Search results for "Lithium oxide"
showing 8 items of 8 documents
A field induced ferromagnetic-like transition below 2.8 K in Li2CuO2: An experimental and theoretical study
1998
The low temperature magnetic properties of the Li2CuO2 compound have been investigated by means of superconducting quantum interference device magnetometry. We find in addition to an antiferromagnetic phase below 9.5 K a ferromagnetic-like steep rise of the magnetization around 2.8 K. The observed low temperature behavior is discussed by considering second and fourth order magnetocrystalline effective anisotropy coefficients, in addition to the exchange couplings reported in the literature. Work at the Institut de Ciencia dels Materials was supported by the Spanish Comisión Interministerial de Ciencia y Technología Grant No. CICYT MAT 96-1037.
Synthesis and host properties of tetragonal Li2Mn2O4 and Li2Co0.4Mn1.6O4
2000
Abstract This paper presents synthesis and electrochemical properties of tetragonal lithium manganese dioxide, Li2Mn2O4 and its cobalt doped analogue Li2Co0.4Mn1.6O4. The materials are compared as host materials for lithium insertion and the behavior during the initial lithium extraction as well as on repeated cycling is presented. These materials show an initial lithium extraction capacity between 200 and 270 mAh/g. On repeated cycling, they are converted into spinel-like lattices with reversible capacities in the range 82–90 mAh/g. As they are chemically compatible with the manganese spinel, they will be well suited as additives compensating for the capacity loss during the initial formin…
Atomic layer deposition of lithium containing thin films
2009
Five different lithium containing compounds, all representing different chemical systems, were studied in order to deposit lithium containing films by atomic layer deposition ALD. The studied compounds were a lithium β-diketonate Li(thd) (thd = 2,2,6,6-tetramethyl-3,5-heptanedionate), a lithium alkoxide LiOtBu (OtBu = tert-butoxide), a lithium cyclopentadienyl LiCp (Cp = cyclopentadienyl), a lithium alkyl n-butyllithium, and a lithium amide lithium dicyclohexylamide. Films containing lithium carbonate (Li2CO3) were obtained from alternate pulsing of Li(thd) and ozone in a temperature range of 185–300 °C. The film composition was analyzed by time-of-flight elastic recoil detection analysis (…
New insight on the lithium hydride–water vapor reaction system
2018
Abstract The reaction of lithium hydride (LiH) powder with pure water vapor (H2O and D2O) was studied by thermogravimetry and in situ infrared spectroscopy at 298 K over a large pressure range. The mean particle size of LiH is around 27 μm. At very low pressure, the hydrolysis starts with the formation of lithium oxide (Li2O). Then, both Li2O and lithium hydroxide (LiOH) are formed on increasing pressure, thus, creating a Li2O/LiOH bilayer. The reaction takes place through the consumption of LiH and the formation of Li2O at the LiH/Li2O interface and through the consumption of Li2O and the formation of LiOH at the Li2O/LiOH interface. Above 10 hPa, only the monohydrate LiOH·H2O is formed. T…
Thermoluminescence study of irradiated lithium orthosilicate
1998
Abstract The thermoluminescental investigations of neutron and gamma irradiated lithium orthosilicate pellets were carried out. It has been shown that the addition of Cr 3+ and Fe 3+ ions with the total concentration up to 2.0 wt.% during preparation of lithium orthosilicate pellets, significantly reduces the formation of radiation defects in irradiated matrix. This phenomena can be explained by the reducing of the formation of primary radiation defects during irradiation due to stimulating the recombination processes by the ions of impurities. Several ion concentration combinations were studied. The thermoluminescental investigations of fast neutron irradiated lithium orthosilicate pellets…
Enhanced interfacial lithium storage in nanocomposites of transition metals with LiF and Li2O: Comparison of DFT calculations and experimental studies
2008
Abstract Me/LiX nanocomposites (Me – transition metal and X = F or O) exhibit extra lithium storage, with pseudo-capacitive behavior and high-rate performance. While LiX surface layers or the interfacial core serves as hosts for extra Li, atoms of contacting transition metal serve as electron sinks, depending on Me electronegativity. To verify the mechanism, we have performed comparative DFT-LCAO calculations on the polar Ti|Li|Li2O(111) and non-polar Cu|Li|LiF(001) interfaces with extra Li atoms inserted inside both 2D interfaces, gradually changing their concentration. Theoretical calculations confirm validity of this interfacial model for explanation of the extra storage capacity at low …
The role of radiolysis products in in situ luminescence of Li2O
1998
Abstract A new phenomenon of an “excess luminescence” (EL) in Li 2 O observed at 4.5–2.5 eV under light ion (H + , He + ) irradiation during the rise of temperature (>573 K ) was studied. The essence of the EL is in the rapid pulse increase of the luminescence intensity. It is proposed that this phenomenon is based on the thermo-dissociation of colloidal Li into Li lattice ions, F + and F 0 centers, and oxygen vacancies. Formed oxygen vacancies capture electrons during the irradiation and form excited F-centers, whose relaxation gives the EL. This phenomenon was reproduced using X-ray irradiation and a sample containing colloidal Li introduced by irradiation with electron accelerator to an …
Investigation on lithium/polymer electrolyte interface for high performance lithium rechargeable batteries
1997
Abstract Performance data of several linear and cross-linked polymer electrolytes are reported and the electrochemical criteria for the selection of electrolytes to be used in electric vehicle lithium metal batteries are discussed. Further, laboratory lithium cells with LiMn2O4 composite cathode were tested to ascertain the effective viability of these polymer in solid-state batteries and preliminary results are reported. This study clearly demonstrates the importance of a broad-based electrochemical characterization in selecting an electrolyte for lithium metal batteries.