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arXiv:0710.5292

Single Molecule Photon Statistics from a Sequence of Laser Pulses

F. Shikerman, He, Yong, Eli Barkai

Published Oct 28, 2007• 0 citations
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Abstract

There are many ways of calculating photon statistics in quantum optics in general and single molecule spectroscopy in particular such as the generating function method, the quantum jump approach or time ordering methods. In this paper starting with the optical Bloch equation, within the paths interpretation of Zoller, Marte and Walls we obtain the photon statistics from a sequence of laser pulses expressed by means of quantum trajectories. We find general expressions for Pn(t) - the probability of emitting n photons up to time t, discuss several consequences and show that the interpretation of the quantum trajectories (i) emphasizes contribution to the photon statistics of the coherence paths accumulated in the delay interval between the pulses and (ii) allows simple classification of the terms negligible under certain physical constraints . Applying this method to the concrete example of two square laser pulses we find the probabilities of emitting 0,1 and 2 photons, examine several limiting cases and investigate the upper and lower bounds of P0(t), P1(t) and P2(t) for a sequence of two strong pulses in the limit of long measurement times. Implication to single molecule non-linear spectroscopy and theory of pairs of photons on demand are discussed briefly.

DOI
10.48550/arxiv.0710.5292

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There are many ways of calculating photon statistics in quantum optics in general and single molecule spectroscopy in particular such as the generating function method, the quantum jump approach or time ordering methods. In this paper starting with the optical Bloch equation, within the paths interpretation of Zoller, Marte and Walls we obtain the photon statistics from a sequence of laser pulses expressed by means of quantum trajectories. We find general expressions for Pn(t) - the probability of emitting n photons up to time t, discuss several consequences and show that the interpretation of the quantum trajectories (i) emphasizes contribution to the photon statistics of the coherence paths accumulated in the delay interval between the pulses and (ii) allows simple classification of the terms negligible under certain physical constraints . Applying this method to the concrete example of two square laser pulses we find the probabilities of emitting 0,1 and 2 photons, examine several limiting cases and investigate the upper and lower bounds of P0(t), P1(t) and P2(t) for a sequence of two strong pulses in the limit of long measurement times. Implication to single molecule non-linear spectroscopy and theory of pairs of photons on demand are discussed briefly.
We investigate photon statistics emerging from the interaction of a two-level system with two laser pulses separated by a delay interval. It is shown that Pn(t){P}_{n}(t)Pn​(t), the probability of emitting nnn photons up to time ttt, may be represented as a summation over quantum trajectories, which allows simple identification of the coherent effect arising from the existence of the delay. We obtain a relation between photon statistics emerging from the interaction with a single pulse and photon statistics emerging from the interaction with two separated pulses with finite delay. In addition, the probabilities of emitting zero, one, and two photons, the expectation number of emissions, ⟨N⟩⟨N⟩⟨N⟩, and Mandel's QQQ parameter are calculated explicitly. The case of two short and strong pulses, the so-called pump and probe setup, yielding up to two photons at most, is considered in detail. We examine different limiting behaviors of the photon statistics and obtain the upper and lower bounds for P0{P}_{0}P0​, P1{P}_{1}P1​, and P2{P}_{2}P2​ in the limit of strong fields. Implications for single-molecule nonlinear spectroscopy and the theory of obtaining pairs of photons on demand are discussed briefly.
We develop the theory of nonlinear spectroscopy for a single molecule undergoing stochastic dynamics and interacting with a sequence of two laser pulses. We find general expressions for the photon counting statistics and the exact solution to the problem for the Kubo-Anderson process. In the limit of impulsive pulses the information on the photon statistics is contained in the molecule's dipole correlation function. The selective limit, the semiclassical approximation, and the fast modulation limit exhibit rich general behaviors of this new type of spectroscopy. We show how the design of external fields leads to insights on ultrafast dynamics of individual molecules that are different from those found for an ensemble.
We investigate theory of single-photon control from a two-level single-molecule source irradiated by laser pulses of various shapes and pulse durations in terms of quantum trajectories which link stochastic dynamics of the radiating source with quantum measurement theory. Using Monte Carlo wave function simulation, we analyze the detailed dissipative dynamics of the single-molecule source and the photon statistics as revealed by repeated Gedanken photon measurement on the single radiating source. We show that much of the photon statistics from the two-level single-molecule single-photon sources, including few-photon emission probability, waiting time distribution, and two-time correlation function of the fluorescent light, can be understood qualitatively from the simple picture of Rabi nutation and pi pulse in terms of pulse areas.
A theory is formulated for time dependent fluctuations of the spectrum of a single molecule in a dynamic environment. In particular, we investigate the photon counting statistics of a single molecule undergoing a spectral diffusion process. Based on the stochastic optical Bloch equation, fluctuations are characterized by Mandel's QQQ parameter yielding the variance of number of emitted photons and the second order intensity correlation function, g(2)(t)g^{(2)}(t)g(2)(t). Using a semi-classical approach and linear response theory, we show that the QQQ parameter can be described by a three-time dipole correlation function. This approach gene ralizes the Wiener-Khintchine formula that gives the average number of fluorescent photons in terms of a one-time dipole correlation function. We classify the time ordering properties of the three-time dipole correlation function, and show that it can be represented by three different pulse shape functions similar to those used in the context of nonlinear spectroscopy. An exact solution is found for a single molecule whose absorption frequency undergoes a two state random telegraph process (i.e., the Kubo-Anderson sudden jump process.) Simple expressions are obtained from the exact solution in the slow and fast modulation regimes based on appropriate approximations for each case. In the slow modulation regime QQQ can be large even in the long time limit, while in the fast modulation regime it becomes small.
We consider the theory of single photon on demand from a two level atom or molecule source. Using optical Bloch equations and the generating function formalism we investigate three approaches to single photon control: (i) the square laser pulse; (ii) the square modulation of absorption frequency; and (iii) the rapid adiabatic following approach investigated in the experiments of Brunel et al., Phys. Rev. Lett., 1999, 83, 2722. We discuss the conditions for obtaining the maximum of the probability of emission of a single photon and a pair of photons, under the constrains of finite field strength and finite interaction time with excitation field. We obtain analytical expression for the probability of emitting zero, one, and two photons for the square pulse, and discuss semi-classical and strongly quantum limiting cases. Numerical results obtained from the generating function formalism are compared with experimental results showing that the two level system approach is suitable for the description of cryogenic temperature single molecules, and that experiments were conducted very close to the optimal conditions.
The stream of photons emitted by a single quantum system such as a molecule or a nanocrystal is often statistically characterized by the distribution of delays between consecutive photons, or by the autocorrelation function of the intensity, or by the distributions of on- and off-times. We derive and discuss general relations between their Laplace transforms, addressing the influence of detection yield and background. Our analytical treatment applies to any distribution of delays and to random telegraph signals, including nonexponential distributions. We examine the special case of systems switching between two states characterized by different distributions of delays, where the switching can obey various statistics. We show that the second-order autocorrelation function keeps track of long-time fluctuations which are obviously lost in averaging the distributions of delays. We apply our formalism to random telegraphs, in particular to those with power-law distributions of on- and/or of off-times, which are encountered in the blinking of single semiconductor nanocrystals.