiac pacemaker based on the coupled effect of triboelectrification and electrostatic induction for the treatment of arrhythmia in large animal models. We show that the capsule-shaped device (1.75 g, 1.52 cc) can be integrated with a delivery catheter for implanting in the right ventricle of a swine through the intravenous route, which effectively converts cardiac motion energy to electricity and maintains endocardial pacing function during the three-week follow-up period. We measure in vivo open circuit voltage and short circuit current of the self-powered intracardiac pacemaker of about 6.0 V and 0.2 μA, respectively. This approach exhibits up-to-date progress in self-powered medical devices and it may overcome the inherent energy shortcomings of implantable pacemakers and other bioelectronic devices for therapy and sensing.

Abstract Highly efficient gas sensors able to detect and identify hazardous gases are crucial for numerous applications. Array of conventional single-output sensors is currently limited by problems including drift, large size, and high cost. Here, we report a sensor with multiple chemiresistive and potentiometric outputs for discriminative gas detection. Such sensor is applicable to a wide range of semiconducting electrodes and solid electrolytes, which allows to tailor and optimize the sensing pattern by tuning the material combination and conditions. The sensor performance is boosted by equipping a mixed-conducting perovskite electrode with reverse potentiometric polarity. A conceptual sensor with dual sensitive electrodes achieves superior three-dimensional (sub)ppm sensing and discrimination of humidity and seven hazardous gases (2-Ethylhexanol, ethanol, acetone, toluene, ammonia, carbon monoxide, and nitrogen dioxide), and enables accurate and early warning of fire hazards. Our findings offer possibilities to design simple, compact, inexpensive, and highly efficient multivariate gas sensors.

The use of epidermal growth factor for wound healing is limited by transdermal permeability, reduction, and receptor desensitization. Here the authors develop a microneedle-based self-powered transcutaneous electrical stimulation system to overcome these challenges.

Filtering capacitors are essential to smooth high voltage alternating current lines but are typically limited to hundreds of volts. Here, the authors demonstrate an aqueous hybrid electrochemical capacitor that can exhibit an operating voltage of 1,000 V when assembled into a device of 670 units.

The spin Hall angle (SHA) is a measure of the efficiency for converting a charge to a spin current is still challenging to tune in situ. Here, the authors demonstrate by introducing a ferroelectric (FE) material in a ferromagnetic/heavy metal stack the SHA can be voltage controled via the polarization of the FE layer.

Flexible devices such as solar cells and nanogenerators are attractive for powering wearable electronics, but waterproof capabilities would extend applications. Here the authors report a bionic stretchable nanogenerator that is capable of harvesting energy and multi-position motion monitoring underwater.

Implantable medical electronic devices are limited by battery lifetime and inflexibility, but self-powered devices can harvest biomechanical energy. Here the authors demonstrate cardiac pacing and correction of sinus arrhythmia with a symbiotic cardiac pacemaker, which is an implanted self-powered pacing system powered by cardiac motion, in a swine.

Bacteria are known to be sensitive to electrical interactions with the environment. Here, the authors report on a study into how the antibacterial properties of carbon-doped titania nanotubes are affected by capacitance after charging with direct and alternating currents.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

A major challenge in chemotherapy is chemotherapy resistance in cells lacking p53. Here we demonstrate that NIP30, an inhibitor of the oncogenic REGγ-proteasome, attenuates cancer cell growth and sensitizes p53-compromised cells to chemotherapeutic agents. NIP30 acts by binding to REGγ via an evolutionarily-conserved serine-rich domain with 4-serine phosphorylation. We find the cyclin-dependent phosphatase CDC25A is a key regulator for NIP30 phosphorylation and modulation of REGγ activity during the cell cycle or after DNA damage. We validate CDC25A-NIP30-REGγ mediated regulation of the REGγ target protein p21 in vivo using p53-/- and p53/REGγ double-deficient mice. Moreover, Phosphor-NIP30 mimetics significantly increase the growth inhibitory effect of chemotherapeutic agents in vitro and in vivo. Given that NIP30 is frequently mutated in the TCGA cancer database, our results provide insight into the regulatory pathway controlling the REGγ-proteasome in carcinogenesis and offer a novel approach to drug-resistant cancer therapy.

Abstract Perovskite/silicon tandem solar cells hold great promise for realizing high power conversion efficiency at low cost. However, achieving scalable fabrication of wide-bandgap perovskite (~1.68 eV) in air, without the protective environment of an inert atmosphere, remains challenging due to moisture-induced degradation of perovskite films. Herein, this study reveals that the extent of moisture interference is significantly influenced by the properties of solvent. We further demonstrate that n-Butanol (nBA), with its low polarity and moderate volatilization rate, not only mitigates the detrimental effects of moisture in air during scalable fabrication but also enhances the uniformity of perovskite films. This approach enables us to achieve an impressive efficiency of 29.4% (certified 28.7%) for double-sided textured perovskite/silicon tandem cells featuring large-size pyramids (2–3 μm) and 26.3% over an aperture area of 16 cm2. This advance provides a route for large-scale production of perovskite/silicon tandem solar cells, marking a significant stride toward their commercial viability.

Abstract Hierarchical compartmentalization, a hallmark of both primitive and modern cells, enables the concentration and isolation of biomolecules, and facilitates spatial organization of biochemical reactions. Coacervate-based compartments can sequester and recruit a large variety of molecules, making it an attractive protocell model. In this work, we report the spontaneous formation of core-shell cell-sized coacervate-based compartments driven by spontaneous evaporation of a sessile droplet on a thin-oil-coated substrate. Our analysis reveals that such far-from-equilibrium architectures arise from multiple, coupled segregative and associative liquid-liquid phase separation, and are stabilized by stagnation points within the evaporating droplet. The formation of stagnation points results from convective capillary flows induced by the maximum evaporation rate at the liquid-liquid-air contact line. This work provides valuable insights into the spontaneous formation and maintenance of hierarchical compartments under non-equilibrium conditions, offering a glimpse into the real-life scenario.

The superstate configuration in all-perovskite tandem solar cells is disadvantageous for long-term stability. Here, the authors reverse the processing order and demonstrate substrate configuration to bury oxidizable narrow-bandgap perovskites, and achieve efficiency of 25.3% with long stability.

Electrical interactions between bacteria and the environment are delicate and essential. In this study, an external electrical current is applied to capacitive titania nanotubes doped with carbon (TNT-C) to evaluate the effects on bacteria killing and the underlying mechanism is investigated. When TNT-C is charged, post-charging antibacterial effects proportional to the capacitance are observed. This capacitance-based antibacterial system works well with both direct and alternating current (DC, AC) and the higher discharging capacity in the positive DC (DC+) group leads to better antibacterial performance. Extracellular electron transfer observed during early contact contributes to the surface-dependent post-charging antibacterial process. Physiologically, the electrical interaction deforms the bacteria morphology and elevates the intracellular reactive oxygen species level without impairing the growth of osteoblasts. Our finding spurs the design of light-independent antibacterial materials and provides insights into the use of electricity to modify biomaterials to complement other bacteria killing measures such as light irradiation. [ABSTRACT FROM AUTHOR]