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Register a new userExcitation of a single atom with exponentially rising light pulses
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Added by
Christian Kurtsiefer
Publication date
2013
fields
Physics
and research's language is
English
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We investigate the interaction between a single atom and optical pulses in a coherent state with a controlled temporal envelope. In a comparison between a rising exponential and a square envelope, we show that the rising exponential envelope leads to a higher excitation probability for fixed low average photon numbers, in accordance to a time-reversed Weisskopf-Wigner model. We characterize the atomic transition dynamics for a wide range of the average photon numbers, and are able to saturate the optical transition of a single atom with ~50 photons in a pulse by a strong focusing technique. For photon numbers of ~1000 in a 15ns long pulse, we clearly observe Rabi oscillations.
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We report on a simple method to prepare optical pulses with exponentially rising envelope on the time scale of a few ns. The scheme is based on the exponential transfer function of a fast transistor, which generates an exponentially rising envelope that is transferred first on a radio frequency carrier, and then on a coherent cw laser beam with an electro-optical phase modulator (EOM). The temporally shaped sideband is then extracted with an optical resonator and can be used to efficiently excite a single Rb-87 atom.
In analogy to transistors in classical electronic circuits, a quantum optical switch is an important element of quantum circuits and quantum networks. Operated at the fundamental limit where a single quantum of light or matter controls another field or material system, it may enable fascinating applications such as long-distance quantum communication, distributed quantum information processing and metrology, and the exploration of novel quantum states of matter. Here, by strongly coupling a photon to a single atom trapped in the near field of a nanoscale photonic crystal cavity, we realize a system where a single atom switches the phase of a photon, and a single photon modifies the atoms phase. We experimentally demonstrate an atom-induced optical phase shift that is nonlinear at the two-photon level, a photon number router that separates individual photons and photon pairs into different output modes, and a single-photon switch where a single gate photon controls the propagation of a subsequent probe field. These techniques pave the way towards integrated quantum nanophotonic networks involving multiple atomic nodes connected by guided light.
We investigate experimentally the effect of quantum resonance in the rotational excitation of the simplest quantum rotor - a diatomic molecule. By using the techniques of high-resolution femtosecond pulse shaping and rotational state-resolved detection, we measure directly the amount of energy absorbed by molecules interacting with a periodic train of laser pulses, and study its dependence on the train period. We show that the energy transfer is significantly enhanced at quantum resonance, and use this effect for demonstrating selective rotational excitation of two nitrogen isotopologues, $ ^{14}N_2$ and $ ^{15}N_2$. Moreover, by tuning the period of the pulse train in the vicinity of a fractional quantum resonance, we achieve spin-selective rotational excitation of para- and ortho-isomers of $ ^{15}N_2$.
Precision sensing, and in particular high precision magnetometry, is a central goal of research into quantum technologies. For magnetometers, often trade-offs exist between sensitivity, spatial resolution, and frequency range. The precision, and thus the sensitivity of magnetometry, scales as $1/sqrt {T_2}$ with the phase coherence time, $T_2$, of the sensing system playing the role of a key determinant. Adapting a dynamical decoupling scheme that allows for extending $T_2$ by orders of magnitude and merging it with a magnetic sensing protocol, we achieve a measurement sensitivity even for high frequency fields close to the standard quantum limit. Using a single atomic ion as a sensor, we experimentally attain a sensitivity of $4.6$ pT $/sqrt{Hz}$ for an alternating-current magnetic field near 14 MHz. Based on the principle demonstrated here, this unprecedented sensitivity combined with spatial resolution in the nanometer range and tunability from direct-current to the gigahertz range could be used for magnetic imaging in as of yet inaccessible parameter regimes.
Quantum effects, prevalent in the microscopic scale, generally elusive in macroscopic systems due to dissipation and decoherence. Quantum phenomena in large systems emerge only when particles are strongly correlated as in superconductors and superfluids. Cooperative interaction of correlated atoms with electromagnetic fields leads to superradiance, the enhanced quantum radiation phenomenon, exhibiting novel physics such as quantum Dicke phase and ultranarrow linewidth for optical clocks. Recent researches to imprint atomic correlation directly demonstrated controllable collective atom-field interactions. Here, we report cavity-mediated coherent single-atom superradiance. Single atoms with predefined correlation traverse a high-Q cavity one by one, emitting photons cooperatively with the atoms already gone through the cavity. Such collective behavior of time-separated atoms is mediated by the long-lived cavity field. As a result, a coherent field is generated in the steady state, whose intensity varies as the square of the number of traversing atoms during the cavity decay time, exhibiting more than ten-fold enhancement from noncollective cases. The correlation among single atoms is prepared with the aligned atomic phase achieved by nanometer-precision position control of atoms with a nanohole-array aperture. The present work deepens our understanding of the collective matter-light interaction and provides an advanced platform for phase-controlled atom-field interactions.
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