Improving lithium-ion cells by replacing polyethylene terephthalate jellyroll tape.

Polyethylene terephthalate (PET) tape is widely used by well-known lithium-ion battery manufacturers to prevent electrode stacks from unwinding during assembly. PET tape is selected since it has suitable mechanical and electrical properties, but its chemical stability has been largely overlooked. In the absence of effective electrolyte additives, PET can depolymerize into its monomer dimethyl terephthalate, which is an unwanted redox shuttle that induces substantial self-discharge in a lithium-ion cell. This study presents a chemical screening experiment to probe the PET decomposition mechanism involving in situ generated methanol and lithium methoxide from dimethyl carbonate, one of the most common electrolyte solvents in lithium-ion cells. By screening other polymers, it is found that polypropylene and polyimide (Kapton) are stable in the electrolyte. Finally, it is demonstrated that reversible self-discharge of LiFePO4-graphite cells can be virtually eliminated by replacing PET jellyroll tape with chemically stable polypropylene tape.

Peat-derived hard carbon electrodes with superior capacity for sodium-ion batteries.

Herein we demonstrate how peat, abundant and cheap biomass, can be successfully used as a precursor to synthesize peat-derived hard carbons (PDCs), applicable as electrode materials for sodium-ion batteries (SIB). The PDCs were obtained by pre-pyrolysing peat at 300-800 °C, removing impurities with base-acid solution treatment and thereafter post-pyrolysing the materials at temperatures (T) from 1000 to 1500 °C. By modification of pre- and post-pyrolysis temperatures we obtained hard carbons with low surface areas, optimal carbonization degree and high electrochemical Na+ storage capacity in SIB half-cells. The best results were obtained when pre-pyrolysing peat at 450 °C, washing out the impurities with KOH and HCl solutions and then post-pyrolysing the obtained carbon-rich material at 1400 °C. All hard carbons were electrochemically characterized in half-cells (vs. Na/Na+) and capacities as high as 350 mA h g-1 at 1.5 V and 250 mA h g-1 in the plateau region (E < 0.2 V) were achieved at charging current density of 25 mA g-1 with an initial coulombic efficiency of 80%.