在分层阴极材料中,阴极排序的上层结构的形成和变化
Yilin Tai1, Guojie Chen2, Yangsheng Li3
1Information Materials and Intelligent Sensing Laboratory of Anhui Province, Leibniz International Joint Research Center of Materials Sciences of Anhui Province, Institutes of Physical Science and Information Technology, Anhui University, Hefei 230601, China.
Nano letters
|February 17, 2025
概括
在,,,氧化物 (LiNi$_{0.5}$Co$_{0.2}$Mn$_{0.3}$O$_{2}$) 阴极材料中的阴极排序形成了一个上层结构,主要由离子驱动. 这种上层结构会对电池循环性能和结构稳定性产生负面影响.
科学领域:
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
- 固态化学 固态化学
背景情况:
- ---氧化 (LiNi$_{0.5}$Co$_{0.2}$Mn$_{0.3}$O$_{2}$或NCM523) 是高能离子电池的关键阴极材料.
- 了解结构特征对于优化电池性能和寿命至关重要.
研究的目的:
- 为了最终证实NCM523.3的上层结构内的序.
- 为了研究在上层结构形成中的作用.
- 评估超结构对电池性能和结构稳定性的影响.
主要方法:
- 使用异常校正传输电子显微镜 (TEM) 识别和描述了阴子排序.
- 使用受控加热来研究订单的增强.
- 进行了电池性能测试,以评估超层结构的影响.
主要成果:
- 获得了NCM523超结构中阴离子排序的明确证据,其特征是特定的波向量.
- 离子被确定为这种超结构的形成必不可少的.
- 虽然超结构没有显著影响电压配置文件,但它对循环性能和结构稳定性产生了不利影响.
结论:
- 该研究阐明了NCM523中超结构的起源,将其归因于受影响的阴离子排序.
- 这些发现突出了这些超结构对三元阴极材料的电化学性能和稳定性的不利影响.
- 这项研究通过了解和减轻结构排序的负面影响,为未来开发先进的阴极材料提供了关键的见解.
相关概念视频
Ionic Crystal Structures
14.1K
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...
14.1K
Metallic Solids
18.2K
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....
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
18.2K
Crystal Field Theory - Octahedral Complexes
26.1K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
26.1K
Crystal Field Theory - Tetrahedral and Square Planar Complexes
41.2K
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
41.2K
Ionic Bonding and Electron Transfer
41.1K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions.
41.1K
Structures of Solids
13.8K
Solids in which the atoms, ions, or molecules are arranged in a definite repeating pattern are known as crystalline solids. Metals and ionic compounds typically form ordered, crystalline solids. A crystalline solid has a precise melting temperature because each atom or molecule of the same type is held in place with the same forces or energy. Amorphous solids or non-crystalline solids (or, sometimes, glasses) which lack an ordered internal structure and are randomly arranged. Substances that...
13.8K


