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Coherent control of excitonic dressed states of semiconductor quantum dot



Andrew Ramsay

Coherent light-matter interactions are often understood in terms of dressed states: states that are a composite of light and matter. Recently, we have made a number of experiments to time-resolve the excitonic dressed states of a single self-assembled InAs quantum dot. We demonstrate the possibility of controlling the composition, and energies of the excitonic dressed states on a picosecond timescale. Furthermore, an experiment illustrating that a Rabi oscillation may be interpreted as a beat between two dressed states was performed.

Category: Research
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S. J. Boyle, A. J. Ramsay*, A. M. Fox, and M. S. Skolnick
University of Sheffield, UK
A. P. Heberle,
University of Pittsburgh, and Corning Inc. USA

Accepted for Physical Review Letters, * Email: a.j.ramsay@shef.ac.uk



Figure 1: Energy-level diagram of exciton-biexciton system

An InAs/GaAs quantum dot is a 20-nm diameter by 3-4 nm high disk of InAs embedded in GaAs. This acts as the proverbial three dimensional finite quantum well, trapping electrons and holes in discrete energy levels. Resonant excitation with a circularly polarized laser creates a spin-polarized electron-hole pair in the dot, known as an exciton. We study a 4-level system as shown in figure 1. The 4 states are: no exciton “0”, spin-(up/down) exciton “X”, and biexciton “XX”. There are two laser pulses: the “control” couples the spin-up exciton and biexciton states, whilst the weaker “probe” pulse monitors the no-exciton to spin-up exciton states.  A photocurrent detection technique is used to the total number of excitons created by the sequence of laser pulses.



Figure 2: (a) Autler-Townes splitting of exciton transition. (b) Anti-crossing of excitonic dressed states

In the first experiment the two pulses are temporally overlapped. The control is tuned to the exciton-biexciton transition, and the photocurrent is measured as a function of the detuning of the probe laser, and the pulse-area of the control. As can be seen in figure 2(a) the control pulse splits the exciton transition into an Autler-Townes doublet with a Rabi-splitting proportional to the pulse-area of the control.  A splitting of up to 0.5 meV was observed.

In the second experiment, the pulse-area of the control is fixed, and the photocurrent is measured as a function of the detuning of both the probe and control pulses. In fig 2(b), an anti-crossing between the sequential absorption of an exciton (0-X) followed by a biexciton (X-XX), and creation of the biexciton through direct two-photon absorption (0-XX) is observed.  This shows that the control laser has mixed the exciton and biexciton states to form dressed states. We now study the Autler-Townes splitting in the time-domain.



 
Figure 3: (left) Adiabatic control of dressed states (right) Time-resolved measurement of Rabi oscillation, a beat between dressed states

To time-resolve the Autler-Townes doublet, the control pulse is tuned to the exciton-biexciton transition, and its pulse-area fixed. The photocurrent is measured as a function of the detuning of the probe, and the inter-pulse time-delay. As can be seen in figure 3(left) the Rabi splitting follows the Gaussian envelope of the control pulse, shown as a red-line, demonstrating that the Rabi splitting and hence the composition of the dressed states adiabatically follows the control laser, on a picosecond timescale. This is encouraging for the prospects of using coherent control schemes based on adiabatic following in semiconductor quantum dots.

The grand finale is to observe a beat between the excitonic dressed states. The time-duration of the probe pulse is reduced. Figure 3(right) shows the photocurrent versus inter-pulse time-delay for a series of different control pulses of different pulse-areas. The clearest interpretation of the data is a time-resolved measurement of the Rabi rotation between the exciton and biexciton states. Where the probe creates an exciton triggering the X-XX Rabi oscillation at a time equal to the negative time-delay, and thus by varying the time-delay one can observe the time evolution of the Rabi rotation.   Because of the experimental difficulties of varying the time duration of a picosecond laser pulse, excitonic Rabi rotations are usually measured as a function of pulse-area by varying the incident laser power. However, Rabi oscillations are generally understood in the time-domain, so it is aesthetically pleasing to observe the Rabi oscillation in the time-domain by optically gating the control field.

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