The optical absorption spectra of spontaneously electrical solids: the case of nitrous oxide.

Phys Chem Chem Phys

Department of Physics and Astronomy, Aarhus University, Ny Munkegade 120, DK-8000 Aarhus, Denmark.

Published: January 2019

AI Article Synopsis

  • The study presents absorption spectra of N2O films across a temperature range of 33 K to 64 K, examining how deposition temperature affects absorption energy.
  • The analysis indicates that the observed shifts are linked to temperature-driven spontaneously electric fields in the films, suggesting that excitons are influenced by these fields up to certain temperatures.
  • Results highlight a potential blockade effect on excitons due to structural defects and provide insights into the regular periodicity of the films, revealing structural changes near the known phase transition at around 47 K to 48 K.

Article Abstract

Absorption spectra of films of N2O, in the range 115-160 nm, are presented for deposition temperatures between 33 K and 64 K. Observed shifts in the absorption energy vs. deposition temperature are analysed in terms of the temperature-dependent spontaneously electrical ('spontelectric') fields present in the films. Using a simple electrostatic theory, we suggest that (i) spectra are associated with Wannier-Mott excitons, (ii) the action of the electric field upon the excitons suffers a blockade at ≤54 K for the C-state and ≤52 K for the D-state of N2O, (iii) the blockade may be attributed to structural defects, which trap excitons, limiting their size and (iv) films form with defect-free regions containing 324 ± 3, 168 ± 46 and 95 ± 1 molecules of N2O at 54 K, 52 K and 50 K respectively, yielding an experimental indication of the scale size of regular periodicity associated with Wannier-Mott excitons. Results demonstrate how the spontelectric effect can be used as a tool for exploring the structure of solids and give a graphic image of the structural changes that take place close to the known phase change at 47 K/48 K.

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Source
http://dx.doi.org/10.1039/c8cp05746jDOI Listing

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