Guang Yang, Lingbo Xu, Can Cui, Xiaodong Pi, Deren Yang, Rong Wang
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引用次数: 0
摘要
熔碱刻蚀已被广泛用于揭示 4H 碳化硅(4H-SiC)中的位错,这促进了对 4H-SiC 单晶中位错密度的识别和统计。然而,4H-SiC 的蚀刻机理被误解得很有限。在这封信中,我们结合熔融-KOH蚀刻、X射线光电子能谱(XPS)和第一原理研究,揭示了4H-SiC硅面和C面的各向异性蚀刻机制。计算得出 4H-SiC C 面和 Si 面的熔融-KOH 蚀刻活化能分别为 25.09 和 35.75 kcal/mol。C 面的熔融-KOH 蚀刻率高于 Si 面。结合 XPS 分析和第一原理计算,我们发现 4H-SiC 的熔融-KOH 蚀刻是由溶解氧氧化 4H-SiC 和熔融 KOH 去除氧化物循环进行的。C 面蚀刻速度较快的原因是 C 面的氧化物不稳定,更容易被熔融碱去除,而不是 C 面更容易被氧化。
Anisotropic etching mechanisms of 4H-SiC: Experimental and first-principles insights
Molten-alkali etching has been widely used to reveal dislocations in 4H silicon carbide (4H-SiC), which has promoted the identification and statistics of dislocation density in 4H-SiC single crystals. However, the etching mechanism of 4H-SiC is limited misunderstood. In this letter, we reveal the anisotropic etching mechanism of the Si face and C face of 4H-SiC by combining molten-KOH etching, X-ray photoelectron spectroscopy (XPS) and first-principles investigations. The activation energies for the molten-KOH etching of the C face and Si face of 4H-SiC are calculated to be 25.09 and 35.75 kcal/mol, respectively. The molten-KOH etching rate of the C face is higher than the Si face. Combining XPS analysis and first-principles calculations, we find that the molten-KOH etching of 4H-SiC is proceeded by the cycling of the oxidation of 4H-SiC by the dissolved oxygen and the removal of oxides by molten KOH. The faster etching rate of the C face is caused by the fact that the oxides on the C face are unstable, and easier to be removed with molten alkali, rather than the C face being easier to be oxidized.