Speciation of Transition Metal Dissolution in Electrolyte from Common Cathode Materials.

Significant capacity loss has been observed across extended cycling of lithium-ion batteries cycled to high potential. One of the sources of capacity fade is transition metal dissolution from the cathode active material, ion migration through the electrolyte, and deposition on the solid-electrolyte interphase on the anode. While much research has been conducted on the oxidation state of the transition metal in the cathode active material or deposited on the anode, there have been limited investigations of the oxidation state of the transition metal ions dissolved in the electrolyte.

Electrochemically derived functionalized graphene for bulk production of hydrogen peroxide.

On-site peroxide generation via electrochemical reduction is gaining tremendous attention due to its importance in many fields, including water treatment technologies. Oxidized graphitic carbon-based materials have been recently proposed as an alternative to metal-based catalysts in the electrochemical oxygen reduction reaction (ORR), and in this work we unravel the role of C=O groups in graphene towards sustainable peroxide formation. We demonstrate a versatile single-step electrochemical exfoliation of graphite to graphene with a controllable degree of oxygen functionalities and thickness, leading to the formation of large quantities of functionalized graphene with tunable rate parameters, such as the rate constant and exchange current density.

Solid-state thermal exfoliation of graphite nano-fibers to edge-nitrogenized graphene nanosheets for oxygen reduction reaction.

We demonstrate a simple, single-step and scalable synthesis of edge-nitrogenated graphene nanosheets (E-N-GNS) through thermal exfoliation of graphite platelet nanofibers (GPNF) in the presence of melamine. This material was characterized using different physical characterization techniques which divulges that, the edges are selectively functionalised with pyridinic and pyrrolic type nitrogens leading to the formation of E-N-GNS. Further, the electrocatalytic activity of E-N-GNS towards oxygen reduction reaction (ORR) in alkaline medium was studied using electrochemical techniques to reveal superior electrocatalytic activity of E-N-GNS towards ORR than that of GPNF, perhaps due to the incorporation of N at the edges.