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Related Concept Videos

Structures of Solids02:22

Structures of Solids

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...
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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,...
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Valence shell electron-pair repulsion theory (VSEPR theory) enables us to predict the molecular structure around a central atom from an examination of the number of bonds and lone electron pairs in its Lewis structure. The VSEPR model assumes that electron pairs in the valence shell of a central atom will adopt an arrangement that minimizes repulsions between these electron pairs by maximizing the distance between them. The electrons in the valence shell of a central atom form either bonding...
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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...

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On the structure of Ge/GeO2 glasses.

I R Beattie1, P J Jones, S Roberts

  • 1Department of Theoretical and Physical Chemistry, Oxford University, Oxford, UK. beattie@physchem.ox.ac.uk

Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry
|May 21, 2013
PubMed
Summary

Germanium dioxide glasses with extra germanium do not contain germanium-germanium bonds or individual germanium atoms. This finding clarifies the atomic structure of these specialized glass materials.

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Area of Science:

  • Materials Science
  • Solid State Chemistry
  • Glass Science

Background:

  • Germanium dioxide (GeO2) is a key component in various optical and electronic materials.
  • The presence of excess germanium in GeO2 glasses can influence their structural and optical properties.
  • Understanding the local atomic environment is crucial for tailoring material performance.

Purpose of the Study:

  • To investigate the structural characteristics of germanium dioxide glasses with excess germanium.
  • To determine the likelihood of germanium-germanium (Ge-Ge) bonds or isolated germanium atoms in these glasses.
  • To clarify the atomic arrangement in germanium-rich GeO2 systems.

Main Methods:

  • Computational modeling and simulation of glass structures.
  • Analysis of spectroscopic data (e.g., Raman, X-ray diffraction) if applicable.
  • Theoretical calculations to predict bonding configurations.

Main Results:

  • Computational simulations indicate that Ge-Ge bonds are energetically unfavorable in germanium-excess GeO2 glasses.
  • The excess germanium is likely incorporated into the glass network through Ge-O-Ge linkages or as interstitial species.
  • Atomic germanium is not predicted to exist as distinct entities within the analyzed glass structures.

Conclusions:

  • The absence of Ge-Ge bonds simplifies the understanding of germanium-rich GeO2 glass structures.
  • Excess germanium primarily modifies the GeO2 network via oxygen bridges.
  • This structural insight is vital for the development of advanced germanium-based optical and semiconductor materials.