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Ionic Crystal Structures02:42

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...
Metallic Solids02:37

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...
Unit Cells01:18

Unit Cells

A crystal's internal structure is an orderly array of atoms, ions, or molecules, and the details of this array significantly influence the solid's properties. In a crystal, periodically repeating 'structural motifs' - which could be atoms, molecules, or groups thereof - create a 'space lattice.' This is essentially a three-dimensional, infinite array of points, each surrounded by its neighbors in an identical way, forming the basic structure of the crystal.A 'unit cell' is a theoretical...
Network Covalent Solids02:18

Network Covalent Solids

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...
Ionic Compounds: Formulas and Nomenclature03:34

Ionic Compounds: Formulas and Nomenclature

An element composed of atoms that readily lose electrons (a metal) can react with an element composed of atoms that readily gain electrons (a nonmetal) to produce ions through complete electron transfer. The compound formed by this transfer is stabilized by the electrostatic attractions (ionic bonds) between the oppositely charged ions.
The Seven Crystal Systems: Overview01:24

The Seven Crystal Systems: Overview

Crystals with various point group symmetries belong to different crystal classes, which are synonymous terms. Despite being in the same class, crystals may have distinct shapes, like cubes and octahedra. There are 32 three-dimensional point groups, all of which are systematically divided into seven crystal systems.The basic cubic crystal system, exemplified by NaCl, features orthogonal vectors (α = β = �� = 90°) of equal lengths (a = b = c). When specific requirements are not imposed on the...

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Updated: Jun 23, 2026

Fabrication and Optimization of Type II Silicon Clathrate Films
06:53

Fabrication and Optimization of Type II Silicon Clathrate Films

Published on: October 14, 2025

Cs(8-x)Si(46): a type-I clathrate with expanded silicon framework.

Aron Wosylus1, Igor Veremchuk, Walter Schnelle

  • 1Max-Planck-Institut für Chemische Physik fester Stoffe, Nöthnitzer Strasse 40, 01187 Dresden, Germany.

Chemistry (Weinheim an Der Bergstrasse, Germany)
|May 15, 2009
PubMed
Summary

The synthesis of cesium silicon clathrate-I (Cs(8-x)Si(46)) was achieved at high pressures and temperatures. This completes the series of alkali metal silicides with this unique structure.

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Area of Science:

  • Materials Science
  • Solid State Chemistry
  • Inorganic Chemistry

Background:

  • Alkali metal silicides with clathrate-I structures are known for M = Na, K, Rb.
  • The synthesis of the cesium analogue, Cs(8-x)Si(46), was previously unachieved under ambient conditions.

Purpose of the Study:

  • To synthesize the binary cesium silicon clathrate-I compound, Cs(8-x)Si(46).
  • To investigate the synthesis conditions required for Cs(8-x)Si(46).
  • To complete the series of M(8-x)Si(46) clathrate-I compounds.

Main Methods:

  • High-pressure synthesis at elevated temperatures.
  • Varying pressure conditions between 2-10 GPa.
  • Heating at 1200 degrees C.

Main Results:

  • Successfully synthesized the binary Cs(8-x)Si(46) clathrate-I compound.
  • Cs(8-x)Si(46) requires elevated pressures (2-10 GPa) for formation, unlike lighter alkali metal silicides.
  • Cesium content increases with applied pressure.

Conclusions:

  • The synthesis of Cs(8-x)Si(46) under high pressure completes the series of binary alkali metal silicides with the clathrate-I structure.
  • High pressure is a critical factor for forming cesium-based clathrate-I silicides.