اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدSpectroscopy of atomic rubidium at 500 bar buffer gas pressure: approaching the thermal equilibrium of dressed atom-light states
389
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We have recorded fluorescence spectra of the atomic rubidium D-lines in the presence of several hundreds of bars buffer gas pressure. With additional saturation broadening a spectral linewidth comparable to the thermal energy of the atoms in the heated gas cell is achieved. An intensity-dependent blue asymmetry of the spectra is observed, which becomes increasingly pronounced when extrapolating to infinitely high light intensity. We interpret our results as evidence for the dressed (coupled atom-light) states to approach thermal equilibrium.
قيم البحث
اقرأ أيضاً
We describe measurements demonstrating laser cooling of an atomic gas by means of collisional redistribution of radiation. The experiment uses rubidium atoms in the presence of several hundred bar of argon buffer gas pressure. Frequent collisions in
the dense gas transiently shift a far red detuned optical field into resonance, while spontaneous emission occurs close to the unperturbed atomic transition frequency. Evidence for the cooling is obtained both via thermographic imaging and via thermographic deflection spectroscopy. The cooled gas has a density above 10$^{21}$ atoms/cm$^3$, yielding evidence for the laser cooling of a macroscopic ensemble of gas atoms.
Photoelectron emission from excited states of laser-dressed atomic helium is analyzed with respect to laser intensity-dependent excitation energy shifts and angular distributions. In the two-color XUV (exteme ultra-violet) -- IR (infrared) measuremen
t, the XUV photon energy is scanned between SI{20.4}{electronvolt} and the ionization threshold at SI{24.6}{electronvolt}, revealing electric dipole-forbidden transitions for a temporally overlapping IR pulse ($sim!SI{e12}{wattper centimetersquared}$). The interpretation of the experimental results is supported by numerically solving the time-dependent Schrodinger equation in a single-active-electron approximation.
We report on the demonstration of Doppler-free polarization spectroscopy of the D2 line of 6Li atoms. Counterintuitively, the presence of an Ar buffer gas, in a certain pressure range, causes a drastic enhancement of the polarization rotation signal.
The observed dependence of the signal amplitude on the Ar buffer pressure and the pump laser power is reproduced by calculations based on simple rate equations. We performed stable laser frequency locking using a dispersion signal obtained by polarization spectroscopy for laser cooling of 6Li atoms.
We report modulation transfer spectroscopy on the D2 transitions in 85Rb and 87Rb using a simple home-built electro-optic modulator (EOM). We show that both the gradient and amplitude of modulation transfer spectroscopy signals, for the 87Rb F=2 to F
=3 and the 85Rb F=3 to F=4 transitions, can be significantly enhanced by expanding the beams, improving the signals for laser frequency stabilization. The signal gradient for these transitions is increased by a factor of 3 and the peak to peak amplitude was increased by a factor of 2. The modulation transfer signal for the 85Rb F=2 to F transitions is also presented to highlight how this technique can generate a single, clear line for laser frequency stabilization even in cases where there are a number of closely spaced hyperfine transitions.
We demonstrate cryogenic buffer-gas cooling of gas-phase methyltrioxorhenium (MTO). This molecule is closely related to chiral organometallic molecules where the parity-violating energy differences between enantiomers may be measurable. The molecules
are produced with a rotational temperature of approximately 6~K by laser ablation of an MTO pellet inside a cryogenic helium buffer gas cell. Facilitated by the low temperature, we demonstrate absorption spectroscopy of the 10.2~$mu$m antisymmetric Re=O stretching mode of MTO with a resolution of 8~MHz and a frequency accuracy of 30~MHz. We partially resolve the hyperfine structure and measure the nuclear quadrupole coupling of the excited vibrational state.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
