The charging capacity of the half cell with lithium metal counter electrode from 0.03 V to I.5 V, that corresponds to the discharge capacity or the full cell was improved to 600 mAh/g, where as that for pristine NiO was 230 mAh/g. This improvement of capacity in the lower voltage region is expected to originate in redox of aluminum ion. The redox activity of aluminum ion was confirmed by ex-situ XANES measurement at Al K edge. The absorption edge of aluminum ion shifted to lower energy direction with discharge from 1560 keV to 1556 keV. With charging (the absorption edge of aluminum shifted back to the initial position. This dearly indicates the redox activity of aluminum ion during charge- discharge. This is the first report of anode material for lithium battery that utilizes redox of aluminum ion as far as we know.
In order to investigate the detailed reaction mechanism, ex-situ XRD and XAFS measurements were, carried out. On the basis of these results, the reaction mechanism of Ni-Al binary metal oxide was concluded as follows. In the higher voltage discharge process (OCV-1.0 V), lithium intercalation into the cation vacancy and lithium ion adsorption to the surface of Ni-Al binary metal oxide with the partial redaction of nickel ion is proceeding. In the lower voltage discharge (1.0-0.03 V), the conversion reaction proceeds with the reduction of Ni and Al ions. In the lower voltage charge process (0.03-1.0 V), only aluminum ion is oxidized to form an intermediate state, where aluminum ion makes complex with surrounding oxide ions. In the higher voltage charge process, nickel metal is oxidized to re-form the Ni-Al binary metal oxide with the rock salt structure.