ABSTRACT
Rechargeable Li-metal/Li-ion all-solid-state batteries due to their high safety levels and high energy densities are in great demand for different applications ranging from portable electronic devices to energy storage systems, especially for the production of electric vehicles. The Li1.5Al0.5Ge1.5(PO4)3 (LAGP) solid electrolyte remains highly attractive because of its high ionic conductivity at room temperature, and thermal stability and chemical compatibility with electrode materials. The possibility of LAGP production by the glass-ceramic method makes it possible to achieve higher total lithium-ion conductivity and a compact microstructure of the electrolyte membrane compared to the ceramic one. Therefore, the crystallization kinetics investigations of the initial glass are of great practical importance. The present study is devoted to the parent glasses for the production of Li1.5+xAl0.5Ge1.5SixP3-xO12 glass-ceramics. The glass transition temperature Tg is determined by DSC and dilatometry. It is found that Tg decreases from 523.4 (x = 0) to 460 °C (x = 0.5). The thermal stability of glasses increases from 111.1 (x = 0) to 188.9 °C (x = 0.3). The crystallization activation energy of Si-doped glasses calculated by the Kissinger model is lower compared to that of Si-free glasses, so glass-ceramics can be produced at lower temperatures. The conductivity of the glasses increases with the growth of x content.
ABSTRACT
Synthesis, thermodynamic properties, and microscopic magnetic model of ilinskite-type KCu5O2(SeO3)2Cl3 built by corner-sharing Cu4 tetrahedra are reported, and relevant magnetostructural correlations are discussed. Quasi-one-dimensional magnetic behavior with the short-range order around 50 K is rationalized in terms of weakly coupled spin ladders (tubes) having a complex topology formed upon fragmentation of the tetrahedral network. This fragmentation is rooted in the non-trivial effect of the SeO3 groups that render the Cu-O-Cu superexchange strongly ferromagnetic even at bridging angles exceeding 110°.
ABSTRACT
We report the synthesis and characterization of the new bismuth iron selenite oxochloride Bi2Fe(SeO3)2OCl3. The main feature of its crystal structure is the presence of a reasonably isolated set of spin S = 5/2 zigzag chains of corner-sharing FeO6 octahedra decorated with BiO4Cl3, BiO3Cl3, and SeO3 groups. When the temperature is lowered, the magnetization passes through a broad maximum at Tmax ≈ 130 K, which indicates the formation of a magnetic short-range correlation regime. The same behavior is demonstrated by the integral electron spin resonance intensity. The absorption is characterized by the isotropic effective factor g ≈ 2 typical for high-spin Fe(3+) ions. The broadening of ESR absorption lines at low temperatures with the critical exponent ß = 7/4 is consistent with the divergence of the temperature-dependent correlation length expected for the quasi-one-dimensional antiferromagnetic spin chain upon approaching the long-range ordering transition from above. At TN = 13 K, Bi2Fe(SeO3)2OCl3 exhibits a transition into an antiferromagnetically ordered state, evidenced in the magnetization, specific heat, and Mössbauer spectra. At T < TN, the (57)Fe Mössbauer spectra reveal a low saturated value of the hyperfine field Hhf ≈ 44 T, which indicates a quantum spin reduction of spin-only magnetic moment ΔS/S ≈ 20%. The determination of exchange interaction parameters using first-principles calculations validates the quasi-one-dimensional nature of magnetism in this compound.
