Abstract
High-entropy ultra-high temperature ceramics (UHTCs) have garnered significant attention for outstanding designability and performance, yet existing strategies remain largely confined to cationic sublattice engineering, leaving the potential of anionic site manipulation unexplored. Herein, we extend the entropy- stabilization paradigm to the anion sublattice by designing a multi-anion Hf0.8Zr0.2B0.1C0.5N0.4 solid solution. The resulting Hf0.8Zr0.2B0.1C0.5N0.4 -SiC ceramic achieves negative ablation rates (-0.049 mg·s-1; -0.287 μm·s-1) under 2600 °C plasma flame exposure, markedly outperforming Hf0.8Zr0.2C-SiC. This exceptional ablation- resistant performance originates from the synergistic effects enabled by multi-anion sublattice engineering. The incorporation of B-C-N intrinsically enhances fracture toughness, while in-situ precipitation of hexagonal graphite during ablation extrinsically arrests cracks through interfacial shear, preventing catastrophic disintegration. Furthermore, the multi-anion matrix undergoes a sequential oxidation process, forming an HfZrBCNO interlayer that acts as an oxygen scavenger. Concurrently, h-BN precipitates at grain boundaries, serving as compliant diffusion barriers that impede oxygen ingress toward SiC. This dual-layer protection mechanism suppresses the active oxidation of SiC (SiC + O2 ® SiO + CO) and promotes the formation of a dense, scouring-resistant HfZrO2-SiO2 composite barrier. By demonstrating simultaneous microstructural toughening and mesoscale oxidation management, this work establishes multi-anion sublattice engineering as a transformative platform for designing next-generation thermal protection materials beyond the limits of conventional entropy-stabilized ceramics.

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