We investigate the fluorescence intensity correlation function of a single CdSe quantum dot (QD) using a start–stop experiment. We observe strong photon antibunching, a signature of non-classical light emission, over a large range of intensities (0.1–100kW/cm2). The lack of coincidence at zero time delay indicates a highly efficient Auger ionization process, which suppresses multi-photon emission in these colloidal QDs. Using careful analysis of the saturation behavior of the coincidence histograms, the absorption cross-section of a single QD has also been derived.
We investigate the fluorescence intensity correlation function of a single CdSe quantum dot (QD) using a start–stop experiment. We observe strong photon antibunching, a signature of non-classical light emission, over a large range of intensities (0.1–100kW/cm2). The lack of coincidence at zero time delay indicates a highly efficient Auger ionization process, which suppresses multi-photon emission in these colloidal QDs. Using careful analysis of the saturation behavior of the coincidence histograms, the absorption cross-section of a single QD has also been derived.
The fluorescence of single colloidal CdSe quantum dots is investigated at room temperature by means of the autocorrelation function over a time scale of almost 12 orders of magnitude. At short time, the autocorrelation function shows a complete antibunching indicating single photon emission and atomic-like behavior. On longer time scales (up to tens of seconds), we measure a bunching effect due to fluorescence intermittency that can not be described by fluctuations between two states with constant rates. The autocorrelation function also exhibits a non-stationary behavior related to power-law distributions of "On" and "Off" times.
We report the experimental observation of photon antibunching in the photoluminescence of a chemically synthesized CdSe/ZnS quantum dot (QD) at room temperature and from a single self-assembled InAs/GaAs QD at 4 K. These results prove that a single quantum dot acts like an artificial atom, with a discrete anharmonic spectrum. Using the quantum regression theorem, we find that the normalized second-order correlation function g(2)(τ) can be described by a single exponential function in the weak-laser excitation regime. From this model we derive that the time constant of the photon antibunching signal is determined by the effective incoherent pump and recombination rates of the nonresonant optically pumped QD.
The fluorescence of single-colloidal CdSe quantum dots is investigated at room temperature by means of the autocorrelation function over a time scale of almost 12 orders of magnitude. Over a short time scale, the autocorrelation function shows complete antibunching, indicating single-photon emission and atomiclike behavior. Over longer time scales (up to tens of seconds), we measure a bunching effect that is due to fluorescence intermittency and that cannot be described by fluctuations between two states with constant rates. The autocorrelation function also exhibits nonstationary behavior related to power-law distributions of On and Off times.
Single photon emission is one of the most striking optical properties of semiconductor quantum dots (QDs), and the corresponding photon anti-bunching effect was observed by non-resonant and resonant photoluminescence experiments in single QDs [1,2]. Up to now, all the measurements reported in the literature focus on the incoherent photoluminescence signal for achieving single photon emission. In this regime, the linewidth of the photoluminescence spectrum is limited to the so-called radiative limit. In this paper, we report on the resonant emission (RE) of the exciton in single InAs/GaAs QDs embedded in a planar microcavity [2]. We present an original type of single photon source based on the coherent laser light scattering by a single QD [3]. Besides the antibunching effect showing the nonclassical nature of the emitted light, we observe that the QD emission spectrum is determined by the spectrum of the resonant excitation laser. Figure (a,b,c) shows high-resolution measurements by Fourier transform spectroscopy of the RE where the data are fitted to the first-order correlation function g(1)(τ) of the RE of a two-level system. The inverse Fourier transform of the g(1)(τ) function allows a direct comparison of the different RE emission profiles in figure (d,e,f). By reducing the resonant excitation power, the Mollow triplet shrinks to a single narrow Lorentzian line, while the relative intensity of this narrow peak increases and tends to overwhelm the RE spectrum. This implies that single QDs can produce single photons with a coherence time that is not limited anymore by the QD electronic properties, resulting in an ultra-coherent character [3]. References [1] P. Michler et al, Science 290, 2282 (2000). [2] H. S. Nguyen et al, Phys. Rev. Lett. (accepted, in press). See arXiv 1109.4304. [3] H. S. Nguyen et al, Appl. Phys. Lett. 99, 261904 (2011).
We report correlation and cross-correlation measurements of photons emitted under continuous wave excitation by a single II–VI quantum dot (QD) grown by molecular-beam epitaxy. A standard technique of microphotoluminescence combined with an ultrafast photon correlation setup allowed us to see an antibunching effect on photons emitted by excitons recombining in a single CdTe∕ZnTe QD, as well as cross correlation within the biexciton (X2)-exciton (X) radiative cascade from the same dot. Fast microchannel plate photomultipliers and a time-correlated single photon module gave us an overall temporal resolution of 140ps better than the typical exciton lifetime in II–VI QDs of about 250ps.
Single photon emission is one of the most striking optical properties of semiconductor quantum dots (QDs), and the corresponding photon anti-bunching effect was observed by non-resonant and resonant photoluminescence experiments in single QDs [1,2,3,4]. Other experiments demonstrated the possibility to use single QDs for the generation of indistinguishable single photons [3]. An important general issue is to reach the so-called fundamental radiative limit. Several strategies have been followed in that sense such as the shortening of population lifetime induced by the Purcell effect [5] or the reduction of pure dephasing by resonant excitation [2,3,4]. Up to now, all the measurements reported in the literature focus on the incoherent photoluminescence signal for achieving single photon emission. In this regime, the linewidth of the photoluminescence spectrum is always limited to the radiative limit. In this paper, we report on the resonant emission (RE) of the exciton in single InAs/GaAs QDs embedded in a planar microcavity, in an orthogonal excitation-detection geometry [4]. We present an original type of single photon source based on the coherent laser light scattering by a single QD [6]. Besides the antibunching effect showing the non-classical nature of the emitted light, we observe that the QD emission spectrum is determined by the spectrum of the resonant excitation laser. We present high-resolution measurements by Fourier transform spectroscopy of the RE where the data are fitted to the first-order correlation function g(1)(τ) of the RE of a two-level system. The inverse Fourier transform of the g(1)(τ) function allows a direct comparison of the different RE emission profiles. We show that, by reducing the resonant excitation power, the so-called Mollow triplet shrinks to a single narrow Lorentzian line, while the relative intensity of this narrow peak increases and tends to overwhelm the RE spectrum. This implies that single QDs can produce single photons with a coherence time that is not limited anymore by the QD electronic properties, resulting in an ultra-coherent character [6]. In conclusion, the resulting " ultra-coherent single photon source " promises high degrees of indistinguishability of the emitted photons which is a crucial requirement for quantum information applications. [1] P. Michler et al., Science 290, 2282 (2000). [2] A. Muller et al., Phys. Rev. Lett. 99, 187402 (2007). [3] S. Ates et al., Phys. Rev. Lett. 103, 167402 (2009). [4] H. S. Nguyen et al., Phys. Rev. Lett. 108, 057401 (2012). [5] C. Santori et al., Nature 419, 594 (2002). [6] H. S. Nguyen et al., Appl. Phys. Lett. 99, 261904 (2011).