Effect of sodium hydroxide pretreatment of NiOx cathodes on the performance of squaraine-sensitized p-type dye-sensitized solar cells

Squaraines are full-organic dyes employed as sensitizers in ptype dye-sensitized solar cells (p-DSSC). Their absorption spectrum shows a wide tunability that ranges from visible to NIR. Sensitization in the NIR region is crucial for exploiting a particularly intense portion of the solar spectrum. In this work three squaraines will be presented and tested as sensitizers in NiO-based p-type DSSC O4_C2, O4_C4 and O4_C12). The structures of the dyes differ for the length of the alkyl side chain (C2, C4 and C12). Alkyl side chains improve the solubility of the dye, influence the extent of dye loading on the electrode and affect the overall efficiency of devices. The generally low stability of squaraines represents a critical issue in view of their employment as sensitizers of p-DSSC. Such a problem becomes even more evident when this class of molecules is bound onto an acidic surface like the one of the photocathode here employed: non-stoichiometric nickel oxide (NiOx). NiOx possesses a quite acidic character because of the high surface concentration of Ni(III) sites. To buffer the surface acidity of NiOx due to the presence of high-valence states of nickel, we considered the electrode pretreatment with sodium hydroxide (NaOH) prior to sensitization. This assures a major stability of the solar cell. At the same time the chemisorbed hydroxyl moieties act as passivating agents of the Ni(III) sites thus diminishing the surface concentration of sites for dye anchoring. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Chromatin-Mediated Regulation of Genome Plasticity in Human Fungal Pathogens

Human fungal pathogens, such as Candida albicans, Aspergillus fumigatus and Cryptococcus neoformans, are a public health problem, causing millions of infections and killing almost half a million people annually. The ability of these pathogens to colonise almost every organ in the human body and cause life-threating infections relies on their capacity to adapt and thrive in diverse hostile host-niche environments. Stress-induced genome instability is a key adaptive strategy used by human fungal pathogens as it increases genetic diversity, thereby allowing selection of genotype(s) better adapted to a new environment. Heterochromatin represses gene expression and deleterious recombination and could play a key role in modulating genome stability in response to environmental changes. However, very little is known about heterochromatin structure and function in human fungal pathogens. In this review, I use our knowledge of heterochromatin structure and function in fungal model systems as a road map to review the role of heterochromatin in regulating genome plasticity in the most common human fungal pathogens: Candida albicans, Aspergillus fumigatus and Cryptococcus neoforman