Crystallographic and TEM Features of a TBC/Ti2AlC MAX Phase Interface after 1300°C Burner Rig Oxidation

A FIB/STEM interfacial study was performed on a TBC/Ti₂AlC MAX phase system, oxidized in an aggressive burner rig test (Mach 0.3 at 1300°C for 500 h). The 7YSZ TBC, a-Al₂O₃TGO, and MAXthal 211 Ti₂AlC base were variously characterized by TEM/STEM, EDS, SADP, and HRTEM. The YSZ was a mix of ‘clean’ featureless and ‘faulted’ high contrast grains. The latter exhibited ferro-elastic domains of high Y content tetragonal t'' variants. No martensite was observed. The TGO was essentially a duplex a-Al₂O₃ structure of inner columnar plus outer equiaxed grains. It maintained a perfectly intact, clean interface with the Ti₂AlC substrate. The Ti₂AlC substrate exhibited no interfacial Al-depletion zone, but rather numerous faults along the basal plane of the hexagonal structure. These are believed to offer a means of depleting Al by forming crystallographic, low-Al planar defects, proposed as Ti_2.5AlC_1.5. These characterizations support and augment prior optical, SEM, and XRD findings that demonstrated remarkable durability for the YSZ/Ti₂AlC MAX phase system in aggressive burner tests.

Keywords:

Subject: Chemistry and Materials Science - Surfaces, Coatings and Films

1. Introduction

The durability of a PS-PVD 7YSZ thermal barrier coating on an alumina-forming Ti₂AlC MAX phase was investigated in a high velocity Mach 0.3 (~ 100 m/s) burner test, burning Jet A fuel at atmospheric pressure. The system survived 500 h at a surface temperature of 1300°C, using 5-h cycles, with no backside cooling. The oxidation was modest, gaining just 2.4 mg/cm², exhibiting well-behaved cubic-linear kinetics (Figure 1).[1]

No indication of TBC failure or spallation was apparent. This was compared to furnace cycling of commercial TBC-Ni(Pt)Al bondcoat-superalloy systems with only 30h life projected at 1300°C, and only 7 μm of Al₂O₃ TGO growth sustained.[2] For the 500h YSZ-MAX phase burner test, optical and SEM microstructural analyses revealed an intact 22 μm Al₂O₃ scale under the TBC at the hot gas impingement face and approximately 14 μm on the bare backside. The exposed backside was somewhat cooler and subject to scale volatility, exhibiting a filamentary, etched scale surface structure, with signs of Ti- and Al-oxide attack by moisture-induced volatilization. The frontside YSZ coating underwent sintering and some phase migration to high-Y cubic and low-Y tetragonal, as demonstrated by Rietveld XRD analyses. The expected transformation of low-Y (t) phase to the detrimental monoclinic phase, associated with TBC spallation and delamination, was not observed. The present FIB-STEM study was initiated to support and enlarge upon those microstructural and XRD phase findings, but on a much finer scale.

2. Materials and Methods

The material, coating, and burner test had been described in detail.[3] Briefly, Kanthal/Sandvik MAXthal 211™ Ti₂AlC material was sectioned from a sintered slab and coated in the Sulzer-Oerlikon-Metco plasma spray physical vapor deposition (PS-PVD) facility at the NASA Glenn Research Center. The burner rig utilized 120 psig (800 kPa) filtered shop air and approximately 1.1 kg (2.5 lb)/min airflow, preheated and mixed with atomized Jet-A fuel. Combustor pressure was 1 psi (6.9 kPa) above ambient to produce a Mach 0.3 flame velocity through a 1 in. (2.54 cm) exit nozzle. Flame temperature was monitored by thermocouple, sample temperature by optical pyrometer (8 μm wavelength for YSZ, emissivity set at 0.92, and 2-color pyrometer for bare Ti₂AlC) controlled ±5° C by a feedback loop. The YSZ-Ti₂AlC interface was estimated as 1244°C and the bare backside was measured as 1216°C. Cycling every 5 h was produced by pivoting the burner apparatus. Inspections and weighing occurred at 1, 10, 15, 25 h, then every 25 h thereafter, as measured on an analytical balance sensitive to 0.01 mg.

The burner and sample are shown in Figure 2. The YSZ coating was exposed face-on (arrow) to the hot gas exhaust of the burner. The 1300°C test control coating surface temperature was targeted at the centerline of the hot zone. The schematic (2b) illustrates the arrangement of the Ni-plating, YSZ TBC top coat, Al₂O₃ scale (TGO), and Ti₂AlC substrate in the polished cross-section with respect to hot gas impingement (arrow). Finally, a montage of the full cross-section (SEM/BSE, 2c) shows actual microstructural features. The positions of the ~ 20 μm long FIB sections was across the TGO at both front and back faces, incorporating interfaces with the TBC and Ti₂AlC matrix. These site-specific sections (TEM foils) at the coated front and uncoated backside were fibbed out using a ZEISS Auriga dual Focused Ion Beam (FIB)/SEM microscope, and are marked as “FIB, I” and “FIB, II”, resp. in Figure 2. The TEM foils were then examined in a Thermo-Fisher Talos F200S Scanning/Transmission Electron Microscope (S/TEM) for detailed microstructural, phase and chemical analyses.

3. Results

3.1. I) YSZ coated, front side

3.1.1. Overview

The TEM microstructure of the TBC coated side of the test bar from the interfacial region “FIB, I” marked in Figure 2 is shown in Figure 3. The TBC coated side of the test bar was not evenly FIB thinned over the YSZ region. Coarsened porosity was evident and heavily streaked from ion milling near the Ni-plate layer. The Al₂O₃ scale (TGO) showed typical dispersed micro-porosity toward the outer half of the scale, some associated with fine, nm-sized Ti- or Zr- rich precipitates. The Ti₂AlC was faulted, but with no dislocations observed on this hot convex side. The YSZ was a mix of large, featureless, cubic grains and smaller, heavily strained and faulted, believed to be ordered t′′ tetragonal. The monoclinic phase was not observed. The faulted grains contained lathe shaped domains with primarily (100) boundaries, some having (110) facets. These fault arrays indicate ferro-elastic domains used to explain high toughness in the 7YSZ t' phase.[4] Moire' patterns from overlapping, slightly offset or rotated variants, 20-100 nm wide, were also prevalent, consistent with imaging theory. Coarsened, intergranular micro-porosity was ubiquitous. This derived from the desirable dispersed intragranular nano-porosity responsible for low thermal conductivity in PVD -type coatings. Local Fe-oxide particles, identified at the Al₂O₃ surface and in the YSZ, may indicate a processing contamination issue. Iron impurities in our PS-PVD coatings had not typically been seen before.

3.1.2. Microstructures, I. Front

The first image (Figure 3) shows the ~ 22 μm thickness of the Al₂O₃ scale (TGO) at the front, burner side. Also present in this foil is a small amount of the adjoining YSZ of the thermal barrier coating on the left and the Ti₂AlC MAX phase substrate on the right. The alumina grains (columnar) are on the order of 5 μm wide at the Ti₂AlC interface and slightly smaller (equiaxed), ~ 3 μm, at the YSZ interface. More detail is presented in Figure 4. The Al₂O₃ -Ti₂AlC interface is very clean and intact (4b). An array of long planar faults is apparent in a Ti₂AlC grain, reflective of the basal faulting that may occur in MAX phases to accommodate stoichiometric variations, discussed later. The image in Figure 4a is from the central portion of the Al₂O₃ scale. It shows a small amount of intragranular porosity, generally finer than the intergranular pores displayed at lower magnification. Many of the pores are seen to be associated with dark nanoparticles, all quite fine on the order of 100 nm. Similar pore-metal features were observed previously for alloy oxidation and may be typical of alumina scales. The white particle in the STEM image (Figure 5) showed high Y, Zr content (5b), with a small Fe peak, and Cu from the support grid. The Y, Zr implies some diffusion from the TBC to the internal region of the scale. By comparison, EDS analysis of the featureless scale revealed a very clean Al, O composition (5c). Additionally, occasional light grey grains in the TBC match contrast with those at the Al₂O₃ scale interface and are believed to be Fe-rich oxide as indicated by EDS. The TGO/YSZ interface is shown in Figure 6 (a-d), with YSZ, Al₂O₃, and a few Fe-rich grains at the interface. These are likely iron-oxide grains formed due to spurious Fe-contamination during coating processing.

The images in Figure 7 shows the YSZ TBC region which is generally a mosaic of 1-2 μm ‘clear’ (C) and adjacent smaller heavily faulted grains (F). The ‘feathery’ nature of the YSZ columns appears to have sintered away. Large 1-2 μm intergranular pores and finer 0.1-0.2 μm pores are prevalent. The faulted grains are also replete with a high density of strain contours, consistent with transformation stresses. Figure 8a presents the SADP of a clean grain (C) and yields a clean cubic pattern for the ZrO₂ fluorite [110] zone axis. Since no (112) reflections are present in this zone axis, no information is obtained regarding the ordered tetragonal phases. A faulted grain (F), also produced a ‘cubic’ [100] zone axis SADP with {100} and {110} reflections present, Figure 8b. This zone axis also shows a multitude of additional reflections. The latter are probably related to two twinned variants of a tetragonal daughter phase with respect to the cubic parent phase. Figure 9 presents an assemblage of lathes believed to be ferro-elastic tetragonal domains. Such arrays can minimize strain energy under stress. [4,5] The <100>, <110> fault planes are seen as domain boundaries, with the FFT zone axis as [100] for the central grain. Another HRTEM image, Figure 9b, reveals multiple parallel lathes of the YSZ phase, ~ 20 nm wide. While the center lath appears featureless, the two bordering it exhibit similar cross-hatch patterns, in colonies, with some resemblance to Moire' fringes. It is speculated that similar overlapping tetragonal colonies make up these structures. Tetragonal YSZ has nearly identical a, c unit cell dimensions, but varying orientations due to oxygen ion shifts along the z-axis.[6] HRTEM images were obtained near that region and produced a nearly orthogonal lattice structure and corresponding FFT diffraction pattern. (Figure 10) The nodes along 〈100〉, Figure 10b, show a spacing of ~ 0.5 nm (5 Ả), approximating the unit cell dimension of 5.1 Å.

3.2. II) Uncoated, backside

3.2.1. Overview

The TEM microstructure of the uncoated backside of the test bar is from the interfacial region marked “FIB, II” in Figure 2. Prior SEM had shown outermost filamentary, exposed alumina grains or Ti-rich scale remnants. However, this surface was not protected enough during FIB milling and appears to be just out of the span of the foil. Within the retained scale, columnar TGO Al₂O₃ grains are nicely imaged, with more equiaxed grains and porosity toward the gas surface. A small number of fine 25 nm -rich spherical particles were dispersed. Some very small Fe-rich particles were observed at the edge of 50 nm nanopores. The Al₂O₃ - Ti₂AlC interface appeared intact and exceptionally clean. No significant detachment or distress at the interface was indicated. Interface faceting followed Al₂O₃ grains. The Ti₂AlC substrate on this end (concave bending) was replete with dislocations and MAX phase stacking faults on the basal (0001) plane. The Al₂O₃ impurity phase, commonly observed as a processing artefact in Al-MAX phases, was conclusively identified by EDS.

3.2.2. Microstructures, II. Back

Figure 11 presents the uncoated backside of the Ti₂AlC sample. The Al₂O₃ TGO grew to ~ 14 μm; this was less than the front face because of the lower backside temperature of ~ 1214°C. The Al₂O₃ grains were again columnar and presented a very clean, faceted interface with Ti₂AlC. EDS of a grain interior, Figure 12a, shows only Al and O, as well as for a particle (P) in the MAX phase. SADP’s of the TGO (12c, d for grains marked A and B) are consistent with trigonal (pseudo-hexagonal) corundum, a=4.8 Ả, c=12.9 Ả, near Z.A. [21-1] and [48-1] respectively. The very fine nm-size TGO particles in the vicinity of the triple point in Figure 13 a, b yield EDS showing Ti (13 d), while that (F) associated with a pore contains Fe (13 c, e).

Figure 14 shows the interior of Ti₂AlC grains having a dispersion of dislocations, consistent with reported bending deformation at temperature. Other grains contain long parallel fault features, Figure 15a. The EDS spectra for Ti₂AlC (T, 15 b) again produced a clean Ti, Al, C result. Accordingly, the SADP of the grain interior (X, 15 c) shows only the Ti₂AlC hexagonal MAX phase, a= 3.1 Ả, c=13.7 Ả, Z.A. = [210]. Whereas, at faulted regions, (Y, 15 d) extra reflections appear for the basal plane along [001], presumably the fault plane. This corresponds to basal plane stacking sequence variations that can occur due to various Ti_xAl_yC_z stoichiometries. Here, the Al atoms are arranged on the c-plane, every 3^rd layer for the 211 compound, then every fourth and fifth layers for decreasing Al stoichiometries corresponding to 312 Ti₃AlC₂ and 413 Ti₄AlC₃ cells.[7,8] The latter are equivalent to c-plane spacings, respectively, of 4/3 and 5/3 that of the basic 3-layer cell having 211 stoichiometry. Increased d-spacings produce inversely decreased reciprocal lattice spacing. In Figure 15d we have minor reflections produced at the fault boundary (Y), along the c-axis, with (007)_fault superposed on the (006)₂₁₁ reflection. Thus, the d-spacing is 7/6 that of the Ti₂AlC 211 phase, or has 3.5 layers/cell, midway between 211 and 312 MAX phase cells. The fault stoichiometry can therefore be surmised to be Ti_2.5AlC_1.5, or Ti₅Al₂C₃.

4. Discussion

4.1. PS-PVD YSZ TBC.

Table 1 compares the XRD phase analyses of this coating with those from an extensive annealing study by Witz, et al.,[9] both determined from Rietveld full XRD pattern fitting. Both indicate a thermally activated transition from the quenched-in metastable t´ tetragonal, with quenched-in Y content, into the equilibrium, low Y tetragonal (t) + high Y cubic (c). Those general trends were repeated from earlier studies. However, a much higher amount of cubic (28-86 % compared to 4-37%) is shown throughout for our coating, as well as almost negligible 0.5% monoclinic after aging at 1300°C. Given the TEM structures showing nearly equal amounts of cubic and faulted tetragonal grains, (Figure 7), one can only surmise that the faulted tetragonal structures are exhibiting a cubic nature in XRD analyses. Initially, (t) identification was based primarily on {400} peak splitting due to increased c/a. Now, the c-axis vacancy ordering that gives rise to the tetragonality appears to be occurring without a change in lattice constants. Thus, ferro-elastic domains appear in HRTEM imaging, but without the classic (400)_c peak splitting in X-ray diffraction patterns. The proximity and distribution of the ‘clear’ and faulted grains is consistent with Y partitioning and phase separation.

The Y content in the various phases was estimated from Rietveld lattice parameters and calibration formulas from the literature. The results based on a c/a calibration are also shown in Table 1. The present coating is seen to have higher as-sprayed YO_1.5 content in the cubic phase compared to that of Witz et al. (n. the 926°C/0.17 h condition here is considered to be essentially as-sprayed). The cubic results from the two studies are similar after 1100°C and 1200°C exposures, at 13-15%, but lower here after 1300°C, at 9% vs 15%.

According to the study by Azzopardi, et al., 2004, [10] for PVD t´ YSZ coatings, the initial metastable tetragonal t′ phase transforms into a mixture of yttria-poor tetragonal phase t and yttria-rich cubic c phase upon thermal aging, as described previously over many years. However, on cooling, the c phase can further transform into an yttria-rich t′′ phase[11] that has tetragonal symmetry but cubic dimensionality. The yttria-poor t phase does not transform to monoclinic, presumably because of the fine grain size and stress constraints on the transformation. That t phase should not be considered ‘non-transformable t′, e.g., upon grinding. To make matters more complex, these t + c phases evolved into a fine, 10 nm banded domain structure.

It is therefore postulated that the present study exhibits faulted t′′ YSZ grains, transformed from cubic parent grains on cooling. A domain structure reflects the three different tetragonal variants possible from a cubic parent, usually shown by dark field imaging using the (112) extra spots. Here they are shown as domain boundaries in HRTEM, with a node spacing of 5 Ả. But the low Y content (9%) is more representative of t′′ rather than equilibrium phase-separated cubic. Martensite has not formed due to the small grain size of any parent structures and was not obvious in the TEM microstructures or previous XRD. The ‘clear’ cubic grains have retained the equilibrium c structure. Further subtleties and delineations are beyond the scope of this work. The presence of these domains, even after extensive thermal exposure, probably contributes to the overall mechanical durability of the coating upon cycling, as does the absence of the disruptive monoclinic transformation.

4.2. Al₂O₃ TGO.

The alumina scales exhibited typical inner columnar grains and more equiaxed outer grains. At the frontside YSZ interface, some Fe-rich scales were observed and presumed to result from some Fe-rich chamber contamination during the initial plasma spray conditions, before deposition. None were seen on the backside. Small included Zr(Y) particles were observed underneath the YSZ coating. Intergranular porosity was present in the equiaxed region, but absent in the columnar region. The interior of the grains was essentially featureless, except for minute amounts of fine, 25-50 nm pores and Fe, or Ti-rich particles. Again, the source of the Fe is believed to be migration from initial PSD-PVD contaminants, whereas the Ti indicates some minute presence from the Ti₂AlC substrate. Considering the 2:1 Ti:Al ratio in the 211 MAX phase, it is remarkable that only this small amount of Ti enters into the scale. This is thought to be a vestige of initial Ti-rich transient oxidation before a healing layer of Al₂O₃ is formed. Oxidation of bare Ti₂AlC in high temperature air or oxygen is well known to produce a TiO₂ or TiAl₂O₄ initial scale before a healing, rate-controlling scale of Al₂O₃ is formed underneath. The exclusion of the typical TiO₂ transient outer layers here suggests that low pO₂ pre-oxidation, expected during initial PS-PVD processing, plays a beneficial role here. The stable, long-term growth of Al₂O₃ at 1300°C is confirmed by the chemical and phase purity of the scale at the Ti₂AlC interface. The Al₂O₃ -Ti₂AlC interfacial regions appeared fully intact, smooth, and atomically bonded. (Unfortunately, the filamentary Al₂O₃ TGO surface resulting from scale volatility on the exposed backside [1] was not included in the optimal portion of this FIB section).

4.3. Ti₂AlC substrate.

The MAX phase substrate was fine grained, exhibited a typical Al₂O₃ processing inclusion, but little chemical/phase diversity. Planar, intragranular (basal plane) faults were common, often nearly perpendicular to the Al₂O₃ -Ti₂AlC interface. These are interpreted as a tendency toward local Ti₃AlC₂ chemistry to accommodate reduced Al content. This mechanism allows for maintaining an intact MAX phase – alumina interface without a distinct depletion layer, as is common for alumina-forming alloys or Cr₂AlC. It is perhaps an indication of the ability of the Ti_xAlC_y MAX phases to supply Al rapidly enough through bulk of the substrate along basal planes to support the growing scale. Preferential Al diffusion along basal planes has been proposed to explain preferential Al₂O₃ scale formation and improved oxidation behavior for textured Ti₂AlC, Ti₃AlC₂, and Ti₃(Si,Al)C₂ MAX phases.[12,13,14,15] Here MAX phase basal planes were aligned perpendicular to the hot pressing direction and served to enhance Al diffusion toward side faces (TSS) in comparison to top faces (TTS). The present SADP diffraction results along [001] on a basal plane fault (Figure 15) suggest a fault stoichiometry of Ti_2.5AlC_1.5. Dislocations were also evident as an indication of the macroscopic plastic deformation that occurred in this sample progressively throughout the 500h test. That was manifested as a 2.3 mm cord-wise deflection across the 6.8 cm burner sample length, as bent by the gas flow. [3] Dislocations and plastic deformation are consistent with high creep rates reported for MAX phase structures above 1200°C.[16]

5. Summary

A Ti₂AlC MAX phase substrate was coated on one side with a 7YSZ TBC by PS-PVD. The sample was oxidized in a Mach 0.3 burner rig at a 1300°C surface temperature for 500 h with no indication of scale or TBC failure. FIB/STEM samples of the intact Al₂O₃ TGO were obtained at the coated front and bare backside. The YSZ was a mix of 1-2 μm ‘clean’ and 0.5-1 μm ‘faulted’ grains with nm-size domains. The domains produced complex SADP; HRTEM revealed {100} and {110} domain boundaries; while XRD had identified primarily ‘cubic cell’ structures. These ferro-elastic domains are believed to represent high Y, tetragonal t′′ YSZ variants generated from the cubic phase on cooldown. No martensite was observed, presumably due to mechanical constraints of fine grain size. The complexity of aged YSZ coatings is a topic requiring intensive study to be fully conclusive. The presence here of ferro-elastic t′′ domains are expected to be beneficial, in the same manner as those widely documented in metastable, ‘non-transformable,’ as-sprayed t′ tetragonal domains. Still, the thermal expansion matching of this YSZ-TGO-MAX phase system presents the largest positive factor for long term, high temperature, cyclic durability. The loss of the strain compliant, PVD ‘feather’ grain structure during sintering, useful for TBC’s on superalloys operated at lower temperatures, has apparently not diminished this durability.

The TGO was essentially α-Al₂O₃, with a duplex structure of outer ~ 0.3 μm equiaxed grains (with intergranular porosity) and inner columnar 0.5 μm grains. The latter showed minimal entrapped fine 25-50 nm porosity and Zr(Y), Fe, or Ti-rich particles. Little interaction with the YSZ was observed. Unfortunately, no information was obtained at the bare backside scale-gas interface because it was outside the span of the FIB section. That surface had exhibited volatility issues (grain boundary etching, filamentary α-Al₂O_3, TiO₂ removal) in previous SEM studies.

The scale maintained a perfectly intact interface with the Ti₂AlC substrate, with no evidence of interfacial porosity or chemical/phase variations. The Ti₂AlC substrate exhibited no depletion zone, but rather numerous crystallographic faults along the basal plane of the hexagonal structure, often in a perpendicular orientation to the interface, extending deep into the grains. These are believed to offer a means of depleting Al by forming a crystallographic planar defect having lower Al stoichiometry in the hexagonal stacking of the Ti_n+1AlC_n MAX phase series. This has wide implications for Al depletion mechanisms in the high temperature oxidation of Ti_n+1AlC_n family of MAX phases.

Author contributions: J. Smialek conceived and organized the research, prepared the manuscript; A. Garg performed the transmission electron microscopy; B. Harder produced the coated sample; M. Cuy performed the high velocity burner rig test.

Funding

These studies were supported by the NASA Fundamental Aeronautics Program.

Acknowledgements

The authors gratefully acknowledge Wayne Jennings for producing the FIB sections.

Conflicts of Interest

The authors declare no conflict of interest.

References

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Figure 1. Weight change performance of YSZ-coated Ti2AlC MAX phase in 1300°C Mach 0.3 burner test. (from Smialek et al., 2020).

Figure 2. Orientation of FIB samples at (I) front and (II) back sides of sample. a) photograph of burner operation showing front side flame impingement. b) schematic of sample cross-section. c) montage of SEM/BSE cross-section images of sample and scale showing TBC coated front side (I) and bare backside (II) after 500 h burner rig test at 1300°C. his is a figure. Schemes follow the same formatting.

Figure 3. TEM Overview of the front side, FIB section I: TBC on left, Ti2AlC MAX phase on right. Avg. scale thickness from prior SEM study was 22 μm, as shown. (500 h at 1300°C).

Figure 4. Features in Al₂O₃ TGO (I): a) fine 50 nm, dispersed intragranular porosity (light) and particles (dark) in Al₂O₃ grains near TBC; b) clean, intact Al₂O₃/Ti₂AlC interface (dashed red line) and 20 closely spaced, highly aligned linear faults in Ti₂AlC grain.

Figure 5. STEM image and EDS of Zr(Y) rich particle embedded in Al₂O₃ (I) grain compared to clear Al₂O₃ region.

Figure 6. STEM image (a) of the TBC/TGO interface (I): elemental rasters (b-d) show Fe-rich particles at interface. (500 h at 1300°C).

Figure 7. TEM image of cubic clear (C) and tetragonal ‘faulted’ (F) submicron YSZ grains in the TBC.

Figure 8. SADP’s of clear (C) [100] and faulted (F) [100] YSZ grains (Figure 7a, b), the latter showing many extra reflections probably related to variants of t´ domain orientation. Here, the primary ‘cubic’ [100] Z.A. reflections are delineated by the 3x3 dashed line grid construction (7c). Extra reflections appear to arise from two twin variants (7d), marked by yellow and aqua grid, slightly off-zone. The trace of possible twin habit planes shown as orthogonal [002] and [020] axes. (a₀ for YSZ is 5.1 Ả for the cubic parent phase and indistinguishable from tetragonal). (The tetragonal structure would, however, allow for forbidden {112} reflections in otherwise cubic patterns due to oxygen ordering along the z-axis).

Figure 9. HRTEM images of ferroelastic domain boundaries in faulted (F) grains. b) with Z.A. = [100]; inset: fast Fourier transform of lattice image. Domain boundaries exhibit {100} and {110} nature with 45° or 90° angles of inclination between themselves. b) other domains to the left of (a).

Figure 10. HRTEM images of domain boundary above Figure 9a; (a) inset: fast Fourier transform of lattice image. (b) enlargement showing node spacing of 5 Ả, corresponding to 5.1 Ả lattice spacing for {100} planes. .

Figure 11. FIB section II: (a) TEM / (b) STEM images of backside of burner sample. Clean, intact Ti₂AlC - Al₂O₃ interface. Columnar TGO grains at interface and equiaxed at gas side; planar faults (F) and included Al₂O₃ particle (P) in Ti₂AlC. (500 h at 1300°C).

Figure 12. EDS spectra of TGO grain (A) and imbedded particle (P) in Figure 11. hkl [21-1] and [481] Z.A. SADP of TGO grains (A) and (B) in Figure 11. Hexagonal Al₂O₃ : a₀ = 4.8Å, c = 12.9Å.

Figure 13. Al₂O₃ TGO triple point region marked O in Figure 11b showing fine ~25 nm Ti- and Fe-rich particles in grains, (a) - (c). EDS spectra of Ti (d) and Fe (e) particles.

Figure 14. Ti₂AlC grains with planar faults (F) and irregular dislocations (D).

Figure 15. STEM image showing (a) the clean, intact Ti₂AlC - Al₂O₃ interface; (b) EDS of the Ti₂AlC phase (T); (c) ‘clean’ [210] Z.A. SADP of the fault-free region (X); and (d) extra spots in SADP of the faulted plane (Y). Ti₂AlC: Hexagonal, a₀ = 3.1 Å, c =1 3.7 Å. The fine spots are regularly spaced at 1/7 (006), indicating a d-spacing of 7/6 d₍₀₀₁₎.

Table 1. Summary of YSZ coating phases after various thermal aging treatments. Rietveld XRD full pattern fitting of for t´, t, c, and m YSZ (wt. %), with corresponding compositions (YO1.5 %): a) from Witz et al., APS. b) this study, PS-PVD.

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