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Dielectric elastomer actuators (DEAs) with large electrically-actuated strain can build light-weight and flexible non-magnetic motors. However, dielectric elastomers commonly used in the field of soft actuation suffer from high stiffness, low strength, and high driving field, severely limiting the DEA’s actuating performance. Here we design a new polyacrylate dielectric elastomer with optimized crosslinking network by rationally employing the difunctional macromolecular crosslinking agent. The proposed elastomer simultaneously possesses desirable modulus (~0.073 MPa), high toughness (elongation ~2400%), low mechanical loss (tan δ m  = 0.21@1 Hz, 20 °C), and satisfactory dielectric properties ( ε r  = 5.75, tan δ e  = 0.0019 @1 kHz), and accordingly, large actuation strain (118% @ 70 MV m −1 ), high energy density (0.24 MJ m −3 @ 70 MV m −1 ), and rapid response (bandwidth above 100 Hz). Compared with VHB TM 4910, the non-magnetic motor made of our elastomer presents 15 times higher rotation speed. These findings offer a strategy to fabricate high-performance dielectric elastomers for soft actuators. Dielectric elastomer actuators (DEAs) with large electrically actuated strain can be used in non-magnetic motors, but high stiffness, poor strength and slow response currently limit the application of DEAs. Here, the authors optimize the crosslinking network in a polyacrylate elastomer to enable a DEA with high toughness and actuation strain and use the polyacrylate to build a motor which can be driven under low electric field.

Metal-free electrocatalysts represent a main branch of active materials for oxygen evolution reaction (OER), but they excessively rely on functionalized conjugated carbon materials, which substantially restricts the screening of potential efficient carbonaceous electrocatalysts. Herein, we demonstrate that a mesostructured polyacrylate hydrogel can afford an unexpected and exceptional OER activity – on par with that of benchmark IrO 2 catalyst in alkaline electrolyte, together with a high durability and good adaptability in various pH environments. Combined theoretical and electrokinetic studies reveal that the positively charged carbon atoms within the carboxylate units are intrinsically active toward OER, and spectroscopic operando characterizations also identify the fingerprint superoxide intermediate generated on the polymeric hydrogel backbone. This work expands the scope of metal-free materials for OER by providing a new class of polymeric hydrogel electrocatalysts with huge extension potentials. Hydrogels are networked hydrophilic polymers with enriched polar groups and confined water but are relatively less explored as electrocatalysts. Here, the authors demonstrate that insulative polymeric hydrogels can be an underlying catalogue of metal-free oxygen evolution electrocatalyst with huge extension potentials.

The uncontrolled dendrite growth and detrimental parasitic reactions of Zn anodes currently impede the large-scale implementation of aqueous zinc ion batteries. Here, we design a versatile quasi-solid-state polymer electrolyte with highly selective ion transport channels via molecular crosslinking of sodium polyacrylate, lithium magnesium silicate and cellulose nanofiber. The abundant negatively charged ionic channels modulate Zn 2+ desolvation process and facilitate ion transport. Moreover, an in-situ formed Zn-Mg-Si medium-entropy alloy on Zn anode allows for an improved Zn nucleation kinetics and homogeneous Zn deposition. These combined advantages of the polymer electrolyte enable Zn anodes to achieve an average Coulombic efficiency of 99.7 % over 2400 cycles and highly reversible cycling up to 600 h with large depth of discharge of 85.6%. The resultant Zn | |V 2 O 5 offers a stable long-term cycling performance and its pouch cell achieves a cycling capacity of 1.13 Ah at industrial-level loading mass of 31.3 mg. The dendrite growth and parasitic reactions on Zn anodes pose significant challenges for the application of aqueous zinc-ion batteries. Here, the authors report a versatile quasi solid-state polymer electrolyte engineered with abundant ion transport channels for enhanced zinc ion battery performance.

Heat stress is being exacerbated by global warming, jeopardizing human and social sustainability. As a result, reliable and energy-efficient cooling methods are highly sought-after. Here, we report a polyacrylate film fabricated by self-moisture-absorbing hygroscopic hydrogel for efficient hybrid passive cooling. Using one of the lowest-cost industrial materials (e.g., sodium polyacrylate), we demonstrate radiative cooling by reducing solar heating with high solar reflectance (0.93) while maximizing thermal emission with high mid-infrared emittance (0.99). Importantly, the manufacturing process utilizes only atmospheric moisture and requires no additional chemicals or energy consumption, making it a completely green process. Under sunlight illumination of 800 W m −2 , the surface temperature of the film was reduced by 5 °C under a partly cloudy sky observed at Buffalo, NY. Combined with its hygroscopic feature, this film can simultaneously introduce evaporative cooling that is independent of access to the clear sky. The hybrid passive cooling approach is projected to decrease global carbon emissions by 118.4 billion kg/year compared to current air-conditioning facilities powered by electricity. Given its low-cost raw materials and excellent molding feature, the film can be manufactured through simple and cost-effective roll-to-roll processes, making it suitable for future building construction and personal thermal management needs. Gan et al. have developed sodium polyacrylate-based films for passive radiative cooling that can be fabricated using atmospheric moisture alone, offering radiative and evaporative cooling, reducing temperatures by up to 5 °C under partly cloudy skies.

Solid-state lithium-metal (Li 0 ) batteries are gaining traction for electric vehicle applications because they replace flammable liquid electrolytes with a safer, solid-form electrolyte that also offers higher energy density and better resistance against Li dendrite formation. Solid polymer electrolytes (SPEs) are highly promising candidates because of their tuneable mechanical properties and easy manufacturability; however, their electrochemical instability against lithium-metal (Li 0 ), mediocre conductivity and poorly understood Li 0 /SPE interphases have prevented extensive application in real batteries. In particular, the origin of the low Coulombic efficiency (CE) associated with SPEs remains elusive, as the debate continues as to whether it originates from unfavoured interfacial reactions or lithium dendritic growth and dead lithium formation. In this work, we use state-of-the-art cryo-EM imaging and spectroscopic techniques to characterize the structure and chemistry of the interface between Li 0 and a polyacrylate-based SPE. Contradicting the conventional knowledge, we find that no protective interphase forms, owing to the sustained reactions between deposited Li dendrites and polyacrylic backbones and succinonitrile plasticizer. Due to the reaction-induced volume change, large amounts of cracks form inside the Li dendrites with a stress–corrosion–cracking behaviour, indicating that Li 0 cannot be passivated in this SPE system. On the basis of this observation, we then introduce additive engineering, leveraging from knowledge of liquid electrolytes, and demonstrate that the Li 0 surface can be effectively protected against corrosion using fluoroethylene carbonate, leading to densely packed Li 0 domes with conformal and stable solid–electrolyte interphase films. Owing to the high room-temperature ionic conductivity of 1.01 mS cm −1 , the high transference number of 0.57 and the stabilized lithium–electrolyte interface, this improved SPE delivers an excellent lithium plating/stripping CE of 99% and 1,800 hours of stable cycling in Li||Li symmetric cells (0.2 mA cm −2 , 1 mAh cm −2 ). This improved cathodic stability, along with the high anodic stability, enables a record high cycle life of >2,000 cycles for Li||LiFePO 4 and >400 cycles for Li||LiCoO 2 full cells. Li-metal surfaces can be effectively protected against corrosion using fluoroethylene carbonate, leading to a conformal and stable solid–electrolyte interphase.

High-performance stretchable conductive fibers are desired for the development of stretchable electronic devices. Here we show a simple spinning method to prepare conductive hydrogel fibers with ordered polymer chain alignment that mimics the hierarchically organized structure of spider silk. The as-prepared sodium polyacrylate hydrogel fiber is further coated with a thin layer of polymethyl acrylate to form a core–shell water-resistant MAPAH fiber. Owing to the coexistence and reversible transformation of crystalline and amorphous domains in the fibers, MAPAH fibers exhibit high tensile strength, large stretchability and fast resilience from large strain. MAPAH fiber can serve as a highly stretchable wire with a conductive hydrogel core and an insulating cover. The stretchability and conductivity of the MAPAH fiber are retained at −35 °C, indicating its anti-freezing property. As a prime example of stretchable conductive fibers, MAPAH fibers will shed light on the design of next generation textile-based stretchable electronic devices. High-performance stretchable conductive fibers are desired for the development of stretchable electronic devices but preparation of conductive hydrogel fibers is challenging. Inspired by spider silk the authors demonstrate here a spinning method to prepare stretchable conductive hydrogel fibers with ordered polymer chain alignment.

Dielectric elastomers, used as driver modules, require high power density to enable fast movement and efficient work of soft robots. Polyacrylate elastomers usually suffer from low power density under low electric fields due to limited response frequency. Here, we propose a bimodal network polyacrylate dielectric elastomer which breaks the intrinsic coupling relationship between dielectric and mechanical properties, featuring relatively high dielectric constant, low Young’s modulus, and wide driving frequency bandwidth (~200 Hz) like silicones. Therefore, an ultrahigh power density (154 W kg −1 @20 MV m −1 , 200 Hz) is realized at low electric field and high resonance frequency, 75 times greater than at 10 Hz. Further, a rotary motor is developed, reaching an impressive speed of 1245 rpm at 19.6 MV m −1 and 125 Hz, surpassing previous acrylate-based motors and entering the high-speed domain of silicone-based motors. These findings offer a versatile strategy to fabricate high-power-density dielectric elastomers for low-electric-field soft actuators. The authors make a bimodal network polyacrylate dielectric elastomer featuring high driving frequency like silicones and thereby a high power density of 154 W kg −1 @20 MV m −1 , 200 Hz. Their rotary motor realizes a maximum rotating speed of 1245 rpm@ 19.6 MV m −1 .

Drought, excessive use of nitrogen fertilizer, and decline in soil organic matter threaten corn production. This study investigated the potential of water retaining agents, inhibitors, and corn stalks in enhancing soil physicochemical properties to bolster corn yield in semi-arid farmlands. In our study, polyacrylamide addition increased the content of ammonium nitrogen (NH4+-N) and nitrate nitrogen (NO3–N) in the seedling stage, exchangeable potassium (K) in the mature stage but decreased the content of available phosphorus (P) in the seedling stage. Potassium polyacrylate addition increased the content of NH4+-N and decreased the content of available P in the seedling stage. The addition of inhibitors decreased the content of NH4+-N and available P in the seedling stage, NO3–N and available P in the jointing stage, and NH4+-N in the mature stage, respectively. Corn stalks returning could maintain soil moisture, decrease the content of NH4+-N in the seedling stage and exchangeable K in the mature stage, and increase the content of available P and exchangeable K in the seedling stage. Combined application of inhibitors and corn stalks could increase soil organic carbon (SOC) and ensure corn yield, which was the best fertilization mode in semi-arid cropland.

The growing need for energy and the depletion of oil wells necessitate advanced Enhanced Oil Recovery (EOR) techniques, particularly water and polymer flooding, which play a crucial role in augmenting hydrocarbon recovery rates. However, water flooding in high-permeability layers often leads to water breakthroughs, reduced sweep efficiency, and the formation of preferential channels, posing significant challenges to oil recovery and reservoir management. Conformance control treatments, including the use of polymer microspheres, offer a promising solution by sealing high-permeability zones and enhancing sweep efficiency. This study focuses on the application of fluorescent polymer microspheres based on polyacrylamide, which is extensively employed in the oil sector as an oil displacement agent. Fluorescent polymers called Poly 400, Poly 200, and Poly 600, incorporating cationic methacrylamide monomers, were synthesized through copolymerization to create amphiphilic polymers with enhanced stability and functionality. These fluorescent polymers were evaluated through flooding tests using a quarter-five-spot model of transparent quartz glass under UV light, allowing for instantaneous measurement and observation of fluorescence intensity. At reservoir conditions, the oil displacement experiments confirm that the incremental oil after water flooding by Poly 400, Poly 200, and Poly 600, is 13.1%, 9.1%, and 6.1% of OOIP respectively. The findings showed that fluorescent polymer microspheres could efficiently target high-permeability layers, adapt to varying pore throat sizes, and improve the plugging rate of high-permeability channels, thereby optimizing oil recovery. A subsequent simulation study using the CMG simulator provided further insights into the efficacy of these fluorescent polymers as EOR agents, revealing their potential to enhance sweep efficiency and enhance oil recovery. Simulation results showed that oil saturation decreased from 68% (initial) to 13.5%, 16.1%, and 18.3% after Poly 400, Poly 200, and Poly 600 flooding respectively. This work highlights the potential of fluorescent polymer microspheres as a valuable tool for EOR applications, offering significant advancements in reservoir management and oil recovery optimization.

Oxide ceramic electrolytes (OCEs) have great potential for solid-state lithium metal (Li 0 ) battery applications because, in theory, their high elastic modulus provides better resistance to Li 0 dendrite growth. However, in practice, OCEs can hardly survive critical current densities higher than 1 mA/cm 2 . Key issues that contribute to the breakdown of OCEs include Li 0 penetration promoted by grain boundaries (GBs), uncontrolled side reactions at electrode-OCE interfaces, and, equally importantly, defects evolution (e.g., void growth and crack propagation) that leads to local current concentration and mechanical failure inside and on OCEs. Here, taking advantage of a dynamically crosslinked aprotic polymer with non-covalent –CH 3 ⋯CF 3 bonds, we developed a plastic ceramic electrolyte (PCE) by hybridizing the polymer framework with ionically conductive ceramics. Using in-situ synchrotron X-ray technique and Cryogenic transmission electron microscopy (Cryo-TEM), we uncover that the PCE exhibits self-healing/repairing capability through a two-step dynamic defects removal mechanism. This significantly suppresses the generation of hotspots for Li 0 penetration and chemomechanical degradations, resulting in durability beyond 2000 hours in Li 0 -Li 0 cells at 1 mA/cm 2 . Furthermore, by introducing a polyacrylate buffer layer between PCE and Li 0 -anode, long cycle life >3600 cycles was achieved when paired with a 4.2 V zero-strain cathode, all under near-zero stack pressure. Self-healing is an appealing property for solid-state battery electrolytes to combat Li metal dendrites that pierce through the solid electrolyte. Here, authors report a self-healing electrolyte and observe its self-repairing kinetics in real-time using advanced microscopy.