Wet Gel Research Articles

Preparation of monolithic silica HPLC columns with truss-structured skeletons and embedded surfactant-templated mesopores

AbstractMonolithic macro/mesoporous silica gels have been prepared via a sol-gel process using triblock copolymer Pluronic P123 (EO20PO70EO20) as a structure-directing agent. In this synthesis, P123 not only induces phase separation to form macroporous structure but also acts as a supramolecular template to form mesopores with precisely controlled shape and size. Obtained was a monolithic silica composed of continuous truss-like columnar skeletons in which cylindrical mesopores are arranged in a 2D-hexagonal symmetry. These monolithic silica gels have extremely high porosity approaching 90% and exhibited high specific surface area and sharp pore size distribution as revealed by N2 sorption measurements. Combinations of the initial composition and the post-gelation treatment on wet gels allowed the control of physical properties of meso- and macropore structures. The monolithic HPLC columns prepared using these silica gels surface-modified by ODS (octadecylsilyl) ligands gave as many as 140,000 theoretical plates/m for the separation of alkylbenzenes in a reversed-phase mode. Very weak dependence of height equivalent to theoretical plate, H, on the mobile phase velocity was also recognized in comparison with conventional particle-packed columns. Graphical Abstract

Development of photoactive ZnS-SiO2 composites on biogenic silica matrix for organic pollutant degradation.

Sulfide ZnS-SiO2 composite photocatalysts with biogenic silica matrix were prepared by sol-gel method based on wet gel and xerogel. FT-IR, SEM, XRD, EDXRF, UV-Vis, and XPS methods were systematically used to characterize the obtained materials. The use of support allowed to obtain stable porous (SBET = 79-105 m2g-1; Vpore = 0.25-0.17 cm3·g-1) ZnS-SiO2 photocatalysts in aqueous solutions. Zn2+ content in methyl orange solution after its degradation was 0.4 MPC. ZnS-SiO2 composites had 3.68-3.70eV band gap. The obtained materials were photoactive under different irradiation conditions (sunlight, UV-light, Xenon light, visible light) due to effective separation of charge carriers (e- and h+). Methyl orange degradation degree under UV light excitation was 35-88%, under sunlight - 11-30%. ZnS-SiO2 composite synthesized using silica xerogel showed a greater photoactivity due to a presence of cone-shaped or cylindrical pores with one open end in its structure and a higher content of ZnS photoactive component. A comparative study of photocatalytic performance of methyl orange degradation by ZnS-SiO2 under UV irradiation was investigated using radical scavengers. •O2- was main active species during MO degradation under UV irradiation, and electrons played additional role during the photocatalytic process.

Porous polyimide composite films containing mesoporous hollow silica nanospheres with ultralow dielectric constant and dissipation loss

Porous polyimide hybrid films with ultralow dielectric constant and dissipation loss were synthesized during chemical imidization and rapid evaporation of polymer solutions. Polyimide (PI) of bis(4-aminophenyl)-1,4-diisopropylbenzene (BISP) and 4,4′-(hexafluoroisopropylidene) diphthalic anhydride (6FDA) were synthesized in N-methylpyrrolidinone (NMP) to yield the corresponding poly(amic acid)s (PAA)s, which were then chemically imidized. To reduce the dielectric properties of the porous PI films, amine-functionalized, surface-modified hollow silica nanoparticles (AHNS) with various sizes from 100 nm to 1 μm, prepared via sol-gel process, were added with PAA at 3, 5, or 10 % weight content, followed by chemical imidization to produce the porous PI/AHNS films. To avoid the high-volume shrinkage of wet gels and maintain the high porosity of the PI with low polarizability, AHNS nanoparticles were added to the porous structure of the PI xerogels as a physical crosslinker. The polyimide hybrid film with 10 nm AHNS nanoparticles at 10 % weight content showed a dielectric constant of 1.151 and a dissipation rate of 0.001 at a frequency of 10 GHz.

Ultrasoft Long-Lasting Reusable Hydrogel-Based Sensor Patch for Biosignal Recording.

Here, we report an ultrasoft extra long-lasting, reusable hydrogel-based sensor that enables high-quality electrophysiological recording with low-motion artifacts. The developed sensor can be used and stored in an ambient environment for months before being reused. The developed sensor is made of a self-adhesive electrical-conductivity-enhanced ultrasoft hydrogel mounted in an Ecoflex-based frame. The hydrogel's conductivity was enhanced by incorporating polypyrrole (PPy), resulting in a conductivity of 0.25 S m-1. Young's modulus of the sensor is only 12.9 kPa, and it is stretchable up to 190%. The sensor was successfully used for electrocardiography (ECG) and electromyography (EMG). Our results indicate that using the developed hydrogel-based sensor, the signal-to-noise ratio of recorded electrophysiological signals was improved in comparison to that when medical-grade silver/silver chloride (Ag/AgCl) wet gel electrodes were used (33.55 dB in comparison to 22.16 dB). Due to the ultra-softness, high stretchability, and self-adhesion of the developed sensor, it can conform to the skin and, therefore, shows low susceptibility to motion. In addition, the sensor shows no sign of irritation or allergic reaction, which usually occurs after long-term wearing of medical-grade Ag/AgCl wet gel electrodes on the skin. Further, the sensor is fabricated using a low-cost and scalable fabrication process.

Novel ternary nanocomposite (TiO2@Fe3O4-chitosan) system for nitrate removal from water: an adsorption cum photocatalytic approach.

Nitrate pollution of water emerging from various anthropogenic activities has become a major environmental concern because of its deleterious effects on natural water resources. The present work deals with the synthesis of the ternary nanocomposite based on chitosan, iron oxide (Fe3O4), and titanium dioxide (TiO2) and its application for the removal of nitrates from model-contaminated water. Fe3O4 derived through a coprecipitation method was incorporated into the chitosan matrix which was fabricated in the form of beads. The wet gel beads were then successfully coated with sol-gel-derived silver-doped titanium dioxide sol followed by drying under suitable conditions to get the functional nanocomposite beads. The synthesized functional materials were further characterized for their structural, morphological, and textural features using X-ray diffraction analysis, physical property measurement (PPMS), Fourier transform infrared (FTIR) analysis, UV visible spectroscopy analysis (UV-vis), BET surface area analysis (BET), field emission scanning electron microscopic (FESEM), and transmission electron microscopy (TEM) analysis. The ternary nanocomposites were further used for the removal of nitrates via adsorption cum photocatalytic reduction technique from the model contaminated water when subjected to an adsorption study under dark conditions and photocatalytic study under UV/visible/sunlight for a definite time. Fe3O4 in the nanocomposite provides enhanced adsorption features whereas the functional coating of titanium dioxide aids in the removal of nitrates through the photocatalytic reduction technique. The functional beads containing 3% Fe3O4 in the wet gel form (CTA-F3) have excellent nitrate removal efficiency of ~ 97% via adsorption cum solar photocatalysis towards the removal of nitrate ions from 50ppm nitrate solution, whereas the dried nanocomposite beads have got a nitrate removal efficiency of ~ 68% in 1h from 100ppm nitrate solution. Continuous flow adsorption cum photocatalytic study was performed further using the oven-dried functional beads in which flow rate and bed height were varied while maintaining the concentration of feed solution as constant. A nitrate removal efficiency of 65% and an adsorption capacity of 4.1 mgg-1 were obtained for the CTA-F3 beads in the continuous flow adsorption cum photocatalysis experiment for up to 5h when using an inlet concentration of 100ppm, bed height 12cm, and flow rate 5.0mlmin-1. A representative fixed-bed column adsorption experiment conducted using CTA-F3 beads for the treatment of a real groundwater sample shows reasonable results for nitrate removal (71.7% efficiency) along with a significant removal rate for the other anions as well. Thus, the novel adsorbent/photocatalyst developed is suitable for the removal of nitrates from water due to the synergistic effect between Fe3O4, chitosan, and titanium dioxide.

Reusable free-standing hydrogel electronic tattoo sensors with superior performance

Recently electronic tattoo sensors have attracted immense interest for health monitoring mainly due to their higher sensing performance than conventional dry sensors, owing to the ultra-low thickness which results in their conformability to the skin. However, their performance is worse than wet sensors. Further, these electronic tattoo sensors are not durable and reusable when free-standing because of their low thickness and being too delicate. Here, we report a remarkably high-performance freestanding, reusable, ultrathin and ultra-soft electronic tattoo sensor made of parylene-hydrogel double layer system with high water retention over extended periods that can be used for the extended period of 6 months. The hydrogel electronic tattoo (HET) sensors consist of electrically conductive self-adhesive hydrogel with a thickness of 20 µm and Young’s modulus of only 31 kPa at 37 °C, allowing for ultra-conformal contact to the skin microscopic features. Our HET sensors are fabricated using a scalable cost-effective method on ordinary tattoo papers and are laminated on the skin like temporary tattoos and were used for electrophysiological signals recording such as electrocardiography (ECG), electromyography (EMG), and skin hydration, temperature sensing. The HET sensors, for the first time, show 234% lower sensor-skin interface impedance (SSII) and significantly lower susceptibility to motion than gold standard medical grade silver/silver chloride wet gel electrodes which are known to have the lowest SSII and susceptibility to motion. Further, the low HET-skin interface impedance leads to a considerably larger signal amplitude and signal-to-noise ratio (SNR) of the electrophysiological signals recorded using HET sensors in comparison with those obtained using gold standard medical grade silver/silver chloride wet gel electrodes. The SNR of some types of electrophysiological signals such as EMG recorded using HET is up to 19 dB higher than gold standard medical grade electrodes due to higher signal amplitude, significantly lower susceptibility of HET to motion and lower motion artifacts. Also, the HET sensor is the first free-standing ultrathin tattoo sensor that can be transferred from the skin to tattoo paper and vice versa many times and the electrophysiological sensing quality remained high during repeated use for over 6 months.

Advanced, high‐performance thermo‐insulating plaster

AbstractThe main purpose of many current studies regarding energy efficiency is the improvement of the thermal resistance of buildings. To fulfill this goal, the development of advanced insulating materials, to be incorporated in the building envelopes, is imperative. Aerogels are ultralight porous materials typically produced via the sol‐gel process followed by supercritical drying of the wet gel. They exhibit very high porosities and a mesoporous‐macroporous structure which endows aerogels with extremely low thermal conductivity. This makes them ideal candidates for ambient thermal insulation applications. However, the cost for aerogel insulation is considerably higher than the one of standard insulation products. In the present work, highly porous aerogel‐like materials based on silica and commercial novolac resin were developed and added to common mortars. The prepared materials were dried under ambient pressure to minimize the manufacturing cost. The bulk density of silica quasi‐aerogels was 0.03 g/cm3–0.09 g/cm3 and that of the novolac resin samples 0.09 g/cm3–0.21 g/cm3. The aerogels were incorporated in mortars and cured for 28 days before measurement of thermal conductivity. The values of the thermal conductivity coefficient of the measured samples were 0.047 W/m K–0.058 W/m K for the silica reinforced mortars and 0.036 W/m K–0.044 W/m K for the novolac reinforced ones.

SiOC foam‐aerogel composites: Optimal balance of lightness and excellent thermal insulation

AbstractFoam‐aerogel composites are synthesized in polymeric, hybrid, and ceramic states by completing the open cells of the foam with a solution forming a wet gel, carbon dioxide (CO2) supercritically dried, and pyrolyzed. Thermal diffusivity measurements are conducted using the laser flash, and for mechanical performance, cold crushing tests are done to obtain compressive strengths. Samples possess a range of specific surface area (SSA) values up to ∼650 m2/g contingent upon the material state, that is, polymeric, hybrid, or ceramic. While SSA values can be deliberately altered, almost all samples demonstrated a total porosity of ∼90 vol%, with superb specific compressive strength reaching around 2 MPa. In addition to adjustable surface characteristics granting hydrophobic and hydrophilic features, the study revealed the potential use of these foam‐aerogel composites as thermal insulators with low thermal conductivities of 0.02 W·m−1·K−1 at RT and 0.05 W·m−1·K−1 at 500°C. When exposed directly to a butane flame gun with a flame temperature reaching ∼1200°C, from the backside of a 5 mm‐thick foam‐aerogel composite, only ∼200°C is recorded, which is lower than a comparable commercial insulator panel tested under the same conditions.

Organic solvents-free and ambient-pressure drying melamine formaldehyde resin aerogels with homogeneous structures, outstanding mechanical strength and flame retardancy

Atmospheric drying method for fabricating aerogels is considered the most promising way for casting aerogels on a large scale. However, the organic solvent exchange, remaining environmental pollution risk, is a crucial step in mitigating the impact of surface tension during the atmospheric drying process, especially for wet gel formed through the alkoxy-derived sol-gel process, such as melamine-formaldehyde resin (MF) aerogel. Herein, a tough polymer-assisted in situ polymerization was proposed to fabricate MF resin aerogel with a combination of mechanical toughness and strength, enabling it to withstand the capillary force during water evaporation. The monolithic MF resin aerogel through the sol-gel method can be directly prepared without additional network strengthening or organic solvent exchange. The resulting MF resin aerogel exhibits a homogeneous as well as hierarchical structure with macropores and mesopores (~6 μm and ~5 nm), high compressive modulus of 31.8 MPa, self-extinguishing property, and high-temperature thermal insulation with 97 % heat decrease for butane flame combustion. This work presents a straightforward and environmentally friendly method for fabricating MF resin aerogels with nanostructures and excellent performance in open conditions, exhibiting various applications.

Comparative catalytic performance of PGM-nanoparticle-doped alumina Xerogels and aerogels for potential application in automotive pollution mitigation

The structural (low density, high porosity), thermal (low thermal conductivity, high temperature stability), and chemical (high degree of tailorability) properties of aerogels make them attractive in a range of applications, including catalysis. The automotive industry relies on three-way-catalysts (TWCs) for automotive pollution mitigation, and TWCs in turn depend heavily on the use of platinum group metals (PGMs). Reduction of the use of PGMs in TWCs would be advantageous. To investigate the effect of aerogel structure and processing on three-way catalytic performance we prepared alumina wet gels doped with ca. 15 nm rhodium and palladium nanoparticles and dried them (1) supercritically to form aerogels and (2) under ambient conditions to form xerogels. Nanoparticle concentration was adjusted to ensure that both forms of the catalyst (aerogel and xerogel) had the same volumetric concentration of PGM after calcination to 800°C. Powder x-ray diffraction and transmission electron microscopy (TEM) confirmed the presence of PGMs. TEM images showed PGM particle agglomeration on the order of 40 to 200 nm in both the aerogel and xerogel materials. Gas adsorption analysis indicated that the aerogels have a surface area of 460 m2/g with most pores in the 2- to 100-nm range, whereas the xerogel surface area was 170 m2/g with a narrow pore distribution around 10 nm. Catalytic performance tests under a range of simulated automotive operating conditions show that, in all cases, the aerogels outperformed the xerogels. The aerogel light-off temperatures (the temperature at which a 50 % conversion is achieved) were 45 to 120 °C lower for the conversion of HCs, 25 to 55 °C lower for the conversion of CO and 40 to 145 °C lower for the conversion of NO. This study provides direct evidence that aerogel processing of catalysts provides catalytic performance benefits separate from the underlying chemistry of the catalysts.

Structure-Activity Relationships toward the Identification of a High-Potency Selective Human Toll-like Receptor-7 Agonist.

Toll-like receptor (TLR)-7 agonists are immunostimulatory vaccine adjuvants. A systematic structure-activity relationship (SAR) study of TLR7-active 1-benzyl-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine led to the identification of a potent hTLR7-specific p-hydroxymethyl IMDQ 23 with an EC50 value of 0.22 μM. The SAR investigation also resulted in the identification of TLR7 selective carboxamide 12 with EC50 values of 0.32 μM for hTLR7 and 18.25 μM for hTLR8. In the vaccination study, TLR7-specific compound 23 alone or combined with alum (aluminum hydroxide wet gel) showed adjuvant activity for a spike protein immunogen in mice, with enhanced anti-spike antibody production. Interestingly, the adjuvant system comprising carboxamide 12 and alum showed prominent adjuvant activity with high levels of IgG1, IgG2b, and IgG2c in immunized mice, confirming a balanced Th1/Th2 response. In the absence of any apparent toxicity, the TLR7 selective agonists in combination with alum may make a suitable vaccine adjuvant.

Separation of Perfluorooctanoic Acid from Water Using Meso- and Macroporous Syndiotactic Polystyrene Gels.

Per- and polyfluoroalkyl substances are an emerging class of contaminants that are environmentally persistent, bioaccumulative, and noxious to human health. Among these, perfluorooctanoic acid (PFOA) molecules are widely found in ground and surface water sources. A novel high surface area, meso- and macroporous syndiotactic polystyrene (sPS) wet gel is used in this work as the adsorbent of PFOA molecules from water at environmentally relevant PFOA concentrations (≤1 μg/L) and cleanse water to below the U.S. EPA's 2023 health advisory limit of 4 parts per trillion (ppt). The sigmoidal shape of the PFOA adsorption isotherm indicates a two-step adsorption mechanism attributed to the strong affinity of PFOA molecules for the sPS surface and molecular aggregation at solid-liquid interfaces or within the pores of the sPS wet gel. The adsorption kinetics and the effects of sPS wet gel porosity, pore size, and pore volume on the removal efficiency are reported. The adsorption kinetics is seen to be strongly dependent on pore size and pore volume.

Flexible and Compressible Nanostructure-Assembled Aramid Nanofiber/Silica Composites Aerogel.

The Applications of silica aerogel are limited due to its brittleness and low strength. As a result, it is essential to strengthen and toughen it. Organic nanofibers are one of the preferred reinforcement materials. In this work, we designed and fabricated flexible and compressible nanostructure-assembled aramid nanofiber/silica composites aerogel (ANF/SiO2 aerogel) to improve the mechanical strength and flexibility of silica aerogel without compromising thermal insulation properties. The aramid nanofiber/silica composite aerogels were prepared by immersing the aramid nanofiber wet gel into the silica sol for a certain period of time followed by freeze drying without solvent replacement. The surface modifier 3-aminopropyltriethoxysilane (APTES) was used as a coupling agent to form chemical linkage between the ANF fiber and silica gel. It was observed that APTES can effectively drive the silica sol to infuse into ANF hydrogel, promoting the assembly of silica gel onto the fiber surface and a uniform distribution in the network of ANF. The compressive resilience, thermal stability, and thermal insulation properties of the composite aerogels were evaluated by inducing the silica aerogel into the ANF network to form a protective layer on the fiber and change the pore structure in the ANF network.

Evaluating Bacterial Nanocellulose Interfaces for Recording Surface Biopotentials from Plants.

The study of plant electrophysiology offers promising techniques to track plant health and stress in vivo for both agricultural and environmental monitoring applications. Use of superficial electrodes on the plant body to record surface potentials may provide new phenotyping insights. Bacterial nanocellulose (BNC) is a flexible, optically translucent, and water-vapor-permeable material with low manufacturing costs, making it an ideal substrate for non-invasive and non-destructive plant electrodes. This work presents BNC electrodes with screen-printed carbon (graphite) ink-based conductive traces and pads. It investigates the potential of these electrodes for plant surface electrophysiology measurements in comparison to commercially available standard wet gel and needle electrodes. The electrochemically active surface area and impedance of the BNC electrodes varied based on the annealing temperature and time over the ranges of 50 °C to 90 °C and 5 to 60 min, respectively. The water vapor transfer rate and optical transmittance of the BNC substrate were measured to estimate the level of occlusion caused by these surface electrodes on the plant tissue. The total reduction in chlorophyll content under the electrodes was measured after the electrodes were placed on maize leaves for up to 300 h, showing that the BNC caused only a 16% reduction. Maize leaf transpiration was reduced by only 20% under the BNC electrodes after 72 h compared to a 60% reduction under wet gel electrodes in 48 h. On three different model plants, BNC-carbon ink surface electrodes and standard invasive needle electrodes were shown to have a comparable signal quality, with a correlation coefficient of >0.9, when measuring surface biopotentials induced by acute environmental stressors. These are strong indications of the superior performance of the BNC substrate with screen-printed graphite ink as an electrode material for plant surface biopotential recordings.

A NiFeSn oxyhydroxide electrocatalyst wet gel for highly efficient water electrolysis in alkaline media

Since the kinetic barrier posed by the oxygen evolution reaction (OER) is a significant obstacle in water-splitting systems, the creation of effective and inexpensive OER electrocatalysts has received considerable research interest. We report the facile synthesis of an amorphized NiFeSn oxyhydroxide wet gel on Ni foam via a gelation-induced embedding method. Its intrinsic pore structure provided a sufficiently large surface area without the need for a binder. The NiFeSn oxyhydroxide wet gel electrocatalyst only needed overpotentials of 253, 301, and 346 mV to produce 100, 200, and 300 mA·cm−2, respectively, for the OER and an overpotential value of 198 mV at 50 mA·cm−2 for the hydrogen evolution reaction. Moreover, an exceptionally low voltage of 1.55 V was required for overall water splitting under alkaline conditions. Enhancement of the catalytic properties of the oxyhydroxide by adding Sn was confirmed by using density functional theory calculations. The nanoporous multi-metallic wet gel can be used to create effective low-cost stable self-supporting electrocatalysts with a high current density for enhanced water electrolysis.

Microneedle Array Electrodes Fabricated With 3D Printing Technology for High-Quality Electrophysiological Acquisition.

Electrophysiological recordings are vital in assessing biological functions, diagnosing diseases, and facilitating biofeedback and rehabilitation. The applications of conventional wet (gel) electrodes often come with some limitations. Microneedle array electrodes (MAEs) present a possible solution for high-quality electrophysiological acquisition, while the prior technologies for MAE fabrication have been either complex, expensive, or incapable of producing microneedles with uniform dimensions. This work employed a projection stereolithography (P μ SL) 3D printing technology to fabricate MAEs with micrometer-level precision. The MAEs were compared with gel and flat electrodes on electrode-skin interface impedance (EII) and performances of EMG and ECG acquisition. The experimental results indicate that the P μ SL 3D printing technology contributed to an easy-to-perform and low-cost fabrication approach for MAEs. The developed MAEs exhibited promising EII and enabled a stable EMG and ECG acquisition in different conditions without inducing skin allergies, inflammation, or injuries. This research lies in the development of a type of customizable MAE with considerable biomedical application potentials for ultra-minimally invasive or non-invasive electrophysiological acquisition.

A study on preparation and properties of fly ash-based SiO2 aerogel material

Using fly ash acid leaching residue as the silicon source, sodium silicate solution was produced by alkali leaching and the wet gel was obtained by the sol-gel method. Hexamethyldisiloxane (HMDSO) was used to modify the surface of the wet gel, thereby reducing the capillary tension during the atmospheric pressure drying process, and finally preparing a silica aerogel material with hydrophobic properties. The effects of different alkali leaching conditions, different sol pH, HMDSO dosage on the aerogel density and the changes of aerogel material properties and composition during the preparation process were investigated, and the reaction mechanism of silica aerogel preparation by atmospheric pressure drying was described. The results showed that the optimum conditions for alkali leaching were 20 wt% NaOH concentration, 2 h reaction time and 100 °C, and the desilication rate was 81.72%; the lowest Silica aerogel density of 108 mg/cm3 at pH 5 to 6; the lowest density of silica aerogel was 110 mg/cm3 at a modifier to wet gel volume ratio of 1:1.4.

Modification of Quartz Ceramics by Applying a Sol-Gel Composition of MgO–Al2O3–ZrO2–SiO2 System

Composite sol-gel materials of the MgO–Al2O3–ZrO2–SiO2 system were synthesized and the processes of their thermal evolution and crystallization were studied. Application of sol-gel compositions of the MgO–Al2O3–ZrO2–SiO2 system to the surface of quartz ceramics leads to a significant increase in the mechanical strength of the material. The processes of thermal evolution of the sol-gel composition were studied using IR spectroscopy, X-ray diffraction, electron microscopy, and energy dispersive analysis. It was shown that the formation of the oxide composite structure of materials begins at the stage of wet gels. Treatment of quartz ceramics with composite sols followed by drying and heat treatment up to 1200°C results in modification of the surface layers of the material, which makes it possible to increase the mechanical strength of the material by more than 20%. Sol-gel modifying compositions, upon drying and subsequent heat treatment, form polycrystalline structures bonded to quartz ceramic particles and consisting of various oxide crystals.

Flexible, Conductive Fabric‐Backed, Microneedle Electrodes for Electrophysiological Monitoring

AbstractMicroneedle‐based electrodes have attracted significant attention due to their potential applications in high‐quality, long‐term electrophysiological monitoring. In this study, micromoulding technology is used to develop a flexible, conductive fabric microneedle (CF–MN) electrode by bonding a conductive textile to polymeric microneedle arrays. The resulting electrode conforms to the curved surfaces of the body, and the use of a conductive textile backing reduces metallization time and costs by 50% over double‐sided dry electrodes. The electrode‐skin impedance of the CF–MN electrodes is significantly lower than that of gel electrodes over a wide frequency range, and tests on healthy volunteers, both at rest and under a range of ambulatory conditions, showed that the electrodes are capable of acquiring electrocardiography (ECG) and electromyography (EMG) signals that have a comparable kurtosis and signal‐to‐noise ratio to those recorded using conventional electrodes, but without the need for skin preparation or the use of a wet gel. The biomechanical properties of the electrode are also characterized. This is the first demonstration of CF–MN electrodes that can ultimately be integrated into clothing, which in turn can facilitate personalized cardiac health management by enabling continuous, long‐term ECG/EMG monitoring during daily activities.

Physically cross-linked chitosan gel with tunable mechanics and biodegradability for tissue engineering scaffold

Chitosan, a cationic polysaccharide, exhibits promising potential for tissue engineering applications. However, the poor mechanical properties and rapid biodegradation have been the major limitations for its applications. In this work, an effective strategy was proposed to optimize the mechanical performance and degradation rate of chitosan gel scaffolds by regulating the water content. Physical chitosan hydrogel (HG, with 93.57 % water) was prepared by temperature-controlled cross-linking, followed by dehydration to obtain xerogel (XG, with 2.84 % water) and rehydration to produce wet gel (WG, with 56.06 % water). During this process, changes of water content significantly influenced the water existence state, hydrogen bonding, and the chain entanglements of chitosan in the gel network. The mechanical compression results showed that the chitosan gel scaffolds exhibited tunable compressive strength (0.3128–139 MPa) and compressive modulus (0.2408–1094 MPa). XG could support weights exceeding 65,000 times its own mass while maintaining structural stability. Furthermore, in vitro and in vivo experiments demonstrated that XG and WG exhibited better biocompatibility and resistance to biodegradation compared with HG. Overall, this work contributes to the design and optimization of chitosan scaffolds without additional chemical crosslinkers, which has potential in tissue engineering and further clinical translation.