Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userRoom-temperature Mechanical Resonator with a Single Added or Subtracted Phonon
75
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
A room-temperature mechanical oscillator undergoes thermal Brownian motion with an amplitude much larger than the amplitude associated with a single phonon of excitation. This motion can be read out and manipulated using laser light using a cavity-optomechanical approach. By performing a strong quantum measurement, i.e., counting single photons in the sidebands imparted on a laser, we herald the addition and subtraction of single phonons on the 300K thermal motional state of a 4GHz mechanical oscillator. To understand the resulting mechanical state, we implement a tomography scheme and observe highly non-Gaussian phase-space distributions. Using a maximum likelihood method, we infer the density matrix of the oscillator and confirm the counter-intuitive doubling of the mean phonon number resulting from phonon addition and subtraction.
rate research
Read More
Narrowband single photons that couple well to atomic ensembles could prove essential for future quantum networks, but the efficient generation of such photons remains an outstanding challenge. We realize a spatially-multiplexed heralded source of single photons that are inherently compatible with the commonly employed D2 line of rubidium. Our source is based on four-wave mixing in hot rubidium vapor, requiring no laser cooling or optical cavities, and generates single photons with high rate and low noise. We use Hong-Ou-Mandel interference to verify the indistinguishability of the photons generated in two different (multiplexed) channels. We further demonstrate a five-fold tunability of the photons temporal width. The experimental results are well reproduced by a theoretical model.
When a gain system is coupled to a loss system, the energy usually flows from the gain system to the loss one. We here present a counterintuitive theory for the ground-state cooling of the mechanical resonator in optomechanical system via a gain cavity. The energy flows first from the mechanical resonator into the loss cavity, then into the gain cavity, and finally localizes there. The energy localization in the gain cavity dramatically enhances the cooling rate of the mechanical resonator. Moreover, we show that unconventional optical spring effect, e.g., giant frequency shift and optically induced damping of the mechanical resonator, can be realized. Those feature a pre-cooling free ground-state cooling, i.e., the mechanical resonator in thermal excitation at room temperature can directly be cooled to its ground state. This cooling approach has the potential application for fundamental tests of quantum physics without complicated cryogenic setups.
The radiation-pressure driven interaction of a coherent light field with a mechanical oscillator induces correlations between the amplitude and phase quadratures of the light. These correlations result in squeezed light -- light with quantum noise lower than shot noise in some quadratures, and higher in others. Due to this lower quantum uncertainty, squeezed light can be used to improve the sensitivity of precision measurements. In particular, squeezed light sources based on nonlinear optical crystals are being used to improve the sensitivity of gravitational wave (GW) detectors. For optomechanical squeezers, thermally driven fluctuations of the mechanical oscillators position makes it difficult to observe the quantum correlations at room temperature, and at low frequencies. Here we present a measurement of optomechanically (OM) squeezed light, performed at room-temperature, in a broad band near audio-frequency regions relevant to GW detectors. We observe sub-poissonian quantum noise in a frequency band of 30 kHz to 70 kHz with a maximum reduction of 0.7 $pm$ 0.1 dB below shot noise at 45 kHz. We present two independent methods of measuring this squeezing, one of which does not rely on calibration of shot noise.
Single molecule spectroscopy aims at unveiling often hidden but potentially very important contributions of single entities to a systems ensemble response. Albeit contributing tremendously to our ever growing understanding of molecular processes the fundamental question of temporal evolution, or change, has thus far been inaccessible, resulting in a static picture of a dynamic world. Here, we finally resolve this dilemma by performing the first ultrafast time-resolved transient spectroscopy on a single molecule. By tracing the femtosecond evolution of excited electronic state spectra of single molecules over hundreds of nanometres of bandwidth at room temperature we reveal their non-linear ultrafast response in an effective 3-pulse scheme with fluorescence detection. A first excitation pulse is followed by a phase-locked de-excitation pulse-pair, providing spectral encoding with 25 fs temporal resolution. This experimental realisation of true single molecule transient spectroscopy demonstrates that two-dimensional electronic spectroscopy of single molecules is experimentally in reach.
We study a general theory of phonon lasing [I. S. Grudinin et al., Phys. Rev. Lett. 104, 083901 (2010)] in coupled optomechancial systems. We derive the dynamical equation of the phonon lasing using supermodes formed by two cavity modes. A general threshold condition for phonon lasing is obtained. We also show the differences between phonon lasing and photon lasing, generated by photonic supermodes and two-level atomic systems, respectively. We find that the phonon lasing can be realized in certain parameter regime near the threshold. The phase diagram and second-order correlation function of the phonon lasing are also studied to show some interesting phenomena that cannot be observed in the common photon lasing with the two-level systems.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
