材料科学
原子层沉积
带隙
X射线光电子能谱
光电子学
固溶体
图层(电子)
薄膜
化学计量学
堆积
沉积(地质)
密度泛函理论
超晶格
宽禁带半导体
化学工程
纳米技术
物理化学
计算化学
冶金
工程类
古生物学
物理
核磁共振
化学
生物
沉积物
作者
Ming‐Wei Liao,Horng‐Tay Jeng,Tsong‐Pyng Perng
标识
DOI:10.1002/adma.202207849
摘要
Nanolamination of GaN and ZnO layers by atomic layer deposition (ALD) is employed to fabricate GaN-ZnO homogenous solid-solution thin films because it offers more precise control of the stoichiometry. By varying the ALD cycle ratios of GaN:ZnO from 5:10 to 10:5, the (GaN)1-x (ZnO)x films with 0.39 ≦ x ≦ 0.79 are obtained. The formation of solid solution is explained based on the atomic stacking and preferred orientation of the layers of GaN and ZnO. However, the growth rates of GaN and ZnO during the lamination process are different from those of pure GaN and ZnO films. It is found that GaN grows faster on ZnO, whereas ZnO grows slower on GaN. The density functional theory (DFT) calculations are performed using a superlattice model for GaN and ZnO laminated layers fabricated by ALD to understand the difference of density of states (DOS) and evaluate the bandgaps for various atomic configurations in the solid-solution films. The band positions are experimentally defined by ultraviolet photoelectron spectroscopy. Significant bandgap reduction of the solid solutions is observed, which can be explained by the DOS from the DFT calculations. Visible-light-driven photocatalytic hydrogen evolution is conducted to confirm the applicability of the solid-solution films.
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