偏心因子
化学
电化学
快离子导体
电解质
碱金属
介电谱
离子电导率
结晶学
分析化学(期刊)
差示扫描量热法
电导率
熔点
电阻率和电导率
物理化学
热力学
电极
电气工程
物理
工程类
色谱法
有机化学
作者
Cyrille Galven,V. Albin,Simon Hubert,Virginie Lair,Armelle Ringuedé,Marie‐Pierre Crosnier‐Lopez,F. Le Berre
标识
DOI:10.1021/acs.inorgchem.3c00932
摘要
Two new acentric oxycarbonates Na6Li4MO4(CO3)4 (M = W and Mo) were synthesized via a conventional solid-state route. Their structure was determined from X-ray diffraction data on single crystals. Na6Li4MO4(CO3)4 (M = W and Mo) crystallizes in the acentric cubic P-43m space group (a ≈ 7.15 Å). It is composed of MLi4O16 units built from MO4 and LiO4 tetrahedra and linked by CO32– groups to form a three-dimensional framework in which Na+ ions are inserted. We showed from differential scanning calorimetry and powder X-ray diffraction experiments that the melting is congruent (T ∼525 °C). In the solid and molten forms, conductivity was measured for both oxycarbonates by electrochemical impedance spectroscopy with three various gas compositions (CO2 100 vol %, CO2–air 70–30 vol %, and CO2–air 20–80 vol %). Each time, the stability of the electrical behavior was checked via heating and cooling cycles. The conductivity of both solid and molten phases is purely ionic and in the same order of magnitude as for the classical molten alkali electrolyte made of Li-Na or Li-K carbonates. As activation energies are also comparable, those new oxycarbonates appear to be promising electrolytes for electrochemical devices.
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