Non-Linear Optical Effects in Molecules.

Abstract

We analyze the evolution of first principle molecular theory in obtaining reliable values of molecular hyperpolarizabilities. Such quantities place severe demands on the capability of quantum chemistry, as large basis sets, frequency dependence, and high levels of electron correlation are all shown to be essential in obtaining observed, gas phase hyperpolarizabilities to within an error of 10%. Ab initio Hartree Fock results are typically in error by nearly a factor of two, while the errors due to the neglect of frequency dependence average about 1O to 3O% depending upon the particular process. It is also shown that for small molecules, standard semiempirical approaches, like INDO and INDO/S, will often not even give the correct sign for hyperpolarizabilities. It is demonstrated that using state of the art correlated, frequency dependent methods, it is possible to provide results to within 10%. Excluding any one of the essential elements, though, destroys the agreement

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Document Details

Document Type
Technical Report
Publication Date
Mar 31, 1996
Accession Number
ADA306197

Entities

People

  • Rodney J. Bartlett

Organizations

  • University of Florida

Tags

Communities of Interest

  • Air Platforms
  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Air Force
  • Chemistry
  • Computational Chemistry
  • Computational Chemistry Methods
  • Density Functional Theory
  • Electro-Optics
  • Frequency
  • Kerr Effects
  • Materials Science
  • Molecular Orbital Theory
  • Optical Properties
  • Optics
  • Quantum Chemistry
  • Quantum Mechanics
  • Semi-Empirical Quantum Chemistry Methods
  • Small Molecules
  • Wave Mixing

Fields of Study

  • Physics

Readers

  • Computational Modeling and Simulation
  • Molecular Photonics/Laser Physics
  • Quantum spin resonance or Electron Paramagnetic Resonance spectroscopy.

Technology Areas

  • Microelectronics
  • Quantum Computing