Pressure dependence of the direct absorption edge of InP
- 15 May 1980
- journal article
- research article
- Published by American Physical Society (APS) in Physical Review B
- Vol. 21 (10), 4879-4883
- https://doi.org/10.1103/physrevb.21.4879
Abstract
The variation of the lowest direct absorption edge of InP with pressure has been measured at room temperature with a diamond anvil cell for pressures up to the phase transition (100 kbar). Both transmission and luminescence techniques were used. The gap varies sublinearly with pressure but linearly with lattice constant: the gap deformation potential so obtained is eV. This result is discussed in the light of theoretical calculations. The observed luminescence intensity remains nearly constant as a function of pressure up to 90 kbar. At this pressure the efficiency begins to decrease thus signaling the crossing of the and conduction-band minima which we estimate to occur at 104 ± 1 kbar. The pressure coefficient of the indirect gap is found to be -(3 ± 1) × eV/bar.
Keywords
This publication has 11 references indexed in Scilit:
- Dependence of the phonon spectrum of InP on hydrostatic pressurePhysical Review B, 1980
- High pressure photoluminescence and resonant Raman study of GaAsSolid State Communications, 1978
- Effect of hydrostatic pressure on the direct absorption edge of germaniumPhysical Review B, 1977
- Pressure dependence of the direct energy gap of GaAsPhysical Review B, 1976
- Dependence of the direct energy gap of GaAs on hydrostatic pressurePhysical Review B, 1975
- Calibration of the pressure dependence of the R1 ruby fluorescence line to 195 kbarJournal of Applied Physics, 1975
- Pressure dependence of energy gaps and refractive indices of tetrahedrally bonded semiconductorsPhysical Review B, 1974
- Bond-orbital model. IIPhysical Review B, 1974
- An Optical Fluorescence System for Quantitative Pressure Measurement in the Diamond-Anvil CellReview of Scientific Instruments, 1973
- Calculation of Energy-Band Pressure Coefficients from the Dielectric Theory of the Chemical BondPhysical Review Letters, 1971