Temperature stable Sm(Nb1-: X Vx )O4(0.0 ≤ x ≤ 0.9) microwave dielectric ceramics with ultra-low dielectric loss for dielectric resonator antenna applications

  • Fang Fang Wu
  • , Di Zhou
  • , Chao Du
  • , Shi Kuan Sun
  • , Li Xia Pang
  • , Biao Bing Jin
  • , Ze Ming Qi
  • , Jobin Varghese
  • , Qiang Li
  • , Xiu Qun Zhang

Research output: Contribution to journalArticlepeer-review

85 Scopus citations

Abstract

Herein, the structure and dielectric properties of Sm(Nb1-xVx)O4 (SNV-x) (0.0 ≤ x ≤ 0.9) ceramics were studied by crystal structure refinement, Raman, transmission electron microscope (TEM), far-infrared/THz reflectivity spectroscopy and microwave dielectric tests. Three kinds of ultra-low dielectric loss and temperature-stable Sm(Nb1-xVx)O4 (0.2 ≤ x ≤ 0.4) ceramics with permittivities of 18.01-16.89, Q × f values of 97 800-75 200 GHz (@∼8.6 GHz), and TCF of -5.6 (x = 0.2), to +2.3 ppm °C-1 (x = 0.3), then -6.3 (x = 0.4) ppm °C-1 were synthesized in this system. It was found that V5+ substitution can reliably induce the phase transition of monoclinic fergusonite (M-fergusonite, I2/a) to tetragonal zircon phase (T-zircon, I41/amd) (x ≈ 0.3), while effectively reducing the phase transition temperature. TEM shows that there were two different orientation domain structures in the M-fergusonite phase, and the widths of the two domain structures get closer with an increase in B-site substitution. Moreover, the variations in permittivity (ϵr), quality factor (Q × f), and the temperature coefficient of resonance frequency (TCF) were strongly related to the crystal distortion and phase transition. Notably, a rectangular dielectric resonator antenna (RDRA) was fabricated with an Sm(Nb0.8V0.2)O4 (SNV-0.2) specimen. The antenna resonated at 27.04 GHz and had a bandwidth of ∼820 MHz (S11 < -10 dB). This system is a good candidate for 5G and future millimeter-wave applications.

Original languageEnglish
Pages (from-to)9962-9971
Number of pages10
JournalJournal of Materials Chemistry C
Volume9
Issue number31
DOIs
StatePublished - 21 Aug 2021

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