Microenvironment modulation of interpenetrating-type hierarchical porous foam carbon by mild-homogeneous activation for H2 storage and CO2 capture under ambient pressure.

Currently, carbon-based porous materials for hydrogen (H2) storage and carbon dioxide (CO2) capture are mostly applied at higher pressures (30-300 bar). However, applications for H2 storage and CO2 capture under ambient pressure conditions are significant for the development of portable, household, and miniaturized H2 energy technologies. This demands a higher standard for the interface microenvironment of adsorbents. Derived from polyurethane foams (PUFs) solid waste, the hierarchical porous foam carbon with interpenetrating-type pore structures exhibits high specific surface area (SBET = 1753 m2/g), abundant oxygen and nitrogen functional groups, and a hierarchical nanopore structure (VUltra = 0.232 cm3/g, VMicro = 0.628 cm3/g and VMeso = 0.186 cm3/g) through the mild-homogeneous sonication-assisted activation process. Under the limited adsorption of pore interface microenvironment composed by hierarchical nanopore structure and dipole-induced interaction (H(Ⅱ)-H(Ⅰ)···N/O and O(Ⅱ) = C(Ⅰ) = O(Ⅱ)···N/O), it exhibits an excellent H2 storage density (2.92 wt% at 77 K, 1 bar) and CO2 capture capacity (5.28 mmol/g at 298 K, 1 bar). This research approach can serve as a reference for the dual-functional design of porous foam carbon, and promote the development of adsorption materials for CO2 capture and energy gas storage under ambient conditions.

Photothermal Conversion of the Oleophilic PVDF/Ti3C2Tx Porous Foam Enables Non-Aqueous Liquid System Applicable Actuator.

Various physical and chemical reaction processes occur in non-aqueous liquid systems, particularly in oil phase systems. Therefore, achieving efficient, accurate, controllable, and cost-effective movement and transfer of substances in the oil phase is crucial. Liquid-phase photothermal actuators (LPAs) are commonly used for material transport in liquid-phase systems due to their remote operability and precise control. However, existing LPAs typically rely on materials like hydrogels and flexible polymers, commonly unsuitable for non-aqueous liquids. Herein, a 3D porous poly(vinylidene fluoride) (PVDF)/Ti3C2Tx actuator is developed using a solvent displacement method. It demonstrates directional movement and controlled material transport in non-aqueous liquid systems. When subject to infrared light irradiation (2.0 W cm-2), the actuator achieves motion velocities of 7.3 and 6 mm s-1 vertically and horizontally, respectively. The actuator's controllable motion capability is primarily attributed to the foam's oil-wettable properties, 3D porous oil transport network, and the excellent photothermal conversion performance of Ti3C2Tx, facilitating thermal diffusion and the Marangoni effect. Apart from multidimensional directions, the actuator enables material delivery and obstacle avoidance by transporting and releasing target objects to a predetermined position. Hence, the developed controllable actuator offers a viable solution for effective motion control and material handling in non-aqueous liquid environments.

All-in-one self-floating porous foams as robust heat-blocking layers for efficient photothermal conversion and solar desalination.

Solar-driven interfacial evaporation is a highly efficient and ecofriendly technology for producing freshwater. Herein, self-floating plasmon Ag/black TiO2/carbon porous layered foams (Ag-BTCFs) were demonstrated as efficient solar-thermal convectors using freeze-drying cast-molding and high-temperature surface hydrogenation strategies. This all-in-one three-dimensional (3D) cross-linked self-floating porous layered foam material with full-spectrum absorption can fully harvest sunlight (∼95.45%) and effectively block heat transfer to its sublayer. The synergy of sufficient utilization of absorbed ultraviolet radiation by black TiO2 (b-TiO2), visible light absorption by Ag nanoparticles (Ag NPs) via localized surface plasmon resonance, and near-infrared absorption by layered-amorphous carbon can achieve full-solar-spectrum absorption to concentrate thermal energy. In addition to their synergistic effect, they are conducive to the relaxation of hot electrons when utilizing photogenerated holes to degrade pollutants in domestic wastewater. The steam generation efficiency of Ag-BTCFs is up to 1.79 kg m-2h-1 due to their solar energy conversion efficiency of 81.74% under 1 sun irradiation, which is five times higher than the evaporation rate of pure water. Notably, the material's efficient ion removal rate of 99.80% for solar desalination indicates its high potential for various applications. This strategy provides new insights for fabricating recyclable heat-blocking layer systems against thermal loss to enhance solar steam generation.

Preparation of Bio-Based Foams with a Uniform Pore Structure by Nanocellulose/Nisin/Waterborne-Polyurethane-Stabilized Pickering Emulsion.

Bio-based porous materials can reduce energy consumption and environmental impact, and they have a possible application as packaging materials. In this study, a bio-based porous foam was prepared by using a Pickering emulsion as a template. Nisin and waterborne polyurethane (WPU) were used for physical modification of 2,2,6,6-tetramethyl piperidine-1-oxyl-oxidized cellulose nanocrystals (TOCNC). The obtained composite particles were applied as stabilizers for acrylated epoxidized soybean oil (AESO) Pickering emulsion. The stability of the emulsion was characterized by determination of the rheological properties and microscopic morphology of the emulsion. The emulsion stabilized by composite particles showed better stability compared to case when TOCNC were used. The porous foam was obtained by heating a composite-particles-stabilized Pickering emulsion at 90 °C for 2 h. SEM (scanning electron microscopy) images showed that the prepared foam had uniformly distributed pores. In addition, the thermal conductivity of the foam was 0.33 W/m·k, which was a significant decrease compared to the 3.92 W/m·k of the TOCNC foam. The introduction of nisin and WPU can reduce the thermal conductivity of the foam, and the physically modified, TOCNC-stabilized Pickering emulsion provides an effective means to preparing bio-based porous materials.

Highly Stretchable Composite Foams via Sustainable Utilization of Waste Tire Rubbers for Temperature-Dependent Electromagnetic Wave Absorption.

Recently, the sustainable utilization of waste resources has become a low-cost and effective strategy to design high-performance functional materials to solve the increasingly serious environmental pollution problem. Herein, the flexible and highly stretchable polyurethane (PU) composite foams assisted by one-dimensional carbon nanotubes (CNTs) and zero-dimensional Fe3O4 were fabricated using waste tire rubbers (WTRs) as reinforcements during a simple self-foaming process. The collaborative introduction of conductive CNTs, magnetic Fe3O4, and WTRs with three-dimensional cross-linked structures enabled the construction of an efficient electronic transmission path and heterointerfaces inside the composite foam. The resulting composite foam possessed a desired minimum reflection loss (RLmin) of −47.43 dB, and also exhibited superior mechanical properties with a tensile strength of >3 MPa and multiple tensile deformation recovery abilities. In addition, increasing the temperature could significantly improve the electromagnetic wave absorption performance of the composite foam. This comprehensive composite foam derived from WTRs has shown a promising development potential for using waste materials to relieve electromagnetic pollution.

Removal of both anionic and cationic dyes from wastewater using pH-responsive adsorbents of L-lysine molecular-grafted cellulose porous foams.

High adsorption efficiency, active to both anionic and cationic dyes and simple desorption are three main challenges of the existed adsorbents for decolorization of the dye-contained wastewaters. Porous foams based on L-lysine (Lys) molecular-grafted cellulose were firstly designed and fabricated to overcome those challenges. Cellulose were grafted with Lys in 1-butyl-3-methylimidazolium chloride (BMIMCl) via a chemical connection resulted from glycidyl methacrylate (GMA). The synthesized cellulose derivative (Cell-g-PGMA-Lys) was regenerated in the morphology of foam by non-solvent induced phase inversion from the BMIMCl-based solutions. The presence of Lys moieties and porous structure of Cell-g-PGMA-Lys were confirmed with a series of instrumental analysis. Both anionic reactive brilliant red X-3B (RBR X-3B) and cationic methylene blue (MB) were effectively adsorbed on and desorbed from Cell-g-PGMA-Lys by adjusting the solution pH value. Cell-g-PGMA-Lys had higher adsorption capacities than most of the reported adsorbents and was easy to separate from the decolorized water. It could be reused many times with little reduction of the adsorption capacity, which remained 86.9% and 92.5% for RBR X-3B and MB respectively after six adsorption-desorption cycles. The isothermal and kinetic adsorption proved that dyes were adsorbed single-layered on Cell-g-PGMA-Lys depending upon the electrostatic interaction between adsorbent and adsorbate.

Tannin foam immobilized with ferric ions for efficient removal of ciprofloxacin at low concentrations.

The presence of ciprofloxacin (CIP) in natural water may cause potential threats to the environment. Adsorption is a convenient and efficient method to remove CIP from aqueous solution. Bayberry tannin (BT), a natural polyphenol, has been utilized in the synthesis of tannin foam (TF) due to its abundant polyphenolic hydroxyls to chelate with metal ions. The obtained TF was subsequently immobilized with Fe3+ via a facile chelative adsorption to fabricate functional tannin foam (TF-Fe), which was highly porous, with a porosity of 78.93%. The Fe species in the TF-Fe featured good dispersity, which were active for chelative adsorption of CIP. The adsorption of CIP on the TF-Fe was a pH-dependent process. At the optimized pH of 7.0, the TF-Fe provided the adsorption capacity of 91.8 mg g-1. When applied in removal of CIP at the low concentration of 2.0 µg mL-1, a high removal efficiency of 96.60% was still obtained, which was superior to commercial activated carbon (28.78%). The adsorption kinetics were well fitted by the pseudo-second-order rate model while the adsorption isotherms were well described by the Langmuir model. The TF-Fe was capable of recycling, which still maintained a high removal efficiency of 92.25% in the 5th cycle.

Oxidized-Polydopamine-Coated Graphene Anodes and N,P Codoped Porous Foam Structure Activated Carbon Cathodes for High-Energy-Density Lithium-Ion Capacitors.

As a tradeoff between supercapacitors and batteries, lithium-ion capacitors (LICs) are designed to deliver high energy density, high power density, and long cycling stability. Owing to the different energy storage mechanisms of capacitor-type cathodes and battery-type anodes, engineering and fabricating LICs with excellent energy density and power density remains a challenge. Herein, to alleviate the mismatch between the anode and cathode, we ingeniously designed a graphene with oxidized-polydopamine coating (LG@DA1) and N,P codoped porous foam structure activated carbon (CPC750) as the battery-type anode and capacitor-type cathode, respectively. Using oxidized-polydopamine to stabilize the structure of graphene, increase layer spacing, and modify the surface chemical property, the LG@DA1 anode delivers a maximum capacity of 1100 mAh g-1 as well as good cycling stability. With N,P codoping and a porous foam structure, the CPC750 cathode exhibits a large effective specific surface area and a high specific capacity of 87.5 mAh g-1. In specific, the present LG@DA1//CPC750 LIC showcases a high energy density of 170.6 Wh kg-1 and superior capacity retention of 93.5% after 2000 cycles. The success of the present LIC can be attributed to the structural stability design, surface chemistry regulation, and enhanced utilization of effective active sites of the anode and cathode; thus, this strategy can be applied to improve the performance of LICs.

Sequential Synthesis Methodology Yielding Well-Defined Porous 75%SrTiO3/25%NiFe2O4 Nanocomposite.

In this research, we reported on the formation of highly porous foam SrTiO3/NiFe2O4 (100-xSTO/xNFO) heterostructure by joint solid-state and sol-gel auto-combustion techniques. The colloidal assembly process is discussed based on the weight ratio x (x = 0, 25, 50, 75, and 100 wt %) of NiFe2O4 in the 100-xSTO/xNFO system. We proposed a mechanism describing the highly porous framework formation involving the self-assembly of SrTiO3 due to the gelation process of the nickel ferrite. We used a series of spectrophotometric techniques, including powder X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), N2 adsorption isotherms method, UV-visible diffuse reflectance spectra (UV-Vis DRS), vibrating sample magnetometer (VSM), and dielectric measurements, to investigate the structural, morphological, optical, magnetic, and dielectric properties of the synthesized samples. As revealed by FE-SEM analysis and textural characteristics, SrTiO3-NiFe2O4 nanocomposite self-assembled into a porous foam with an internally well-defined porous structure. HRTEM characterization certifies the distinctive crystalline phases obtained and reveals that SrTiO3 and NiFe2O4 nanoparticles were closely connected. The specific magnetization, coercivity, and permittivity values are higher in the 75STO/25NFO heterostructure and do not decrease proportionally to the amount of non-magnetic SrTiO3 present in the composition of samples.

Ultralight Biomass Porous Foam with Aligned Hierarchical Channels as Salt-Resistant Solar Steam Generators.

The creation of solar steam generators with both high energy conversion efficiency and desired salt-resistant performance is essential for practical desalination. Herein, we report for the first time the fabrication of polypyrrole-coated biomass porous foam as efficient solar steam generators. The as-prepared foams possess a low thermal conductivity of 0.022 W M-1 K-1 for alkali-treated corn straw (CSA) and 0.027 W M-1 K-1 for both microwave- and alkali-treated corn straw (CSMA). Based on their high light absorption (95-100%), superhydrophilic wettability, excellent thermal insulation, and unique aligned channels, the foams show excellent energy conversion efficiency of 89.74, 91.08, and 91.54% for the polypyrrole-coated CSA (P-CSA) and 96.8, 97.05, and 98.32% for the polypyrrole coated CSMA (P-CSMA) at light intensities of 1, 2, and 3 kW m-2, respectively. Importantly, thanks to their aligned hierarchical channels, our generators show extraordinary salt-resistant performance, e.g., the energy conversion efficiencies of P-CSA and P-CSMA were measured to be 62.30 and 94.7% in 20 wt % NaCl at 1 kW m-2 irradiation, respectively. Furthermore, no obvious salt accumulation was observed after 30 d of continuous operation at real sunlight irradiation, implying an outstanding long-term stability for practical solar steam generation.

Flexible 3D Porous MXene Foam for High-Performance Lithium-Ion Batteries.

2D transition-metal carbides and nitrides, named MXenes, are promising materials for energy storage, but suffer from aggregation and restacking of the 2D nanosheets, which limits their electrochemical performance. In order to overcome this problem and realize the full potential of MXene nanosheets, a 3D MXene foam with developed porous structure is established via a simple sulfur-template method, which is freestanding, flexible, and highly conductive, and can be directly used as the electrode in lithium-ion batteries. The 3D porous architecture of the MXene foam offers massive active sites to enhance the lithium storage capacity. Moreover, its foam structure facilitates electrolyte infiltration for fast Li+ transfer. As a result, this flexible 3D porous MXene foam exhibits significantly enhanced capacity of 455.5 mAh g-1 at 50 mA g-1 , excellent rate performance (101 mAh g-1 at 18 A g-1 ), and superior ultralong-term cycle stability (220 mAh g-1 at 1 A g-1 after 3500 cycles). This work not only demonstrates the great superiority of the 3D porous MXene foam but also proposes the sulfur-template method for controllable constructing of the 3D foam from 2D nanosheets at a relatively low temperature.

Piezoelectric Material-Polymer Composite Porous Foam for Efficient Dye Degradation via the Piezo-Catalytic Effect.

Piezoelectric nanomaterials have been utilized to realize effective charge separation for degrading organic pollutants in water under the action of mechanical vibrations. However, in particulate form, the nanostructured piezoelectric catalysts can flow into the aqueous pollutant and limit its recyclability and reuse. Here, we report a new method of using a barium titanate (BaTiO3, BTO)-polydimethylsiloxane composite porous foam catalyst to address the challenge of secondary pollution and reusable limits. Piezo-catalytic dye degradation activity of the porous foam can degrade a Rhodamine B (RhB) dye solution by ∼94%, and the composite material exhibits excellent stability after repeated decomposition of 12 cycles. It is suggested that under ultrasonic vibrations, the piezoelectric BTO materials create separated electron-hole pairs that react with hydroxyl ions and oxygen molecules to generate superoxide (•O2-) and hydroxyl (•OH) radicals for organic dye degradation. The degradation efficiency of RhB is associated with the piezoelectric constant, the specific surface area, and the shape of the material.

Fabricating carbon-nanotubes-based porous foam for superoxide electrochemical sensing through one-step hydrothermal process induced by phytic acid.

The detection of superoxide anions (O2•-) is widely considered as a potential way for cancer diagnosis and the development of enzyme-mimic catalysts is the main challenge in the establishment of electrochemical sensors for O2•- sensing in real samples. Here we present a novel enzyme- and metal-free electrochemical catalyst for superoxide (O2•-) sensing based on the widely-used carbon nanotubes (CNT). Through a one-step hydrothermal process induced by phytic acid (PA), CNT-based porous foam (PACNTF) was successfully obtained. Characterizations demonstrated the enhanced defect and disorder degree of PACNTF after PA treatment, which leaded to the increased active sites of PACNTF for electron transfer and the adhesion of O2•- during the electrochemical process. As a result, the PACNTF presented higher conductivity and larger current response toward O2•- sensing when compared with CNT precursor and CNTF without PA treatment. The sensitivity of PACNTF/SPCE was calculated to be 1230 µA cm-2 mM-1 in the linear range of 0-193.6 µM (R2 = 0.965) and 373 µA cm-2 mM-1 in the linear range of 193.6-1153.6 µM (R2 = 0.995) with a limit of detection of 0.16 µM (S/N = 3). Further, the PACNTF/SPCE presented fast response toward cell-released O2•- stimulated by Zymosan A. The above results indicated that the fabricated sensor holds potential usage in biological samples.

Light-Triggered CO2 Breathing Foam via Nonsurfactant High Internal Phase Emulsion.

Solid materials for CO2 capture and storage have attracted enormous attention for gaseous separation, environmental protection, and climate governance. However, their preparation and recovery meet the problems of high energy and financial cost. Herein, a controllable CO2 capture and storage process is accomplished in an emulsion-templated polymer foam, in which CO2 is breathed-in under dark and breathed-out under light illumination. Such a process is likely to become a relay of natural CO2 capture by plants that on the contrary breathe out CO2 at night. Recyclable CO2 capture at room temperature and release under light irradiation guarantee its convenient and cost-effective regeneration in industry. Furthermore, CO2 mixed with CH4 is successfully separated through this reversible breathing in and out system, which offers great promise for CO2 enrichment and practical methane purification.

Light and Strong Hierarchical Porous SiC Foam for Efficient Electromagnetic Interference Shielding and Thermal Insulation at Elevated Temperatures.

A novel light but strong SiC foam with hierarchical porous architecture was fabricated by using dough as raw material via carbonization followed by carbothermal reduction with silicon source. A significant synergistic effect is achieved by embedding meso- and nanopores in a microsized porous skeleton, which endows the SiC foam with high-performance electromagnetic interference (EMI) shielding, thermal insulation, and mechanical properties. The microsized skeleton withstands high stress. The meso- and nanosized pores enhance multiple reflection of the incident electromagnetic waves and elongate the path of heat transfer. For the hierarchical porous SiC foam with 72.8% porosity, EMI shielding can be higher than 20 dB, and specific EMI effectiveness exceeds 24.8 dB·cm3·g-1 at a frequency of 11 GHz at 25-600 °C, which is 3 times higher than that of dense SiC ceramic. The thermal conductivity reaches as low as 0.02 W·m-1·K-1, which is comparable to that of aerogel. The compressive strength is as high as 9.8 MPa. Given the chemical and high-temperature stability of SiC, the fabricated SiC foam is a promising candidate for modern aircraft and automobile applications.

Well-dispersed Pt cubes on porous Cu foam: high-performance catalysts for the electrochemical oxidation of glucose in neutral media.

The investigation of highly efficient catalysts for the electrochemical oxidation of glucose is the most critical challenge to commercialize nonenzymatic glucose sensors, which display a few attractive superiorities including the sufficient stability of their properties and the desired reproducibility of results over enzyme electrodes. Herein we propose a new and very promising catalyst: Pt cubes well-dispersed on the porous Cu foam, for the the electrochemical oxidation reaction of glucose in neutral media. The catalyst is fabricated in situ on a homemade screen-printed carbon electrode (SPCE) substrate through initially synthesizing the three-dimensional (3D) porous Cu foam using a hydrogen evolution assisted electrodeposition strategy, followed by electrochemically reducing the platinic precursor simply and conveniently. Field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) proofs demonstrate that Pt cubes, with an average size (the distance of opposite faces) of 185.1 nm, highly dispersed on the macro/nanopore integrated Cu foam support can be reproducibly obtained. The results of electrochemical tests indicate that the cubic Pt-based catalyst exhibits significant enhancement on the catalytic activity towards the electrooxidation of glucose in the presence of chloride ions, providing a specific activity 6.7 times and a mass activity 5.3 times those of commercial Pt/C catalysts at -0.4 V (vs. Ag/AgCl). In addition, the proposed catalyst shows excellent stability of performance, with only a 2.8% loss of electrocatalytic activity after 100 repetitive measurements.