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相关概念视频

Ionic Crystal Structures02:42

Ionic Crystal Structures

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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...
14.9K
Metallic Solids02:37

Metallic Solids

18.9K
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....
18.9K
Network Covalent Solids02:18

Network Covalent Solids

14.6K
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
14.6K
Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

44.8K
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,...
44.8K
Lattice Centering and Coordination Number02:33

Lattice Centering and Coordination Number

10.0K
The structure of a crystalline solid, whether a metal or not, is best described by considering its simplest repeating unit, which is referred to as its unit cell. The unit cell consists of lattice points that represent the locations of atoms or ions. The entire structure then consists of this unit cell repeating in three dimensions. The three different types of unit cells present in the cubic lattice are illustrated in Figure 1.
Types of Unit Cells
Imagine taking a large number of identical...
10.0K
Trends in Lattice Energy: Ion Size and Charge02:54

Trends in Lattice Energy: Ion Size and Charge

24.3K
An ionic compound is stable because of the electrostatic attraction between its positive and negative ions. The lattice energy of a compound is a measure of the strength of this attraction. The lattice energy (ΔHlattice) of an ionic compound is defined as the energy required to separate one mole of the solid into its component gaseous ions. For the ionic solid sodium chloride, the lattice energy is the enthalpy change of the process:
24.3K

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具有四角孔的单层集群离子链网络.

Haoyang Li1, Qichen Lu2,3, Fenghua Zhang1

  • 1Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry, Tsinghua University, Beijing, China.

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概括

研究人员使用聚氧甲酸盐 (POM) 集群开发了全新的无机多孔二维材料. 基于Mn的材料显示出特有的氧化催化活性,由作为电子缓冲器的POM集群实现.

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科学领域:

  • 材料科学 材料科学 材料科学
  • 纳米技术纳米技术
  • 催化剂是一种催化剂.

背景情况:

  • 具有内在孔隙的二维 (2D) 材料对于催化和电子学至关重要.
  • 由于功能复杂性,在使用无机连接器创建全无机2D网络方面存在差距.

研究的目的:

  • 引入一类新的二维全无机多孔网络:集群离子链网络 (CIN).
  • 调查聚氧甲 (POM) 集群对这些网络电子和催化性能的影响.

主要方法:

  • 使用PW10M2 (M = Mn,Co) POM集群作为节点和端盖剂合成单层CIN.
  • 合成CINs的电子和带结构的表征.
  • 评估催化活性,特别是氧化,并对反应机制进行计算分析.

主要成果:

  • 成功构建了2D全无机CIN与集成的POM集群.
  • 在POM集成后观察到电子和带结构的显著变化.
  • 基于Mn的CIN显示了对托卢氧化具有很高的催化活性 (超过1.45 mmol g-1 h-1).

结论:

  • POM集群可以作为"超原子"封闭剂,使得功能全无机二维网络的创建成为可能.
  • POM集群的"电子缓冲"效应稳定了活性位点,并降低了催化作用的激活能量.
  • 这项工作为设计具有独特电子性质的先进催化材料提供了新的途径.