Polyacrylamide Hydrogel Research Articles

Integrin Subtypes and Lamellipodia Mediate Spatial Sensing of RGD Ligands during Cell Adhesion.

Understanding how the spatial distribution of adhesive ligands regulates cell behavior is crucial for designing biomaterials. This study investigates how precisely controlled ligand spacing affects cell spreading and integrin subtype engagement. Using engineered polyacrylamide hydrogels with gold nanoparticle arrays, we explored the impact of RGD ligand spacings (30 and 150 nm) on human mesenchymal stromal cells. Cells exhibited distinct morphological behaviors: smaller spacings promoted larger spreading areas, while larger spacings resulted in elongated shapes with reduced spreading. Mechanistically, we found that the α5β1 integrin, not the αvβ3 integrin, played a central role in mediating these responses, alongside lamellipodia formation. Our findings provide critical insights into the spatial sensing of ligands, highlighting the influence of ligand spacing on cellular mechanotransduction and integrin-specific responses. This work advances the understanding of cell-material interactions and offers potential strategies for designing biomaterials to guide cell behavior in tissue engineering.

Boosting Dendrite‐Free Zinc Anode with Strongly Polar Functional Group Terminated Hydrogel Electrolyte for High‐Safe Aqueous Zinc‐Ion Batteries

AbstractAqueous zinc‐ion batteries (AZIBs) have become a promising energy storage device due to their low cost and high security. However, the severe dendrite growth and side reactions on metallic zinc (Zn) anode hamper their commercial implementation. Herein, a strongly electronegative trifluoroborate anion (─BF3−) functionalized polyacrylamide hydrogel (PAME) is well‐designed and constructed as the quasi‐solid‐state electrolyte to overcome these obstacles. The PAME chain segments terminated with strongly polar functional groups promote the conversion of water molecules from free water to bound water through the enhanced hydrogen bonding interaction to alleviate the side reactions. Furthermore, the PAME electrolyte featured with hierarchically porous structure and enhanced electrostatic interaction among the ─BF3− groups, and Zn2+ ions homogenizes the high‐flux Zn ion transport and induce the uniform deposition to restrain dendrite growth. Consequently, the assembled Zn‖PAME‖Zn batteries deliver remarkable cycling stability over 1800 h at 1 mA cm−2 and 900 h at 15 mA cm−2. Additionally, the constructed Zn‖PAME‖MnO2 full cells achieve a reversible capacity of 202 mAh g−1 at 2.0 A g−1 with a capacity retention rate of 91.4% over 500 cycles. This work sheds light on constructing the strongly polar hydrogel electrolyte to boost free‐dendrite Zn anodes for long‐lifespan AZIBs.

Poroelastic fracture of polyacrylamide hydrogels: Enhanced crack tip swelling driven by chain scission

The deformation of hydrogels is accompanied by water migration, a process that plays a crucial role in their fracture behaviors. Previous investigations primarily focus on how the water migration between the environment and hydrogel affects the fracture of hydrogels. Herein, a novel mechanism of the rate-dependent fracture of hydrogels induced by interior water migration is uncovered. Notched polyacrylamide (PAAm) hydrogels are stretched at various stretch rates in both oil and deionized (DI) water environments. Notably, the critical stretches to crack propagation are positively correlated with the stretch rates in both the two environments. This rate-dependent fracture is attributed to the crack tip swelling of PAAm hydrogels. Delayed fracture tests conducted in oil further verify the co-existence of delayed fracture and rate-dependent fracture resulted from interior water migration in PAAm hydrogels. The experimental findings are interpreted by considering the imperfection of a real polymer network, in which the scission of short chains in the region neighboring the crack tip reduces the average crosslinking density locally, thereby greatly amplifying the degree of crack tip swelling and its influence on the fracture of hydrogels. A constitutive model coupling the evolution of polymer network and the diffusion of water molecules is proposed, which can predict the crack tip swelling of notched PAAm hydrogels through the finite element method. Assuming that the decrease in fracture toughness is positively related to the swelling along the crack propagation surface, the predicted normalized fracture toughness matches the experimental results of PAAm hydrogels stretched in water well, and satisfies those in oil environment qualitatively. This work highlights the significant influence of interior water migration on the fracture of hydrogels and provides insights that may guide the design of hydrogels with enhanced fracture resistance.

A diode-like integrated hydrogel for piezoionic generators and sensors

Wearable sensing electronic devices based on hydrogel are gradually developing towards multifunction and portability, however, efficiently harvesting energy from the surrounding environment to power traditional hydrogel-based wearable electronic devices is a major challenge. The assembly of multilayer heterogeneous hydrogels is a potential strategy to address this challenge. Herein, inspired by the structure of diodes, a diode-like integrated hydrogel composed of a three-tier structure of anionic polyelectrolyte hydrogel, polyacrylamide hydrogel and cationic polyelectrolyte hydrogel is developed. By the connection of polyacrylamide hydrogel, the composite hydrogel exhibits excellent structural stability and mechanical properties. Notably, due to the introduction of MXene ion-conducting microchannels, the directional transport of free cations and anions ionized by anionic and cationic polyelectrolytes is achieved, thereby improving the conductivity (74.58 mS/cm), sensing (gauge factor = 7.47) and piezoionic output performance of the composite hydrogel. The composite hydrogel-based sensor can sense tiny facial movements and recognize the direction of human movement, and the composite hydrogel-based piezoionic generator exhibit more efficient mechanical-electric conversion performance, which can output the maximum voltage of 1410mV, current of 28 μA, and power density of 2.9mW/m2 for a composite hydrogel of 5×5 cm2. The integration of multilayer heterogeneous hydrogels proposes a versatile strategy for the development of high-performance hydrogel-based self-powered sensing electronic devices, expanding the application of hydrogels in artificial intelligence and human-computer interaction.

Experimental and simulation study on hygroscopic hydrogel-based thermal management of electronic device

With the increasing power of electronic devices, thermal management has become crucial for their operational efficiency and lifespan. In this work, we have demonstrated a sorption-based thermal management strategy enabled by hygroscopic hydrogel. The polyacrylamide (PAM) hydrogel impregnated with LiCl (PAM-LiCl) was attached to a silicon wafer. And Pt metal circuits were coated to the silicon wafer to measure the temperature variations under different heat flux densities. The results show that the hydrogel can effectively reduce the surface temperature. At a heating power of 0.3 W/cm2, the temperature control duration reached 30 min, with an average effective heat transfer coefficient of 65.5 W/(m2·K) and an effective heat storage density of 171 J/cm2. Additionally, we developed and validated a multiphysics model considering desorption and vapor diffusion within the hydrogel. Numerical results indicate that during the desorption cooling process, the surface heat transfer resistance and the internal diffusion resistance play a dominant role. Additionally, we analyzed the effects of material properties, structure parameters, and operating conditions on the thermal management performance. This study helps to understand the key points of sorption-based thermal management technology and guide the design and optimization of sorption-based thermal management system.

Hybrid Hydrogels of Polyacrylamide and Self-assembly Photodynamic Nanoparticles with Diverse Adhesion for Infected Chronic Wound Healing.

The healing of infected wounds is challenging for patients. In this paper, a hybrid hydrogel with strong tissue adhesion, self-healing, and antibiosis without antibiotics was developed as a dressing to promote the healing of infected chronic wounds. Acrylamide (PAM) was polymerized with N,N-methylene bis(acrylamide) (BIS) as the substrate, and self-assembled nanoparticles of carboxymethyl chitosan and chlorin e6 (CMCS/Ce6 NPs) trapped with magnesium (Mg2+) ions were dispersed in the hydrogel substrate. CMCS/Ce6 NPs provided favorable photodynamic antibiosis via the production of reactive oxygen species (ROS) under NIR irradiation. The hybrid hydrogels exhibited excellent self-healing properties, diverse adhesion, and biocompatibility. The in vivo results indicated that the hybrid hydrogel accelerated wound healing significantly via comprehensive factors of photodynamic antibiosis of CMCS/Ce6 NPs, cell proliferation promotion by Mg2+, good bioadhesion, and moisture retention of the PAM hydrogel, which promoted collagen deposition and blood vessel maturation.

Mechanosensitive Differentiation of Human iPS Cell-Derived Podocytes.

Stem cell fate decisions, including proliferation, differentiation, morphological changes, and viability, are impacted by microenvironmental cues such as physical and biochemical signals. However, the specific impact of matrix elasticity on kidney cell development and function remains less understood due to the lack of models that can closely recapitulate human kidney biology. An established protocol to differentiate podocytes from human-induced pluripotent stem (iPS) cells provides a promising avenue to elucidate the role of matrix elasticity in kidney tissue development and lineage determination. In this study, we synthesized polyacrylamide hydrogels with different stiffnesses and investigated their ability to promote podocyte differentiation and biomolecular characteristics. We found that 3 kPa and 10 kPa hydrogels significantly support the adhesion, differentiation, and viability of podocytes. Differentiating podocytes on a more compliant (0.7 kPa) hydrogel resulted in significant cell loss and detachment. Further investigation of the mechanosensitive proteins yes-associated protein (YAP) and synaptopodin revealed nuanced molecular distinctions in cellular responses to matrix elasticity that may otherwise be overlooked if morphology and cell spreading alone were used as the primary metric for selecting matrices for podocyte differentiation. Specifically, hydrogels with kidney-like rigidities outperformed traditional tissue culture plates at modulating the molecular-level expression of active mechanosensitive proteins critical for podocyte health and function. These findings could guide the development of physiologically relevant platforms for kidney tissue engineering, disease modeling, and mechanistic studies of organ physiology and pathophysiology. Such advances are critical for realizing the full potential of in vitro platforms in accurately predicting human biological responses.

Leveraging Deep Learning and Generative AI for Predicting Rheological Properties and Material Compositions of 3D Printed Polyacrylamide Hydrogels.

Artificial intelligence (AI) has the ability to predict rheological properties and constituent composition of 3D-printed materials with appropriately trained models. However, these models are not currently available for use. In this work, we trained deep learning (DL) models to (1) predict the rheological properties, such as the storage (G') and loss (G") moduli, of 3D-printed polyacrylamide (PAA) substrates, and (2) predict the composition of materials and associated 3D printing parameters for a desired pair of G' and G". We employed a multilayer perceptron (MLP) and successfully predicted G' and G" from seven gel constituent parameters in a multivariate regression process. We used a grid-search algorithm along with 10-fold cross validation to tune the hyperparameters of the MLP, and found the R2 value to be 0.89. Next, we adopted two generative DL models named variational autoencoder (VAE) and conditional variational autoencoder (CVAE) to learn data patterns and generate constituent compositions. With these generative models, we produced synthetic data with the same statistical distribution as the real data of actual hydrogel fabrication, which was then validated using Student's t-test and an autoencoder (AE) anomaly detector. We found that none of the seven generated gel constituents were significantly different from the real data. Our trained DL models were successful in mapping the input-output relationship for the 3D-printed hydrogel substrates, which can predict multiple variables from a handful of input variables and vice versa.

Congelation- and dehydration-tolerant, mechanically robust hydrogel electrolyte for durable iontronic sensors operating in open air and freezing temperatures over wide strain and pressure ranges

Conventional hydrogels have limitations in mechanical properties and are susceptible to loss of elasticity and conductivity caused by congelation and dehydration, limiting their practical uses for application in high-stress environments, open air, and freezing temperatures. This study introduces a mechanically robust, dehydration- and congelation-tolerant, and ionically conductive hydrogel electrolyte, practical for iontronic sensors working in wide pressure and strain ranges under open-air and freezing temperatures. This hydrogel electrolyte is fabricated through a reconstruction process comprising a drying-induced densification of double-network hydrogel of alginate and polyacrylamide, a structure fixation by Fe3+ crosslinking, and a Li+ infiltration. The resultant hydrogel electrolyte is tolerant to dehydration and congelation and mechanically robust, with strength and elastic modulus of a few mega-pascals comparable to those of non-conductive elastomers/rubbers used as dielectric materials. Therefore, the hydrogel electrolyte-based iontronic sensors demonstrate exceptional sensitivity and stability under compression and tension and across a wide temperature range. Further, the sensor demonstrates their practical applicability in high-stress environments from kg-range human weight to ton-range car weight. These achievements evince that iontronic sensors, based on mechanically robust and ionically conductive hydrogel electrolytes tolerant to congelation and dehydration, can be employed for practical applications.

Fast On-Site Speciation and High Spatial Resolution Imaging of Labile Arsenic in Freshwater and Sediment Using the DGT-SERS Sensor.

Diffusive gradients in thin films (DGT) technique is renowned for in situ passive sampling but not for rapid on-site analysis, whereas surface-enhanced Raman spectroscopy (SERS) excels in ultrasensitive on-site detection but is limited by substrate contamination from complex matrices. Here, a hierarchical nanostructure of silver (Ag) mirror-supported large Ag nanoparticles (∼120 nm) was grown in situ in polyacrylamide hydrogel with a restricted pore size (PAM/Ag mirror/AgNPs) to serve as both the DGT binding phase and the SERS substrate. The substrate exhibited a maximum electric field enhancement factor of 9.9 × 108 and a signal relative standard error of 4.8%. Using the DGT-SERS sensor, As(III) and As(V) in freshwater were simultaneously detected at limits of 0.9 and 0.8 μg L-1, respectively, applicable across a wide range of environmental conditions. The DGT-SERS effectively mitigated the interfacial reduction of As(V) caused by humic acid by excluding it from plasmonic hotspots through size exclusion of the diffusive layer. The Raman analysis of a DGT sample in the field requires only 2 s using a portable spectrometer without DGT device disassembly. More importantly, the DGT-SERS captured the first two-dimensional image of As(III) and As(V) in one DGT at the micron scale resolution, revealing their spatially supplementary distribution patterns at the sediment-water interface. This study paves the way for next-generation speciation imaging DGT and the application of SERS in complex environments.

Magnetically Driven Hydrogel Surfaces for Modulating Macrophage Behavior.

During the host response toward implanted biomaterials, macrophages can shift phenotypes rapidly upon changes in their microenvironment within the host tissue. Exploration of this phenomenon can benefit significantly from the development of adequate tools. Creating cell microenvironment alterations on classical hydrogel substrates presents challenges, particularly when integrating them with cell cultivation and monitoring processes. However, having the capability to dynamically manipulate the cell microenvironment on biomaterial surfaces holds significant potential. We introduce magnetically actuated hydrogels (MadSurface) tailored to induce reversible stiffness changes on polyacrylamide hydrogel substrates with embedded magnetic microparticles in a time-controllable manner. Our investigation focused on exploring the potential of magnetic fields and MadSurfaces in dynamically modulating macrophage behavior in a programmable manner. We achieved a consistent modulation by subjecting the MadSurface to a pulsed magnetic field with a frequency of 0.1 Hz and a magnetic field flux density of 50 mT and analyzed exposed cells using flow cytometry and ELISA. At the single-cell level, we identified a subpopulation for which the dynamic stiffness conditions in conjunction with the pulsed magnetic field increased the expression of CD206 in M1-activated THP-1 cells, indicating a consistent shift toward the M2 anti-inflammatory phenotype on MadSurface. At the population level, this effect was mostly hindered in the culture period utilized in this work. The MadSurface approach advances our understanding of the interplay between magnetic field, cell microenvironment alterations, and macrophage behavior.

Polyacrylamide Hydrogels as Versatile Biomimetic Platforms to Study Cell‐Materials Interactions

Polyacrylamide Hydrogels as Versatile Biomimetic Platforms to Study Cell‐Materials Interactions

Geometric constraint of mechanosensing by modification of hydrogel thickness prevents stiffness-induced differentiation in bone marrow stromal cells.

Extracellular matrix (ECM) stiffness is fundamental in cell division, movement and differentiation. The stiffness that cells sense is determined not only by the elastic modulus of the ECM material but also by ECM geometry and cell density. We hypothesized that these factors would influence cell traction-induced matrix deformations and cellular differentiation in bone marrow stromal cells (BMSCs). To achieve this, we cultivated BMSCs on polyacrylamide hydrogels that varied in elastic modulus and geometry and measured cell spreading, cell-imparted matrix deformations and differentiation. At low cell density BMSCs spread to a greater extent on stiff compared with soft hydrogels, or on thin compared with thick hydrogels. Cell-imparted matrix deformations were greater on soft compared with stiff hydrogels or thick compared with thin hydrogels. There were no significant differences in osteogenic differentiation relative to hydrogel elastic modulus and thickness. However, increased cell density and/or prolonged culture significantly reduced matrix deformations on soft hydrogels to levels similar to those on stiff substrates. This suggests that at high cell densities cell traction-induced matrix displacements are reduced by both neighbouring cells and the constraint imposed by an underlying stiff support. This may explain observations of the lack of difference in osteogenic differentiation as a function of stiffness.

Structure regulation of oxidized soybean cellulose nanocrystals/poly-acrylamide hydrogel and its application potential in wound dressing

The development of functional dressings based on natural polysaccharide-based hydrogels remains a great challenge, and the specific roles of gel composition and drug-controlled release mechanisms were unclear. In this study, oxidized soybean cellulose nanocrystals (CNCs)/poly-acrylamide (PAM) hydrogel was prepared. The proportion of CNCs, crosslinkers, and water in the system was regulated to fine-tune the rheological performances, texture properties, transparency, and micro-network structures of CNCs/PAM hydrogel, and further explored its application potential in the field of wound dressings. It was found that CNCs improved the rigidity and adhesion of hydrogels, crosslinkers improved the network density, and water promoted the softening and fluidity of hydrogels. The effective filling of CNCs in the composite hydrogel was verified by FTIR, XRD, and NMR. Furthermore, the pH responsiveness and drug-loading potential of the smart hydrogel were tested by swelling and drug-controlled release experiments, elucidating drug-release dynamic mechanisms during the wound healing process. The inhibition zones (>7 mm) of gram-positive/negative bacteria and cell viability (>100 %) assay showed satisfactory biocompatibility, as the hydrogel effectively accelerated wound healing in a wound model. These results elucidated the regulation mechanism of the structures of CNCs/PAM hydrogel and revealed the application potential of CNCs/PAM hydrogel in wound dressings.

A high temperature-resistant, strong, and self-healing double-network hydrogel for profile control in oil recovery

Hydrogels are widely used in profile control to plug high-permeability zones in oil recovery. In this study, a novel double-network (DN) hydrogel is developed for profile control. The two networks of the prepared hydrogel are polyacrylamide (PAAm) crosslinked by N,N’-Methylenebisacrylamide (MBAA) and konjac glucomannan (KGM) crosslinked by borax (B), respectively. The two networks are interconnected by their interpenetrating structures and hydrogen bonds. Based on the results of a series of evaluation experiments, the AAm/KGM DN hydrogels developed in this study exhibit a strong mechanical strength with their fracture stresses exceeding 0.137 MPa. Meanwhile, the AAm/KGM DN hydrogels can remain thermally stable after being heated at 130 °C for 24 h, indicating the good high-temperature resistance of the new sample. Moreover, the prepared AAm/KGM DN hydrogels present excellent self-healing performance due to the abundant hydrogen bonds in their structures, which helps form stable and long-term plugging in porous media. In addition, the pure PAAm hydrogel and the AAm/KGM DN hydrogel are sheared into two dispersed particle gel (DPG) suspensions to investigate their plugging performances. The results demonstrate that the AAm/KGM DN DPG can effectively plug a high-permeability sandpack with a plugging efficiency of 93.2 %, while the pure AAm DPG can only provide a much lower plugging efficiency of 60.5 %. The AAm/KGM DN hydrogel developed in this study, with its high mechanical strength, high-temperature resistance, and self-healing capability, offers a promising new candidate for profile control in oil recovery.

Metal welding-inspired phase change self-healing strategy applied to high-modulus hydrogel composites

The self-healing efficiencies of polymers are inversely proportional to their modulus, as the recovery of the polymer network heavily relies on the mobility of polymer chains. Therefore, reinvigorated by the metal welding, we have developed S-PAM-SA-x supercooling hydrogels, consisting of polyacrylamide hydrogel networks and inorganic CH3COONa·3H2O phase change materials. Subsequently, rigid self-healing H-PAM-SA-x composites were achieved via self-actuated crystallization-related phase change from the supersaturated hydrogels, resulting in a significant enhancement in mechanical properties. Notably, the Young’s modulus experienced an astonishing increase from 0.07 to 387.1 MPa. The H-PAM-SA-130 % composites demonstrated satisfactory self-healing performance based on the phase change of melting and crystallization, as the dominant mechanical carrier was found to be the crystal lattice rather than the PAM network. Leveraging the reversible nature of melting and crystallization, the same position can undergo multiple healing cycles without compromising self-healing efficiencies. Moreover, this distinctive dynamic phase change process significantly expands the range of functional applications, encompassing self-healing, adhesion, and patterns’ replication among others.

Relation of synthesis and fatigue property in elastic soft materials

Fatigue has long been studied for many materials, but many aspects are not well understood. Our recent study of the distinct roles of crosslinks and entanglements in the synthesis-property relation of a polymer network under monotonic load leads to a fundamental question: how do crosslinks and entanglements affect the synthesis-property relation of a polymer network under cyclic load? Here we study the relation of synthesis and fatigue property of elastic soft materials without precut cracks. We prepare polyacrylamide hydrogels by free radical polymerization as a model system, and swell the hydrogels in water to equilibrium or to a certain amount of polymer content. The synthesis parameters include the crosslinker-to-monomer molar ratio and the water-to-monomer molar ratio in the precursor, as well as the polymer content in the hydrogel. Three series of hydrogels are prepared. For each hydrogel, the stress-stretch curve under cyclic stretch of various amplitudes and the number of cycles to rupture are measured, giving four properties: fatigue life, endurance stretch, endurance stress, and endurance work. When the crosslinker-to-monomer molar ratio in the precursor is high, the degree of network imperfection on average is low. When the water-to-monomer molar ratio in the precursor is low, the number of entanglements per polymer segment on average is large. We show that crosslinks decrease the susceptibility to fatigue and entanglements increase the endurance stress. By contrast, both crosslinks and entanglements negligibly affect the endurance stretch and the endurance work.

PIEZO1 mediates matrix stiffness-induced tumor progression in kidney renal clear cell carcinoma by activating the Ca2+/Calpain/YAP pathway

ObjectiveThe significance of physical factors in the onset and progression of tumors has been increasingly substantiated by a multitude of studies. The extracellular matrix, a pivotal component of the tumor microenvironment, has been the subject of extensive investigation in connection with the advancement of KIRC (Kidney Renal Clear Cell Carcinoma) in recent years. PIEZO1, a mechanosensitive ion channel, has been recognized as a modulator of diverse physiological processes. Nonetheless, the precise function of PIEZO1 as a transducer of mechanical stimuli in KIRC remains poorly elucidated. MethodsA bioinformatics analysis was conducted using data from The Cancer Genome Atlas (TCGA) and the Clinical Proteomic Tumor Analysis Consortium (CPTAC) to explore the correlation between matrix stiffness indicators, such as COL1A1 and LOX mRNA levels, and KIRC prognosis. Expression patterns of mechanosensitive ion channels, particularly PIEZO1, were examined. Collagen-coated polyacrylamide hydrogel models were utilized to simulate varying stiffness environments and study their effects on KIRC cell behavior in vitro. Functional experiments, including PIEZO1 knockdown and overexpression, were performed to investigate the molecular mechanisms underlying matrix stiffness-induced cellular changes. Interventions in the Ca2+/Calpain/YAP Pathway were conducted to evaluate their effects on cell growth, EMT, and stemness characteristics. ResultsOur findings indicate a significant correlation between matrix stiffness and the prognosis of KIRC patients. It is observed that higher mechanical stiffness can facilitate the growth and metastasis of KIRC cells. Notably, we have also observed that the deficiency of PIEZO1 hinders the proliferation, EMT, and stemness characteristics of KIRC cells induced by a stiff matrix. Our study suggests that PIEZO1 plays a crucial role in mediating KIRC growth and metastasis through the activation of the Ca2+/Calpain/YAP Pathway. ConclusionThis study elucidates a novel mechanism through which the activation of PIEZO1 leads to calcium influx, subsequent calpain activation, and YAP nuclear translocation, thereby contributing to the progression of KIRC driven by matrix stiffness.

Synergistic Effect Between 0D CQDs and 2D MXene to Enhance the Photothermal Conversion of Hydrogel Evaporators for Efficient Solar Water Evaporation, Photothermal Sensing and Electricity Generation.

Solar-powered interfacial water evaporation is a promising technique for alleviating freshwater stress. However, the evaporation performance of solar evaporators is still constrained by low photothermal conversion efficiency and high water evaporation enthalpy. Herein, 0D carbon quantum dots (CQDs) are combined with 2D MXene to serve as a hybrid photothermal material to enhance the light absorption and photothermal conversion ability, meanwhile sodium carboxymethyl cellulose (CMC)/polyacrylamide (PAM) hydrogels are used as a substrate material for water transport to reduce the enthalpy of water evaporation. The synergistic effect in 0D CQDs/2D MXene hybrid photothermal materials accelerate the carrier transfer, inducing efficient localized surface plasmon resonance (LSPR) effect. This results in the enhanced photothermal conversion efficiency. The integrated hydrogel evaporators demonstrate a high evaporation rate (1.93 and 2.86kgm-2h-1 under 1 and 2 sunlights, respectively) and low evaporation enthalpy (1485Jg-1). In addition, the hydrogel evaporators are applied for photothermal sensing and temperature difference power generation (TEG). The TEG device presents an efficient output power density (230.7mWm-2) under 1 sunlight. This work provides a feasible approach for regulating and controlling the evaporation performances of hydrogel evaporators, and gives a proof-of-concept for the design of multipurpose solar evaporation systems.

Sliding on Slide-Ring Gels

Recent investigations have pointed to physical entanglements that greatly outnumber chemical crosslinks as key sources of energy dissipation and low friction in hydrogel networks. Slide-ring gels are an emerging class of hydrogels described by their mobile crosslinks, which are formed by rings topologically constrained to slide along linear polymer chains within the network. These materials have enjoyed decades of study by polymer chemists but have been underexplored by the tribology community. In this work, we synthesized a pseudo-rotaxane crosslinker from poly(ethylene glycol) diacrylate (PEG-diacrylate) and α-cyclodextrin-acrylate followed by hydrogel networks by connecting the sliding crosslinks with polyacrylamide chains. The mechanical and tribological properties of slide-ring hydrogels were investigated using a custom-built microtribometer. Slide-ring hydrogels exhibit unique behavior compared to conventional covalently crosslinked polyacrylamide hydrogels and offer a vast design space for future investigations.Graphical