TEM and DFT study of basal-plane inversion boundaries in SnO2-doped ZnO

IF 1.4 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS
Vesna Ribić, A. Rečnik, G. Dražič, M. Podlogar, Z. Branković, G. Branković
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引用次数: 3

Abstract

In our recent study (Ribic et al. 2020) we reported the structure of inversion boundaries (IBs) in Sb2O3-doped ZnO. Here, we focus on IBs that form in SnO2-doped ZnO. Using atomic resolution scanning transmission electron microscopy (STEM) methods we confirm that in SnO2-doped ZnO the IBs form in head-to-head configuration, where ZnO4 tetrahedra in both ZnO domains point towards the IB plane composed of a close-packed layer of octahedrally coordinated Sn and Zn atoms. The in-plane composition is driven by the local charge balance, following Pauling's principle of electroneutrality for ionic crystals, according to which the average oxidation state of cations is 3+. To satisfy this condition, the cation ratio in the IB-layer is Sn4+: Zn2+=1:1. This was confirmed by concentric electron probe analysis employing energy dispersive spectroscopy (EDS) showing that Sn atoms occupy 0.504 ? 0.039 of the IB layer, while the rest of the octahedral sites are occupied by Zn. IBs in SnO2-doped ZnO occur in the lowest energy, IB3 translation state with the cation sublattice expansion of ?IB(Zn-Zn) of +91 pm with corresponding O-sublattice contraction ?IB(O-O) of -46 pm. Based on quantitative HRTEM and HAADF-STEM analysis of in-plane ordering of Sn and Zn atoms, we identified two types of short-range distributions, (i) zigzag and (ii) stripe. Our density functional theory (DFT) calculations showed that the energy difference between the two arrangements is small (~6 meV) giving rise to their alternation within the octahedral IB layer. As a result, cation ordering intermittently changes its type and the direction to maximize intrinsic entropy of the IB layer driven by the in-plane electroneutrality and 6-fold symmetry restrictions. A long-range in-plane disorder, as shown by our work would enhance quantum well effect to phonon scattering, while Zn2+ located in the IB octahedral sites, would modify the bandgap, and enhance the in-plane conductivity and concentration of carriers. Keywords
SnO2掺杂ZnO衬底平面反转边界的TEM和DFT研究
在我们最近的研究(Ribic et al. 2020)中,我们报道了sb2o3掺杂ZnO的反转边界(IBs)结构。在这里,我们关注的是在sno2掺杂ZnO中形成的IBs。利用原子分辨率扫描透射电子显微镜(STEM)方法,我们证实了在sno2掺杂的ZnO中,IB形成头对头构型,其中两个ZnO结构域的ZnO4四面体指向由八面体配位的Sn和Zn原子紧密堆积层组成的IB平面。面内组成由局部电荷平衡驱动,遵循鲍林离子晶体的电中性原理,根据该原理,阳离子的平均氧化态为3+。为了满足这一条件,ib层中的阳离子比为Sn4+: Zn2+=1:1。利用能谱(EDS)的同心电子探针分析证实了这一点,表明Sn原子占据了0.504 ?而其余的八面体位被Zn占据。sno2掺杂ZnO中的IBs发生在能量最低的IB3平移态,阳离子亚晶格扩展- IB(Zn-Zn)为+91 pm,对应的o -亚晶格收缩- IB(O-O)为-46 pm。基于定量HRTEM和HAADF-STEM对Sn和Zn原子的面内有序分析,我们确定了两种短程分布类型,即(i)之字形和(ii)条纹。我们的密度泛函理论(DFT)计算表明,这两种排列之间的能量差很小(~6 meV),导致它们在八面体IB层内交替。结果表明,在平面内电中性和6重对称约束的驱动下,阳离子的排序会间歇性地改变其类型和方向,从而使IB层的本征熵最大化。我们的工作表明,长程面内无序会增强量子阱对声子散射的效应,而位于IB八面体位置的Zn2+会改变带隙,提高载流子的面内电导率和浓度。关键字
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来源期刊
Science of Sintering
Science of Sintering 工程技术-材料科学:硅酸盐
CiteScore
2.50
自引率
46.70%
发文量
20
审稿时长
3.3 months
期刊介绍: Science of Sintering is a unique journal in the field of science and technology of sintering. Science of Sintering publishes papers on all aspects of theoretical and experimental studies, which can contribute to the better understanding of the behavior of powders and similar materials during consolidation processes. Emphasis is laid on those aspects of the science of materials that are concerned with the thermodynamics, kinetics and mechanism of sintering and related processes. In accordance with the significance of disperse materials for the sintering technology, papers dealing with the question of ultradisperse powders, tribochemical activation and catalysis are also published. Science of Sintering journal is published four times a year. Types of contribution: Original research papers, Review articles, Letters to Editor, Book reviews.
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