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Scientific Reports

Single-photon emission of two-level system via rapid adiabatic passage

Qiang Miao, Yujun Zheng

Published Sep 7, 2016• 6 citations
Publisher

Abstract

In this paper, we present a high quality single-photon source based on the two-level system undergoing rapid adiabatic passage (RAP). A trigger strategy (sweet region) is suggested to optimize the single-photon emission and explain a counter-intuitive phenomenon on the optimal parameters. The RAP strategy of single-photon source is robust against control error and environmental fluctuation.

DOI
10.1038/srep32827

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The linear Stark effect on a single molecule allows us to sweep its frequency through resonance with a fixed laser frequency by applying a sinusoidal RF voltage on two electrodes. If the conditions of adiabatic following are fulfilled, we can prepare the excited molecular state with near certainty. Spontaneous emission from this state gives rise to a single photon. With our current experimental conditions, up to 75% of the sweeps lead to the emission of a single photon. Since the adiabatic passage is done on command, the molecule performs as a high rate source of triggered photons. The experimental results are in quantitative agreement with quantum Monte Carlo simulations.

AIP conference proceedings•Jan 1, 2001•1 citation
In this paper, we present a high quality single-photon source based on the two-level system undergoing rapid adiabatic passage (RAP). A trigger strategy (sweet region) is suggested to optimize the single-photon emission and explain a counter-intuitive phenomenon on the optimal parameters. The RAP strategy of single-photon source is robust against control error and environmental fluctuation.
We demonstrate deterministic and robust generation of pulsed resonance fluorescence single photons from a single InGaAs quantum dot using the method of rapid adiabatic passage. Comparative study is performed with transform-limited, negatively chirped and positively chirped pulses, identifying the last one to be the most robust against fluctuation of driving strength. The generated single photons are background free, have a vanishing two-photon emission probability of 0.3% and a raw (corrected) two-photon Hong-Ou-Mandel interference visibility of 97.9% (99.5%), reaching a precision that places single photons at the threshold for fault-tolerant surface-code quantum computing. The single-photon source can be readily scaled up to multi-photon entanglement and used for quantum metrology, boson sampling and linear optical quantum computing.
Single photons are attractive candidates of quantum bits (qubits) for quantum computation and are the best messengers in quantum networks. Future scalable, fault-tolerant photonic quantum technologies demand both stringently high levels of photon indistinguishability and generation efficiency. Here, we demonstrate deterministic and robust generation of pulsed resonance fluorescence single photons from a single semiconductor quantum dot using adiabatic rapid passage, a method robust against fluctuation of driving pulse area and dipole moments of solid-state emitters. The emitted photons are background-free, have a vanishing two-photon emission probability of 0.3% and a raw (corrected) two-photon Hong-Ou-Mandel interference visibility of 97.9% (99.5%), reaching a precision that places single photons at the threshold for fault-tolerant surface-code quantum computing. This single-photon source can be readily scaled up to multiphoton entanglement and used for quantum metrology, boson sampling, and linear optical quantum computing.
We use the method of adiabatic following to prepare a single molecule in its fluorescing excited state. Spontaneous emission from this state gives rise to a single photon. With our current experimental conditions, up to 7474%74 of the sweeps lead to the emission of a single photon. Since the adiabatic passage is done on command, the molecule performs as a high rate source of triggered photons. The experimental results are in quantitative agreement with quantum Monte Carlo simulations.
The generation of single photons using solid-state quantum emitters is pivotal for advancing photonic quantum technologies, particularly in quantum communication. As the field continuously advances toward practical use cases and beyond shielded laboratory environments, specific demands are placed on the robustness of quantum light sources during operation. In this context, the robustness of the quantum light generation process against intrinsic and extrinsic effects is a major challenge. Here, we present a robust scheme for the coherent generation of indistinguishable single-photon states with very low photon number coherence using a three-level system in a semiconductor quantum dot. Our approach combines the advantages of adiabatic rapid passage and stimulated two-photon excitation. We demonstrate robust quantum light generation while maintaining the prime quantum-optical quality of the emitted light state. Moreover, we highlight the immediate advantages of the implementation of various quantum cryptographic protocols.
The generation of non-classical states of light [1] is an important scientific challenge with many potential applications. For example, squeezed states of light [2] have generated much interest in the past decade, because measurements can be performed with noise levels that are lower than those available with classical light. A particularly novel non-classical source of light is a triggered single-photon source: a source that has the property to emit with a high degree of certainty one (and only one) photon at a user-specified time. Such a deterministic source of single photons can be important for quantum information processing [3], quantum cryptography [4] and certain quantum computation problems [5]. A single quantum emitter such as a molecule or an atom is a good potential source because it can emit only one photon at a time. The emitted light is antibunched [6, 7] and consists of single photons separated by random time intervals, which depend on the excited state lifetime and on the pumping rate. Thus triggered emission of single photons can be obtained with controlled excitation of a single emitter. The first demonstration of a single photons source [8] using a single molecule in a solid is based on a rapid adiabatic passage method [9] to excite the molecule. In the effective spin picture, the Bloch vector follows the driving magnetic field adiabatically if the laser-molecule frequency detuning is swept slowly through the resonance. Since the passage inverts the field, the system goes from the ground to the excited state. From this fluorescent state the molecule can emit only a single photon. The molecular resonance is swept by Stark effect at fixed laser frequency. This is done easily by applying a radio frequency electric field to the molecule. The results showed photon states with statistics that differ radically from those of coherent states. But this method requires cryogenic temperatures (2K) since narrow zero phonon lines are needed for the adiabatic following. At room temperature a source of triggered single photons based on the concept of pulsed optical excitation of a single highly fluorescent molecule has been demonstrated [10]. A short pulse of green laser light pumps the molecule from the ground state to a vibronically excited level of the first electronic excited state. After fast (ps) relaxation to the lowest electronic excited state, the molecule subsequently emits a single photon. A frequency-doubled mode-locked Nd-YAG laser is used to pump highly stable single terrylene molecules contained in a p-terphenyl molecular crystal where they are protected from exposure to diffusing quenchers (such as oxygen). The result shows that the photons are emitted after the laser pulses at times separated by the laser repetition time within the lifetime of terrylene in p-terphenyl. Since the pump pulse width is very short compared to the fluorescence lifetime, the probability of two (or more) photon emission per pulse is always zero. At the maximum laser power, 90% of the laser pulses lead to a single photon emission. The parameters of this source (repetition rate and single photon generation probability) were limited only by the laser system used; nevertheless, this performance already surpasses that of previous work. The high performance combined with the vanishing two photon emission probability and the simplicity of this source suggests that it can be considered for a variety of quantum optical experiments and for secure quantum cryptography [11]. Semiconductor quantum dots (QD) are other potential systems for single photon generation [12]. QDs are often referred to as “artificial atoms” because many of their optical properties, such as ultranarrow transitions, arise from discrete, atomic-like energy levels [13, 14]. To reinforce this analogy a study of the photon antibunching in this system was needed. QDs differ from atoms and molecules since the creation of multiple excitons is possible in QDs. Consequently, if two electron-hole pairs can radiatively recombine, the simultaneous emission of two photons from a QD is then possible. Thus different regimes of photon statistics were expected because the probability of multiple exciton creation depends on excitation intensity. The fluorescence intensity correlation function of a single CdSe quantum dot has been investigated [15] using a coincidence setup (start-stop experiment). A strong photon antibunching has been observed over a large range of intensities (0.1-100 kW/cm2). The lack of coincidence at zero time delay indicates a highly efficient Auger ionization process [16], which suppresses multi-photon emission in these colloidal quantum dots. This result shows that room temperature single photon sources can be achieved with colloidal nanoparticles.
The linear Stark effect on a single molecule allows us to sweep its frequency through resonance with a fixed laser frequency by applying a sinusoidal RF voltage on two electrodes. If the conditions of adiabatic following are fulfilled, we can prepare the excited molecular state with near certainty. Spontaneous emission from this state gives rise to a single photon. With our current experimental conditions, up to 75% of the sweeps lead to the emission of a single photon. Since the adiabatic passage is done on command, the molecule performs as a high rate source of triggered photons. The experimental results are in quantitative agreement with quantum Monte Carlo simulations.