Unlocking Four-electron Conversion in Tellurium Cathodes for Advanced Magnesium-based Dual-ion Batteries.

Magnesium (Mg) batteries hold promise as a large-scale energy storage solution, but their progress has been hindered by the lack of high-performance cathodes. Here, we address this challenge by unlocking the reversible four-electron Te0/Te4+ conversion in elemental Te, enabling the demonstration of superior Mg//Te dual-ion batteries. Specifically, the classic magnesium aluminum chloride complex (MACC) electrolyte is tailored by introducing Mg bis(trifluoromethanesulfonyl)imide (Mg(TFSI)2), which initiates the Te0/Te4+ conversion with two distinct charge-storage steps. Te cathode undergoes Te/TeCl4 conversion involving Cl- as charge carriers, during which a tellurium subchloride phase is presented as an intermediate. Significantly, the Te cathode achieves a high specific capacity of 543 mAh gTe -1 and an outstanding energy density of 850 Wh kgTe -1, outperforming most of the previously reported cathodes. Our electrolyte analysis indicates that the addition of Mg(TFSI)2 reduces the overall ion-molecule interaction and mitigates the strength of ion-solvent aggregation within the MACC electrolyte, which implies the facilized Cl- dissociation from the electrolyte. Besides, Mg(TFSI)2 is verified as an essential buffer to mitigate the corrosion and passivation of Mg anodes caused by the consumption of the electrolyte MgCl2 in Mg//Te dual-ion cells. These findings provide crucial insights into the development of advanced Mg-based dual-ion batteries.

Cellular uptake of biotransformed graphene oxide into lung cells.

Due to its high surface area and convenient functionalization, graphene oxide has many potential applications in biomedicine, especially as a drug carrier. However, knowledge about its internalization inside mammalian cells is still limited. Graphene oxide cellular uptake is a complex phenomenon affected by factors such as the size of the particle and modifications of its surface. Moreover, nanomaterials introduced into living organisms interact with biological fluids' components. It may further alter its biological properties. All these factors must be considered when the cellular uptake of potential drug carriers is considered. In this study, the effect of graphene oxide particle sizes on internalization efficiency into normal (LL-24) and cancerous (A549) human lung cells was investigated. Moreover, one set of samples was incubated with human serum to determine how the interaction of graphene oxide with serum components affects its structure, surface, and interaction with cells. Our findings indicate that samples incubated with serum enhance cell proliferation but enter the cells with lesser efficiency than their counterparts not incubated with human serum. What is more affinity towards the cells was higher for larger particles.

Structural and Charge Transport Properties of Composites of Phosphate-Silicate Protonic Glass with Uranyl Hydroxy-Phosphate and Hydroxy-Arsenate Obtained by Mechano-Chemical Synthesis Undergoing Hydration Changes.

The introduction of the hydrogen economy, despite its obvious technological problems, creates a need for a significant number of niche-focused solutions, such as small-sized (10-100 W) fuel cells able to run on hydrogen of lesser purity than what is considered a standard in the case of PEMFCs. One of the solutions can be derived from the fact that an increase in the operational temperature of a cell significantly decreases its susceptibility to catalyst poisoning. Electrolytes suitable for the so-called medium temperature operational range of 120-400 °C, hence developed, are neither commercialized nor standardized. Among them, phosphate silicate protonically conductive glasses were found not only to reveal interestingly high levels of operational parameters, but also, to exhibit superior chemical and electrochemical stability over their polymeric counterparts. On the other hand, their mechanical properties, including cracking fragility, still need elaboration. Initial studies of the composite phosphate silicate glasses with uranyl-based protonic conductors, presented here, proved their value both in terms of application in fuel cell systems, and in terms of understanding the mechanism governing the charge transport mechanism in these and similar systems. It was found that whereas systems containing 10-20 wt% of the crystalline additive suffer from significant instability, materials containing 45-80 wt% (with an optimum at 60%) should be examined more thoughtfully. Moreover, the uranyl hydrogen phosphate was found to surpass its arsenate counterpart as an interesting self-healing behavior of the phase structure of the derived composite was proved.

Silver-Graphene Oxide Nanohybrids for Highly Sensitive, Stable SERS Platforms.

Graphene oxide-silver nanoparticle nanohybrids were synthesized by simple reduction of the silver nitrate and graphene oxide (GO) mixture in water using the mild reducing agent ascorbic acid. The concentration of ascorbic acid was varied to verify the possible influence of the GO surface composition on the efficiency of the hybrid material as substrates for surface enhanced Raman spectroscopy (SERS). Furthermore, the composites were conditioned in ammonia solution or in potassium hydroxide diluted solution. For comparison, the graphene oxide-silver nanoparticle composite has been synthesized using the ammonia-treated GO. All materials were characterized using spectroscopic and microscopic methods including UV-Vis, infrared, and Raman spectroscopy and scanning electron microscopy. The SERS efficiency of the nanohybrids was tested using 4-aminothiophenol (PATP). The optimal synthesis conditions were found. Ammonia and potassium peroxide drop-casted on the composite changed the SERS properties. The sample treated with KOH showed the best SERS enhancement. The variation of the SERS enhancement was correlated with the shape of the UV-Vis characteristics and the surface structure of the composites.

Elemental imaging of heterogeneous inorganic archaeological samples by means of simultaneous laser induced breakdown spectroscopy and laser ablation inductively coupled plasma mass spectrometry measurements.

Multilayered fragments of murals were used to evaluate the usefulness of two laser-based instrumental methods: laser induced breakdown spectroscopy (LIBS) and laser ablation (LA) inductively coupled plasma mass spectrometry (ICP-MS) for elemental imaging of unique historic samples. Simultaneous LA/LIBS measurements with the use of 266nm Nd:YAG laser were performed on cross-sections of mediaeval Nubian objects with specific blue painting layers including either Egyptian blue (CaCuSi4O10) or lapis lazuli (Na8-10Al6Si6O24S2-4). A combined use of both laser-based methods allowed for clear distinguishing of blue pigments based on visual imaging of a chemical composition of heterogeneous archaeological inorganic samples. The identification of the pigments was confirmed with Raman spectroscopy.