Kunihisa Shima

Structural and Functional Analysis of Surface Film on Li Anode in Vinylene Carbonate-Containing Electrolyte

The lithium cycling efficiencies of the lithium anode in the ethylene carbonate (EC)-based electrolytes were improved by adding vinylene carbonate (VC) to the electrolyte. We analyzed the surface films of deposited lithium on a nickel substrate in a VC-containing electrolyte with scanning electron microscopy, Fourier transform infrared spectroscopy, two-dimensional nuclear magnetic resonance, gel permeation chromatography, and X-ray photoelectron spectroscopy. The corresponding surface films comprise various polymeric species including poly-(vinylene carbonate) [poly-(VC)], oligomeric VC, and a ring-opened polymer of VC. Furthermore, the surface film of carbon double bonds (C = C-O) and lithium carboxylate (RCOOLi) as reduction products of VC were formed on deposited lithium. These structures of the surface film on the lithium anode were similar to those on the graphite anode. At elevated temperatures, the VC-containing electrolyte led to the formation of surface films comprising poly(VC). The VC-derived polymeric surface film, which exhibited gel-like morphology, could prevent the deleterious reaction which occurs between deposited lithium and the electrolyte, resulting in an enhanced lithium cycling efficiency.

Electrochemical properties of quaternary ammonium borodiglycolates and borodioxalates

Abstract Quaternary ammonium borodiglycolates and borodioxalates were prepared by the reaction of quaternary ammonium tetrahydroxyborates with glycolic acid and oxalic acid, respectively. These compounds are used as the electrolyte salts of aluminum electrolytic capacitors. Their molar conductivities, limiting molar conductivities and oxidation potentials in γ-butyrolactone were higher than those of borodisalicylates and borodicatecholates due to the lack of aromatic rings. Their film-forming ability of anodic aluminum oxide in γ-butyrolactone electrolytes containing a small amount of water was poor, because both anodic dissolution and oxidation occurred simultaneously.