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Related Concept Videos

Network Covalent Solids02:18

Network Covalent Solids

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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.
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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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Light-induced Patterning and Grafting for Slippery Surfaces based on Silane-coated Nanoporous Structures
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Hexagonal silicon grown from higher order silanes.

Yizhen Ren1, Philipp Leubner1, Marcel A Verheijen1,2

  • 1Eindhoven University of Technology, Department of Applied Physics, Eindhoven, The Netherlands.

Nanotechnology
|March 7, 2019
PubMed
Summary
This summary is machine-generated.

Tetrasilane (Si4H10) enables faster, non-tapered growth of defect-free hexagonal silicon shells on gallium phosphide nanowires at lower temperatures compared to disilane (Si2H6). This advancement offers improved material quality and growth efficiency.

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Semiconductor Growth

Background:

  • Epitaxial growth of hexagonal silicon (Si) shells on semiconductor nanowires is crucial for advanced electronic and optoelectronic devices.
  • Previous research primarily utilized disilane (Si2H6) as a silicon precursor, with limitations in growth rate and control.

Purpose of the Study:

  • To explore tetrasilane (Si4H10) as a superior precursor for epitaxially growing defect-free hexagonal silicon shells.
  • To investigate and compare the growth kinetics and mechanisms of silicon shells using tetrasilane versus disilane.
  • To achieve non-tapered silicon shells with enhanced growth rates at lower temperatures.

Main Methods:

  • Epitaxial growth of hexagonal silicon shells on wurtzite gallium phosphide (GaP) nanowires.
  • Utilized two silicon precursors: tetrasilane (Si4H10) and disilane (Si2H6).
  • Analyzed growth kinetics across two temperature regimes (415 °C-600 °C and 600 °C-735 °C) and determined activation energies.

Main Results:

  • Identified two distinct surface reaction mechanisms (adsorbate interaction and chemisorption) for both precursors at different temperatures.
  • Tetrasilane exhibited a lower activation energy (1.5 ± 0.1 eV) compared to disilane (2.4 ± 0.2 eV) in the low-temperature regime.
  • Achieved non-tapered silicon shells with over 50 times higher growth rates below 460 °C using tetrasilane, significantly reducing inverse tapering observed with disilane.

Conclusions:

  • Tetrasilane (Si4H10) is a highly effective precursor for growing high-quality, defect-free hexagonal silicon shells.
  • The use of tetrasilane allows for significantly faster growth rates and improved shell morphology at lower temperatures.
  • This advancement in silicon shell growth using tetrasilane holds promise for reduced impurity incorporation and enhanced device performance.