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Register a new userReal-time optimal quantum control of mechanical motion at room temperature
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The ability to accurately control the dynamics of physical systems by measurement and feedback is a pillar of modern engineering. Today, the increasing demand for applied quantum technologies requires to adapt this level of control to individual quantum systems. Achieving this in an optimal way is a challenging task that relies on both quantum-limited measurements and specifically tailored algorithms for state estimation and feedback. Successful implementations thus far include experiments on the level of optical and atomic systems. Here we demonstrate real-time optimal control of the quantum trajectory of an optically trapped nanoparticle. We combine confocal position sensing close to the Heisenberg limit with optimal state estimation via Kalman filtering to track the particle motion in phase space in real time with a position uncertainty of 1.3 times the zero point fluctuation. Optimal feedback allows us to stabilize the quantum harmonic oscillator to a mean occupation of $n=0.56pm0.02$ quanta, realizing quantum ground state cooling from room temperature. Our work establishes quantum Kalman filtering as a method to achieve quantum control of mechanical motion, with potential implications for sensing on all scales. In combination with levitation, this paves the way to full-scale control over the wavepacket dynamics of solid-state macroscopic quantum objects in linear and nonlinear systems.
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Quantum control of a system requires the manipulation of quantum states faster than any decoherence rate. For mesoscopic systems, this has so far only been reached by few cryogenic systems. An important milestone towards quantum control is the so-called strong coupling regime, which in cavity optomechanics corresponds to an optomechanical coupling strength larger than cavity decay rate and mechanical damping. Here, we demonstrate the strong coupling regime at room temperature between a levitated silica particle and a high finesse optical cavity. Normal mode splitting is achieved by employing coherent scattering, instead of directly driving the cavity. The coupling strength achieved here approaches three times the cavity linewidth, crossing deep into the strong coupling regime. Entering the strong coupling regime is an essential step towards quantum control with mesoscopic objects at room temperature.
We report quantum ground state cooling of a levitated nanoparticle in a room temperature environment. Using coherent scattering into an optical cavity we cool the center of mass motion of a $143$ nm diameter silica particle by more than $7$ orders of magnitude to $n_x=0.43pm0.03$ phonons along the cavity axis, corresponding to a temperature of $12~mu$K. We infer a heating rate of $Gamma_x/2pi = 21pm 3$ kHz, which results in a coherence time of $7.6~mu$s -- or $15$ coherent oscillations -- while the particle is optically trapped at a pressure of $10^{-6}$ mbar. The inferred optomechanical coupling rate of $g_x/2pi = 71$ kHz places the system well into the regime of strong cooperativity ($C approx 5$). We expect that a combination of ultra-high vacuum with free-fall dynamics will allow to further expand the spatio-temporal coherence of such nanoparticles by several orders of magnitude, thereby opening up new opportunities for macrosopic quantum experiments.
We create an ultracold-atoms-based cavity optomechanical system in which as many as six distinguishable mechanical oscillators are prepared, and optically detected, near their ground states of motion. We demonstrate that the motional state of one oscillator can be selectively addressed while preserving neighboring oscillators near their ground states to better than 95% per excitation quantum. We also show that our system offers nanometer-scale spatial resolution of each mechanical element via optomechanical imaging. This technique enables in-situ, parallel sensing of potential landscapes, a capability relevant to active research areas of atomic physics and force-field detection in optomechanics.
Quantum mechanical phenomena, such as electronic coherence and entanglement, play a key role in achieving the unrivalled efficiencies of light-energy conversion in natural photosynthetic light-harvesting complexes, and triggered the growing interest in the possibility of organic quantum computing. Since biological systems are intrinsically heterogeneous, clear relations between structural and quantum-mechanical properties can only be obtained by investigating individual assemblies. However, single-molecule techniques to access ultrafast coherences at physiological conditions were not available so far. Here we show by employing femtosecond pulse-shaping techniques that quantum coherences in single organic molecules can be created, probed, and manipulated at ambient conditions even in highly disordered solid environments. We find broadly distributed coherence decay times for different individual molecules giving direct insight into the structural heterogeneity of the local surroundings. Most importantly, we induce Rabi-oscillations and control the coherent superposition state in a single molecule, thus performing a basic femtosecond single-qubit operation at room temperature.
Utilizing the tools of quantum optics to prepare and manipulate quantum states of motion of a mechanical resonator is currently one of the most promising routes to explore non-classicality at a macroscopic scale. An important quantum optomechanical tool yet to be experimentally demonstrated is the ability to perform complete quantum state reconstruction. Here, after providing a brief introduction to quantum states in phase space, we review and contrast the current proposals for state reconstruction of mechanical motional states and discuss experimental progress. Furthermore, we show that mechanical quadrature tomography using back-action-evading interactions gives an $s$-parameterized Wigner function where the numerical parameter $s$ is directly related to the optomechanical measurement strength. We also discuss the effects of classical noise in the optical probe for both state reconstruction and state preparation by measurement.
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