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Formation of metastable calcite-type barium carbonate during low-temperature decomposition of (Ba,Ti)-precursor complexes

机译:(Ba,Ti)-前体配合物的低温分解过程中亚稳方解石型碳酸钡的形成

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摘要

(Ba,Ti)-precursor complexes, important for the production of advanced BaTiO_3 perovskite-type materials, undergo structural transformations and complex reactions during their thermal decomposition. Based on XRD phase analysis, combined with Rietveld refinement of crystal structure data, and on IR analysis, the intermediate formation of calcite-type BaCO_3 is evidenced, which can be explained by the stabilization of this metastable modification in the form of an oxycarbonate phase down to room temperature. Two possible processes, leading to such an oxycarbonate, are discussed: (i) partial substitution of CO_3~(2-) by O~(2-) in the anionic sublattice, and (ii) topotaxial formation of calcite-type structural domains of BaCO_3 by templating with oxygen-deficient titanates, resulting in the oxide-carbonate intergrowth structures.
机译:对高级BaTiO_3钙钛矿型材料的生产很重要的(Ba,Ti)前体配合物在其热分解过程中会发生结构转变和复杂的反应。基于XRD相分析,结合Rietveld晶体结构数据的精炼,以及IR分析,证实了方解石型BaCO_3的中间形成,这可以通过碳酸盐向下转化形式稳定这种亚稳修饰来解释。到室温。讨论了导致这种碳酸盐的两种可能的过程:(i)在阴离子亚晶格中用O〜(2-)部分取代CO_3〜(2-),以及(ii)偏方形成方解石型结构域。通过用缺氧的钛酸盐进行模板化来生成BaCO_3,从而形成氧化物-碳酸盐共生结构。

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