The Simpler the Better: Ultrafast Air-Plasma Synthesis of 3D Crosslinked Graphene Nanoscroll-Nanosheet Aerogels at Room Temperature for Capacitive Deionization.

Graphene nanoscroll (GNS) is an important 1D tubular form of graphene-derivative materials, which has garnered widely attention. However, conventional fabrication methods commonly suffer from complex processing and time-consuming. Herein, with graphene oxide (GO) as a precursor, the study puts forward a facile air-plasma synthesis strategy to fabricate 3D graphene nanoscroll-nanosheet aerogels (GSSA). It is demonstrated that without using any chemical additives, a highly efficient reduction-exfoliation-scrolling process can be achieved all-in-one at room temperature within 1 s. The GNSs "grew" from 2D graphene sheets and firmly cross-linked them together, and they not only provide a shortcut path for electron transport but also act as intrinsic spacers to prevent restacking of graphene sheets. When using as an electrode material for capacitive deionization (CDI), GSSA exhibits excellent merits of salt-removal performance. These findings open a new pathway to large-scale synthesis of high-quality and high-purity GNS-based materials with promising applications in CDI and beyond.

Solid-state atomic hydrogen as a broad-spectrum RONS scavenger for accelerated diabetic wound healing.

Hydrogen therapy shows great promise as a versatile treatment method for diseases associated with the overexpression of reactive oxygen and nitrogen species (RONS). However, developing an advanced hydrogen therapy platform that integrates controllable hydrogen release, efficient RONS elimination, and biodegradability remains a giant technical challenge. In this study, we demonstrate for the first time that the tungsten bronze phase H0.53WO3 (HWO) is an exceptionally ideal hydrogen carrier, with salient features including temperature-dependent highly-reductive atomic hydrogen release and broad-spectrum RONS scavenging capability distinct from that of molecular hydrogen. Moreover, its unique pH-responsive biodegradability ensures post-therapeutic clearance at pathological sites. Treatment with HWO of diabetic wounds in an animal model indicates that the solid-state atomic H promotes vascular formation by activating M2-type macrophage polarization and anti-inflammatory cytokine production, resulting in acceleration of chronic wound healing. Our findings significantly expand the basic categories of hydrogen therapeutic materials and pave the way for investigating more physical forms of hydrogen species as efficient RONS scavengers for clinical disease treatment.

Reduced Graphene Oxide Coating LiFePO4 Composite Cathodes for Advanced Lithium-Ion Battery Applications.

Recently, the application of LiFePO4 (LFP) batteries in electric vehicles has attracted extensive attention from researchers. This work presents a composite of LFP particles trapped in reduced graphene oxide (rGO) nanosheets obtained through the high-temperature reduction strategy. The obtained LiFePO4/rGO composites indicate spherical morphology and uniform particles. As to the structure mode of the composite, LFP distributes in the interlayer structure of rGO, and the rGO evenly covers the surface of the particles. The LFP/rGO cathodes demonstrate a reversible specific capacity of 165 mA h g-1 and high coulombic efficiency at 0.2 C, excellent rate capacity (up to 10 C), outstanding long-term cycling stability (98%) after 1000 cycles at 5 C. The combined high electron conductivity of the layered rGO coating and uniform LFP particles contribute to the remarkable electrochemical performance of the LFP/rGO composite. The unique LFP/rGO cathode provides a potential application in high-power lithium-ion batteries.

Investigation of construction and characterization of carboxymethyl chitosan - sodium alginate nanoparticles to stabilize Pickering emulsion hydrogels for curcumin encapsulation and accelerating wound healing.

Limitations in compatibility and effectiveness in delivering bioactive compounds often make it prohibitively difficult to apply Pickering emulsions in wound dressing. In this research, we prepared Pickering emulsion composite hydrogels based on carboxymethyl chitosan - sodium alginate (CMCS-SA) nanoparticles (NPs) stabilized Pickering emulsions, poloxamer 407 (PLX), and curcumin (CUR). CMCS-SA NPs were prepared and used to stabilize Pickering emulsion. The stability of Pickering emulsion improved with the increase of the concentration of NPs, and was highly sensitive to ionic strength change. This Pickering emulsion remained stable at various temperatures. After curcumin were introduced into the emulsion, 0.6% CMCS-SA NPs Pickering emulsion showed controlled release of curcumin in vitro. The CMCS-SA-PLX-CUR hydrogels also exhibited smooth surface and dense structure. This composite hydrogels has antibacterial properties against Escherichia coli and Staphylococcus aureus. Moreover, the CMCS-SA-PLX-CUR hydrogels improved wound healing and increased expression of Ki67 and CD31. RT-qPCR results indicated that the mRNA levels of α-SMA and TGF-ß1 in the CMCS-SA-PLX-CUR group were downregulated, while the mRNA levels of TGF-ß3 increased. The present study suggests that the potentials of CMCS-SA-PLX-CUR hydrogels are promising in protecting bioactive components and wound care management.

Ultrahigh Content Boron and Nitrogen Codoped Hierarchically Porous Carbon Obtained from Biomass Byproduct Okara for Capacitive Deionization.

Capacitive deionization (CDI) is an environmentally friendly, energy efficient, and low cost water purification technique in comparison with other conventional techniques, and it has attracted considerable attention in recent years. Here, we use biomass byproduct okara as the starting material to fabricate a boron and nitrogen codoped hierarchically porous carbon (BNC) with ultrahigh heteroatom contents and abundant in-plane nanoholes for CDI application. With the interconnected hierarchical porous structure, the BNC not only exhibits a large surface area (647.0 m3 g-1) for the adsorption of ions but also offers abundant ion transport channels to access the entire internal surface. Meanwhile, the ultrahigh dopants' content of B (11.9 at%) and N (14.8 at%) further gives rise to the increased surface polarity and enhanced capacitance for BNC. Owing to these favorable properties, BNC exhibits top-level salt adsorption capacity (21.5 mg g-1) and charge efficiency (59.5%) at the initial NaCl concentration of ∼500 mg L-1. Moreover, we performed first-principle simulations to explore the different effects between N-doping and N,B-codoping on the capacitive property, which indicate that the boron and nitrogen codoping of carbon can largely increase the quantum capacitance over the double layer capacitance. The results of this work suggest a promising prospect for the BNC material in practical CDI application.