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MicroPL optical setup

Professor Robert Taylor

Emeritus Professor of Condensed Matter Physics

Research theme

  • Photovoltaics and nanoscience

Sub department

  • Condensed Matter Physics

Research groups

  • Quantum Optoelectronics
Robert.Taylor@physics.ox.ac.uk
Telephone: 01865 (2)72230
Clarendon Laboratory, room 164
orcid.org/0000-0003-2578-9645
  • About
  • Teaching
  • Positions available
  • Publications

Lasing in perovskite nanocrystals

Image of transverse modes from lasing nanocrystals
Nano Research, 14, 108, 2021

Relevance of dephasing processes for the ultrafast rise of emission from resonantly created excitons in quantum wells

Physica Status Solidi (B) Basic Research 204:1 (1997) 35-38

Authors:

S Haacke, G Hayes, RA Taylor, B Deveaud, R Zimmermann, I Bar-Joseph

Abstract:

We present a comparative study of time-integrated four-wave-mixing and femtosecond emission under resonant, excitation on excitons in weakly disordered GaAs quantum wells. At highest exciton densities when dephasing dominates the spectral width (homogeneous broadening), we find that the rise time of the incoherent luminescence signal is given by T2/2. At lowest densities, optical coherence times approach the exciton radiative lifetime (15 to 20 ps). This confirms our previous result that coherent resonant Rayleigh scattering is responsible for the short rise time of the excitonic emission. We also show clear evidence for dephasing due to exciton-phonon interaction, as the rise time of the emission decreases dramatically when the sample temperature is increased.
More details from the publisher

Resonant femtosecond emission from quantum well excitons: The role of rayleigh scattering and luminescence

Physical Review Letters 78:11 (1997) 2228-2231

Authors:

S Haacke, RA Taylor, R Zimmermann, I Bar-Joseph, B Deveaud

Abstract:

We study the ultrafast properties of secondary radiation of semiconductor quantum wells under resonant excitation. We show that the exciton density dependence allows one to identify the origin of secondary radiation. At high exciton densities, the emission is due to incoherent luminescence with a rise time determined by exciton-exciton scattering. For low densities, when the distance between excitons is much larger than their diameter, the temporal shape is independent of density and rises quadratically, in excellent agreement with recent theories for resonant Rayleigh scattering. © 1997 The American Physical Society.
More details from the publisher

Direct observation in the temporal domain of relaxation oscillations in a semiconductor laser

PHYSICA STATUS SOLIDI B-BASIC RESEARCH 204:1 (1997) 574-576

Authors:

T Hessler, S Haacke, JL Pleumeekers, PE Selbmann, MA Dupertuis, B Deveaud, P Doussiere, M Bachmann, JY Emery, T Ducellier, RA Taylor
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Efficient intersubband scattering via carrier-carrier interaction

PHYSICA STATUS SOLIDI B-BASIC RESEARCH 204:1 (1997) 159-161

Authors:

M Hartig, S Haacke, PE Selbmann, B Deveaud, RA Taylor, L Rota
More details from the publisher

Femtosecond luminescence of semiconductor nanostructures

Optica Publishing Group (1997) qthd.2

Authors:

B Deveaud, S Haacke, M Hartig, R Ambigapathy, I Bar Joseph, RA Taylor

Abstract:

Luminescence has been quite widely used for the study of semiconductor nanostructures, and more especially time resolved luminescence, due to the ease to get a luminescence signal. The interpretation of the results however is sometimes quite complex, and one generally finds that some care has to be taken for the results to be meaningful. In particular, the homogeneity of the excited density over the detected luminescence signal is a quite important parameter, also it is often desirable to work at the lowest possible densities.
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