Property evolutions of Si/mixed Yb2Si2O7 and Yb2SiO5 environmental barrier coatings completely wrapping up SiCf/SiC composites under 1300 °C water vapor corrosion

A bi-layer environmental barrier coating (EBC) consisting of silicon(Si) bond coat/mixed ytterbium disilicate (Yb₂Si₂O₇) and ytterbium monosilicate (Yb₂SiO₅) topcoats has been successfully prepared to completely wrap up the SiC_f/SiC composites and the protective effects of such EBC have been evaluated by soaking them in a mixed 50% O₂ and 50% H₂O corrosive gases at 1300 °C for various times. In topcoats, Yb₂Si₂O₇ is the major phase, providing good thermal expansion coefficient (CTE) matching with composite substrate and thus excellent thermal shock resistance, whereas Yb₂SiO₅ is the dispersing minor phase, providing improved water vapor corrosion resistance. The completely wrapping up of SiC_f/SiC composites by above EBC system is employed to avoid direct exposure to the corrosive conditions, making it possible to evaluate the genuine protection effects of current EBCs. Under 1300 °C water vapor corrosion, the mass change, the phase composition and the evolution of microstructure are investigated, which suggest that the bi-layer EBC has excellent performance on protecting SiC_f/SiC composites from water vapor corrosion at 1300 °C.     

High-Temperature thermochemical interactions of molten silicates with Yb2Si2O7 and Y2Si2O7 environmental barrier coating materials

The thermochemical behavior of EBC candidate materials yttrium disilicate (Y₂Si₂O₇) and ytterbium disilicate (Yb₂Si₂O₇) was evaluated with three calcium-magnesium-aluminosilicate (CMAS) glasses possessing CaO:SiO₂ ratios relevant to gas turbine systems. Pellet mixtures of 50 mol% EBC powder to 50 mol% CMAS glass powder were heat treated at 1200°C, 1300°C, and 1400°C. The products of these interactions were evaluated using X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy. Above glass melting temperatures, exposure of the disilicates primarily resulted in dissolution into the molten glass followed by precipitation of a Ca₂RE₈(SiO₄)₆O₂ (RE = Yb³⁺, Y³⁺) apatite-type silicate and/or rare earth disilicate. In glasses with high CaO concentrations, apatite readily forms while the disilicate material is consumed by the reaction. As CaO content decreases, the disilicate phase becomes the main reaction product. Overall, reactions with yttrium disilicate favored more apatite crystallization than ytterbium disilicate. The viability of using these disilicates in various operating environments is discussed.     

Synthesis and characterization of ytterbium oxide: A novel CMAS-resistant environmental barrier coating material

Demand for more powerful aircraft promotes development of ceramic matrix composites and environmental barrier coating (EBC). A promising EBC material, ytterbium oxide (Yb₂O₃), was fabricated by hot pressing, and its properties were systemically investigated. The evaluation of thermal properties provides a baseline for the application of Yb₂O₃ on SiC_f/SiC or Al₂O_3f/Al₂O₃ composites. The performance in water vapor and molten calcium–magnesium–aluminosilicate (CMAS) environments indicates its excellent durability in harsh environment. Compared with rare-earth silicates, the thermochemical interactions between ytterbium oxide and CMAS changed greatly with the absence of silicon oxide. Reactions of ytterbium oxide with CMAS form several reaction products, including apatite, garnet, and silicocarnotite. The crystallization of garnet and silicocarnotite could effectively consume and solidify the CMAS melt, which prevents the melt infiltration and mitigates the further corrosion.     

Yttrium Bearing Silicon Carbide Matrices for Robust Ceramic Composites

Application of SiC‐based ceramic matrix composites (CMCs) in combustion environments demands the use of an environmental barrier coating (EBC) to prevent volatilization of the protective SiO₂ scale in flowing water vapor. The EBC only provides protection while present on the surface; cracking and spallation of the coating leaves the underlying SiC vulnerable to the oxidation–volatilization processes. A robust matrix material chemically tailored to regrow a yttrium silicate scale in the event of EBC loss has been developed by incorporating yttrium bearing species including YB₂, Y₂O₃, and Y₅Si₃ into the SiC. During oxidation a borosilicate glass helps seal cracks while Y₂O₃ and SiO₂ react to form Y₂Si₂O₇ for environmental protection. Candidate compositions were oxidized for 10 min to 100 h at 1400°C and for 24 h at 1500°C to understand the scale growth. The prospects for effectively applying this approach in CMCs are discussed.     

Characterization of Yb2Si2O7–Yb2SiO5 composite environmental barrier coatings resultant from in situ plasma spray processing

Plasma spraying of multicomponent materials produces shifts in coating composition associated with differential vaporization of constituent elements within the strong thermal gradients of the process. This effect is quite noticeable in rare-earth silicates which are now widely being employed as Environmental Barrier Coatings (EBCs) for SiC based ceramic components of turbine engines. Of particular interest is the preferential volatilization of SiO₂ during thermal plasma spraying Yb₂Si₂O₇ (ytterbium disilicate) coatings which leads to the deviation from stoichiometry of the desired disilicate composition resulting in a mixed phase coating consisting of Yb₂Si₂O₇ plus Yb₂SiO₅ (ytterbium monosilicate). Recent work has shown that presence of monosilicate can be beneficial as its evolution from amorphous, metastable to stable crystalline phase can lead to crack healing during high temperature exposure, however, careful control of the chemistry and architecture may be needed. In this work a 50/50 mol% Yb₂Si₂O₇–Yb₂SiO₅ composite coating has been targeted through in situ decomposition during plasma spray from stoichiometric Yb₂Si₂O₇ powder. The as sprayed amorphous coating reverts to crystalline upon thermal treatment passing through a metastable state identified by XRD and Raman spectroscopy. The transition to the final stable phases results in a mixed phase coating comprising of 46/54 mol% Yb₂Si₂O₇–Yb₂SiO₅ composite that is thermo-mechanically stable with the underlying bond coated silicon coated SiC substrate.     

SiC modified self-healing ytterbium disilicate materials for potential environmental barrier coating application

Environmental barrier coatings (EBCs) are crucial to the reliability and durability of SiC_f/SiC composite components seeking applications in hot sections of next-generation advanced aero-engines. The cracks initiated and developed in EBCs owing to various reasons during service greatly undermine their lifespans. To address this problem, in this work, silicon carbide (SiC) in the forms of particles and whiskers with various amounts have been introduced to ytterbium disilicate (Yb₂Si₂O₇), the mainstream EBC topcoat materials, so as to gain some self-healing potential. The results reveal that, the SiC inclusions in Yb₂Si₂O₇ in the presence of ytterbium monosilicate (Yb₂SiO₅) can trigger the following reactions. Specifically, SiC self-healing agents are oxidized to form viscous SiO₂, which actively reacts with Yb₂SiO₅ upon encountering it, forming Yb₂Si₂O₇. This has brought twofold beneficial effects including ① silicon supplementation of disilicate topcoat, whose silicon element tends to be “dragged out” by water vapor, leading to the deterioration of thermal mismatch; as well as ② crack self-healing resulting from the volume expansion induced by the above reactions. Then the two aspects of self-healing agents, namely the “promptness” and “sustainability,” have been discussed in detail. The former is unveiled to be more pertinent to the repairing of large cracks, whilst the latter is more relevant to the self-healing of tiny cracks at initiation or early stage of propagation. The current work sheds some lights on the design and development of more durable and robust EBCs with self-healing capability.     

Interaction of CMAS on thermal sprayed ytterbium disilicate environmental barrier coatings: A story of porosity

Molten calcium magnesium alumina-silicates (CMAS) represent a challenge for the current generation of rare earth silicates environmental barrier coatings (EBCs). Their interaction with ytterbium disilicate (Yb₂Si₂O₇) free-standing coatings deposited using thermal spraying technique has been studied to further understand the reaction mechanisms. Three coatings, deposited with different porosity levels and thickness, representing traditional EBCs (<3% porosity and ～350 μm thickness) and abradable coatings (～20% porosity and 500–1000 μm thickness) were exposed to CMAS at 1350 °C. The results show that higher porosity levels facilitates CMAS infiltration in the first hour of exposure, in combination with infiltration through the inter-splat boundaries. Preferential dissolution of ytterbium monosilicate (Yb₂SiO₅) takes place, forming a 10–15 μm Ca₂Yb₈(SiO₄)₆O₂ apatite layer as the reaction product, producing a network of fine porosity (<10 μm) as the inter-splat boundary material is consumed. After exposure for 48 h, CMAS has completely infiltrated all three coatings, with apatite crystals present across the coatings, up to a depth of ～550 μm. Despite the extensive CMAS infiltration and apatite formation, no damage could be observed in any of the coatings, providing a promising first step for environmental barrier abradable coatings.     

Steam oxidation and microstructural evolution of rare earth silicate environmental barrier coatings

A primary failure mode for environmental barrier coatings (EBCs) on SiC ceramic matrix composites (CMCs) is the oxidation of the intermediate Si-bond coating, where the formation of SiO₂ at the bond coating–EBC interface results in debonding and spallation. This work compares the microstructure evolution and steam oxidation kinetics of the Si-bond coating beneath yttrium/ytterbium disilicate ((Y/Yb)DS) and ytterbium disilicate/monosilicate (YbDS/YbMS) EBCs to better understand the impact of EBC composition on oxidation kinetics. After 500 1-h cycles at 1350°C, (Y/Yb)DS displayed a decreasing concentration of the monosilicate minor phase and increasing concentration of porosity as furnace cycling time increased, whereas the YbDS/YbMS EBC displayed negligible microstructural evolution. For both EBC systems, thermally grown oxide growth rates in steam were found to increase by approximately an order magnitude compared to dry air oxidation. The (Y/Yb)DS EBC displayed a reduced steam oxidation rate compared to YbDS/YbMS.     

Mechanical properties and microstructure of Yb2SiO5 environmental barrier coatings under isothermal heat treatment

Yb₂SiO₅ (ytterbium monosilicate) top coatings and Si bond coat layer were deposited by air plasma spray method as a protection layer on SiC substrates for environmental barrier coatings (EBCs) application. The Yb₂SiO₅-coated specimens were subjected to isothermal heat treatment at 1400 °C on air for 0, 1, 10, and 50 h. The Yb₂SiO₅ phase of the top coat layer reacted with Si from the bonding layer and O₂ from atmosphere formed to the Yb₂Si₂O₇ phase upon heat treatment at 1400 °C. The oxygen penetrated into the cracks to form SiO₂ phase of thermally grown oxide (TGO) in the bond coat and the interface of specimens during heat treatment. Horizontal cracks were also observed, due to a mismatch of the coefficient of thermal expansion (CTE) between the top coat and bond coat. The isothermal heat treatment improves the hardness and elastic modulus of Yb₂SiO₅ coatings; however, these properties in the Si bond coat were a little bit decreased.     

Thermal Properties of Rare‐Earth Monosilicates for EBC on Si‐Based Ceramic Composites

Rare‐earth (RE) monosilicates are promising candidates as environmental barrier coating (EBC) materials for ceramic matrix composites for aerospace applications. Five rare‐earth monosilicate materials have been investigated: Y₂SiO₅, Gd₂SiO₅, Er₂SiO₅, Yb₂SiO₅, and Lu₂SiO₅ produced from RE oxides and silica starting materials pressed and sintered at 1580°C under flowing air. Relative densities above 94% were obtained for all samples and ceramics were made containing 85–100 wt% of the RE monosilicate according to X‐ray diffraction (XRD) with RE disilicates as the second phase in the Gd, Yb, and Lu silicate systems. Microstructures were characterized using scanning electron microscopy and XRD, and thermal properties measured including specific heat, thermal expansion, and thermal diffusivity. For the first time, specific heat capacity values are reported for the monosilicates [0.45–0.69 J·(g·K)^?1]. Thermal expansion coefficients (TECs) of the dense samples ranged between 5.9 and 10.3 × 10^?6 K^?1 measured for 473 to 1473 K. All EBCs have low thermal conductivities [1.8 W·(m·K)^?1 or less] making them excellent EBC insulators.     

Thermo-mechanical properties and CMAS resistance of (Ho0.4Yb0.3Lu0.3)2SiO5 solid solution for environmental barrier coating applications

Rare earth monosilicate (RE₂SiO₅) is one of the most promising candidates as an environmental barrier coating (EBC) for SiC_f/SiC ceramic matrix composites. But single-component RE₂SiO₅ is hard to meet the multiple and harsh performance requirements of EBC which brings a significant challenge to their applications. Based on our previous research on single-component RE₂SiO₅ ceramics, (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ solid solution was designed and successfully fabricated in this work. Doping of multiple RE elements endows (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ with excellent thermal insulation properties and matched thermal expansion coefficient with SiC_f/SiC substrates. In addition, it exhibits lower elastic modulus and comparable hardness than that of single-component RE₂SiO₅. (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ also presents good resistance to calcium-magnesium alumino-silicates (CMAS) corrosion. Rational composition design allows (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ to retain the merits of single-component RE₂SiO₅ while taking advantage of the solid solution effect. The results of this work suggest (Ho_0.4Yb_0.3Lu_0.3)₂SiO₅ as a promising EBC candidate.     

Self-crack healing ability and strength recovery in ytterbium disilicate/silicon carbide nanocomposites

The SiO₂ volatility and SiC recession in hydrocarbon-rich combustion atmosphere is the main problem of SiC-reinforced ceramics when they are utilized as coating materials for gas turbine blades. The composite of Yb₂Si₂O₇-Yb₂SiO₅/SiC is expected as a self-crack healing material that can avoid this problem because the monosilicate can react with the SiO₂ glass to form disilicate and hence further reinforce the composite. In this study, the composites, fabricated with various morphology of SiC nanofillers, were precracked and then heat-treated in an oxidizing environment to activate their crack healing behavior. The healing effect as a function of filler morphology and annealing time was investigated. Healing mechanism and future applications of these composites were also discussed.     

Effects of the chemistry of coating and substrate on the steam oxidation kinetics of environmental barrier coatings for ceramic matrix composites

Environmental barrier coatings (EBCs) are an enabler for SiC/SiC ceramic matrix composites (CMCs) in gas turbines by protecting CMCs from environmental degradation. A critical EBC failure mode is the EBC spallation due to a build-up of elastic strains caused by the formation of SiO₂ scale, known as TGO (thermally grown oxide). H₂O, a byproduct of combustion reactions, accelerates the TGO-induced EBC failure by increasing TGO growth rates by orders of magnitude. NASA’s approach to improve the EBC life, therefore, is to reduce TGO growth rates. NASA discovered that modifying the TGO chemistry by modifying the EBC chemistry of Gen 2 EBC (Si / Yb₂Si₂O₇) reduces the TGO thickness by up to ～80 %. A study was undertaken to understand the oxidation mechanism of modified Gen 2 EBCs as well as to investigate the effect of EBC and CMC chemistry on TGO growth rates. This study confirmed the previously proposed TGO-controlled oxidation mechanism of modified Gen 2 EBCs and determined the correlations between the EBC and CMC chemistry, TGO chemistry, and TGO growth rates.     

Calcium-Magnesium-Aluminosilicate (CMAS) corrosion resistance of high entropy rare-earth phosphate (Lu0.2Yb0.2Er0.2Y0.2Gd0.2)PO4: A novel environmental barrier coating candidate

Single phase (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄ was synthesized, and its thermal properties and CMAS resistance were investigated to explore its potential as an environmental barrier coating (EBC) candidate. The high entropy phosphate (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄ displays a lower thermal conductivity (2.86 W m⁻¹ K⁻¹ at 1250 K) than all the single component xenotime phase rare-earth phosphates. Interaction of (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄ pellets with CMAS at 1300 °C led to the formation of a dense and uniformed Ca₈MgRE(PO₄)₇ reaction layer, which halted the CMAS penetration into the bulk pellet. At 1400 and 1500 °C the (Lu_0.2Yb_0.2Er_0.2Y_0.2Gd_0.2)PO₄-CMAS corrosion showed CMAS penetrating beyond the reaction layer into the bulk pellet via the grain boundaries, and SiO₂ precipitates remaining at the pellet surface. The effects of duration, temperature, and compositions on the resistance against CMAS corrosion are discussed within the context of optimizing materials design and performance of high entropy rare-earth phosphates as candidates for advanced EBC applications.     

Rare earth silicate environmental barrier coatings for SiC/SiC composites and Si3N4 ceramics

Rare earth silicates have been investigated to evaluate their potential as an advanced environmental barrier coating (EBC) having higher temperature capability than current EBCs. Volatility data in high steam environments indicate that rare earth monosilicates (RE₂SiO₅; RE: rare earth element) have lower volatility than the current barium strontium aluminum silicate (BSAS) EBC top coat in combustion environments. Rare earth silicates also exhibit superior chemical compatibility compared to BSAS. The superior chemical compatibility and low volatility are key attributes to achieve higher temperature capability. The chemical compatibility is especially critical for EBCs on Si₃N₄ because of the high chemical reactivity of some of the oxide additives in Si₃N₄. In simulated combustion environments, EBCs with a rare earth monosilicate top coat exhibit superior temperature capability and durability compared to the current state-of-the art EBCs with a BSAS top coat.     

High-temperature interactions of desert sand CMAS glass with yttrium disilicate environmental barrier coating material

A calcium-magnesium aluminosilicate (CMAS) glass was prepared by melting a sample of desert sand to evaluate the high-temperature interactions between molten CMAS and yttrium disilicate (Y₂Si₂O₇), an environmental barrier coating (EBC) candidate material. Cold-pressed pellets of 80?wt% Y₂Si₂O₇ powder and 20?wt% CMAS glass powder were heat treated at 1200?°C, 1300?°C, 1400?°C and 1500?°C for 20?h in air. The resulting phases were evaluated using powder X-ray diffraction. In the second set of experiments, free standing hot-pressed Y₂Si₂O₇ substrates with cylindrical wells were filled with CMAS powder to a loading of ~35?mg/cm² and heat treated in air at 1200?°C, 1300?°C, 1400?°C and 1500?°C for 20?h. Scanning electron microscopy, energy-dispersive spectroscopy and electron microprobe analysis were used to evaluate the microstructure and phase compositions of specimens after heat treatment. An oxyapatite silicate (Ca₂Y₈(SiO₄)₆O₂) phase was identified in all specimens after CMAS exposure regardless of heat treatment temperature. Apatite appeared to form by dissolution of Y₂Si₂O₇ into molten CMAS, reacting with CaO in the melt according to the reaction 4Y₂Si₂O₇ +?2CaO → Ca₂Y₈(SiO₄)₆O₂ +?2SiO₂, and followed by precipitation of the apatite phase.     

Thin single-phase yttrium-based environmental barrier coating systems for SiC/SiC CMCs

Two thin yttrium silicate-based EBC systems for SiC/SiC CMCs that comprised of three layers were produced via (reactive) magnetron sputtering with pure yttrium disilicate (YDS) and yttrium mono silicate (YMS) layers. The systems survived 1000 1-hour furnace cycle tests at 1250 °C in air interrupted by active cooling for 10 min. One system showed partial delamination of the YMS. The YDS intermediate layer stopped deleterious reactions among YMS and silicon and the silica formation did not cause spallation of the silicates. Some vertical cracks in YMS left possible attack paths for water vapor. Rapid water vapor testing was performed at 1250 °C in 100 vol% water vapor at 10 m/s for 2 h. This test proved that a thin but hermetic and phase pure YMS top layer can protect the system from volatilization: single phase X2-YMS was not attacked by steam whereas a mixed β-YDS/X2-YMS coating showed volatilization of SiO₂.     

Crack-healing behaviour of MoSi2 dispersed Yb2Si2O7 environmental barrier coatings

MoSi₂ doped Yb₂Si₂O₇ composites were designed to extend the lifetime of Yb₂Si₂O₇ environmental barrier coatings (EBCs) via self-healing cracks during high-temperature applications. Yb₂Si₂O₇–Yb₂SiO₅–MoSi₂ composites with different mass fractions were prepared by applying spark plasma sintering. X-ray diffraction results confirmed that the composites consisted of Yb₂Si₂O₇, Yb₂SiO₅, and MoSi₂. The thermal expansion coefficients (CTEs) of the composites increased with an increase in the MoSi₂ content. The average CTE of the 15 wt% MoSi₂ doped Yb₂Si₂O₇ composite was 5.24 × 10^?6 K^?1, indicating that it still meets the CTE requirement of EBC materials. After being pre-cracked by using the Vickers indentation technique, the samples were annealed for 0.5 h at 1100 or 1300 °C to evaluate the crack-healing ability. Microstructural studies showed that cracks in 15 wt% MoSi₂ doped Yb₂Si₂O₇ composites were fully healed during annealing at 1300 °C. Two mechanisms may be responsible for crack healing. First, the cracks were filled with SiO₂ glass formed by MoSi₂ oxidation. Second, the formed SiO₂ continued to react with Yb₂SiO₅ to form Yb₂Si₂O₇, which can cause cracks to heal owing to volumetric expansion. The Yb₂Si₂O₇ formation with smaller volume expansion is more beneficial.     

Influence of phase composition on microstructure and thermal properties of ytterbium silicate coatings deposited by atmospheric plasma spray

In this study, ytterbium silicate coatings with different compositions were designed by controlling the Yb₂O₃/ SiO₂ ratio and fabricated by atmospheric plasma spray. The microstructure and thermal properties of these coatings were characterized. Results showed that the Yb₂O₃-rich coatings contained Yb₂O₃ and Yb₂SiO₅ phases, which were characterized by Yb₂O₃ columnar grains, obvious interfaces between splats and many microcracks. The SiO₂-rich coatings were composed of Yb₂SiO₅ and Yb₂Si₂O₇ phases, which were composed of well bonded splats with many spherical pores. The Yb₂O₃-rich coatings had higher coefficient of thermal expansion values and lower thermal conductivities than the SiO₂-rich coatings. The SiO₂-rich coatings presented much better thermal cycling resistance than the Yb₂O₃-rich coatings. The relationship among phase composition, microstructure and thermal properties of ytterbium silicate coatings was analyzed. The results of this study may provide some clues for designs and applications of rare-earth silicates as environmental barrier coatings.     

Enhancing CMAS corrosion resistance of PS-PVD Si/Yb2Si2O7 EBCs via Al-modification

Enhancing the resistance to molten silicate corrosion is crucial for the long service life of environmental barrier coatings (EBCs). In this study, we used the Al-modification technique to enhance the CMAS corrosion resistance of Si/Yb₂Si₂O₇ coatings prepared by plasma spray-physical vapor deposition. The results show that the Al-modified Yb₂Si₂O₇ coating had higher resistance to CMAS corrosion than the Yb₂Si₂O₇ coating annealed at 1300 ℃ for 100 h, which is related to the refractory mullite and Yb₂Mg(AlO₂)₂O₃ generated during the CMAS exposure of Al-modified Yb₂Si₂O₇ coating. The Al-modified Yb₂Si₂O₇ coating also exhibited excellent resistance to oxygen penetration. The Al-modification technology provides the direction for the corrosion resistance of Yb₂Si₂O₇ system to CMAS.