The pyrochlore-type solid-solution formation in a BiMgCuTaO system, synthesized for the first time, is observed at ≤ 0.56. High-temperature X-ray diffraction showed that the pyrochlore phase exists in air up to 1080 °C, where its thermal decomposition leads to the segregation of (Mg,Cu)TaO. The thermal expansion coefficients of the end member, BiMgCuTaO, increase from 3.3 × 10 °C at room temperature up to 8.7 × 10 °C at 930 °C. Rietveld refinement confirmed that the pyrochlore crystal structure is disordered with space group 3̅:2 ( = 8, no. 227). Doping with copper results in a modest expansion of the cubic unit cell, promotes sintering of the ceramic materials, and induces their red-brown color. X-ray photoelectron spectroscopy demonstrated that the states of Bi(III) and Mg(II) are not affected by doping, and the effective charge of tantalum cations is lower than +5, while the Cu(II) states coexist with Cu(I). The electron spin resonance spectra display a single line with = 2.2, ascribed to the dipole-broadened Cu signal. The dielectric permittivity of BiMgCuTaO ceramics may achieve up to ∼10, with the dielectric loss tangent varying in the range from 0.2 up to 12. Multiple dielectric relaxations are found at room temperature and above for all samples.

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http://dx.doi.org/10.1021/acs.inorgchem.1c03053DOI Listing

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