A world-wide growing concern relates to the rising levels of CO₂ in the atmosphere that leads to devastating consequences for our environment. In addition to reducing emissions, one alternative strategy is the conversion of CO₂ (via the CO₂ Reduction Reaction, or CO₂RR) into added-value chemicals, such as CO, HCOOH, C₂H₅OH, CH₄, and more. Although this strategy is currently not economically feasible due to the high stability of the CO₂ molecule, significant progress has been made to optimize this electrochemical conversion, especially in terms of finding a performing catalyst. In fact, many noble and non-noble metal-based systems have been investigated but achieving CO₂ conversion with high faradaic efficiency (FE), high selectivity towards specific products (e.g., hydrocarbons), and maintaining long-term stability is still challenging. The situation is also aggravated by a concomitant hydrogen production reaction (HER), together with the cost and/or scarcity of some catalysts. This review aims to present, among the most recent studies, some of the best-performing catalysts for CO₂RR. By discussing the reasons behind their performances, and relating them to their composition and structural features, some key qualities for an “optimal catalyst” can be defined, which, in turn, will help render the conversion of CO₂ a practical, as well as economically feasible process.

Ce:YAG nanostructures (Ce:YAG = Cerium in Yttrium Aluminium Garnet), easy to control and shape, have been prepared via templating approach using natural and synthetic materials (i.e. paper, cotton wool and glass wool) previously soaked with a gel-like metals precursor and then thermally treated to achieve the wished morphology. The final material, otherwise difficult to process, can be easily moulded, it is lightweight, portable and forms, at the nanoscale, homogeneous layers of interconnected but not agglomerated nanoparticles (15 ± 5 nm). Using the same synthetic route, called Urea-Glass-Route, but in absence of a template, extremely pure Ce:YAG nanoparticle (45 ± 5 nm) can be also prepared, highly crystalline and well-defined in size and shape. Both structural and optical properties of the final materials were investigated, showing high optical quality. The support allows the production of a multifunctional material with mouldable shape and potential lighting application for large structures combining the strength, chemical durability, fire resistance, and translucency of glass fibres. Last, but not least, the synthetic path also allows an easy scaling up of the process: the first, key step for practical application of nanosized rare-earth doped YAG on large scale.

Iron carbide (Fe₃C) is a ceramic magnetic material with high potential for applications in different fields, including catalysis, medicine imaging, coatings, and sensors. Despite its interesting properties, it is still somehow largely unexplored, probably due to challenging synthetic conditions. In this contribution, we present a sol-gel-based method that allows preparing different Fe₃C@C nanocomposites with tailored properties for specific applications, in particular, we have focused on and discussed potential uses for adsorption of noxious gas and waste removal. Nanocomposites were prepared using readily available and “green” sources, such as urea, simple and complex sugars, and chitosan. The nanocomposite prepared from chitosan was found to be more efficient for CO₂ uptake, while the sample synthetized from cellulose had optimal capability for dye absorption and waste oil removal from water.

Graphite oxidation to graphene oxide (GO) is carried out using methods developed by Brodie (GO-B) and Hummers (GO-H). However, a comparison of the antibacterial properties based on the physicochemical properties has not been performed. Therefore, this paper outlines a comparative analysis of GO-H and GO-B on antibacterial efficacy against Gram-positive and Gram-negative bacterial cultures and biofilms in an aqueous environment and discusses which of the properties of these GO nanomaterials have the most significant impact on the antibacterial activity of these materials. Synthesis of GO with Brodie’s and modified Hummers’ methods was followed by an evaluation of their structural, morphological, and physicochemical properties by Raman, FTIR, UV–vis spectroscopy, and X-ray diffraction (XRD). The GO-B surface appeared more oxidized than that of GO-H, which could be crucial for interactions with bacteria. According to our results, GO-B demonstrated notably superior anti-biofilm efficacy. Despite its higher production cost, GO-B exhibits more excellent capabilities in combating bacterial biofilms than GO-H.