Interconnected Macropores Research Articles

Selective oxygen-doping in self-supportive carbon electrode by electrochemical oxidation for electrocatalytic synthesis of hydrogen peroxide

We report the selective introduction of oxygen-containing functional groups for two-electron oxygen reduction reaction (2e-ORR) in self-supportive carbon electrode using electrochemical oxidation method. The optimal electrode shows hydrogen peroxide (H2O2) selectivity up to 95 %. CO is found active to control 2e-ORR selectivity and mechanism of oxygen species variation is elucidated by in situ infrared reflection absorption spectroscopy. We further improve mass transfer by introducing highly interconnected macropores in electrode, which shows H2O2 yield of 144 mmol cm−2 h−1 and Faradaic efficiency of nearly 100 %. These may inspire advanced active electrode creation for applications through selective electrochemical doping and structural design.

Development and characterization of ceramic-polymeric hybrid scaffolds for bone regeneration: incorporating of bioactive glass BG-58S into PDLLA matrix

In recent years, there has been a notable surge of interest in hybrid materials within the biomedical field, particularly for applications in bone repair and regeneration. Ceramic-polymeric hybrid scaffolds have shown promising outcomes. This study aimed to synthesize bioactive glass (BG-58S) for integration into a bioresorbable polymeric matrix based on PDLLA, aiming to create a bioactive scaffold featuring stable pH levels. The synthesis involved a thermally induced phase separation process followed by lyophilization to ensure an appropriate porous structure. BG-58S characterization revealed vitreous, bioactive, and mesoporous structural properties. The scaffolds were analyzed for morphology, interconnectivity, chemical groups, porosity and pore size distribution, zeta potential, pH, in vitro degradation, as well as cell viability tests, total protein content and mineralization nodule production. The PDLLA scaffold displayed a homogeneous morphology with interconnected macropores, while the hybrid scaffold exhibited a heterogeneous morphology with smaller diameter pores due to BG-58S filling. The hybrid scaffold also demonstrated a pH buffering effect on the polymer surface. In addition to structural characteristics, degradation tests indicated that by incorporating BG-58S modified the acidic degradation of the polymer, allowing for increased total protein production and the formation of mineralization nodules, indicating a positive influence on cell culture.

Macroporous, Highly Hygroscopic, and Leakage-Free Composites for Efficient Atmospheric Water Harvesting.

Hygroscopic composites based on hygroscopic salts and hydrogels are promising for atmospheric water harvesting (AWH), but their relatively low water production and possible salt leakage hinder real applications. Here, we report highly hygroscopic and leakage-free composites from loading LiCl into emulsion-templated sodium alginate and poly(vinyl alcohol) hydrogels with macroporous structures and interpenetrating polymer networks. The resulting composites exhibited an enhanced moisture uptake (up to 3.4 g g-1) and leakage-free behavior even at an extremely high relative humidity (RH) of 90%. Moreover, the composites showed accelerated adsorption, with high adsorption (0.803 g g-1 water at 25 °C and 90% RH within 1 h) and desorption due to the emulsion-templated, highly interconnected macropores. The hygroscopic composites obtained 1.12 g g-1 water per adsorption-desorption collection cycle and showed high reusability, without obvious deterioration in adsorption, desorption, and collection after 10 cycles. With the presence of carbon nanotubes, solar-driven AWH could be realized, without the requirement of additional energy. The highly hygroscopic and leakage-free composites with enhanced and accelerated adsorption and desorption are excellent candidates for efficient AWH.

Micron-Sized Thiol-Functional Polysilsesquioxane Microspheres with Open and Interconnected Macropores: Preparation, Characterization and Formation Mechanism.

Polysilsesquioxane (PSQ) microspheres have shown promise in many fields, but previous studies about porous PSQ microspheres are scarce. Herein, we fabricated novel micron-sized thiol-functional polysilsesquioxane (TMPSQ) microspheres with open and interconnected macropores by combining inverse suspension polymerization with two-step sol-gel and polymerization-induced phase separation processes, without using phase-separation-promoting additives or sacrificial templates. The chemical composition of the TMPSQ microspheres was confirmed using FTIR and Raman spectroscopy. The morphology of the TMPSQ microspheres was characterized using SEM and TEM. TGA was employed to test the thermal stability of the TMPSQ microspheres. Mercury intrusion porosimetry and nitrogen adsorption-desorption tests were performed to investigate the pore structure of the TMPSQ microspheres. The results showed that the TMPSQ microspheres had open and interconnected macropores with a pore size of 839 nm, and the total porosity and intraparticle porosity reached 70.54% and 43.21%, respectively. The mechanism of porous generation was proposed based on the morphological evolution observed using optical microscopy. The macropores were formed through the following four steps: phase separation (spinodal decomposition), coarsening, gelation, and evaporation of the solvent. The macropores can facilitate the rapid mass transfer between the outer and inner spaces of the TMPSQ microspheres. The TMPSQ microspheres are promising in various fields, such as catalyst supports and adsorbents.

Leaf‐Mimicking Superstructured Porous Membrane with Multiple Bioactive Pro‐Healing Functions for Effective Guided Bone Regeneration

AbstractBarrier membrane, a key material for guided bone regeneration surgery, is applied between soft and hard tissue interfaces in complex oral environment. The abilities to integrate contradictory requirements and self‐regulate the local microenvironment are highly desirable for barrier membrane but remain challenging to achieve. Herein, inspired by the leaf's hierarchical multifunctional synergy, a kind of superstructured porous membrane (SPM), integrating asymmetric surface pores, interconnected macropores and functional micropores, is developed based on the combination of breath figure and phase separation. For the SPM, the densely porous layer can inhibit penetration of soft tissue cells and maintain osteogenic space, and the loosely porous layer with interconnected microporous channels can effectively promote the adhesion and proliferation of osteoblasts, help to transport nutrients, and expose functional components. Meanwhile, porous carbon nanospheres introduced into SPM as multifunctional core components can ameliorate the undesirable microenvironment by scavenging reactive oxygen species, repairing bioelectrical environment, and killing bacteria, thus achieving multiple bioactive pro‐healing functions for efficient bone regeneration in vivo. These findings can open an appealing avenue for developing high‐performance barrier membranes as well as many other implant materials.

An efficient fabrication method of lightweight aramid nanofibrous aerogels for high-efficient sound absorption and thermal properties

The aramid nanofibrous aerogels (ANFs) have various application prospects due to their ultra-light, high porosity and excellent properties of aramid fibers. However, the preparation of ANFs requires long preparation time and their ultra-dense pore structure leads to poor sound penetration and high sound energy reflectivity, which ultimately makes the overall sound absorption performance of ANFs poor. Therefore, a strategy for synthesis of ANFs is designed to achieve light weight, excellent thermal insulation performance and significantly improve sound absorption properties. This strategy combines cell pulverizing, pump-filtration molding, and directional freezing to ensure structural strength of the aerogel without the addition of cross-linking agents, and this process enables the ANFs to introduce in macro-pores while keeping nano-pores. The structure of multi-layered pores effectively reduces the reflectivity of incident acoustic energy and improves the sound absorption coefficient. The interconnected macro-pores and interlaced small pores of ANFs provide good sound absorption performance (sound absorption average (SAA) = 0.338), excellent flame retardant and thermal insulation properties (thermal conductivity = 0.0635 W (m*K)−1) with ultralight (density = 40.5 mg cm−3) in a thinner thickness (15 mm), which extend the potential of ANFs in areas of noise control and thermal insulation. In addition, the structure of multi-scaled pores can also be formed inside other aerogels by using the method of cell pulverization and filtration preparation, which can be helpful for improving their properties of thermal insulation and sound absorption.

Multifunctional amphibious superhydrophilic-oleophobic cellulose nanofiber aerogels for oil and water purification

Aerogels are of a popular choice for oil-water separation and water purification due to their attractive properties, such as lightweight, large surface area, and high porosity. Developing robust aerogels with multifunctional characteristics is highly desirable but remains challenging nowadays. Herein, we develop a facile one-pot condensation strategy for the fabrication of superhydrophilic-oleophobic (SHI-OP) composite aerogels using cellulose nanofibers (CNF), 3-glycidy-loxypropyl trimethoxysilane (GPTMS), polyethyleneimine (PEI) and fluorine-contained compound (FS-60). The resulted aerogels exhibit a directional lamellar structure with interconnected macropores, super-lightweight with high porosity of 98.30 % and low density of 0.0256 g·cm−3. Also, the aerogels are mechanically durable against repeated compression. Meanwhile, the amphibious SHI-OP feature of the composite aerogels in both air and water states enables them to not only absorb trace amount of water from contaminated oils, but also separate oil-water mixtures with separation efficiency of over 99 % and high permeation flux of over 9060 L/m2·h. Moreover, the aerogels also show excellent dye adsorption capability and reusability toward anionic dyes with a maximum adsorption capacity of 1245.68 mg/g. Such robust and multifunctional aerogels with special surface wettability provide good opportunity for liquid purification and dye-containing wastewater treatment.

Intravascular elimination of circulating tumor cells and cascaded embolization with multifunctional 3D tubular scaffolds.

The primary tumor ("root") and circulating tumor cells (CTCs; "seeds") are vital factors in tumor progression. However, current treatment strategies mainly focus on inhibiting the tumor while ignoring CTCs, resulting in tumor metastasis. Here, we design a multifunctional 3D scaffold with interconnected macropores, excellent photothermal ability and perfect bioaffinity as a blood vessel implantable device. When implanted upstream of the primary tumor, the scaffold intercepts CTCs fleeing back to the primary tumor and then forms "micro-thrombi" to block the supply of nutrients and oxygen to the tumor for embolization therapy. The scaffold implanted downstream of the tumor efficiently captures and photothermally kills the CTCs that escape from the tumor, thereby preventing metastasis. Experiments using rabbits demonstrated excellent biosafety of this scaffold with 86% of the CTC scavenging rate, 99% of the tumor inhibition rate and 100% of CTC killing efficiency. The multifunctional 3D scaffold synergistically inhibits the "root" and eliminates the "seeds" of the tumor, demonstrating its potential for localized cancer therapy with few side effects and high antitumor efficacy.

Three-dimensionally ordered macroporous ZSM-5 zeolite supported high-dispersed Ni2P: Highly active catalyst for quinoline hydrodenitrogenation

Zeolite catalysts have shown significant advantages in hydrogenation reactions due to their ordered pore structure and abundant acid sites. Common zeolites exhibit pore accessibility limited to microporous states, which restricts their application in diffusion-limited processes. In this study, a steam-seeding-assisted colloidal crystal template (SSAC) method was used to prepare ZSM-5 zeolite with a three-dimensionally ordered macroporous (3DOM) structure, which was then loaded with nickel phosphide for hydrodenitrogenation reactions. SEM and TEM characterization demonstrated that the prepared zeolite material possessed a highly ordered 3DOM structure with interconnected macropores. XRD, FT-IR, and BET analysis indicated that the macroporous zeolite material exhibited a typical MFI structure, mesoporous channels, and a higher specific surface area. The high external surface area facilitated the formation of uniformly sized Ni2P nanoparticles on the zeolite surface. The introduction of macroporous structures also leads to suitable Brönsted acid and Lewis acid sites in zeolite materials. The resultant Ni2P/3DOMZSM-5 catalyst exhibited higher reaction rate constants and TOF (10.87×10−2 μmolg−1s−1 and 1.5×10−3s−1, respectively) compared to other zeolite catalysts and commercial catalysts.

Coupling of reasonable micro-defect structure and multiple chemisorption sites for boosting the K+ storage capacity in dual-carbon potassium ion hybrid capacitors

Construction of hierarchical porous (meso‑microporous) carbonaceous anodes with reasonable-sized defects and rich active sites is important for enhancing K+ storage capacity. Here, we propose a strategy that can expand the microporous defects and synchronously introduce multiple chemisorption sites to synthesize phosphorus-nitrogen double-doped foamed porous carbon (PN-FPC). Interlaced and interconnected macropores in PN-FPC can effectively promote long-range mass transfer, while ultrathin carbon bubble walls with abundant meso‑micropores and chemisorption sites can maximize the utilization of active sites. Density-functional theory (DFT) calculations show that the P, N double-doped synergistically rational micro-defect structure significantly contributes to the reversible adsorption-desorption of K+. More importantly, the potassium-ion hybrid capacitors (PIHCs) composed of P, N double-doped activated porous carbon (PN-FAPC) as cathode and pre-activated PN-FPC as anode exhibited ultra-high energy density (155.6 Wh kg−1), power density (17,000 W kg−1), and ultra-long lifetime (90.9 % capacity retention after 10,000 cycles). This study not only provides new insights for the convenient synthesis of advanced carbonaceous anode materials, but also provides a deeper understanding for revealing the charge storage mechanism of PIHCs.

Hierarchical Nano-Electrocatalytic Reactor for High Performance Polysulfides Redox Flow Batteries.

The aqueous polysulfides is an important Earth-abundant and multielectron redox couple to construct high capacity density and low-cost aqueous redox flow batteries (RFB) ; nevertheless, the sluggish conversion and kinetic behavior of S2-/Sx2- result in a low power density output and poor active material utilizations. Herein, we present nanoconfined self-assembled ordered hierarchical porous Co and N codoped carbon (OHP-Co/NC) as an electrocatalytic reactor to enhance the mass transfer and redox activity of aqueous polysulfides. Finite element method simulation proves that the OHP-Co/NC with interconnected macropores and mesopores exhibits an enhanced mass transfer and delivers a larger redox electrolyte utilization of 50.1% compared to 23.3% of conventional Co/NC. Notably, the OHP-Co/NC obtained at 850 °C delivers the smallest redox peak potential difference (ΔE = 99 mV). Comparison studies of in operando Raman for aqueous polysulfides in the redox electrolyte and in situ electrochemical Raman on the single OHP-Co/NC particle for the adsorbed polysulfides were carried out. And it confirms that the OHP-Co/NC-850 catalyst has a strong adsorption of S42- and can retard the strong disproportionation and hydrolysis behavior of polysulfides on the electrocatalyst interface. Therefore, the polysulfide/ferrocyanide RFB with an OHP-Co/NC-850 based membrane-electrode assembly (MEA) exhibited a high power density of 110 mW cm-2, as well as a steady capacity retention over 99.7% in 300 cycles.

Hierarchical porosity design enables highly recyclable and efficient Au/TiO2 composite fibers for photodegradation of organic pollutants

Titanium dioxide (TiO2) nanomaterials are ideal for photocatalytic degradation of organic pollutants but remain infeasible for industrial and municipal wastewater treatment because they cannot simultaneously satisfy two essential criteria for practical application, i.e., high performance and good recyclability. Here, we design and create hierarchically porous TiO2 fibers by dual-polymer templating sol–gel electrospinning combined with precise control over crystallization. The produced fibers own unique interconnected macropores throughout the fiber body that enable significantly enhanced light absorption and unlimited mass transport, making them ideal hosts for anchoring plasmonic nanoparticles (NPs). The Au NP-coupled TiO2 fibers have photocatalytic efficiencies up to 6.6 times higher than plain TiO2 fibers, showing comparable ability as commercial P25 nanopowder in photodegrading methyl blue (MB) and achieving complete decomposition of methyl orange (MO) in 90 min while P25 degrades only 66% MO. Unlike P25 or anatase TiO2 nanopowders that non-reversibly disperse/aggregate in water, our composite fibers can be recollected through natural sedimentation, and their superior performance remains for at least six cycles. This work offers a practical and feasible design for high-performance recyclable photocatalysts for industrial-scale water treatment.

Bioactive Glasses-Based Nanozymes Composite Macroporous Cryogel with Antioxidative, Antibacterial, and Pro-Healing Properties for Diabetic Infected Wound Repair.

The treatment for diabetic ulcers still remains a big clinic challenge owing to the adverse repair microenvironment. Bioactive glasses (BGs) play an important role in the late stages of healing due to their ability to promote vascularization and collagen fiber deposition, but fail to improve infection and oxidative stress in the early stage.Therefore, it is critical to develop a material involved in regulating the whole healing phases. In this work, BGs-based nanozymes (MnO2 @PDA-BGs) with antioxidation, antibacterial and pro-healing abilities are synthesized by the redox deposition of MnO2 on mesoporous BGs. Afterward, cryogel with the interconnected macropore structure is fabricated by the polymerization of methacrylate anhydride gelatin (GelMA) at -20 °C. MnO2 @PDA-BGs are loaded into the cryogel to obtain nanocomposite cryogel (MnO2 @PDA-BGs/Gel) with multiple enzymes-like- activities to eliminate reactive oxygen species (ROS). Besides, MnO2 @PDA-BGs/Gel has intensive peroxidase-like activity under acidic condition and near infrared photothermal responsiveness to achieve excellent antibacterial performance. Cells experiments demonstrate that MnO2 @PDA-BGs/Gel recruits L929s and promotes their proliferation. Furthermore, MnO2 @PDA-BGs/Gel eliminates intracellular overexpressed ROSand maintains the viability of L929s. Animal experiments confirm that MnO2 @PDA-BGs/Gel promotes wound healing and avoided scarring by killing bacteria, reversing inflammation, promoting vascularization, and improving the deposition of collagen III.

Preparation of a poly(2-acrylamido-2-methyl-1-propanesulfonic acid)-grafted polyurethane sponge using atmospheric pressure plasma-induced graft polymerization and its catalytic properties for the acetalization of glycerol to solketal

Poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (poly(AMPS)) bearing a sulfo group was grafted onto a polyurethane sponge by an argon atmospheric-pressure plasma treatment and subsequent graft polymerization. Thus, a novel poly(AMPS)-grafted polyurethane sponge was developed as a heterogeneous acid catalyst for organic synthesis. The average grafting amount was 0.0277 kg-polymer/kg-substrate. The surface properties of the polyurethane sponge changed considerably, from hydrophobic to hydrophilic. The poly(AMPS)-grafted sponge successfully catalyzed the acetalization of glycerol with acetone to produce the desired solketal. The reaction rate was analyzed using a pseudo-first-order kinetic model, and the apparent reaction rate constant, k, and apparent activation energy were determined. The k value for the poly(AMPS)-grafted sponge was one order of magnitude larger than that for the EDGA-co-AMPS gel (EDGA: ethoxy diethyleneglycol acrylate). The poly(AMPS)-grafted sponge with interconnected submillimeter-sized macropores and high porosity (98%) exhibits excellent diffusional permeability. In addition, the structural features of the sponge provide advantages such as a negligible pressure drop and easy handling during the reaction process. This study provides a strategy for the use of polymers grafted onto sponges as catalysts.

Experimental Investigation on the Impact of Coal Fines Migration on Pores and Permeability of Cataclastic Coal.

During the production process of coalbed methane, the generation and migration of coal fines can obstruct fractures in coal reservoirs and reduce their permeability. In order to investigate the effects of coal fines migration on the porosity and permeability of coal reservoirs, we conducted core water flooding experiments, low-field nuclear magnetic resonance (NMR), and low-temperature N2 adsorption experiments to study the variations in porosity and permeability of cataclastic coal during coal fines migration and the impact of coal fines migration on porosity and permeability. The experimental results reveal that the initial porosity ratio of cataclastic coal exhibits the characteristics of micropore > macropore > transitional pore > mesopore, with the pore types being predominantly fissured. The porosity of pores larger than 1000 nm and those larger than 10,000 nm exhibit consistent trends before and after water flooding, indicating that the blockage or unblocking of pores with radius larger than 10,000 nm by coal fines can also cause blockage or unblocking of some interconnected macropore. The early stage of flooding is the main period for coal fines migration and production in cataclastic coal, during which the mass concentration of coal fines production is higher and some macropores and fractures become blocked, resulting in a larger decrease in porosity. The higher the initial permeability of cataclastic coal samples with a larger end-face fracture density, the more similar the variations in porosity and permeability of pores larger than 10,000 nm during the flooding experiment, indicating that coal fines mainly block interconnected pores and fractures with radius larger than 10,000 nm through migration, thereby reducing permeability. This study provides a theoretical basis for the efficient production of coalbed methane.

Batch and fixed bed adsorption of methylene blue onto foamed metakaolin-based geopolymer: A preliminary investigation

Synthetic dyes, represent a serious hazard for the aquatic environments and groundwater system. The removal of dyes by the adsorption process avoids the production of sludge and secondary toxic compounds and offers high efficiency and very short operational times. In the present work, cationic Methylene Blue (MB) dye was used as a model pollutant to investigate the adsorption properties of a foamed geopolymer. The adsorbent has an apparent density of 0,75 g/cm3. It is characterized by a complex system of spherical and interconnected macro-pores with a mesopore volume of 0.143 cm³ /g that favors the mass transport and a pHpzc equal to 8.2. Batch and fixed granular bed column tests were carried out. The maximum MB uptake, in batch experiments, was 40.0 mg/g. Removal efficiency was around 95% up to a MB concentration of 25 mg/L. The pseudo second order kinetic model and Langmuir isotherm model better describe MB adsorption onto geopolymer. Fixed granular bed column tests were carried out by varying the initial dye concentration at a constant flow rate and bed height. Results are better fitted by Yoon and Nelson model. The obtained results demonstrate that foamed geopolymers are good candidates for the removing MB from aqueous solutions.

Enhanced invertase binding from baker's yeast via cryogels included boronic acids.

Invertase, an industrially significant glycoenzyme, was purified from baker's yeast using poly (2-Hydroxyethyl methacrylate) [PHema-Pba] cryogels functionalized with boronic acid. At subzero temperatures, PHema-Pba cryogels were synthesized and characterized using swelling tests, scanning electron microscopy, and Fourier-transform infrared spectroscopy. The surface area of the PHema-Pba cryogels was 14 m2/g with a swelling ratio of 88.3% and macroporosity of 72%. The interconnected macropores of PHema-Pba cryogels were shown via scanning electron microscopy. Invertase binding capacity of PHema-Pba cryogel was evaluated by binding studies in different pH, temperature, and interaction time conditions and the maximum Invertase binding of PHema-Pba cryogel was found as 15.2mg/g. and 23.7 fold Invertase purification was achieved from baker's yeast using PHema-Pba cryogels. The results show that PHema-Pba cryogels have high Invertase binding capacity and may be used as an alternative method for enzyme purification via boronate affinity systems.

High-density triple-phase contact points for enhanced photocatalytic CO2 reduction to methanol

The efficiency of photocatalytic CO2 reduction reaction (PCRR) is restricted by the low solubility and mobility of CO2 in water, poor CO2 adsorption capacity of catalyst, and competition with hydrogen evolution reaction (HER). Recently, hydrophobic modification of the catalyst surface has been proposed as a potential solution to induce the formation of triple-phase contact points (TPCPs) of CO2 (gas phase), H2O (liquid phase), and catalysts (solid phase) near the surface of the catalyst, enabling direct delivery of highly concentrated CO2 molecules to the active reaction sites, resulting in higher CO2 and lower H+ surface concentrations. The TPCPs thus act as the ideal reaction points with enhanced PCRR and suppressed HER. However, the initial synthesis of triple-phase photocatalysts tends to possess a lower bulk density of TPCPs due to the simple structure leading to limited active points and CO2 adsorption sites. Here, based on constructing a hydrophobic hierarchical porous TiO2 (o-HPT) with interconnected macropores and mesopores structure, we have significantly increased the density of TPCPs in a unit volume of the photocatalyst. Compared with hydrophobic macroporous TiO2 (o-MacPT) or mesoporous TiO2 (o-MesPT), the o-HPT with increased TPCP density leads to enhanced photoactivity, enabling a high methanol production rate with 1111.5 µmol g−1 h−1 from PCRR. These results emphasize the significance of high-density TPCPs design and propose a potential path for developing efficient PCRR systems.

Coupling Uniform Pore Size And Multi‑Chemisorption Sites: Hierarchically Ordered Porous Carbon For Ultra‐Fast And Large Zinc Ion Storage

AbstractConstructing hierarchically ordered macro/meso−microporous structures of carbonaceous cathode with matchable pore size and adequate active sites is significant toward large Zn2+ storage, but remains a formidable challenge. Herein, a new perspective is reported for synthesizing phosphorus and nitrogen dual‐doped hierarchical ordered porous carbon (PN‐HOPC) by eliminating the micropore confinement effect and synchronously introducing multi‐chemisorption sites. The interconnected macropore can effectively facilitate long‐distance mass transfer, and meso−microporous wall can promote accessibility of active sites. Density functional theory (DFT) calculations identify that the P and N co‐doping markedly contributes to the reversible adsorption/desorption of zinc ions and protons. Consequently, the optimized PN‐HOPC exhibits outstanding Zn2+ storage capabilities in terms of high capacity (211.9 mAh g−1), superb energy density (169.5 Wh kg−1), and ultralong lifespan (99.3% retention after 60 000 cycles). Systematic ex situ measurements integrating with in situ Raman spectroscopy and electrochemical quartz crystal microbalance (EQCM) techniques elucidate that the superior electrochemical capability is ascribed to the synergistic effect of the Zn2+, H+, and SO42− co‐adsorption mechanism, as well as invertible chemical adsorption. This study not only provides new insights to design advanced carbon materials toward practical applications but also sheds lights on a deeper understanding of charge storage mechanism for zinc‐ion capacitors (ZICs).

Gelatin-based spongy and compressive resistant cryogels with shape recovery ability as ideal scaffolds to support cell adhesion for tissue regeneration

Methacryloyl gelatin (GelMA) was blended with dextran methacrylate (DexMA) to produce polymer networks with interconnected macropores via cryostructuring and radical crosslinking of the polymers at subzero temperatures. The experimental set-up was optimized to allow the formation of monolithic networks characterized by highly uniform structure with interconnected macropores. The total polymers mass, the amount of the gel-forming reagents and particularly the rheological properties of GelMA resulted the most critical factors for the fabrication of homogeneous and not collapsed scaffolds. Indeed, only the use of GelMA with very low gelation temperature resulted in the formation of uniform monolithic cryogels. However, blending with DexMA produced general worsening of the mechanical properties of the scaffolds, due to DexMA interference with secondary structuring of GelMA during the cryogelation process. DexMA also had negative effect on the ability of the cryogel to support growth and proliferation of HaCat cells, bringing to slower cell adhesion to the scaffold.