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The polyacrylic acid/tungsten oxide (PAA/WO3) composite films with good electrochromic properties have been prepared by a layer-by-layer method. The porous PAA layers were used as a template for the deposition of WO3, and finally, the composite film showed a network structure with high porosity. The electrochromic performance of the PAA/WO3 composite film was investigated by means of cyclic voltammogram (CV), chronoamperometry (CA), and transmittance measurements. The PAA/WO3 film also exhibited a remarkable electrochromism ability with the reversible color change from transparent colorless to dark blue and the transmittance change from 83% to 24% at 620 nm. This research provided a cost-effective approach for the preparation of PAA/WO3 composite films with controllable microstructure and good electrochromic property.

Hydrogen is regarded as one of the most promising energy sources of the future, due to its low-cost, zero-pollution, and high-heat value. Nevertheless, traditional methods of storing hydrogen are commonly accompanied by the risk of leaks and explosions, so how to store and transport hydrogen safely and efficiently is a critical issue that needs to be addressed. Solid-state hydrogen storage is the most attractive way to store hydrogen in nanomaterials by chemical or physical adsorption, which has the advantages of high energy density and good safety. Here, a rational Ni–Zn bimetallic MOF has been constructed by a straightforward synthetic technique, in which the Zn atom was partially replaced by the Ni atom. The micropore rate of the Ni–Zn bimetallic MOFs is higher than that of ZIF-8. In addition, the presence of Ni provides more unsaturated metal sites and strengthens the bonding between hydrogen molecules and Ni, effectively improving the hydrogen storage capacity of Ni–Zn bimetallic MOFs. The experimental results show that the hydrogen adsorption capacity of Ni–Zn bimetallic MOFs can reach 1.35 wt% at 77 K and 1 bar. [ABSTRACT FROM AUTHOR]

One of the most promising methods for capturing carbon dioxide (CO2) is solid physical adsorption, which is an efficient and simple technique. The key to effective CO2 capture is the development of high-performance solid adsorbents with excellent CO2 adsorption capacity, CO2/N2 selectivity, and rapid adsorption/desorption kinetics. In this paper, a Mg-MOF-74/sodium alginate composite aerogel was prepared by loading Mg-MOF-74 on sodium alginate sheets followed by directional freeze-drying. The composite aerogel exhibited a hierarchical porous structure, in which sodium alginate provided an open mesoporous/macroporous structure that promoted diffusion and contact with the active center of CO2. The Mg-MOF-74 micropores/mesopores promoted the strong interaction between CO2 and the adsorbent in the micropore and rapid mass transfer of CO2 to the adsorbent through the mesopores. The experimental data showed that MSA-6 achieved CO2 adsorption of 2.461 mmol·g–1 at 298 K. Furthermore, the CO2/N2 adsorption selectivity of MSA-6 reached 35.108, indicating its strong CO2 selective adsorption potential. [ABSTRACT FROM AUTHOR]

Rapid and safe disinfection and exudate management are two major challenges in infected wound care. Therefore, in this work, we developed a novel wound dressing via encapsulating ZIF-8-derived carbon nanoparticles in a hydrophilic nanofiber sponge to address severe wound infection and heavy exudate problems. The dressing can effectively kill bacteria through chemo-photothermal synergistic therapy. Meanwhile, the hydrophilic nanofiber sponge can quickly absorb wound exudate around the wound and accelerate the evaporation rate of liquid through the photothermal effect and its own structure; therefore, it is possible to remove excess liquid and regulate its wetness. In this way, it prevents the problem of wound overhydration often caused by hydrophilic dressings. In our experiment, the dressing showed good antibacterial performance and biocompatibility in vitro and could effectively control wound infection, absorb wound exudate and promote skin wound healing in vivo. Its good therapeutic effect is not only due to effective infection control and wound exudate management, but also because the structure of nanofibers similar to an extracellular matrix provides basic physical support and structural signals conducive to skin tissue regeneration. [ABSTRACT FROM AUTHOR]

Constructing heterostructure in nanomaterials is a scientific and efficient method to optimize the electrochemical properties of supercapacitors. Carbon aerogels (CAs) can enhance electrical conductivity and ion diffusion because of their three-dimensional porous structure, which is useful for fabricating electrodes. The moderate nanoheterostructures in aerogel nanomaterials have made great contributions to the optimization of application performance. Herein, a simple method for constructing the MnO2 nanoparticle/CA (MnO2/CA) heterostructure is proposed. The MnO2/CA heterostructure exhibits outstanding electrochemical capability in a three-electrode system, with a specific capacitance of 384 F/g, higher than 201 F/g of the CA, at a current density of 0.5 A/g. When MnO2/CA is used as a symmetric supercapacitor, it also exhibits a high energy density and power density, with the highest energy density of 33.78 Wh/kg. The prepared MnO2/CA shows improved performance for synergies in providing a high specific capacity and long cycle life. [ABSTRACT FROM AUTHOR]

The cost of CO2 separation and energy consumption can be decreased through the use of CO2 adsorption. Due to the electron-rich heteroatoms in its network, polyimide (PI) has a remarkable affinity for CO2. Polyethylene glycol (PEG) can increase the layer spacing of polymers, so as to change the mass transfer of CO2 in it. Furthermore, the ether bond (-O-) in PEG has good affinity for CO2. In this study, PEG-1000 was introduced into PI aerogel by mild sol-gel method at low temperature, and freeze-drying was used to produce PI/PEG composite aerogels with directional pore structure. The effect of PEG-1000 content and directional pore structure of the PI/PEG composite aerogels on CO2 adsorption performance were further studied. The L-PI/PEG-4 composite aerogel, which contains 4 g PEG and is directionally frozen in liquid nitrogen, has a CO2 adsorption capacity of 16.76 cm3/g at 25°C and 1 bar. L-PI/PEG-4 aerogel also exhibits high CO2/N2 selectivity and adsorption cycle stability. [ABSTRACT FROM AUTHOR]

High CO2 concentration in atmosphere causes serious environmental issues, and carbon capture and storage technologies have attracted attention as a means to reduce the atmospheric CO2 concentration. Metal-organic frameworks (MOFs) can potentially be used for CO2 adsorption, but their poor stability and microporosity limit their applications. Herein, a novel strategy was proposed to combine a cellulose aerogel and hierarchically-porous MOFs (HP-MOFs) with larger pores. According to this strategy, a series of microcrystalline cellulose/HP-UIO-66-NH2 hybrid aerogels (MC-HUN-X) was constructed by adding a modulator (monocarboxylic acid, MA), followed by the in-situ growth of HP-UIO-66-NH2 on a cellulose aerogel. By adjusting the chain length of MA, the structure–function relationship between pore size and the CO2 adsorption capacity of MC-HUN-X was explored. The results showed that the CO2 adsorption capacity increased first and then decreased upon increasing the MOFs pore size, while the adsorption selectivity of CO2 continuously increased. Among all samples, MC-HUN-4 with a moderate pore size had the highest CO2 adsorption capacity (1.90 mmol/g at 298 K and 1 bar) and adsorption selectivity (13.02 and 2.40 for CO2/N2 and CO2/CH4). The combination with a cellulose aerogel endowed MC-HUN-X with excellent mechanical stability and reusability. Cellulose/HP-UIO-66-NH2 hybrid aerogel with larger aperture sizes of MOF showed excellent adsorption capacity and selectivity for CO2, and the combination with aerogel could effectively improve the mechanical stability and reusability. [ABSTRACT FROM AUTHOR]