A multifunctional Ag NPs/guar gum hydrogel as versatile platform for catalysts, antibacterial agents, and construction of oil-water separation interfaces.

The frequently encountered wastewater contaminations, including soluble aromatic compound and dye pollutants, pathogenic bacteria, and insoluble oils, have resulted in significant environmental and human health issues. It poses a challenge to utilize identical materials for the treatment of complex wastewater. Herein, in this research, multifunctional Ag NPs/guar gum hybrid hydrogels were fabricated using a facile in situ reduction and self-crosslinking method for efficient remediation of complex wastewater. The Ag NPs/guar gum hybrid hydrogel showed remarkable remodeling, adhesive, and self-healing characteristics, which was favorable for its versatile applications. The combination of Ag NPs with the guar gum skeleton endowed the hybrid hydrogel with exceptional catalytic activity for reducing aromatic compounds and dye pollutants, as well as remarkable antibacterial efficacy against pathogenic bacteria. In addition, the Ag NPs/guar gum hybrid hydrogel could be employed to coat a variety of substrates, including cotton fabrics and stainless steel meshes. The hydrogel coated cotton fabrics and meshes presented superhydrophilicity/underwater superoleophobicity, excellent antifouling capacity, and outstanding recyclability, which could be successfully applied for efficient separation of oil-water mixtures. The findings of this work provide a feasible and cost-effective approach for the remediation of intricate wastewater.

Highly stable and reversible Zn anodes enabled by an electrolyte additive of sucrose.

Aqueous zinc-ion batteries (ZIBs) are one of the most promising candidates for electric energy storage devices due to their merits of low cost and high safety. However, the notorious side reactions and dendrite formation on zinc anodes impede the commercialization of ZIBs. In this work, a cheap and edible electrolyte additive sucrose is applied to address the above issues. Sucrose with hydroxyl groups can react as zincophilic sites to adsorb Zn2+. As verified by Raman and FT-IR spectroscopy, the solvation structure of Zn2+ and the hydrogen bonds can be regulated by the sucrose molecule. The weakened solvated structure of Zn2+ and lowered coupling degree between Zn2+ and SO42- can inhibit the hydrogen evolution reaction (HER) and the generation of the sulfate by-product. Furthermore, a solid electrolyte interphase (SEI)-like ion buffer layer is formed because of the preferentially adsorbed sucrose, which can increase the nucleation overpotential and equalize the ion distribution. The enriched Zn nucleation sites and inhibited 2D diffusion of Zn2+ resulting from the sucrose additive enable uniform Zn deposition. Thus, improved performances of symmetric Zn||Zn, asymmetric Zn||Cu and Zn||VO2 cells are realized. The Zn||Zn cell exhibits a highly reversible cycling performance for 1200 h and 400 h at 5 mA cm-2/1 mA h cm-2 and 10 mA cm-2/5 mA h cm-2, respectively. This work provides a readily available and edible additive to improve the performance of ZIBs.

Mussel-Inspired Ag NPs Immobilized on Melamine Sponge for Reduction of 4-Nitrophenol, Antibacterial Applications and Its Superhydrophobic Derivative for Oil-Water Separation.

A functional material integrated with a variety of functions is highly desired in wastewater treatment. In this research, a mussel-inspired method of immobilizing silver nanoparticles on the skeleton of a melamine sponge is proposed and applied for water remediation. Ag NPs were reduced in situ and grown on a polydopamine-modified melamine sponge. The catalytic reduction of 4-nitrophenol (4-NP) in the presence of the obtained MS-PDA-Ag was evaluated, and the results demonstrated that the MS-PDA-Ag presented high catalytic reduction activity. In addition, the monolithic MS-PDA-Ag presents excellent reusability with no remarkable decrease in catalytic efficiency after multiple reuses. Owing to the immobilized Ag NPs, the MS-PDA-Ag can also effectively inhibit the growth of bacteria against both gram-positive and gram-negative species, making it possible for bacteria elimination in polluted water. To further explore the possibility of utilizing the MS-PDA-Ag for versatile applications, a superhydrophobic derivative (S-MS-PDA-Ag) was prepared by coating a low-surface-energy substance (octadecanethiol) on the surface of MS-PDA-Ag. The obtained S-MS-PDA-Ag presents the capacities of oil/organics adsorption and water repellence, which can separate the insoluble oil/organics from water. The melamine sponge immobilized with Ag NPs demonstrates prominent catalytic reduction of 4-NP, antibacterial activity and the superhydrophobic derivative presents the capacity of insoluble oil/organics separation from oil-water mixtures, exhibiting high potential in the remediation of polluted water.

Sulfur-doped honeycomb-like carbon with outstanding electrochemical performance as an anode material for lithium and sodium ion batteries.

Sulfur-doped honeycomb-like 3D porous carbon (SHC) from bagasse waste is efficiently synthesized using a simple, economically feasible and environmentally friendly approach. SHC, which has a unique porous structure with the coexistence of macro-, meso- and micropore structures, affords facile storage and transport channels for both Li+ and Na+. As an anode material for lithium ion batteries (LIBs), SHC provides a superior electrochemical reversible specific capacity (690.9 mAh g-1 at 0.1 A g-1 after 100 cycles and 229 mAh g-1 after 500 cycles at 5 A g-1). When used as an anode for sodium ion batteries (SIBs), SHC exhibits an excellent reversible specific capacity of 505.8 mAh g-1 at 0.1 A g-1 after 100 cycles and 108 mAh g-1 after 500 cycles at 5 A g-1. This study demonstrates a simple strategy to synthesize SHC with excellent electrochemical performance for LIBs and SIBs from natural waste materials.

New strategy to prepare hollow silica microspheres with tunable holes on the shell wall.

Hollow silica microspheres with holes of tunable numbers and sizes on the shell wall were prepared in this study. Clusters with positively charged polystyrene (PS) microspheres as the central spheres (CSs) and negatively charged PS spheres as the "halo" spheres (HSs) were formed via electrostatic interactions and utilized as a template. In the subsequent silica coating process, only CS was selectively coated; hence, after calcination, porous hollow silica microspheres were obtained.