Benzophenone-3 grafted chitosan (CS-BP-3) was successfully synthesized and applied as an antibacterial coating for the first time. The grafting mechanism is based on the reaction between ketone and primary amine to form imine derivatives and the chemical structure of grafted chitosan was studied by Fourier transform infrared (FTIR) spectroscopy. Water solubility of BP-3 is enhanced after covalently grafted on chitosan and consequently renders the chitosan coating with UV blocking property. Results of thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) further confirmed the thermal stability of BP-3 modified chitosan is enhanced. The CS-BP-3 coating was applied on a variety of substrates of glass, plastics, wood, and metal. The surface features of the coatings such as morphology, water contact angle (WCA), and surface roughness were investigated. The optical and thermal stabilities of the coatings under UV irradiation were studied for 16 h. Antibacterial activity of CS-BP-3 was evaluated against both Gram-negative and Gram-positive bacteria. And the results of bacterial inhibition by CS-BP-3 coating indicate its potential for future application in food packaging.

Chitosan (CS), an edible and non-toxic natural biopolymer, has been widely used in food preservation attributed to its intrinsic antimicrobial, biodegradable, and excellent film-forming properties. In this work, we report photocatalyst-loaded chitosan coating on commercial polyethylene (PE) film with enhanced antimicrobial properties for food packaging application. To improve the chemical stability of zinc oxide (ZnO) photocatalyst in acidic chitosan matrix, a thin layer (1–5 nm) of amorphous tin oxide (SnOx) was coated on ZnO nanoparticles. Consequently, the charge transfer efficiency of ZnO is improved and most of the surface defects are retained according to the studies of UV–Vis and fluorescence spectroscopy. The thin SnOx coating on ZnO was observed by high-resolution transmission electron microscopy (HRTEM) and its effects on crystallinity and particle size of ZnO were examined using X-ray diffraction (XRD) and particle sizer, respectively. The addition of ZnO@SnOx particles in chitosan coating increases water contact angle (WCA) and enhances thermal stability of chitosan coating. The antimicrobial activity of chitosan, ZnO-SnOx nanoparticles, and CS-ZnO@SnOx coated PE films were examined against both Gram-negative (E. coli, A. faecalis) and Gram-positive (S. aureus, B. subtilis) bacteria. Compared to the limited antimicrobial effects of chitosan, ZnO-SnOx demonstrates an improved inhibition effect on bacterial growth over 48 h period under light. For the CS-ZnO@SnOx nanocomposite coated PE films, no inhibition zone was observed due to the limitation of disc diffusion method. Meanwhile, there were no bacterial colonies found to develop on the film, rendering this CS nanocomposite coating a good candidate for food packaging applications.

PEGylation is regarded as a common antifouling strategy and the effect is normally linked with surface hydrophilicity of the coatings. Herein, the biopolymer chitosan (CS) was grafted by polyethylene glycol (PEG) of different chain lengths (molecular weight 200, 4 k and 100 k Da) to verify if the hydrophilicity of CS-PEG coatings is crucial in determining antifouling activities and if PEG chain length influences biofouling in marine environment. Properties of copolymers such as melting points and crystallinity are affected by grafting PEG. The water contact angle (WCA) of CS-PEG coatings increases with the chain length of grafted PEG, from 27° to 58°. Photocatalyst of zinc oxide-silver (ZnO/Ag) was also studied and its embedment (2 % to CS-PEG) renders the surface of CS-PEG coatings more hydrophobic with WCA increased from 52° to 86°. Antibacterial, anti-diatom, and anti-biofilm activities of the coatings were evaluated in natural sea water. The bacterial density on CS-PEG coatings was dramatically reduced to 4 × 104 compared to the control of 7 × 104 ind/mm2, and further to 2 × 104 for CS-PEG-ZnO/Ag coatings. CS-PEG coatings also strongly inhibit diatoms (120–200 ind/mm2), but the inclusion of ZnO/Ag did not obviously enhance such effect (50–150 ind/mm2). The findings provide useful insights for designing polymer-based antifouling coatings.

Multiple and hierarchical manganese (Mn)-based Prussian blue analogues obtained on different substrates are successfully prepared using a universal, facile, and simple strategy. Different functional groups and surface charge distributions on carbon cloth have significant effects on the morphologies and nanostructures of Mn-based Prussian blue analogues, thereby indirectly affecting their physicochemical properties. Combined with the advantages of the modified carbon cloth and the nanostructured Mn-based Prussian blue analogues, the composite with negative surface charge formed by the electronegativity differences shows good electrochemical properties, leading to improvement in charge efficiency during capacitive desalination. An asymmetric device fabricated with Mn-based Prussian blue analogue-modified F-doped carbon cloth as the cathode and acid-treated carbon cloth as the anode presents the highest salt adsorption capacity of 10.92 mg g-1 with a charge efficiency of 82.28% and the lowest energy consumption of 0.45 kW h m-3 at 1 V due to the main influencing factor from the negative surface charge leading to co-ion expulsion boosting the capacitive deionization performance. We provide insights for further exploration of the relationship between second-phase materials and carbon cloth, while offering some guidance for the design and preparation of electrodes for desalination and beyond. 

Highly efficient and environmentally friendly multifunctional electrode materials for application in super -capacitors to electrocatalysis are important for advances in the future of electrical energy storage and green hydrogen production. This work reports a simple growth strategy to obtain hierarchical P(Ni, Co, Fe) modified electrodes by phosphating a core/shell composite of nickel-cobalt (NiCo) Prussian blue analogues fabricated through an in situ self-sacrificial growth process. Due to the unique microstructure, abundant surface-active sites, and enhanced interfacial conductivity, the hybrid electrode exhibits specific capacitance as high as 1125.8 F g-1 (3.7 F cm-2) at 2 mA cm-2, excellent rate capability and improved cycling stability (97.1% retention capacitance after 5000 cycles at 50 mA cm-2 and 89.9% after continuous 5000 cycles at 100 mA cm-2). Furthermore, the hybrid structure shows excellent oxygen evolution reaction performance with an overpotential of 252 mV at 100 mA cm-2 and 283 mV at 300 mA cm-2, with a low Tafel slope of 68 mV dec- 1, and overall water splitting abilities with a cell voltage of 1.55 V at 100 mA cm-2. This work provides insights into the design of next -generation high-performance multifunctional electrode materials by controlling the surface/interface of multi -component structures for enhancing their properties.