MnTi co-doping in Mg2Al4Si5O18 ceramics enhances Q factor and improves temperature stability with a τf value closer to zero

Abstract

Co-doping of ions effectively modulates structures and properties of functional ceramic materials. This study fabricated the Mg2Al4Si5−x(Mn0.5Ti0.5)xO18 (0 ≤ x ≤ 0.16) ceramic via solid-state reaction method and achieved remarkable dielectric properties, with values of εr = 4.907, Q × f = 159 681 GHz, and τf = −21.075 ppm °C−1. The intricate connection between microwave dielectric characteristics and crystalline framework received comprehensive examination through the lens of the complex chemical bond theory. The dielectric constant (εr) of Mg2Al4Si5−x(Mn0.5Ti0.5)xO18 (0 ≤ x ≤ 0.16) ceramics primarily depends on material density, bond ionization, and ionic polarization capacity. The quality factor (Q × f) rose 2.24-fold due principally to enhanced lattice energy, with this Q × f value also correlating to the symmetry of [Si4Al2] and [O6] hexagonal rings within the pyroxene crystal structure. The temperature coefficient of the resonant frequency (τf) is mainly attributed to the bond energy and deformation of the [MgO6] octahedra. This study innovatively employs (Mn0.5Ti0.5)4+ to co-dope the Si4+ sites in Mg2Al4Si5O18 based on ionic radius matching, achieving synergistic optimization of Q × f and τf. These findings offer critical guidance for developing silica ceramics featuring elevated Q × f values and near-zero τf characteristics for 6G communication systems.

Graphical abstract: MnTi co-doping in Mg2Al4Si5O18 ceramics enhances Q factor and improves temperature stability with a τf value closer to zero

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Article information

Article type
Paper
Submitted
07 Jan 2026
Accepted
09 Feb 2026
First published
10 Feb 2026

J. Mater. Chem. C, 2026, Advance Article

MnTi co-doping in Mg2Al4Si5O18 ceramics enhances Q factor and improves temperature stability with a τf value closer to zero

K. Ding, Y. Li, L. Fan, X. Liu, H. Wang, J. Yan, L. Xu, W. Chen, X. Wang, Y. Lai, J. Li and Y. Liao, J. Mater. Chem. C, 2026, Advance Article , DOI: 10.1039/D6TC00047A

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