We report on an easy, fast, eco-friendly, and reliable method for the synthesis of reduced graphene oxide/SnO2 nanocomposite as cathode material for application in microbial fuel cells (MFCs). The material was prepared starting from graphene oxide that has been reduced to graphene during the hydrothermal synthesis of the nanocomposite, carried out in a microwave system. Structural and morphological characterizations evidenced the formation of nanocomposite sheets, with SnO2 crystals of few nanometers integrated in the graphene matrix. Physico-chemical analysis revealed the formation of SnO2 nanoparticles, as well as the functionalization of the graphene by the presence of nitrogen atoms. Electrochemical characterizations put in evidence the ability of such composite to exploit a cocatalysis mechanism for the oxygen reduction reaction, provided by the presence of both SnO2 and nitrogen. In addition, the novel composite catalyst was successfully employed as cathode in seawater-based MFCs, giving electrical performances comparable to those of reference devices employing Pt as catalyst.

In the field of dye-sensitized solar cells, polymer electrolytes are among the most studied materials due to their ability to ensure both high efficiency and stability, the latter being a critical point of these devices. Hundreds of polymeric matrices have been proposed over the years, and their functionalization with several groups, the variation of their molecular weight and the tuning of the crosslinking degree have been investigated. However, the true effect that polymeric matrices have on the cell parameters has often been addressed superficially, and hundreds of papers justify the obtained results with a simple bibliographic reference to other systems (sometimes completely different). This work proposes a system of nanoscale growth and crosslinking of a polymer electrolyte inside a nanostructured photoanode. Electrochemical and photovoltaic parameters are carefully monitored as a function of thickness and degree of penetration of the electrolyte. The results derived from this study refute many clichés generally accepted and taken for granted in many literature articles, and – for the first time – a compromise between the amount of polymer, cell efficiency and stability is achieved.

The aim of this work is to investigate the development of nanofiber mats, based on intrinsically conductive polymers (ICPs), which show simultaneously a high electrical conductivity and mandatory insoluble water properties. In particular, the nanofibers, thanks to their properties such as high surface area, porosity, and their ability to offer a preferential pathway for electron flow, play a crucial role to improve the essential characteristics ensured by ICPs. The nanofiber mats are obtained by electrospinning process, starting from a polymeric solution made of polyethylene oxide (PEO) and poly(styrene sulfonate) (PEDOT:PSS). PEO is selected not only as a dopant to increase the electrical/ionic conductivity, as deeply reported in the literature, but also to ensure the proper stability of the polymeric jet, to collect a dried nanofiber mat. Moreover, in the present work, two different treatments are proposed in order to induce crosslinking between PEO chains and PEDOT:PSS, made insoluble into water which is the final sample. The first process is based on a heating treatment, conducted at 130°C under nitrogen atmosphere for 6 h, named the annealing treatment. The second treatment is provided by UV irradiation that is effective to induce a final crosslinking, when a photoinitiator, such as benzophenone, is added. Furthermore, we demonstrate that both crosslinking treatments can be used to verify the preservation of nanostructures and their good electrical conductivity after water treatment (i.e., water resistance). In particular, we confirm that the crosslinking method with UV irradiation results to being more effective than the standard annealing treatment. Indeed, we demonstrate that the processing time, required to obtain the final crosslinked nanofiber mats with a high electrical conductance, results to being smaller than the one needed during the heating treatment.