Exploring Zinc-Doped Manganese Hexacyanoferrate as Cathode for Aqueous Zinc-Ion Batteries.

Aqueous zinc-ion batteries (AZiBs) have emerged as a promising alternative to lithium-ion batteries as energy storage systems from renewable sources. Manganese hexacyanoferrate (MnHCF) is a Prussian Blue analogue that exhibits the ability to insert divalent ions such as Zn2+. However, in an aqueous environment, MnHCF presents weak structural stability and suffers from manganese dissolution. In this work, zinc doping is explored as a strategy to provide the structure with higher stability. Thus, through a simple and easy-to-implement approach, it has been possible to improve the stability and capacity retention of the cathode, although at the expense of reducing the specific capacity of the system. By correctly balancing the amount of zinc introduced into the MnHCF it is possible to reach a compromise in which the loss of capacity is not critical, while better cycling stability is obtained.

Irreversible deformation of hyper-crosslinked polymers after hydrogen adsorption.

Hyper-crosslinked polymers (HCPs) have been produced by the Friedel-Crafts reaction using anthracene, benzene, carbazole or dibenzothiophene as precursors and dimethoxymethane as crosslinker, and the effect of graphene oxide (GO) addition has been studied. The resulting HCPs were highly microporous with BET areas (ABET) between 590 and 1120 m2g-1. The benzene-derived HCP (B1FeM2) and the corresponding composite with GO (B1FM2-GO) exhibited the highest ABET and were selected to study their hydrogen adsorption capacities in the pressure range of 0.1 - 14 MPa at 77 K. The maximum H2 excess uptake was 2.1 and 2.0 wt% for B1FeM2 and B1FeM2-GO, respectively, at 4 MPa and 77 K. The addition of GO reduced the specific surface area but increased the density of the resultant HCP-GO composites, which is beneficial for practical applications and proves that materials giving higher gravimetric storage capacities are not necessarily those that offer higher volumetric capacities. H2 adsorption-desorption cycles up to 14 MPa showed irreversible deformation of both HCP and HCP-GO materials, which calls into question their application for hydrogen adsorption at pressures above 4 MPa.

Cytotoxicity of Nucleotide-Stabilized Graphene Dispersions on Osteosarcoma and Healthy Cells: On the Way to Safe Theranostics Agents.

An appealing strategy that overcomes the hydrophobicity of pristine graphene and favors its interaction with biological media is colloidal stabilization in aqueous medium with the support of a biomolecule, such as flavin mononucleotide (FMN), as exfoliating/dispersing agent. However, to establish FMN-stabilized graphene (PG-FMN) as suitable for use in biomedicine, its biocompatibility must be proved by a complete assessment of cytotoxicity at the cellular level. Furthermore, if PG-FMN is to be proposed as a theranostic agent, such a study should include both healthy and tumoral cells and its outcome should reveal the nanomaterial as selectively toxic to the latter. Here, we provide an in-depth comparative in vitro analysis of the response of Saos-2 human sarcoma osteoblasts (model tumor cells) and MC3T3-E1 murine preosteoblasts (undifferentiated healthy cells) upon incubation with different concentrations (10-50 µg mL-1) of PG-FMN dispersions constituted by flakes with different average lateral size (90 and 270 nm). Specifically, the impact of PG-FMN on the viability and cell proliferation, reactive oxygen species (ROS) production, and the cellular incorporation process, cell-cycle progression, and apoptosis has been evaluated. PG-FMN was found to be toxic to both types of cells by increasing ROS production and triggering cell-cycle arrest. The present results constitute a cautionary tale on the need to establish the effect of a nanomaterial not only on tumor cells but also on healthy ones before proposing it as anticancer agent.

Boosting the Performance of Graphene Cathodes in Na-O2 Batteries by Exploiting the Multifunctional Character of Small Biomolecules.

Graphene aerogels derived from a biomolecule-assisted aqueous electrochemical exfoliation route are explored as cathode materials in sodium-oxygen (Na-O2 ) batteries. To this end, the natural nucleotide adenosine monophosphate (AMP) is used in the multiple roles of exfoliating electrolyte, aqueous dispersant, and functionalizing agent to access high quality, electrocatalytically active graphene nanosheets in colloidal suspension (bioinks). The surface phenomena occurring on the electrochemically derived graphene cathode is thoroughly studied to understand and optimize its electrochemical performance, where a cooperative effect between the nitrogen atoms and phosphates from the AMP molecules is demonstrated. Moreover, the role of the nitrogen atoms in the adenine nucleobase of AMP and short-chain phosphate is unraveled. Significantly, the use of such cathodes with a proper amount of AMP molecules adsorbed on the graphene nanosheets delivers a discharge capacity as high as 9.6 mAh cm-2 and performs almost 100 cycles with a considerably reduced cell overpotential and a coulombic efficiency of ≈97% at high current density (0.2 mA cm-2 ). This study opens a path toward the development of environmentally friendly air cathodes by the use of natural nucleotides which offers a great opportunity to explore and manufacture bioinspired cathodes for metal-oxygen batteries.