1. Introduction
For TBCs, a low thermal conductivity and sintering rate, a good phase stability and adherence, as well as compatibility with the thermal expansion coefficient (TEC) are typical criteria [
1,
2,
3]. Recently, as a novel material for TBCs, La
2(Zr
0.7Ce
0.3)
2O
7 (LZ7C3) with matching parameters has elicited people’s wide concern and consideration. The significance of LZ7C3 has been certified and reviewed through a significant amount of research, whether in powder or in coating form. Yin et al. studied the hot corrosive behavior of La
2(Zr
0.7Ce
0.3)
2O
7 using a salt mixture (Na
2SO
4 + V
2O
5) [
4]. Che et al. devoted their work to the investigation of the structural and thermophysical properties of La
2(Zr
0.7Ce
0.3)
2O
7 through a molecular dynamic simulation, as well as through other experiments [
5]. Wang et al. prepared nano-sized La
2(Zr
0.7Ce
0.3)
2O
7 using the hydrothermal method and evaluated its relevant performance compared with 8YSZ and La
2Zr
2O
7 [
6]. Such previous studies have demonstrated that La
2(Zr
0.7Ce
0.3)
2O
7 is a promising material for the application of TBCs.
In fact, the performance of the powders/coatings is not only reliant upon their structures and components but also bound by their morphologies and particle sizes; thus, selecting a suitable synthesis method is essential to improving TBC properties. Furthermore, relevant reports have identified that some properties of TBC materials are influenced by extrinsic and intrinsic factors; for instance, the sintering rate is closely related to the activation energy for crystal growth (AECG), the micro-strain (MS) limits crystal growth behavior, and the chemical factors (such as adsorbed atoms) can change the surface energy and influence the correlation properties further [
7]. Additionally, such factors are more or less affected by synthetic routes, therefore implying that the influence of synthetic processes is not ignorable.
Nano-sized particles, on the other hand, differ obviously from their bulk counterparts due to their highly specific surface area, their greater grain boundaries, and their quantum effect. The larger S
BET (specific surface area) leads to a faster reaction rate and enhances the strength properties, the grain boundary is well correlated to the TEC of the material [
8], and the quantum effect is conducive to improving the relevant natures [
9], implying that the thermal as well as mechanical properties of the nano-sized materials notably improved in comparison with their corresponding bulk counterparts. At this point, various synthesis methods have been developed in order to obtain nanopowders with different particle diameters, size distributions, and morphologies. Among these methods, the hydrothermal and sol-gel techniques stand out due to their main advantages: low cost, simplicity, and ability to control the parameters of the reaction [
10,
11]. To those authors’ knowledge, nevertheless, there is a lack of information concerning the influences of the synthetic processes on the thermophysical properties of La
2(Zr
0.7Ce
0.3)
2O
7. Since the physicochemical properties of powders are controlled by the reaction environment and the nucleation process, adopting an advisable method in order to create high-performance powders is important.
The present study looks at the systematic comparisons, as described here, for La2(Zr0.7Ce0.3)2O7. The study also looks at the effects of the synthetic processes (sol-gel and hydrothermal processes) on the thermophysical properties, such as the phase structure, the thermal conductivity, TEC, the anti-sintering properties, the micro-strain, AECG, etc., as well as their related mechanisms that are also discussed in detail.
3. Results and Discussion
Figure 1 presents the TG-DSC profiles of LZ7C3-HT and LZ7C3-SG from room temperature up to 1200 °C. Despite that these curves display a similar shape, some tiny distinctions can also be found. The total mass loss in LZ7C3-HT is 40–42%, which is slightly higher than that in LZ7C3-SG (39–41%). The major mass losses corresponding to the two remarkable exothermic peaks are around 195 and 423 °C for the DSC curves, which can be attributed to the removal of the water molecule and the decomposition of organic substances (citric acid, ethanol, and so on) [
12,
13]. No significant endothermic or exothermic peaks can be found above 550 °C for the TG and DSC curves, implying that such behaviors are completed.
Figure 2a,b give the XRD patterns of LZ7C3-HT and LZ7C3-SG powders calcined at various temperatures. All diffraction peaks of both samples are well matched with a pyrochlore structure (JCPDS 17-0450). The peaks around 28.7, 32.9, 35.9, 43.5, and 47.4° can be well indexed to the (222), (400), (331), (511), and (440) planes of the pyrochlore structure, respectively. No traces of other impurities can be detected in the whole test temperature range, suggesting that both samples possess an excellent thermal stability. Additionally, LZ7C3-HT displays better crystallinity than LZ7C3-SG, which can be attributed to the pressure in the autoclave generated during the heating reaction [
14]. It is worth noting that, compared with LZ7C3-HT, the peak positions of LZ7C3-SG show a tiny blue shift (
Figure 2c), implying a mismatch in lattice parameters between both samples. For this, the lattice parameters of LZ7C3-HT and LZ7C3-SG were further calculated, and the determined values were 10.81 and 10.84 Å, respectively. The Raman spectra of both samples sintered at 1300 °C were also investigated to further verify the phase structure, as shown in
Figure 2d. It has been confirmed that rare earth zirconates with a pyrochlore structure possess six vibration modes, corresponding to the A
1g, E
g, and 4T
2g modes. In our cases, the spectra of both samples are remarkably similar with the exception of the peak intensity. The band located at 292 cm
−1 belongs to the E
g mode, and the two residual bands around 386 and 495 cm
−1 can be assigned to the 2T
2g mode. For the other three modes (A
1g and 2T
2g), they are too weak at a normal pressure and are almost invisible [
6]. In addition, no obvious characteristic peaks of other structures can be observed in both curves, meaning pure pyrochlore structures for both samples.
For a comparison of the thermophysical properties of LZ7C3-HT and LZ7C3-SG, the as-prepared powders were compacted at 230 MPa and then sintered at different temperatures.
Figure 3 shows the relative densities and volume shrinkages of both samples, and the detailed measurement processes are described in Ref. [
3]. The relative density of LZ7C3-HT is smaller than that of LZ7C3-SG, as seen in all of the test temperature points (
Figure 3a). For both samples, the increase in relative density is obvious before reaching 1200 °C and then becomes gradual as the temperature further increases. At 1400 °C, the relative density determined for LZ7C3-HT is 83–84%, which is lower than that of LZ7C3-SG (88–89%). On the other hand, the volume shrinkage of both samples decreases simultaneously as the temperature increases, as shown in
Figure 3b. Such results are consistent with the conclusion reported by Cao [
15]. On the other hand, the volume shrinkage of LZ7C3-HT is 11–12% after heat-treatment at 1400 °C, while the corresponding value of LZ7C3-SG is 13–14%.
The SEM micrographs of the as-prepared powders and the surface of the compacted bodies of LZ7C3-HT and LZ7C3-SG calcined at 1400 °C are shown in
Figure 4. Clearly, the selected synthetic methods have obvious effects on the morphologies of the samples (
Figure 4a,b). LZ7C3-HT exhibits spherical particles with a uniform size, while LZ7C3-SG exhibits entirely different microstructures, and the polyhedron agglomerates are dominant. Moreover, the morphology of the compacted body surface can give us some information about the anti-sintering property of the material. As shown in
Figure 4c, LZ7C3-HT shows a uniform particle size and well-defined boundaries compared with those of LZ7C3-SG. It is worth stressing that some micropores can also be observed on the surface of the body and are beneficial for improving the TEC of the coatings. Additionally, despite LZ7C3-SG (
Figure 4d) possessing a denser body structure and larger particle size, no abnormal growths can be found and the boundaries are still clear. By contrast, LZ7C3-HT possesses a superior anti-sinterability than LZ7C3-SG.
As known to all, cation diffusion affects the densification/grain growth of materials [
16]. The mainstream mechanisms include two aspects: the solute drag mechanism and the lattice distortion mechanism. For the former, the space charge layer can be formed at the grain boundary region, which can impede on the grain boundary migration. For the latter, the mismatch in ionic radii will lead to the distortion of the lattice [
17]. As illustrated in Ref. [
18], for the crystals, the local distortions give rise to the nonhomogeneous micro-strain that is accompanied by variations in some characteristics of XRD peaks, such as peak broadening. The micro-strain can bring the mobility of cations down and further affect the densification/grain growth of the materials [
19]. Moreover, the different nucleation processes and the interactions between the inorganic precursor molecules during the nucleation processes that originate from different synthetic routes can also cause a mismatch in the micro-strain. At this point, the contributions of the crystal size and the micro-strain need to be considered. The Scherrer equation cannot work well for such cases and should be modified so the following relation can be obtained [
20].
Here
β,
θ,
λ,
L, and
ε are the full width half maximum, diffraction angle, wavelength of X-ray radiation, average size, and micro-strain, respectively, and K is set at 0.9, generally. Based on Equation (3), L and ε can be calculated based on the slope of
βcos
θ vs. 2sin
θ.
Figure 5 represents the relationship between
βcos
θ and 2sin
θ with different peaks and temperatures, and 2
ε (the slope of straight line) and kλ/L (intercept) can be obtained from the curves. For the micro-strain, the values of LZ7C3-HT determined from 1000 to 1400 °C are 0.4698 ± 0.0008, 0.2132 ± 0.0005, 0.0983 ± 0.0003, 0.0792 ± 0.0002, and 0.0747 ± 0.0001. Meanwhile, the corresponding values of LZ7C3-SG are 0.1647 ± 0.0008, 0.1215 ± 0.0004, 0.1027 ± 0.0003, 0.0839 ± 0.0002, and 0.0802 ± 0.0001. Additionally, the average crystal sizes (nm) of both samples are calculated and displayed in
Table 1.
Generally, the micro-strain is mainly derived from local distortions of the atoms in the lattice, including dislocations, defects, and grain boundaries. As we know that for LZ7C3, La
2O
3 dissolves in ZrO
2 and CeO
2 crystal lattice by substitution solid solution, La
3+ as the dopants, will be expelled and occupy the surface sites due to the “self-purification” mechanism, resulting in a reinforced grain boundary defect density and a large micro-strain. Thus, the grain boundary microstructure is the dominant contribution to the micro-strain in this study [
21]. After annealing at a higher temperature however, the rearrangement of the local position of the atoms and the decrease in the density of the grain boundary defects will result in the release of the micro-strain. Consequently, the micro-strain decreases as the temperature increases. Interestingly, it should be noted from
Figure 5, that the obtained values of both samples show different trends with 1200 °C as the inflection point. Below 1200 °C, the values of LZ7C3-HT are larger than those of LZ7C3-SG, which may be due to the faster nucleation based on the synthesis conditions of the hydrothermal method [
22]. With a reinforced nucleation rate, La
2O
3 rapidly dissolves in ZrO
2 and CeO
2 crystals, and transfers to the surface sites, enhancing the grain boundary defect density, and brings a large micro-strain. Besides, the morphology of LZ7C3-HT is more uniform than that of LZ7C3-SG, According to Rush’s report [
23], the high micro-strain with a small particle size may be closely bound with S
BET and the morphology of materials. On the other hand, for the high temperature zone, the micro-strain values of LZ7C3-HT and LZ7C3-SG are quite the opposite. From
Table 1, it is noteworthy that the mean particle sizes of both samples exhibit the consistent trend with the micro-strain. Above 1200 °C, the average particle sizes of LZ7C3-SG are larger than those of LZ7C3-HT, and the mismatch becomes larger and larger, demonstrating that LZ7C3-SG possesses a more rapid growth rate than LZ7C3-HT. Nevertheless, a fast crystal growth rate will cause lattice distortion, forming more defects, and resulting in a larger micro-strain.
Furthermore, as stated in our previous studies [
16,
24], regarding the TBC materials, there are two competitive aspects in the crystal growth processes which are known as crystallization and sintering. Crystallization can impede the densification of materials, while sintering will lead to the degradation of its thermophysical performance due to the absence of micropores and microcracks. Thus, the activation energy of the crystal growth (AECG) of the TBC materials should be investigated in-depth. To this end, AECG of both samples were calculated based on Equation (4) with the mean crystal size (as shown in
Table 1) obtained through Equation (3) [
24]:
Here,
Dt and
D0 correspond to the mean particle sizes for the initial and final temperatures, respectively. R is the gas constant, and T denotes the temperature. Based on Equation (4), the plot of Ln (
Dt/
D0) vs. 1000/T for the two samples is exhibited in
Figure 6, and AECG (Q) can be obtained from the slope. The values determined based on the above equation were found to be 99.31 ± 0.04 and 53.84 ± 0.05 KJ mol
−1 for LZ7C3-HT and LZ7C3-SG, respectively. It is worth noting that the greater AECG means a slower crystal growth rate, which offers a better anti-resistance property for the materials. It is recognized that the crystal growth behavior is closely tied to defects, oxygen vacancies, micro-strain, and so on. For the La
2(Zr
0.7Ce
0.3)
2O
7 system, La
3+ will be expelled to the surface, enhancing the grain boundary defect density and micro-strain; both factors have substantial effects on the crystal growth behavior [
25]. As mentioned above, LZ7C3-HT possesses a larger micro-strain than LZ7C3-SG below 1200 °C and the large micro-strain can impede the formation of necks between particles to form big particles, leading to a bigger AECG. On the other hand, above 1200 °C, based on studies by Leite et al. [
26], who proposed a grain-rotation-induced grain coalescence model for the growth of nanocrystalline materials, assuming that the crystallographic orientations of the grains are in agreement, the rotation of the particles gives rise to a coherent interface among neighboring particles, allowing for single, large grains to form through the elimination of the grain boundaries of the particles. In our cases, in comparison with LZ7C3-SG, LZ7C3-HT exhibits smaller particle sizes and more regular morphologies, causing more complicated grain boundaries. To eliminate the grain boundaries in order to form big particles, more energy is required, and thus, the AECG of LZ7C3-HT is larger than that of LZ7C3-SG for high temperature ranges.
Figure 7 presents the thermal expansion coefficients and thermal conductivities of LZ7C3-HT and LZ7C3-SG under different temperatures, respectively. Obviously, the changes in both parameters show an opposing trend as the temperature increases. For each temperature point, LZ7C3-HT has higher TEC values than LZ7C3-SG. For example, the value of LZ7C3-HT at 1300 °C is 11.43 ± 0.06 × 10
−6 K
−1, while the corresponding value of LZ7C3-SG is 11.23 ± 0.05 × 10
−6 K
−1. This difference may be attributed to the small crystal size and the regular morphology of LZ7C3-HT. According to Rupp’s report [
27], for nanocrystallites, the TEC is dependent upon the microstructure of the grain boundary. The larger the grain boundary defect density is, the more enhanced the TEC will be. The vibrational motion of the atom is sensitive to its surrounding coordinates. The enhanced static shift in the atoms and the bigger micro-strain lead to an increased TEC. On the other hand, the thermal conductivities determined for LZ7C3-HT and LZ7C3-SG are 0.81 ± 0.03 and 0.84 ± 0.02 W m
−1 K
−1, respectively.