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Conductive and self-healing hydrogels are among the emerging materials that mimic the human skin and are important due to their probable prospects in soft robots and wearable electronics. However, the mechanical properties of the hydrogel matrix limit their applications. In this study, we developed a physicochemically dual cross-linked chemically modified-cellulose nanofibers-carbon nanotubes/polyacrylic acid (TOCNF-CNTs/PAA) hydrogel. The TOCNFs acted both as a nanofiller and dispersant to increase the mechanical strength of the PAA matrix and break the agglomerates of the CNTs. The final self-healing and conductive TOCNF-CNTs/PAA-0.7 (mass ratio of CNTs to AA) hydrogel with a uniform texture exhibited highly intrinsic stretchability (breaking elongation to ca. 850%), enhanced tensile properties (ca. 59 kPa), ideal conductivity (ca. 2.88 S m− 1) and pressure sensitivity. Besides, the composite hydrogels achieved up to approximately 98.36% and 99.99% self-healing efficiency for mechanical and electrical properties, respectively, without any external stimuli. Therefore, the as-designed multi-functional self-healing hydrogels, combined with stretching, sensitivity, and repeatability, possess the ability to monitor human activity and develop multifunctional, advanced, and commercial products such as wearable strain sensors, health monitors, and smart robots.Graphic abstract

Seawater electrolysis is a viable method for producing hydrogen on a large scale and low-cost. However, the catalyst activity during the seawater splitting process will dramatically degrade as salt concentrations increasing. Herein, CoP is discovered that could reject chloride ions far from catalyst in electrolyte based on molecular dynamic simulation. Thus, a binder-free electrode is designed and constructed by in-situ growth of homogeneous CoP on rGO nanosheets wrapped around the surface of Ti fiber felt for seawater splitting. As expected, the as-obtained CoP/rGO@Ti electrode exhibits good catalytic activity and stability in alkaline electrolyte. Especially, benefitting from the highly effective repulsive Cl − intrinsic characteristic of CoP, the catalyst maintains good catalytic performance with saturated salt concentration, and the overpotential increasing is less than 28 mV at 10 mA cm −2 from 0 M to saturated NaCl in electrolyte. Furthermore, the catalyst for seawater splitting performs superior corrosion-resistance with a low solubility of 0.04%. This work sheds fresh light into the development of efficient HER catalysts for salinity tolerance hydrogen evolution. Seawater electrolysis for hydrogen production is limited by the poor salinity tolerance of catalysts. CoP was found to repel chlorine while attracting H2O molecules to form a thin layer on the catalyst surface, thus constructing a corrosion-resistant CoP/rGO@Ti catalyst for seawater splitting.

Using GIMMS NDVI3g+ data (1982–2022) together with ERA5-Land temperature and precipitation, this study examined long-term vegetation dynamics in the Indus River Basin (IRB) and used a residual trend framework for cautious first-order attribution. Basin-averaged NDVI increased significantly at 0.0061 per decade (p < 0.05), and 65.5% of the basin showed greening, mainly in irrigated croplands and river-adjacent agricultural zones, whereas 12.6% showed degradation concentrated in rapidly urbanizing areas, cryosphere margins, and desert fringes. Partial correlation and residual analyses indicate that climate-related enhancement was most evident in upper-elevation cryosphere transition zones and some lower-basin barren lands, whereas non-climatic residual effects were especially important in intensively managed agricultural landscapes. Because the attribution model includes only temperature and precipitation, the residual component is interpreted here as a non-climatic residual rather than a direct measure of human activity. The study, therefore, provides a spatially explicit basin-wide assessment of vegetation change while highlighting the uncertainty and interpretation limits of residual-based attribution.

The human skin, an important sensory organ, responds sensitively to external stimuli under various harsh conditions. However, the simultaneous achievement of mechanical/thermal sensitivity and extreme environmental tolerance remains an enormous challenge for skin‐like hydrogel‐based sensors. In this study, a novel skin‐inspired hydrogel–elastomer hybrid with a sandwich structure and strong interfacial bonding for mechanical–thermal multimode sensing applications is developed. An inner‐layered ionic hydrogel with a semi‐interpenetrating network is prepared using sodium carboxymethyl cellulose (CMC) as a nanofiller, lithium chloride (LiCl) as an ionic transport conductor, and polyacrylamide (PAM) as a polymer matrix. The outer‐layered polydimethylsiloxane (PDMS) elastomers fully encapsulating the hydrogel endow the hybrids with improved mechanical properties, intrinsic waterproofness, and long‐term water retention (>98%). The silane modification of the hydrogels and elastomers imparts the hybrids with enhanced interfacial bonding strength and integrity. The hybrids exhibit a high transmittance (~91.2%), fatigue resistance, and biocompatibility. The multifunctional sensors assembled from the hybrids realize real‐time temperature (temperature coefficient of resistance, approximately −1.1% °C−1) responsiveness, wide‐range strain sensing capability (gauge factor, ~3.8) over a wide temperature range (from −20°C to 60°C), and underwater information transmission. Notably, the dual‐parameter sensor can recognize the superimposed signals of temperature and strain. The designed prototype sensor arrays can detect the magnitude and spatial distribution of forces and temperatures. The comprehensive performance of the sensor prepared via a facile method is superior to that of most similar sensors previously reported. Finally, this study develops a new material platform for monitoring human health in extreme environments. A skin‐inspired hydrogel–elastomer hybrids with a sandwich structure and strong interfacial bonding is developed. The hybrids integrating high transparency, fatigue resistance, freezing resistance, anti‐dehydration, waterproofness, and biocompatibility are assembled into multi‐functional dual‐parameter sensors for real‐time temperature responsiveness, wide‐range strain sensing, and underwater information transmission.

Nanocellulose-borax-polyvinyl alcohol (PVA) hybrid foams were prepared using a facile approach in an aqueous medium followed by a freeze-casting technique. Nanocellulose was well-dispersed in the PVA-borax (PB) matrix and acted as a cross-linking agent and nanofiller to bridge the 3D network, leading to enhanced mechanical and thermal performance. The effects of particle size, aspect ratio, surface charge and crystallinity on the microstructure and performance were investigated. With the increasing size and aspect ratio, cellulose nanofiber-PB foam with a density of ~0.110 g/cm 3 exhibited the most pronounced honeycomb-like structure with a porosity of 92.2%, the smallest cell diameter (~0.93 μm) and the highest mechanical strength (bearing more than 7560 times its own weight). Chemical cross-linking of nanocellulose-PVA foams with borax led to uniform porous structure, small pores and high mechanical strength. Possible lyophilization-induced assembly mechanisms, relationships between microstructure and mechanical properties, and complexation reactions between building blocks are proposed.

Intrinsic self-healing and highly stretchable electro-conductive hydrogels demonstrate wide-ranging utilization in intelligent electronic skin. Herein, we propose a new class of strain sensors prepared by cellulose nanofibers (CNFs) and graphene (GN) co-incorporated poly (vinyl alcohol)-borax (GN-CNF@PVA) hydrogel. The borax can reversibly and dynamically associate with poly (vinyl alcohol) (PVA) and GN-CNF nanocomplexes as a cross-linking agent, providing a tough and flexible network with the hydrogels. CNFs act as a bio-template and dispersant to support GN to create homogeneous GN-CNF aqueous dispersion, endowing the GN-CNF@PVA gels with promoted mechanical flexibility, strength and good conductivity. The resulting composite gels have high stretchability (break-up elongation up to 1000%), excellent viscoelasticity (storage modulus up to 3.7 kPa), rapid self-healing ability (20 s) and high healing efficiency (97.7 ± 1.2%). Due to effective electric pathways provided by GN-CNF nanocomplexes, the strain sensors integrated by GN-CNF@PVA hydrogel with good responsiveness, stability and repeatability can efficiently identify and monitor the various human motions with the gauge factor (GF) of about 3.8, showing promising applications in the field of wearable sensing devices.

Recently, with the development of personal wearable electronic devices, the demand for portable power is miniaturization and flexibility. Electro-conductive hydrogels (ECHs) are considered to have great application prospects in portable energy-storage devices. However, the synergistic properties of self-healability, viscoelasticity, and ideal electrochemistry are key problems. Herein, a novel ECH was synthesized by combining polyvinyl alcohol-borax (PVA) hydrogel matrix and 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-cellulose nanofibers (TOCNFs), carbon nanotubes (CNTs), and polyaniline (PANI). Among them, CNTs provided excellent electrical conductivity; TOCNFs acted as a dispersant to help CNTs form a stable suspension; PANI enhanced electrochemical performance by forming a \"core-shell\" structural composite. The freeze-standing composite hydrogel with a hierarchical 3D-network structure possessed the compression stress (~152 kPa) and storage modulus (~18.2 kPa). The composite hydrogel also possessed low density (~1.2 g cm ), high water-content (~95%), excellent flexibility, self-healing capability, electrical conductivity (15.3 S m ), and specific capacitance of 226.8 F g at 0.4 A g . The fabricated solid-state all-in-one supercapacitor device remained capacitance retention (~90%) after 10 cutting/healing cycles and capacitance retention (~85%) after 1000 bending cycles. The novel ECH had potential applications in advanced personalized wearable electronic devices.

Electroluminescent (EL) devices are of great significance for expanding the application range of optoelectronics. However, the realization of EL devices with environment-tolerance, stretchability, mechanical cycling stability, self-adhesion, biocompatibility, and high dielectric constant still remains a challenge. Herein, a type of EL device with enhanced comprehensive performances composing of a chlorinated barium titanate/phosphor/polydimethylsiloxane (Cl-BT/phosphor/PDMS) luminescent layer sandwiched between two silver nanowire-cellulose nanocrystal with II crystalline allomorph/Triton X-100 modified polydimethylsiloxane (AgNW-CNC II/TX-PDMS) electrodes fabricated through a full solution-processing strategy is proposed. Environmentally-friendly CNC II with high transmittance acts as an antioxidant, dispersant and film-former for AgNWs. The hydrophilic modification of TX to PDMS imparts the electrodes with self-adhesion, high stretchability, as well as strong interfacial bonding between TX-PDMS and AgNW-CNC II. The electrodes achieve skin-like modulus by adjusting TX content, endowing the EL devices with a high compliance (186 kPa of Young’s modulus). The luminescent layer with Cl-BT exhibits a high dielectric constant (19) and luminance (up to 72 cd m −2 ). The assembled EL device with excellent cyclic stability (luminance retention 85% after 400 cycles), durability (luminance retention >94% after 400 min) and stretchability (88% luminance at 200% strain) can work properly at broad temperatures (−20 ~ 70 °C) and underwater. This biocompatible and self-adhesive EL device demonstrates great potential for implantable biomedical devices and wearable displays under harsh environments.

Bioderived poly(lactic acid) (PLA) is a promising alternative for fossil-based polymers, but its poor hydrophilicity, high brittleness, and low heat-resistance are problems for its utilization. In this work, bleached softwood kraft pulp (BSKP) fiber was adopted to modify PLA with MAPP as the coupling agent, with BSKP accounting for 10 wt% to 50 wt%. Internal mixing (IM) was applied to mix the PLA/fiber blend instead of screw grinding. The thermal and mechanical properties of the composites were assessed. The IM process was proven qualified for its effective dispersion of BSKP fibers in the PLA matrix. At a fiber loading of 50 wt%, IM-processed composites acquired satisfactory tensile strength (50.49 MPa, slightly higher than PLA) and Young’s modulus (2.56 GPa, 45.8% higher than PLA). The pulp fillers matched PLA matrix well for the characteristic temperatures in thermal decomposition. The BSKP/PLA composites were thermally strengthened by pulp fibers characterized by higher content of residues. The fibers improved the interfacial crystallinity of PLA in the composites (i.e., from 5.22% to 11.86%). The increased crystallinity resulted in enhanced stiffness or weaker damping performance of the composites. In conclusion, natural plant fibers are a feasible option to modify PLA for extended applications.

Integration of solar cell and secondary battery cannot only promote solar energy application but also improve the electrochemical performance of battery. Lithium–sulfur battery (LSB) is an ideal candidate for photoassisted batteries owing to its high theoretical capacity. Unfortunately, the researches related the combination of solar energy and LSB are relatively lacking. Herein, a freestanding photoelectrode is developed for photoassisted lithium–sulfur battery (PALSB) by constructing a heterogeneous structured Au@N‐TiO2 on carbon cloths (Au@N‐TiO2/CC), which combines multiple advantages. The Au@N‐TiO2/CC photoelectrode can produce the photoelectrons to facilitate sulfur reduction during discharge process, while generating holes to accelerate sulfur evolution during charge process, improving the kinetics of electrochemical reactions. Meanwhile, Au@N–TiO2/CC can work as an electrocatalyst to promote the conversion of intermediate polysulfides during charge/discharge process, mitigating induced side reactions. Benefiting from the synergistic effect of electrocatalysis and photocatalysis, PALSB assembled with an Au@N‐TiO2/CC photoelectrode obtains ultrahigh specific capacity, excellent rate performance, and outstanding cycling performance. What is more, the Au@N‐TiO2/CC assembled PALSB can be directly charged under light illumination. This work not only expands the application of solar energy but also provides a new insight to develop advanced LSBs. Photoassisted lithium–sulfur battery (PALSB) can promote the solar energy application. A freestanding Au@N‐TiO2/carbon cloths (CC) photoelectrode for PALSB cannot only work as a photocatalyst that produces the electrons and holes to facilitate the reduction and evolution of sulfur, but also can work as an electrocatalyst to promote the conversion of intermediate polysulfides during charge/discharge process.