纤锌矿晶体结构
X射线吸收精细结构
掺杂剂
X射线光电子能谱
协调数
扩展X射线吸收精细结构
钪
材料科学
结晶学
氧烷
晶体结构
氮化物
X射线吸收光谱法
分析化学(期刊)
离子
吸收光谱法
化学
无机化学
兴奋剂
谱线
纳米技术
核磁共振
光谱学
六方晶系
量子力学
色谱法
物理
光电子学
有机化学
天文
图层(电子)
作者
Asaf Cohen,Junying Li,Hagai Cohen,Ifat Kaplan‐Ashiri,Sergey Khodorov,Ellen Wachtel,Igor Lubomirsky,Anatoly I. Frenkel,David Ehre
出处
期刊:ACS applied electronic materials
[American Chemical Society]
日期:2024-01-19
卷期号:6 (2): 853-861
被引量:4
标识
DOI:10.1021/acsaelm.3c01390
摘要
The local environments of Sc and Y in predominantly ⟨002⟩ textured, Al1–xDoxN (Do = Sc, x = 0.25, 0.30 or Y, x = 0.25) sputtered thin films with wurtzite symmetry were investigated using X-ray absorption (XAS) and photoelectron (XPS) spectroscopies. We present evidence from the X-ray absorption fine structure (XAFS) spectra that, when x = 0.25, both Sc3+ and Y3+ ions are able to substitute for Al3+, thereby acquiring four tetrahedrally coordinated nitrogen ligands, i.e., coordination number (CN) of 4. On this basis, the crystal radius of the dopant species in the wurtzite lattice, not available heretofore, could be calculated. By modeling the scandium local environment, extended XAFS (EXAFS) analysis suggests that when x increases from 0.25 to 0.30, CN for a fraction of the Sc ions increases from 4 to 6, signaling octahedral coordination. This change occurs at a dopant concentration significantly lower than the reported maximum concentration of Sc (42 mol % Sc) in wurtzite (Al, Sc)N. XPS spectra provide support for our observation that the local environment of Sc in (Al, Sc)N may include more than one type of coordination.
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