Ba0.4Sr0.6SnO3的合成和复杂介电性质,具有棘状微观结构的陶
Wei Li1, Xiaoyu Wu1, Ziheng Huang1
1School of Physics and Electronic Information, Yantai University, Yantai 264005, China.
Materials (Basel, Switzerland)
|January 8, 2025
概括
这项研究合成了类似棘的矿陶,揭示了微观结构和兴奋剂如何影响介电性质. 这些发现提供了有关先进陶材料结构性质关系的见解.
科学领域:
- 材料科学 材料科学 材料科学
- 固态化学 固态化学
- 陶工程 陶工程 陶工程
背景情况:
- 矿酸陶对于电子应用至关重要.
- 了解结构-属性关系是优化性能的关键.
- 定制微观结构和组成会影响介电行为.
研究的目的:
- 合成矿Ba0.4Sr0.6SnO3陶具有独特的棘状微观结构.
- 为了研究这种微观结构和A位点兴奋剂对介电性质的影响.
- 阐明控制介电行为和阻抗特征的机制.
主要方法:
- 陶合成的固态反应方法.
- 用X射线衍射 (XRD) 进行相位纯度分析.
- 射线光电子光谱 (XPS) 用于化学状态的确定.
- 介电光谱和阻抗分析用于属性表征.
主要成果:
- 在Ba0.4Sr0.6SnO3陶中成功合成了一种独特的棘状微观结构.
- 介电常数和损耗受到A位点兴奋剂和棘状微观结构的显著影响.
- 界面极化和介电松被归因于Sn4+-Sn2+对,氧空缺和具有特定激活能量的缺陷.
- 阻抗光谱显示了颗粒边界,颗粒和棘状结构的明显阻力.
结论:
- 这项研究确立了独特的棘状微观结构与矿酸陶的介电性质之间的明显联系.
- 接口极化和与缺陷相关的放松机制是观察到的介电行为的主要驱动因素.
- 这些发现为设计针对电子应用的定制介电反应的先进矿陶提供了基础.
更多相关视频
11:17Spark Plasma Sintering Apparatus Used for the Formation of Strontium Titanate Bicrystals
Published on: February 9, 2017
9.8K
06:49Radio Frequency Magnetron Sputtering of GdBa2Cu3O7âˆ'ÃŽ ´/ La0.67Sr0.33MnO3 Quasi-bilayer Films on SrTiO3 STO Single-crystal Substrates
Published on: April 12, 2019
7.6K
相关概念视频
Ionic Crystal Structures
Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Metallic Solids
Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
Structural Isomerism
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Valence Bond Theory
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
Imperfections in Crystal Structure: Stoichiometric Point Defects
Schottky defects arise when some lattice points in a crystal, such as those in NaCl, remain unoccupied, creating lattice vacancies without disturbing the overall electrical neutrality of the crystal. This defect is common in ionic crystals where the positive and negative ions are similar in size, as seen in sodium chloride and cesium chloride. The presence of Schottky defects enables the crystal to conduct electricity to a small extent through an ionic mechanism. Electric fields cause nearby...
Imperfections in Crystal Structure: Non-Stoichiometric Defects
Non-stoichiometric defects refer to a type of defect in the crystal structure of a compound where the ratio of its constituent elements deviates from the ideal stoichiometric ratio. There are two main types of non-stoichiometric defects: metal excess defects and metal deficiency defects.Metal excess defects occur when there is a slight surplus of metal ions than what is required by the stoichiometric ratio of the compound. For example, heating a sodium chloride crystal in sodium vapor results...
