SYNTHESIS, INVESTIGATION AND CONDUCTIVE PROPERTIES OF ALLUAUDITE-RELATED PHASES

N. Strutynska, А. Spivak, R. Kuzmin, M. Slobodyanik
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Abstract

Complex oxide phosphates Na1.5Co1.5Fe1.5(PO4)3, Na1.75Co1.75Fe1.25(PO4)3, Na2Co2Fe(PO4)3 and Li0.25Na1.75Co2Fe(PO4)3, belonging to the alluaudite structural type (monoclinic system, space group C2/c) were synthesized by the melting method with further annealing of the homogenous glasses at a temperature 600°C. According to powder X-ray diffraction data the partial substitution of sodium cations by lithium cations in the initial phosphate matrix Na2Co2Fe(PO4)3 led to decreasing of lattice parameters for Li0.25Na1.75Co2Fe(PO4)3 (a = 11.7572(3) Å, b = 12.4528(4) Å, c = 6.4416(2) Å and β = 113.911(1)°). The FTIR-spectroscopy results confirmed the presence of PO4-tetrahedra in the composition of prepared phases. Modes in the regions of 400–600 cm-1 and 900–1000 cm–1 were assigned to symmetric and asymmetric stretching vibrations of phosphate tetrahedron in the alluaudite-type structure, respectively. The effect of partial substitution of sodium cations by lithium cations in the phosphate matrix Na2Co2Fe(PO4)3 as well as the decrease of sodium cations amounts in the alluauditerelated structure for the phases of Na1.5Co1.5Fe1.5(PO4)3 and Na1.75Co1.75Fe1.25(PO4)3 on the conductive properties of compounds were analyzed. It was found that increasing of sodium cations amount in the channels of the alluaudite-related structure leads to an increase of the specific conductivity from 0.011 Om-1m-1 for Na1.75Co1.75Fe1.25(PO4)3 to 0.15 Om–1m–1 for Na2Co2Fe(PO4)3 at a temperature of 550 °C. It was also found that partial substitution of sodium cations by lithium cations in the initial phosphate matrix Na2Co2Fe(PO4)3 no significant influence on conductivity of phase Li0.25Na1.75Co2Fe(PO4)3 (σ = 0.095 Оm–1m–1 at a temperature of 550 °C). In the case of phosphates Na1.75Co1.75Fe1.25(PO4)3 and Li0.25Na1.75Co2Fe(PO4)3 decreasing of conductive properties in the temperature ranges 190–250 °С and 550–590 °С, respectively are caused by contribution of different components in general conductivity. The synthesized phases can be used in the development of materials with conductive properties.
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冲积土相关相的合成、研究及其导电性能
在600℃温度下对均质玻璃进一步退火,采用熔融法制备了具有单斜晶系、空间群为C2/c的复配氧化物磷酸盐Na1.5Co1.5Fe1.5(PO4)3、Na1.75Co1.75Fe1.25(PO4)3、Na2Co2Fe(PO4)3和Li0.25Na1.75Co2Fe(PO4)3。粉末x射线衍射数据表明,初始磷酸基Na2Co2Fe(PO4)3中钠离子部分被锂离子取代导致Li0.25Na1.75Co2Fe(PO4)3晶格参数下降(a = 11.7572(3) Å, b = 12.4528(4) Å, c = 6.4416(2) Å, β = 113.911(1)°)。红外光谱结果证实了所制备相中存在po4 -四面体。在400 ~ 600 cm-1和900 ~ 1000 cm-1区域,分别为冲积型结构中磷酸盐四面体的对称和非对称拉伸振动模态。分析了磷酸基Na2Co2Fe(PO4)3中钠离子被锂离子部分取代的影响,以及Na1.5Co1.5Fe1.5(PO4)3和Na1.75Co1.75Fe1.25(PO4)3相的冲泡相关结构中钠离子数量的减少对化合物导电性能的影响。结果表明,在550℃时,随着冲蚀相关结构通道中钠离子数量的增加,Na1.75Co1.75Fe1.25(PO4)3的比电导率从0.011 Om-1m-1提高到0.15 Om-1m-1。在初始磷酸盐基体Na2Co2Fe(PO4)3中,锂离子部分取代钠离子对Li0.25Na1.75Co2Fe(PO4)3相的电导率无显著影响(550℃时σ = 0.095 Оm-1m-1)。磷酸盐Na1.75Co1.75Fe1.25(PO4)3和Li0.25Na1.75Co2Fe(PO4)3在190 ~ 250°С和550 ~ 590°С范围内导电性能下降,分别是由于不同组分对总电导率的贡献所致。合成相可用于导电材料的研制。
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