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Abstract The outbreak of the Coronavirus disease 2019 (COVID‐19) pandemic has highlighted the importance of developing antiviral surface coatings that are capable of repelling pathogens and neutralizing them through self‐sanitizing properties. In this study, a novel coating design based on few‐layer graphene (FLG) is proposed and silver‐decorated micro copper flakes (CuMF) that exhibit both antibacterial and antiviral properties. The role of sacrificial anode surfaces and intrinsic graphene defects in enhancing the release of metal ions from CuMF embedded in water‐based binders is investigated. In silico analysis is conducted to better understand the molecular interactions of pathogen‐repelling species with bacterial or bacteriophage proteins. The results show that the optimal amount of CuMF/FLG in the coating leads to a significant reduction in bacterial growth, with reductions of 3.17 and 9.81 log for Staphylococcus aureus and Escherichia coli, respectively. The same coating also showed high antiviral efficacy, reducing bacteriophage phi6 by 5.53 log. The antiviral efficiency of the coating is find to be doubled compared to either micro copper flakes or few‐layer graphene alone. This novel coating design is versatile and can be applied to various substrates, such as personal protective clothing and face masks, to provide biocidal activity against both bacterial and viral pathogens.

Abstract Today, tris‐s‐triazine based graphitic carbon nitride (g‐C3N4) is a new research hot topic. It has a unique electronic band structure, high physicochemical stability, large surface area, and is “earth‐abundant.” These and other properties have made it a highly researched material especially for visible light photocatalysis and photodegradation applications and as the starting material from which to develop novel electrochemical sensing platforms. In this review, the state‐of‐the‐art technologies utilizing tris‐s‐triazine graphitic carbon nitride as a tailorable signal‐transducing nanostructured material for sensing applications is presented in detail. Initially, the electronic structure of g‐C3N4, morphologies, doping, heterojunctions, its combination with other carbon materials, and defect formation, is described, which is followed by a discussion on its role in electrochemiluminescence, photoelectrochemical, fluorescence sensors and gas sensors as a signal transducer with appropriate examples. This review concludes with a discussion summarizing state‐of‐the‐art and both future perspectives and challenges at the cutting edge of this research.

Layers of titania are the critical components in sensitized photovoltaics. The transfer of electrons occurs from the dye molecule to the external circuit through a transparent conducting oxide, namely fluorine-doped tin oxide (FTO). Porosity, interparticle connectivity, and the titania films’ defects play a vital role in assessing the dye-sensitized solar cells’ (DSSCs) performance. The conventional methods typically take several hours to fabricate these layers. This is a significant impediment for the large-scale manufacture of DSSCs. This step can be reduced to a few hours by a microwave sintering process and may facilitate the rapid fabrication of the critical layers for sensitized photovoltaics, thus, boosting the prospects for the commercialization of these devices. In the present study, we aimed to perform different heat treatments (conventional and microwave) on the titania films with different temperatures to understand the phase formation, transmittance, and porosity without losing the titania’s interparticle connectivity. The solar cell performance of microwave-sintered titania films is comparatively higher than that of conventionally sintered titania films.