Abstract

AbstractNovel scheelite‐type [Ca0.55(Nd1‐xBix)0.3]MoO4 (0.2 ≤ x ≤ 0.95) ceramics were prepared using the solid‐state reaction method. According to the X‐ray diffraction data, a solid solution was formed in 0.2 ≤ x ≤ 0.95 and all the samples belong to pure scheelite phase with the tetragonal structure. As revealed by Raman spectroscopy, the number of vibrational modes decreased with the increase in x value, which further indicated that Bi3+ ions occupied A‐site of scheelite structure. As the x value increased, the sintering temperature decreased from 740°C to 660°C; the permittivity increased from 12.6 to 20.3; the Qf value first decreased slightly and gradually remained stable. Based on the infrared reflectivity spectrum analysis, the calculated permittivity derived from the fitted data shared the same trend with the measured value. The [Ca0.55(Nd0.05Bi0.95)0.3]MoO4 ceramic sintered at 660 °C attained a near‐zero value temperature coefficient ~τf (−7.1 ppm/°C) and showed excellent microwave dielectric properties with a ɛr ~ 20.3 and a Qf ~ 33 860 GHz, making this system a promising candidate in the ultralow temperature cofired ceramic (ULTCC) technology.

Highlights

  • Microwave device is an important part of the modern wireless communication system, with the 5th generation wireless systems coming

  • When the x value increases, the sintering temperature of the sample gradually decreases from 740°C to 660°C, and the average grain size of the sample decreases from 3.16 μm to 2.78 μm

  • These results indicate that the Bi3+ ion derived from Bi2O3 could effectively lower the sintering temperature and refine grains

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Summary

Introduction

Microwave device is an important part of the modern wireless communication system, with the 5th generation wireless systems coming. The peaks located at 321, 885cm−1 become narrow and these results may indicate that the introduction of (Nd1-xBix)3+ ions made the MoO4 tetrahedron become distorted, which possibly affect the position of peaks and lead to the decrease in Raman vibrational modes.

Results
Conclusion

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