Effect of Lithium Silicate Addition on the Microstructure and Crack Formation of LiNiCoMnO Cathode Particles.

The microstructure of LiNiCoMnO cathode materials was controlled by the addition of lithium silicate, and the influence on the cycle performance and the rate capability was investigated. Si was not included within the lattice, but localized at the grain boundaries of the primary particles and the pores inside the secondary particles. The addition of the lithium silicate greatly decreased the density of the pores between the primary particles and improved the density of the secondary particles.

The effects of alloying and segregation for the reactivity and diffusion of oxygen on Cu3Au(111).

We report results of the segregation induced by the adsorption of O2 and the barrier of the formation of Cu2O in Cu3Au(111) with an experimental and theoretical approach. Oxidation by a hyperthermal O2 molecular beam (HOMB) was investigated by X-ray photoemission spectroscopy in conjunction with a synchrotron light source. From the incident-energy dependence of the measured O-uptake curve, dissociative adsorption of O2 is less effective on Cu3Au(111) than on Cu(111).

Initial stages of Cu3Au(111) oxidation: oxygen induced Cu segregation and the protective Au layer profile.

We report results of our experimental and theoretical studies on the Au concentration profile of Cu3Au(111) during oxidation by a hyperthermal O2 molecular beam at room temperature, using X-ray photoemission spectroscopy (XPS), in conjunction with synchrotron radiation (SR), and density functional theory (DFT). Before O2 exposure, we observe strong Au segregation to the top layer, i.e.

The temperature dependence of Cu2O formation on a Cu(110) surface with an energetic O2 molecular beam.

We report a study of the surface temperature (T(s)) dependence of Cu(2)O formation on a Cu(110) surface induced by a hyperthermal O(2) molecular beam (HOMB), using x-ray photoemission spectroscopy in conjunction with synchrotron radiation. From the T(s) dependence of the O uptake curves, the direct dissociative adsorption process mainly contributes to the formation of the p(2 × 1)-O structure with an O coverage (Θ) of 0.5 ML for 2.

Kinetics and dynamics in physisorption of CH3Cl on HOPG: surface temperature and molecular orientation dependence.

We report a study of kinetics and dynamics in physisorption of CH(3)Cl on a highly-oriented pyrolytic graphite (HOPG). Thermal energy atom scattering (TEAS) was used to probe the kinetics of thermal CH(3)Cl adsorption on HOPG during the coverage evolution. The desorption energy of CH(3)Cl on HOPG changes from 0.