ALD Zn(O,S) Thin Films' Interfacial Chemical and Structural Configuration Probed by XAS

被引:16
作者
Dadlani, Anup L. [1 ]
Acharya, Shinjita [2 ]
Trejo, Orlando [2 ]
Prinz, Fritz B. [2 ,3 ]
Torgersen, Jan [2 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
基金
奥地利科学基金会;
关键词
X-ray absorption near edge structure (XANES); Zn(O; S); atomic layer deposition (ALD); ternary oxide films; electronic structure; CU(IN; GA)SE-2; SOLAR-CELL; BUFFER LAYERS; ELECTRONIC-STRUCTURE; DAMP-HEAT; THICKNESS;
D O I
10.1021/acsami.6b04000
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The ability to precisely control interfaces of atomic layer deposited (ALD) zinc oxysulfide (Zn(O,S)) buffer layers to other layers allows precise tuning of solar cell performance. The O K- and S K-edge X-ray absorption near edge structure (XANES) of similar to 24 nm thin Zn(O,S) films reveals the chemical and structural influences of their interface with ZnO, a common electrode material and diffusion barrier in solar cells. We observe that sulfate formation at oxide/sulfide interfaces is independent of film composition, a result of sulfur diffusion toward interfaces. Leveraging sulfurs diffusivity, we propose an alternative ALD process in which the zinc precursor pulse is bypassed during H2S exposure. Such a process yields similar results to the nanolaminate deposition method and highlights mechanistic differences between ALD sulfides and oxides. By identifying chemical species and structural evolution at sulfide/oxide interfaces, this work provides insights into increasing thin film solar cell efficiencies.
引用
收藏
页码:14323 / 14327
页数:5
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