Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userHigh order Coherence Functions and Spectral Distributions as given by the Quantum Theory of Laser Radiation
78
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
We propose and demonstrate a method for measuring the time evolution of the off-diagonal elements $rho_{n,n+k}(t)$ of the reduced density matrix obtained from the quantum theory of the laser. The decay rates of the off-diagonal matrix element $rho_{n,n+k}(t)$ (k=2,3) are measured for the first time and compared with that of $rho_{n,n+1}(t)$, which corresponds to the linewidth of the laser. The experimental results agree with the quantum theory of the laser.
rate research
Read More
A metasurface hologram combines fine spatial resolution and large viewing angles with a planar form factor and compact size. However, it suffers coherent artifacts originating from electromagnetic cross-talk between closely packed meta-atoms and fabrication defects of nanoscale features. Here, we introduce an efficient method to remove all artifacts by fine-tuning the spatial coherence of illumination. Our method is implemented with a degenerate cavity laser, which allows precise, continuous tuning of spatial coherence over a wide range with little variation in emission spectrum and total power. We find the optimal degree of spatial coherence to remove the coherent artifacts of a meta-hologram while maintaining the image sharpness. This work paves the way to compact and dynamical holographic display free of coherent defects.
We address the issue of the second-order coherence of single surface plasmons launched by a quantum source of light into extended gold films. The quantum source of light is made of a scanning fluorescent nanodiamond hosting five nitrogen-vacancy (NV) color centers. By using a specially designed microscopy that combines near-field optics with far-field leakage-radiation microscopy in the Fourier space and adapted spatial filtering, we find that the quantum statistics of the initial source of light is preserved after conversion to surface plasmons and propagation along the polycrystalline gold film.
We observe a new regime of coherent XUV radiation generation in noble gases induced by femtosecond pulses at very high intensities. This XUV emission has both a reduced divergence and spectral width as compared to high-order harmonic generation (HHG). It is not emitted at a moderate intensity of the driving pulses where only high-order harmonics are generated. At high driving intensities, the additional XUV comb appears near all harmonic orders and even exceeds the HHG signal on the axis. The peaks are observed in several gases and their frequencies do not depend on the driving intensity or gas pressure. We analyze the divergence, spectral width and spectral shift of this XUV emission. We show that these specific features are well explained by high-order parametric generation (HPG) involving multiphoton absorption and combined emission of an idler THz radiation and an XUV beam with remarkably smooth spatial and spectral characteristics.
We demonstrate injection-locking of 120mW laser diodes operating at 397nm. We achieve stable operation with injection powers of ~100uW and a slave laser output power of up to 110mW. We investigate the spectral purity of the slave laser light via photon scattering experiments on a single trapped Ca40 ion. We show that it is possible to achieve a scattering rate indistinguishable from that of monochromatic light by filtering the laser light with a diffraction grating to remove amplified spontaneous emission.
We show that high-order harmonics generated from molecules by intense laser pulses can be expressed as the product of a returning electron wave packet and the photo-recombination cross section (PRCS) where the electron wave packet can be obtained from simple strong-field approximation (SFA) or from a companion atomic target. Using these wave packets but replacing the PRCS obtained from SFA or from the atomic target by the accurate PRCS from molecules, the resulting HHG spectra are shown to agree well with the benchmark results from direct numerical solution of the time-dependent Schrodinger equation, for the case of H$_2^+$ in laser fields. The result illustrates that these powerful theoretical tools can be used for obtaining high-order harmonic spectra from molecules. More importantly, the results imply that the PRCS extracted from laser-induced HHG spectra can be used for time-resolved dynamic chemical imaging of transient molecules with temporal resolutions down to a few femtoseconds.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
