Investigating the ultralow dielectric loss of spinel-like and modified orthorhombic perovskite ceramic structures for microwave applications

ABSTRACT This study prepared ultralow electron-loss perovskites with spinel-like structures via a solid-state reaction. The (Mg0.95Co0.05)2(Ti0.95Sn0.05)O4 (MCTS) ceramic exhibited approximate values for ultrahigh quality factor, permittivity, and negative temperature coefficient (τf) of 310,000 GHz, 14.25, and −48.1 ppm/oC, respectively. To bring the τf closer to zero, a trace amount of (Ca0.95Sr0.05)(Ti0.97Sn0.03)O3 (CSTS) perovskite was added to MCTS during ceramic manufacturing. CSTS exhibited a permittivity of 92 and a large positive τf value of 810 ppm/°C. A 0.92MCTS–0.08CSTS hybrid ceramic sintered at 1325°C achieved remarkable microwave dielectric properties of εr ~18.42, Q×f ~ 237,000 GHz and τf ~3.72 ppm/°C. This mixed ceramic has significant potential for applications in manufacturing microwave devices.


Introduction
Zn 2 SnO 4 has a spinel-type structure [1][2][3][4][5][6][7][8], which is readily obtained via the solid synthesis of initial oxides or decomposition of appropriate double salts.It exhibits high thermal stability and is chemically and structurally characterized, having numerous microwave communication applications, such as patch antennas and wireless communication.However, dielectric substrates of microwave components are limited in their size, gain, and efficiency.When using microwave components, the following three dielectric properties of a material should be considered: low dielectric loss, permittivity, and temperature-independent resonant frequency, i.e. near-zero τ f .Low-loss and high-performance ceramics have been extensively studied.For instance, the (1-x) [Li 2 Ti 0.98 Mg 0.02 O 2.96 F 0.04 −1 wt%Nb 2 O 5 ]-xLi 3 Mg 2 NbO 6 ceramics with a near-zero τ f have been reported [9].The phase composition, microstructure evolution, and microwave dielectric performance were determined as functions of x and the sintering temperature.Ultralow-loss Li 3 Mg 3 NbO 7 ceramics with an orthorhombic rock-salt structure and optimized density (97.7%) have been prepared using a solid-state reaction method [10].The permittivity was mainly affected by the relative density and average ionic polarization, and the total quality factor and other microwave dielectric properties of perovskites were affected by losses, including conduction, radiation dielectrics, and surface waves.(ABO 3 ), and spinel (A 2 BO 4 ) are common structures in perovskite ceramics [11,12]; however, small amounts of additives have been mixed with ceramics to improve their microwave dielectric properties.In previous studies, two low-temperature sintering and high-performing microwave dielectric ceramics were prepared by adding small amounts of V 2 O 5 and 0.6CuO-0.4B 2 O 3 sintering additives to Li 2 Ti 0.75 (Mg 1/3 Nb 2/3 ) 0.25 O 3 (LTMN 0.25 ) [13].Furthermore, an improved (Mg 0.95 Co 0.05 ) 2 TiO 4 ceramic was prepared using a small amount of Co 2+ instead of Mg 2+ in a Mg 2 TiO 4 perovskite [14].The quality factor Q × f of an (Mg 0.95 Co 0.05 ) 2 TiO 4 ceramic lies in the range 140,000-296,000 GHz; however this type of perovskite has a negative τ f .Therefore, a (Ca 1-x Sr x )(Ti 0.97 Sn 0.03 )O 3 perovskite material with a positive τ f is selected for mixed-phase doping [15].Reportedly, the (Ca 0.95 Sr 0.05 )(Ti 0.97 Sn 0.03 )O 3 (CSTS) ceramic has the following microwave dielectric properties: ε r = 91.23,Q × f = 5200 GHz, and τ f = 810 ppm/°C.Similarly, the microwave dielectric properties of (Mg 0.95 Co 0.05 ) 2 (Ti 0.95 Sn 0.05 )O 4 (MCTS) are as follows: ε r = 14.25,Q × f = 310000 GHz, and τ f = −48.1 pm/°C.To bring τ f closer to zero, a hybrid ceramic, 0.92MCTS-0.08CSTSwas formed by mixing CSTS and MCTS perovskites.This hybrid ceramic was used as the microwave ceramic substrate in an ISM band filter.Several analyses were performed using X-ray diffraction (XRD, Cu Kα at 40 kV and 40 mA, Siemens) method, scanning electron microscopy (SEM, Philips XL-40FEG), HP8757D network analyzer, and HP8350 sweep oscillator.

Experimental procedure
The (1-y)MCTS and yCSTS ceramics were prepared via a traditional solid-state reaction using CoO (>99.7%),TiO 2 (>99.9%),CaO (>99.7%),MgCO 3 (>99.7%),SrO (>99.7%),CaCO 3 (>99.7%),and SnO 2 (>99.7%) as raw Based on this equivalent chemical composition, (1-y)MCTS and yCSTS powders were prepared based on the designed composition and mixed with zirconia balls and ethanol solution in a planetary grinder for 12 h.The prepared powders were dried and calcined in air within a temperature range of 1000-1100°C for 4 h before being mixed in the molar fraction of (1-y)MCTS and yCSTS and stirred for 12 h.Under a pressure of 20 MPa, the mixed powder containing 3 wt% and 10% polyvinyl alcohol (PVA 500, Showa, Japan) solution as an adhesive was pressed into oblate spheroid particles of diameter and thickness 1.1 and 0.5 cm, respectively.Thereafter, the pressed particles were sintered within a temperature range of 1250-1400°C for 4 h to form a (1-y)MCTS-yCSTS hybrid ceramic and cooled to room temperature in a furnace.The heating and cooling rates of heaters were set to 10 °C/min.Subsequently, XRD and SEM were used to analyze the crystal structure of the sintered ceramics and surface morphologies of the samples, respectively.The relative densities of the samples were estimated using the Archimedes method, whereas the microwave dielectric properties were measured using a network analyzer based on the Hakki -Coleman [16] and Courtney [17] methods.Furthermore, τ f was estimated within a temperature range of 25-80°C as follows: where f 80 and f 25 are the resonant frequencies at 80 and 25°C, respectively.

Results and discussion
The MCTS ceramic has a crystalline and spinel-like structure in the tetragonal P4_122 space group; however, it possesses two inequivalent (Mg 0.95 Co 0.05 ) 2 + sites.At the first site, an (Mg 0.95 Co 0.05 ) 2 + cation is bonded to six O 2 − anions to form an (Mg 0.95 Co 0.05 )O₆ octahedra that shares corners with six equivalent (Mg 0.95 Co 0.05 )O₄ tetrahedral.The two edges of the octahedra are adjacent to equivalent (Mg 0.95 Co 0.05 )O₆ octahedra and other four edges are adjacent to equivalent (Ti 0.97 Sn 0.03 )O₆ octahedra.At the second site, an (Mg 0.95 Co 0.05 ) 2 + cation is bonded to four O 2 − anions to form an (Mg 0.95 Co 0.05 )O₄ tetrahedra that share corners with six equivalent (Mg 0.95 Co 0.05 )O₆ octahedra or equivalent (Ti 0.97 Sn 0.03 )O₆ octahedra.Similarly, there exist two nonequivalent O 2 sites.At the first site, O 2 − is bonded to three (Mg 0.95 Co 0.05 ) 2 + cations and a (Ti 0.97 Sn 0.03 ) 4 + cation in a rectangular see-saw-like geometry.At the second site, O 2 − is bonded to two Mg 2 + cations and two equivalent Ti 4 + cations in a distorted rectangular see-saw-like geometry.Figure 1 shows the crystal structure of the MCTS ceramic.Figure 2 shows the XRD patterns of the (1-y)MCTS-yCSTS ceramic sintered at 1325°C for 4 h.The type of secondary phase may depend on the ion diameter, dopant content, and sintering temperature.Secondary phases may influence the microstructure, chemical composition, and mechanical and electrical properties of the ceramics.The appearance of (Mg 0.95 Co 0.05 )(Ti 0.95 Sn 0.05 )O 3 as secondary phases may degrade their microwave properties compared to MCTS.The XRD patterns revealed the presence of (1-y)MCTS and yCSTS hybrid phases in these samples.The XRD patterns of (1-y)MCTS-yCSTS ceramics sintered at 1325°C were similar for various y values.In Figure 2 Figure 3 shows the absence of angular displacement in the 0.92MCTS-0.08CSTSceramic.
Figure 4 shows the SEM images of 0.92MCTS-0.08CSTSceramics sintered at various temperatures.The increase in grain size is not significant when the sintering temperature ranges from 1250 to 1275°C.The uniform grains transform to non-uniform grains when the sintering temperature increases from 1375 to 1400°C.Furthermore, a decrease in pores at the grain boundaries can be observed as the sintering temperature increases from 1250 to 1300°C.An anoxic atmosphere is easily formed at such high temperatures, and the evaporation of SnO 2 , such as the reaction 2SnO 2 (g) → 2SnO (g) + O 2 , may lead to a higher porosity [18].Pores at the grain boundaries decrease the ceramic density [19].The 0.92MCTS-0.08CSTShybrid ceramics sintered at 1375°C were distinguished using the energy dispersive X-ray (EDX) analysis in combination with SEM (Figure 5).Table 1 shows the compositional data for regions A and B. The grain morphology of well-developed 0.92MCTS-    the relative densities of (1-y)MCTS -yCSTS hybrid ceramics sintered at various temperatures for 4 h.As the sintering temperature increases up to 1325°C, the relative density increases to a maximum value of 98% (y = 0.08) and then decreases.Figure 5 shows the decrease in relative density owing to the abnormal growth of grains.
Figure 7 shows that the variations in permittivity and relative density are mutually consistent.When the sintering temperature increases to 1325°C, ε r attains its maximum value before decreasing slightly.For the 0.88MCTS-0.12CSTSceramic sintered from 1250 to 1325°C for 4 h, ε r increased from 18.11 to a maximum of 21.77.Table 2 presents the microwave dielectric properties of the (1-y)MCTS -yCSTS ceramics sintered at 1325°C for 4 h.As y increased from 0.08 to 0.12, the ε r value of the (1-y)MCTS -yCSTS ceramic increased from 18.42 to a maximum of 21.77.
The main causes of microwave dielectric losses include lattice vibration modes, porosity, density, secondary phases, impurities, and lattice defects.The factors minimizing the Q × f value can be categorized into internal and external losses.The former is caused by the interaction between polar phonon vibrations in crystals and microwave electric fields, whereas the latter includes ordered and disordered transitions, pore densities, grain sizes, oxygen vacancies, and impurity phases in the ceramics.The defect-free single crystal exhibited the highest intrinsic Q-value, which could be accurately described within the microwave frequency range using the classical damping oscillator model.Using the one-phonon absorption approximation, the model yielded the following approximate reciprocal relationship between Q × f and the dielectric:   where the frequency f should be approximately limited to the phonon engine frequency (10 12 Hz) at room temperature for effective estimation.Reportedly, the extrapolation of Eq. ( 3) can yield a satisfactory Q-value for well-machined ceramics at room temperature, ranging from microwave to megahertz frequencies that are 1-4 orders of magnitude lower than the optical phonon engine frequency.The experimental results yield the following relationship between Q × f and ε r : Therefore, the increase rate of ε r in Q × f is fairly smooth compared to the Q × f values in Eq. ( 4), which can be attributed to external factors.Reportedly, porous dielectrics deteriorate the Q × f value, and the degree of their influence depends on the dielectric type.
For ceramics possessing low Q × f values of the order 10 3 GHz, the effect of porosity on Q can be described as Q ¼ Q o ð1 À 1:5PÞ, where Q o is the intrinsic quality factor measured by microwave reflectance spectroscopy and P is the porosity.However, for ceramics possessing high Q × f values of the order 10 5 -10 6 GHz, such as polycrystalline Al 2 O 3 ceramics, even a small amount of porosity can significantly reduce the Q value according to the following equation: where Q o is the full-density dielectric quality factor 1.565 × 10 −5 , A 0 is a constant 6.3 × 10 −3 , and P is the porosity.Figure 8 shows the Q × f values of (1-y)MCTS-yCSTS ceramics sintered at different temperatures.These values increased till the sintering temperature attained a maxima of 1325°C and then decreased with increasing sintering temperature.A maximum Q × f value of 237,211 GHz was obtained for the 0.92MCTS-0.08CSTSceramic sintered at 1325°C.The degradation of Q × f values can be attributed to abnormal grain growth at excessively high sintering temperatures, as shown in Figure 4. Furthermore, the Q × f value decreases with increasing CSTS content, i.e. the y value increases.This is because the Q × f value of a CSTS ceramic is lower than that of an MCTS ceramic and less than 5,000 GHz.Reportedly, microwave dielectric loss is affected by the sum of the intrinsic and extrinsic losses.The former is caused by lattice vibration modes, crystal structure, and dielectric polarization, whereas the latter is caused by secondary phases, grain boundaries, oxygen vacancies, densification, and porosity.The relationship between the microstructure of a material and sintering temperature affects the properties of phase formation.Liquid-phase sintering with glass additives is an inexpensive and effective method for reducing the sintering temperature.At lower sintering temperatures, the product content was low and the grain size was relatively small, indicating no phase formation.When the temperature increased to 1375°C, the size of each grain remained the same, i.e. a phase was formed.Additionally, the microstructure attained maximum densification, rendering obtaining the optimal Q × f value difficult.
As the sintering temperature continued to increase, the Q × f value decreased owing to excessive grain growth.As the CSTS content increased, the overall Q × f value decreased owing to the low Q × f value of the CSTS.The occurrence of the secondary phase (Mg 0.95 Co 0.05 )(Ti 0.97 Sn 0.03 )O 3 reduced the Q × f value below that of (Mg 0.95 Co 0.05 ) 2 (Ti 0.97 Sn 0.03 )O 4 .
Figure 9 shows the τ f values of (1-y)MCTS-yCSTS ceramics sintered at various temperatures.The τ f value was affected by material composition, additives, and second phase.Because the τ f values of MCTS and CSTS were −47.5 and + 810 ppm/°C, respectively, the increase in CSTS content led to a more positive τ f value.Hence, a zero τ f value can be achieved by adjusting the CSTS content in the (1-y)MCTS-yCSTS ceramic.When the 0.92MCTS-0.08CSTSceramic was sintered within a temperature range of 1250-1400°C for 4 h, the τ f value was approximately 3.79 ppm/ o C, which is close to zero, indicating good temperature stability.When the y value increased from 0.08 to 0.12, the τ f value of the (1-y)MCTS-yCSTS ceramic varied from 3.79 to 22.22 ppm/°C, as shown in Table 2.  Figure 10 shows the physical layout of the designed filter with a center frequency of 2.4 GHz, and Table 3 lists the simulation results.Compared with FR4 and alumina, using the 0.92MCTS-0.08CSTSceramic as the filter reduced the size and insertion loss to 0.37 dB.This design method can facilitate electromagnetic simulators (HFSS) to accomplish filter design and determine the physical size of the filter.

Conclusions
This study incorporated CSTS into MCTS to form the (1-y)MCTS-yCSTS hybrid ceramic with an adjustable τ f value and dielectric varying with y.The primary and secondary crystal phases were the (1-y)MCTS-yCSTS and (Mg 0.95 Co 0.05 )(Ti 0.95 Sn 0.05 )O 3 ceramics, respectively.At a sintering temperature of 1325°C, the 0.92MCTS-0.08CSTSceramics exhibited excellent microwave dielectric properties with the following parameters: permittivity ~ 18.42; Q × f ~ 237,211 GHz; τ f ~3.79 ppm/°C.Therefore, the 0.92MCTS-0.08CSTSceramic is suitable for fabricating microwave devices.The proposed dielectric combination has a negligible dielectric loss, and its dielectric and temperature characteristics render it promising for practical applications in microwave and next-generation communication systems.