اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدTwo-dimensional spectral interpretation of time-dependent absorption near laser-coupled resonances
78
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We demonstrate a two-dimensional time-domain spectroscopy method to extract amplitude and phase modifications of excited atomic states caused by the interaction with ultrashort laser pulses. The technique is based on Fourier analysis of the absorption spectrum of perturbed polarization decay. An analytical description of the method reveals how amplitude and phase information can be directly obtained from measurements. We apply the method experimentally to the helium atom, which is excited by attosecond-pulsed extreme ultraviolet light, to characterize laser-induced couplings of doubly-excited states.
قيم البحث
اقرأ أيضاً
We present an implementation of a time-dependent multiconfiguration self-consistent-field (TD-MCSCF) method [R. Anzaki et al., Phys. Chem. Chem. Phys. 19, 22008 (2017)] with the full configuration interaction expansion for coupled electron-nuclear dy
namics in diatomic molecules subject to a strong laser field. In this method, the total wave function is expressed as a superposition of different configurations constructed from time-dependent electronic Slater determinants and time-dependent orthonormal nuclear basis functions. The primitive basis functions of nuclei and electrons are strictly independent of each other without invoking the Born-Oppenheimer approximation. Our implementation treats the electronic motion in its full dimensionality on curvilinear coordinates, while the nuclear wave function is propagated on a one-dimensional stretching coordinate with rotational nuclear motion neglected. We apply the present implementation to high-harmonic generation and dissociative ionization of a hydrogen molecule and discuss the role of electron-nuclear correlation.
We report the observation of double-quantum coherence signals in a gas of potassium atoms at twice the frequency of the one-quantum coherences. Since a single atom does not have a state at the corresponding energy, this observation must be attributed
to a collective resonance involving multiple atoms. These resonances are induced by weak inter-atomic dipole-dipole interactions, which means that the atoms cannot be treated in isolation, even at a low density of $10^{12}$ cm$^{-3}$.
Using TRIUMFs off-line laser ion source test stand with a system of tunable titanium sapphire lasers, the polarization dependence of laser resonance ionization has been investigated using beryllium. A significant polarization dependence was observed
for the excitation path $^1$S$_0$$rightarrow$$^1$P$^{circ}_1$$rightarrow$$^1$S$_0$, which are typical transitions for alkaline and alkaline-like elements. This polarization dependence was further verified on Be radioactive isotopes at TRIUMFs isotope separator and accelerator facility (ISAC). Laser polarization was proven to be an important parameter in operating resonance ionization laser ion sources (RILIS). The polarization spectroscopy was preformed off-line both on the 2p$^2$ $^1$S$_0$ autoionizing (AI) state and high-$n$ Rydberg states of the $2sns$ $^1S_0$ and $2snd$ $^1D_2$ series. The energy of the 2p$^2$ $^1$S$_0$ AI state and ionization potential (IP) of beryllium were extracted as 76167(6)~cm$^{-1}$ and 75192.59(3)~cm$^{-1}$. Polarization spectroscopy can be used to determine the $J$ values of newly found states in in-source spectroscopy of the complex/radioactive alkaline-like elements such as Ra, Sm, Yb, Pu and No.
We calculate resonances in three-body systems with attractive Coulomb potentials by solving the homogeneous Faddeev-Merkuriev integral equations for complex energies. The equations are solved by using the Coulomb-Sturmian separable expansion approach
. This approach provides an exact treatment of the threshold behavior of the three-body Coulombic systems. We considered the negative positronium ion and, besides locating all the previously know $S$-wave resonances, we found a whole bunch of new resonances accumulated just slightly above the two-body thresholds. The way they accumulate indicates that probably there are infinitely many resonances just above the two-body thresholds, and this might be a general property of three-body systems with attractive Coulomb potentials.
In expanding universes, the entanglement entropy must be time-dependent because the background geometry changes with time. For understanding time evolution of quantum correlations, we take into account two distinct holographic models, the dS boundary
model and the braneworld model. In this work, we focus on two-dimensional expanding universes for analytic calculation and comparison. Although two holographic models realize expanding universes in totally different ways, we show that they result in the qualitatively same time-dependence for eternal inflation. We further investigate the time-dependent correlations in the radiation-dominated era of the braneworld model. Intriguingly, the holographic result reveals that a thermal system in the expanding universe is {it dethermalized} after a critical time characterized by the subsystem size.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
