LiTi2NbO7 was synthesized from CsTi2NbO7 by direct Cs+/Li+ ion exchange and subsequent thermal decomposition of the hydrated form. Neutron powder diffraction data were collected at high-resolution (ILL, France) and analyzed by Rietveld refinements and Fourier difference techniques, revealing a layer-like crystal structure (orthorhombic Pbnm, a = 9.2476(6), b = 16.955(2), c = 3.7542(2) Å) partly similar to that of monoclinic LiTi3O7. Lithium is tetrahedrically coordinated and bridges adjacent layers of (Ti,Nb)O6 octahedra. Nb atoms are strongly ordered in one of the three independent sites available for Ti/Nb, thus compensating for the unbalance of negative charge from the surrounding O atoms. Electrochemical measurements were performed on a LiTi2NbO7 electrode vs. Li/Li+ couple. Overlapping Ti4 +/Ti3 + and Nb5 +/Nb4 + redox processes occur around 1.4 V, with a specific charge of 245 mAh/g (about 2.8 electrons per f.u.) in the 2.30 to 1.15 V range. Charge-discharge cycling results show a reversible and stable specific capacity of 220 mAh/g at low current density, indicating that this material is a promising alternative to Li4Ti5O12 spinel for reversible anode applications in lithium batteries.
Catti, M., Pinus, I., Ruffo, R., Salamone, M., Mari, C. (2016). A novel layered lithium niobium titanate as battery anode material: Crystal structure and charge-discharge properties. SOLID STATE IONICS, 295, 72-77 [10.1016/j.ssi.2016.08.001].
A novel layered lithium niobium titanate as battery anode material: Crystal structure and charge-discharge properties
CATTI, MICHELE
;PINUS, ILYASecondo
;RUFFO, RICCARDO;SALAMONE, MATTEO MARCOPenultimo
;MARI, CLAUDIO MARIAUltimo
2016
Abstract
LiTi2NbO7 was synthesized from CsTi2NbO7 by direct Cs+/Li+ ion exchange and subsequent thermal decomposition of the hydrated form. Neutron powder diffraction data were collected at high-resolution (ILL, France) and analyzed by Rietveld refinements and Fourier difference techniques, revealing a layer-like crystal structure (orthorhombic Pbnm, a = 9.2476(6), b = 16.955(2), c = 3.7542(2) Å) partly similar to that of monoclinic LiTi3O7. Lithium is tetrahedrically coordinated and bridges adjacent layers of (Ti,Nb)O6 octahedra. Nb atoms are strongly ordered in one of the three independent sites available for Ti/Nb, thus compensating for the unbalance of negative charge from the surrounding O atoms. Electrochemical measurements were performed on a LiTi2NbO7 electrode vs. Li/Li+ couple. Overlapping Ti4 +/Ti3 + and Nb5 +/Nb4 + redox processes occur around 1.4 V, with a specific charge of 245 mAh/g (about 2.8 electrons per f.u.) in the 2.30 to 1.15 V range. Charge-discharge cycling results show a reversible and stable specific capacity of 220 mAh/g at low current density, indicating that this material is a promising alternative to Li4Ti5O12 spinel for reversible anode applications in lithium batteries.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.