INVESTIGATION OF RADIATIVE AND NONRADIATIVE TRANSITIONS IN LASER CRYSTALS.

Abstract

Spontaneous emission probabilities for magnetic- and electric-dipole transitions from excited states of Pr(3+), Nd(3+), Tm(3+) in LaF3 and Pr(3+), Nd(3+), Eu(3+), Tm(3+) in Y2O3 are calculated using the treatment of Judd and Ofelt. Intermediate coupled states and empirical intensity parameters were used. The calculated radiative decay probabilities are compared with fluorescence lifetimes measured at low rare-concentrations, where ion pair relaxation is negligible, to predict quantum efficiencies and test the theory. The agreement between radiative and observed lifetimes is generally satisfactory for those low-lying excited states where unit quantum efficiency is expected; the agreement is less satisfactory for higher excited states. The approximations and limitations inherent in the approach, possible breakdown of the closure assumption, and effects of the neglect of crystal-field interactions are discussed. A decrease in quantum efficiency with decreasing importance of nonradiative decay by multiphonon emission. A general computational program to calculate energy level schemes, absorption and fluorescence intensities, and quantum efficiencies of rare-earth ions is outlined. Techniques for investigating fluorescence decays in the nanosecond time domain are described briefly. (Author)

Document Details

Document Type
Technical Report
Publication Date
Aug 01, 1967
Accession Number
AD0712310

Entities

People

  • Marvin J. Weber

Organizations

  • RTX

Tags

DTIC Thesaurus Topics

  • Absorption
  • Agreements
  • Efficiency
  • Emission
  • Energy Levels
  • Fluorescence
  • Intensity
  • Nanosecond Time
  • Probability
  • Quantum Efficiency
  • Time
  • Time Domain
  • Transitions

Fields of Study

  • Physics

Readers

  • Electronics Engineering
  • Materials Science and Engineering.
  • Quantum spin resonance or Electron Paramagnetic Resonance spectroscopy.

Technology Areas

  • Directed Energy
  • Directed Energy - Lasers
  • Quantum Computing