With the continuous pursuit of higher efficiency and larger thrust-to-weight ratio in aero-gas-turbine engines, the turbine inlet temperature has already exceeded 1300 ℃, imposing increasingly stringent requirements on the thermal resistance and protective capability of hot-section structural materials. Environmental barrier coatings (EBCs) have become a crucial technology to ensure efficient and reliable service of ceramic matrix composite (CMC) turbine components under such extreme working conditions. However, the service environment of EBCs is exceptionally complex. Coatings are continuously exposed to corrosive gaseous species within combustion products, among which the ingression and reaction of molten calcium-magnesium-aluminum-silicate (CMAS) deposits represent one of the most detrimental degradation mechanisms.
To mitigate CMAS-induced deterioration, numerous strategies have been proposed, including compositional modification (doping, high-entropy ceramics), structural design optimization (multilayer or graded coatings), and surface engineering (laser or ion beam treatments). Although these approaches can improve corrosion resistance to some extent, most of them inevitably alter the coating chemistry or structural system, which tends to induce thermal expansion mismatch with the substrate and promotes premature failure during thermal cycling. Therefore, how to enhance CMAS-corrosion resistance while maintaining thermomechanical compatibility remains a critical challenge. Laser glazing (LG) is a surface-modification technique that locally melts and rapidly solidifies the coating surface to form a dense glaze layer. It improves surface compactness and seals microdefects without altering the coating composition, thereby presenting a promising method for improving CMAS-corrosion resistance. In this work, laser glazing is introduced to enhance the CMAS-resistance of EBCs, and the CMAS-corrosion behavior together with the underlying improvement mechanisms are systematically investigated.
SiC ceramic substrates were purchased from Fuzhou Pengkun Optoelectronics Co., Ltd. The samples were cylindrical (diameter 25.4 mm, thickness 3 mm) and mechanically grit-blasted prior to coating deposition. Yb2Si2O7/Si (YbDS) EBCs were deposited on the substrates by atmospheric plasma spraying (APS). Commercial Yb2Si2O7 and Si powders (Shanghai Shuitian Materials Technology Co., Ltd.) were used, and the bond coat consisted of 90% (in mass fraction) Si and 10% Yb2Si2O7. A picosecond ultraviolet pulsed-laser system was subsequently applied to modify the surface microstructure of APS YbDS coatings. Four sets of parameters (L1-L4) were obtained by adjusting the laser power (6 W or 20 W) and scanning speed (100-300 mm/s). CMAS bulk material was synthesized by high-temperature melting. CMAS powder was mixed with ethanol and uniformly brushed onto the coating surface, followed by drying to achieve a coating mass of 5 mg/cm2. The coated samples were exposed at 1350 ℃ for 10, 60 h, and 120 h. After corrosion, the evolution of microstructure and phase composition was analyzed to reveal the degradation behavior.
The APS-prepared YbDS coating exhibited a surface roughness of ~3.7 μm and a porosity of ~4.87%, with typical APS defects such as pores, unmelted particles, and microcracks. After laser glazing, four modified surfaces were obtained. Among them, sample L2 demonstrated the most favorable structural morphology and was selected for subsequent corrosion tests. The L2 coating showed a reduced surface roughness of ~1.824 μm and a homogeneous, dense glaze layer of ~9.6 μm thickness. Moreover, the glazed surface phase completely transformed from Yb2Si2O7 to Yb2SiO5. During CMAS corrosion, the YbDS coating surface was continuously covered by a loose mixture of Ca2Yb8(SiO4)6O2 and CMAS residual glass. In contrast, the laser-modified L2 coating was covered by a compact Ca2Yb8(SiO4)6O2 reaction layer. After corrosion, both coatings displayed Ca2Yb8(SiO4)6O2 and secondary Yb2Si2O7 phases; however, their structural evolution differed significantly. After 120 h of corrosion, the YbDS coating suffered severe structural degradation, including interfacial delamination and partial spallation in cross-sectional observations. Conversely, the L2 coating maintained structural integrity, and its corrosion depth was consistently lower under the same conditions.
The improved CMAS resistance of the L2 coating can be attributed to three synergistic mechanisms: Surface densification, Laser glazing produced a dense, continuous glaze layer that sealed APS-induced pores and cracks, effectively delaying CMAS infiltration pathways; Protective reaction-layer formation, The Yb2SiO5 glaze reacted with CMAS to form a dense Ca2Yb8(SiO4)6O2 layer, which further hindered molten-salt penetration ;Enhanced non-wettability, Laser glazing significantly reduced surface roughness and improved hydrophobicity. As a result, molten CMAS appeared as aggregated hemispherical droplets rather than fully spreading, making it more easily removed by high-velocity gas flow during service.
The findings of this study demonstrate that laser glazing effectively enhances the CMAS-corrosion resistance of YbDS coatings. The improvement originates from the combined effects of surface densification, pore/crack sealing, phase transformation to Yb2SiO5, and subsequent formation of a compact Ca2Yb8(SiO4)6O2 reaction layer during corrosion. Additionally, the smoother and less wettable glazed surface reduces the adhesion and spreading tendency of CMAS, enabling molten deposits to be removed more easily under aerodynamic forces. As a result, the degradation rate of the coating is substantially suppressed, delaying the propagation of corrosion-induced cracks and maintaining structural integrity over prolonged exposure. Moreover, the laser-induced modifications do not alter the coating architecture or introduce thermal expansion mismatch, making the technique compatible with existing EBC design frameworks. Overall, laser glazing represents a promising strategy for improving the durability and service lifetime of EBC systems in next-generation high-temperature aero-engine applications.
| 科 Family | 属数 Number of genus | 种数 Number of species | 占总种数比例 Percentage of total species (%) | 属 Genus | 种数 Number of species | 占总种数比例 Percentage of total species (%) |
|---|---|---|---|---|---|---|
| 鹅膏菌科Amanitaceae | 2 | 11 | 5.26 | 鹅膏菌属 Amanita | 10 | 4.78 |
| 小菇科 Mycenaceae | 2 | 12 | 5.74 | 丝盖伞属 Inocybe | 5 | 2.39 |
| 多孔菌科 Polyporaceae | 8 | 14 | 6.70 | 蜡蘑属 Laccaria | 5 | 2.39 |
| 红菇科 Russulaceae | 3 | 23 | 11.00 | 小皮伞属 Marasmius | 6 | 2.87 |
| 小菇属 Mycena | 11 | 5.26 | ||||
| 光柄菇属 Pluteus | 5 | 2.39 | ||||
| 红菇属 Russula | 17 | 8.13 | ||||
| 栓菌属 Trametes | 5 | 2.39 |