A Novel Electrochemical Differentiation between Exosomal-RNA of Breast Cancer MCF7 and MCF7/ADR-Resistant Cells.

Cancer is considered one of the most burdensome diseases affecting lives and, hence, the economy. Breast cancer is one of the most common types of cancer. Patients with breast cancer are divided into two groups: one group responds to the chemotherapy, and the other group resists the chemotherapy.

Anionic/nonionic surfactants for controlled synthesis of highly concentrated sub-50 nm polystyrene spheres.

Polystyrene nanospheres are of great importance in 3D hard templating along with many other fields like pharmaceuticals and coatings. Therefore, it is important to be able to prepare polystyrene beads with different sphere sizes that suit each application. In this work, the emulsion polymerization method was used to prepare monodispersed polystyrene (PS) spheres with an average size of 50 nm, using styrene monomer, sodium dodecyl sulfate (SDS) and polyvinylpyrrolidone (PVP) as surfactants, and potassium persulfate (KPS) as the initiator.

Tungsten oxide/fullerene-based nanocomposites as electrocatalysts and parasitic reactions inhibitors for VO/VO in mixed-acids.

The relatively high cost of all-vanadium redox flow batteries (VRFBs) limits their widespread deployment. Enhancing the kinetics of the electrochemical reactions is needed to increase the power density and energy efficiency of the VRFB, and hence decrease the kWh cost of VRFBs. In this work, hydrothermally synthesized hydrated tungsten oxide (HWO) nanoparticles, C, and C/HWO were deposited on carbon cloth electrodes and tested as electrocatalysts for the VO/VO redox reactions.

Mechanistic effects of blending formic acid with ethanol on Pd activity towards formic acid oxidation in acidic media.

The direct formic acid fuel cell (DFAFC) is one of the most promising direct liquid fuel cells. Pd is the most active catalyst towards formic oxidation, however, it suffers from CO-like poisoning and instability in acidic media. Blending formic acid with ethanol is known to synergistically enhance the Pt catalytic activity of Pt.

Correction: Fullerene C as a novel electrocatalyst for VO/VO and chlorine evolution inhibitor in all-vanadium redox flow batteries.

Correction for 'Fullerene C76 as a novel electrocatalyst for VO2+/VO2+ and chlorine evolution inhibitor in all-vanadium redox flow batteries' by Farah A. El Diwany et al., Chem.

Fullerene C as a novel electrocatalyst for VO/VO and chlorine evolution inhibitor in all-vanadium redox flow batteries.

We report, for the first time, the superior electrocatalytic activity of fullerene C towards VO/VO in all-vanadium redox flow batteries. Results show a 99.5% and 97% decrease in charge transfer resistance, compared to treated and untreated carbon cloth.

Nanoengineered Ir@Pt Nanoparticles with Controlled Pt Shell Coverages for Direct Methanol Electro-Oxidation.

The design and application of bimetallic alloy nanoparticles (NPs) for electrocatalytic applications are challenged by the need to clearly identify and understand the individual effect of each component. In the present work, the focus has been on PtIr NPs, with alloyed NPs being previously shown to be active toward the methanol oxidation reaction (MOR), but for which the mode of action of the Ir component remains uncertain. We have therefore nanoengineered a family of Ir@Pt NPs, using a modified polyol method, to control the Pt shell coverage (up to 2 monolayers) and thus to allow the separation of the bifunctional and electronic effects of Ir on the Pt activity.

Clarifying the role of Ru in methanol oxidation at Ru(core)@Pt(shell) nanoparticles.

The catalytic activity of Rucore@Ptshell nanoparticles (NPs) towards CO oxidation, a strongly adsorbed intermediate that compromises the performance of direct methanol fuel cells, is known to be significantly better than at Pt alone. However, a systematic study aimed at understanding the beneficial effect of Ru on Pt during the methanol oxidation reaction (MOR) has not been carried out as yet. Here, Rucore@Ptshell NPs, having a controlled Ptshell coverage of zero to two monolayers and two different Rucore sizes (2 and 3 nm), were synthesized using the simple polyol method to determine the precise role and impact of Ru on the MOR in 0.

Novel electrochemical fingerprinting methods for the precise determination of Pt(shell) coverage on Ru(core) nanoparticles.

The surface composition of nanoparticles is critical in defining their chemical and electrochemical properties. However, there are a limited number of tools that can rapidly and reliably establish these important characteristics at this small scale. In the present work, a series of Rucore@Ptshell nanoparticles (2 or 3 nm diameter Ru core, 0 to 2 monolayers of Pt in the shell layer) were synthesized and several novel electrochemical fingerprinting methods were developed to determine the Pt shell characteristics.