Crystal structures, chemical bond features, and Raman vibrations of Li2Co2Mo3O12 microwave dielectric ceramics with low sintering temperature

Li2Co2Mo3O12 (LCMO) ceramics were synthesized using the solid-state reaction method. X-ray diffraction analysis results indicated that the sole crystalline phase present in the ceramics was LCMO, which belongs to the orthorhombic structure of the Pnma space group. The sample, which was sintered at 850 degrees C, demon-strated outstanding microwave dielectric properties, with an er value of 8.95, a Q x f value of 43 200 GHz, and a t(f) value of -71.3 ppm/degrees C. It was found that while the main factor influencing er was ionic polarizability, sintering density had a lesser effect on it. Furthermore, Q x f was primarily affected by relative density, and there was no significant relationship between packing fraction and this property. The higher the degree of distortion of the [Li/CoO6] octahedron is, the poorer the tf value of LCMO ceramics. Additionally, the microwave dielectric properties of LCMO ceramics were intrinsically linked to ionicity, lattice energy, bond energy, and thermal expansion coefficient of chemical bonds, with Mo-O bonds being the primary factor affecting these properties, as supported by analysis using chemical bonding theories. Mo-O bond vibration dominated the Raman spectra. Good chemical compatibility between silver and LCMO ceramics was demonstrated through our co-firing experiment.

Automated summary

Li2Co2Mo3O12 (LCMO) ceramics were synthesized using the solid-state reaction method, and their microwave dielectric properties and influencing factors were studied. It was found that ionic polarizability was the main factor affecting the dielectric constant (er), while relative density had a significant impact on the quality factor (Q x f). In addition, the microwave dielectric properties of LCMO ceramics were closely related to ionicity, lattice energy, bond energy, and thermal expansion coefficient of chemical bonds.