In typical epitaxial quantum dots (QDs) the ideally degenerate optical excitons are energy split, preventing the formation of two-photon entanglement in a biexciton decay. We use an external field, here a continuous-wave laser tuned to the QD in the ac Stark limit, to cancel the splitting and create two-photon entanglement. Quantum-state tomography is used to construct the two-photon density matrix. When the splitting is removed it satisfies well-known entanglement tests. Our approach shows that polarization-entangled photons can be routinely produced in semiconductor nanostructures.

Ultrashort laser pulses have thus far been used in two distinct modes. In the time domain, the pulses have allowed probing and manipulation of dynamics on a subpicosecond time scale. More recently, phase stabilization has produced optical frequency combs with absolute frequency reference across a broad bandwidth. Here we combine these two applications in a spectroscopic study of rubidium atoms. A wide-bandwidth, phase-stabilized femtosecond laser is used to monitor the real-time dynamic evolution of population transfer. Coherent pulse accumulation and quantum interference effects are observed and well modeled by theory. At the same time, the narrow linewidth of individual comb lines permits a precise and efficient determination of the global energy-level structure, providing a direct connection among the optical, terahertz, and radio-frequency domains. The mechanical action of the optical frequency comb on the atomic sample is explored and controlled, leading to precision spectroscopy with an appreciable reduction in systematic errors.Ultrashort laser pulses have given a remarkably detailed picture of photophysical dynamics. In studies of alkali atoms (1) and diatomics (2) in particular, coherent wave packet motion has been observed and even actively controlled. However, the broad bandwidth of these pulses has prevented a simultaneous high-precision measurement of state energies. At the expense of losing any direct observation or control of coherent dynamics, precision spectroscopy enabled by continuous wave (cw) lasers has been one of the most important fields of modern scientific research, providing the experimental underpinning of quantum mechanics and quantum electrodynamics.This trade-off between the time and frequency domains might seem fundamental, but in fact it results from pulse-to-pulse phase fluctuations in laser operation. The recent introduction of phase-stabilized, widebandwidth frequency combs based on modelocked femtosecond lasers has provided a direct connection between these two domains (3, 4). Many laboratories have constructed frequency combs that establish optical frequency markers directly linked to a microwave or optical standard, covering a variety of spectral intervals. Atomic and molecular structural information can now be probed over a broad spectral range, with vastly improved measurement precision and accuracy enabled by this absolute frequency-based approach (5). One of the direct applications is the development of optical atomic clocks (6-8). To date, however, traditional cw laserbased spectroscopic approaches have been essential to all of these experiments, with frequency combs serving only as reference rulers (9).Here we take advantage of the phasestable femtosecond pulse train to bridge the fields of high-resolution spectroscopy and ultrafast dynamics. This approach of direct frequency comb spectroscopy (DFCS) uses light from a comb of appropriate structure to directly interrogate a multitude of atomic levels and to study time-dependent quantum coherence. DFCS allows time-resol...

The dynamic response of InAs/GaAs self-assembled quantum dots (QDs) to strain is studied experimentally by periodically modulating the QDs with a surface acoustic wave and measuring the QD fluorescence with photoluminescence and resonant spectroscopy. When the acoustic frequency is larger than the QD linewidth, we resolve phonon sidebands in the QD fluorescence spectrum. Using a resonant pump laser, we have demonstrated optical frequency conversion via the dynamically modulated QD, which is the physical mechanism underlying laser sideband cooling a nanomechanical resonator by means of an embedded QD.

We demonstrate a new heterodyne Michelson interferometer design for displacement measurements capable of fringe interpolation accuracy of one part in 36 000. Key to this level of accuracy are the use of two acousto-optic modulators for heterodyne frequency generation and digital signal processing demodulation electronics. We make a direct comparison of our interferometer to a commercial interferometer based on a Zeeman-stabilized laser, and show that the residual periodic errors in ours are two orders of magnitude lower than those in the commercial unit. We discuss electronically induced optical cross talk and optical feedback as sources of periodic error. Our new interferometer is simple, robust, and readily implemented.