Lifetime of metastable fluorine atoms

For laser collimation of neutral F atoms, a resonance transition cycle between the metastable and the upper excited states (3s⁴ P _5/2?3p⁴ D ⁰ _7/2) can be used as a two-level closed system. We have determined the lifetime of the metastable state (3s⁴ P _5/2) in F atoms by measuring the decay curve of the fluorescence intensity as a function of distance from the plasma source. Combining the measured velocity of F radicals from the Doppler shift of the fluorescence peak, we have obtained the lifetime of the F metastable state as 3.7±0.5 μs. With this short metastable lifetime of F radicals, the simple Doppler cooling method using spontaneous light force is not practical for laser collimation of F radicals. Use of stimulated light force may be necessary to collimate F radical beams in a short distance. Received: 4 July 2000 / Published online: 13 September 2000     

Laser cooling of a single Ca+ ion: Observation of quantum jumps

This paper describes trapping and laser cooling of a Ca⁺ ion in an rf quadrupole ion trap. A single Ca⁺ ion is laser cooled to below 130 mK and quantum jumps are observed by exciting the ion into the metastable D _5/2 state via the P _3/2 state. The lifetime of the metastable D _5/2 state is estimated from the distribution of the dark periods of the quantum-jump signal. Collision-induced jumps between the metastable D _3/2 state and the D _5/2 state in a background gas are also directly observed.     

Optimizing the production of metastable calcium atoms in a magneto-optical trap

We investigate the production of long-lived metastable (4³ P ₂ ) calcium atoms in a magneto-optical trap (MOT) operating on the 4¹ S ₀ ?4¹ P ₁ transition at 423 nm. For excited 4¹ P ₁ atoms a weak decay channel into the triplet states 4³ P ₂ and 4³ P ₁ exists via the 3¹ D ₂ state. The undesired 4³ P ₁ atoms decay back to the ground state within 0.4 ms and can be fully recaptured if the illuminated trap volume is sufficientlylarge. We obtain a flux of above 10¹⁰ atoms/s into the 4³ P ₂ state. We find that our MOT lifetime of 23 ms is mainly limited by this loss channel, and thus the 4³ P ₂ production is not hampered by inelastic collisions. If we close the loss channel by repumping the 3¹ D ₂ atoms with a 671 nm laser back into the MOT cycling transition, a non-exponential 72 ms trap decay is observed, indicating the presence of inelastic two-body collisions between 4¹ S ₀ and 4¹ P ₁ atoms. Received: 10 July 2001 / Revised version: 22 October 2001 / Published online: 23 November 2001     

Laser cooling with electromagnetically induced transparency: application to trapped samples of ions or neutral atoms

A novel method of ground-state laser cooling of trapped atoms utilizes the absorption profile of a three- (or multi-) level system that is tailored by a quantum interference. With cooling rates comparable to conventional sideband cooling, lower final temperatures may be achieved. The method was experimentally implemented to cool a single Ca⁺ ion to its vibrational ground state. Since a broad band of vibrational frequencies can be cooled simultaneously, the technique will be particularly useful for the cooling of larger ion strings, thereby being of great practical importance for initializing a quantum register based on trapped ions. We also discuss its application to different level schemes and for ground-state cooling of neutral atoms trapped by a far-detuned standing wave laser field. Received: 10 July 2001 / Published online: 23 November 2001     

Measurement of the Rb D2 transition linewidth at ultralow temperature

The Rb D2 linewidth was studied using atoms cooled to a temperature of 50 μK that were contained in a magneto-optical trap. The transmission of a probe laser through the atom cloud was monitored using a CCD detector. The frequency of the probe laser was scanned across the resonance using an acousto-optic modulator. The observed lineshape was very well fitted by a Lorentzian function. The full width half maximum linewidth was examined as a function of the optical depth and the probe laser intensity. The extrapolated value at zero optical depth 6.062 ± 0.017 MHz corresponds to a 5P_3/2 lifetime of 26.25 ± 0.07 ns. This result agrees with lifetimes found in experiments that measured the temporal decay of fluorescence or photoassociation spectroscopy and is somewhat below the result of a relativistic many body perturbation calculation.     

A laser system for the excitation of rubidium Rydberg states using second harmonic generation in a PPLN waveguide crystal

We report on a laser system at a wavelength of 495 nm which is suitable for the excitations of low lying Rydberg states of rubidium atoms. The system is based on frequency doubling of a seeded diode laser in a periodically poled waveguide crystal. We achieve an output power of up to 35 mW and prove the single-frequency performance by direct two photon laser spectroscopy of the rubidium 14D _5/2 and 14D _3/2 states. The measured fine structure splitting is consistent with quantum defect theory calculations.     

Spectroscopy of Te2 with modulation transfer: Reference lines for precision spectroscopy in Yb+ at 467 nm

Modulation-transfer spectroscopy is used to observe resonances in ¹³⁰Te₂ near 467 nm. A signal-to-noise ratio of 500 is obtained with 1 mW laser power and with a time constant of 10 ms; the lineshapes are investigated in detail for different demodulation phases. The signal can be used to servolock a blue dye ring laser at 467 nm on a ¹³⁰Te₂ resonance which serves as reference line for precision spectroscopy on single, trapped Yb⁺ ions at 467 nm.     

Stimulated emission of a laser photon by the excited states of a three-level atom

We study the stimulated emission spectra arising from the emission of a laser photon by two excited states of a three-level atom interacting with a laser field at low intensities. The lifetimes of the stimulated photons emitted by the two excited states are much longer than those emitted spontaneously, while the intensities of the induced peaks take negative values indicating that amplification occurs at low frequencies. The ratio of the intensities of the light emitted by the excited states |3 > and |2 > of the atom is proportional to (₃/₂)^1/2, where ₃ and ₂ are the radiative decay rates of the spontaneously emitted photons by the excited states |3 > and |2 > into the ground state |1 > of the atom, respectively. An absorption spectrum is induced into the ground state of the atom by the laser field. The competition between induced absorption and stimulated emission at low frequencies without population inversion is considered in the low-intensity limit of the laser field. It is shown that for values of ₃/₂ > 1 the relative intensity (height) of the induced peak takes positive values implying that the process of the induced absorption dominates. As the ratio ₃/₂ increases, the height of the induced peak decreases and vanishes for values of ₃/₂ < 400. For values of ₃/₂ > 400, the height of the induced peak becomes negative indicating that the process of the stimulated emission (amplification) is likely to occur at low frequencies. The computed spectra are graphically presented and discussed.Issued as NRCC No. 39088     

Spectral properties of Pr3+ ions in Bi2(MoO4)3 crystal

A Bi₂(MoO₄)₃ single crystal doped with Pr³⁺ ions has been grown by the Czochralski technique. The polarized absorption and fluorescence spectra as well as the fluorescence decay curve of Pr³⁺ ions in the crystal were measured at room temperature. The spectroscopic parameters, including the Judd–Ofelt intensity parameters Ω_t (t=2, 4, and 6), spontaneous emission probabilities, fluorescence branching ratios, radiative lifetimes, stimulated emission cross sections, and fluorescence quantum efficiencies, were calculated. The spectral properties related to laser performance of this crystal were analyzed. The ¹ D ₂ multiplet of the crystal may be a good upper level for a solid-state laser.     

Yb:铅锌镧碲酸盐玻璃的热学、光谱和激光性质

研究了摩尔组分为70TeO2₂-(20-x)ZnO-xPbO-5La2₂O3_{3-25K22O-25Na22O（x=0，5，10，15，20）的新型多元铅 锌镧碲酸盐激光玻璃，外掺Yb22O33为玻璃摩尔组分的1％.测试了 试样的物理性质及吸收光谱、荧光光谱和荧光寿命，计算了Yb3+3+的吸收截面、受激发射截面、荧光有效线宽等 关键词： 3+掺杂碲酸盐玻璃')" href="#">Yb3+³⁺掺杂碲酸盐玻璃 光谱性质 热稳定性}     

Nonlinear spectroscopy with a vertical-cavity surface-emitting laser (VCSEL)

We have evaluated the suitability of a vertical-cavity surface-emitting laser diode (VCSEL) for spectroscopic applications. Despite its low output power it is possible to observe narrow resonances in a saturated absorption spectroscopy experiment on the cesium D ₂ transition at 852 nm, limited in width by the laser linewidth of several tens of MHz. High modulation efficiency of the VCSEL allows us to create modulation sidebands at 9.2 GHz frequency via direct modulation of the laser injection current. Using the carrier and either one of the sidebands coherent population trapping (CPT) resonances in a buffered cesium vapor can be prepared with linewidths below 130 Hz. With this very compact setup we have studied the dependence of CPT resonance position and linewidth as a function of optical detuning and find evidence of the influence of the excited state hyperfine structure. Received: 30 April 1999 / Revised version: 25 June 1999 / Published online: 30 November 1999     

Effect of Tm concentration on the tunability of the YLF laser in the 1.9 µm region

We describe the continuous-wave (cw) operation of a LiYF₄ laser based on crystals doped with different concentrations of Tm³⁺. We observed the fluorescence spectra from the upper laser level when the crystal is placed inside the laser resonator, in the same optical environment of the coherent emission. We measured the laser intensity as a function of pump power and obtained a 24% slope efficiency by selecting a suitable orientation of the crystal. Using all this information, we were able to demonstrate laser tunability at 1.9 µm in a 50 cm^–1 wide interval.     

Tunable single-frequency operation of a diode-pumped vertical external-cavity laser at the cesium D<Subscript>2</Subscript> line

We report on a diode-pumped vertical external-cavity surface-emitting laser emitting around 852 nm for Cesium atomic clocks experiments. We have designed a 7-quantum-well semiconductor structure optimized for low laser threshold. An output power of 330 mW was achieved for 1.1 W of incident pump power. Furthermore, a compact setup was built for low-power single-frequency emission. We obtained an output power of 17 mW in a single longitudinal mode, exhibiting both broad (9 nm) and continuous (14 GHz) tunability around the Cesium D₂ line. The laser frequency has been stabilized on an atomic transition with residual frequency fluctuations ∼300 kHz. Through a beatnote experiment the −3 dB laser linewidth has been measured to <500 kHz over 10 ms.     

Resonant coupling in the van der Waals interaction between an excited alkali atom and a dielectric surface: an experimental study via stepwise selective reflection spectroscopy

We present a detailed experimental study of the evaluation of the van der Waals (vW) atom-surface interaction for high-lying excited states of alkali-metal atoms (Cs and Rb), notably when they couple resonantly with a surface-polariton mode of the neighbouring dielectric surface. This report extends our initial observation [Phys. Rev. Lett. 83, 5467 (1999)] of a vW repulsion between Cs(6D_3/2) and a sapphire surface. The experiment is based upon FM selective reflection spectroscopy, on a transition reaching a high-lying state from a resonance level, that has been thermally pumped by an initial one-photon step. Along with a strong vW repulsion fitted with a blue lineshift, -160±25 kHz μm³ for Cs(6D_3/2) in front of a sapphire surface (with a perpendicular c-axis), we demonstrate a weaker vW repulsion (-32±5 kHz μm³) for Cs(6D_3/2) in front of a YAG surface, as due to a similar resonant coupling at 12 μm between a virtual atomic emission (6D_3/2-7P_1/2) and the surface polariton modes. A resonant behaviour of Rb(6D_5/2) in front of a sapphire surface exists also because of analogous decay channels in the 12 μm range. Finally, one demonstrates that fused silica, nonresonant for a virtual transition in the 12 μm range and hence weakly attracting for Cs(6D_3/2), exhibits a resonant behaviour for Cs(9S_1/2) as due to its surface polariton resonance in the 8-9 μm range. The limiting factors that affect both the accuracy of the theoretical prediction, and that of the fitting method applied to the experimental data, are discussed in the conclusion. Received 16 January 2003 / Received in final form 25 March 2003 Published online 5 May 2003     

Isotope selective loading of an ion trap using resonance-enhanced two-photon ionization

We have demonstrated that resonance-enhanced two-photon ionization of atomic beams provides an effective tool for isotope selective loading of ions into a linear Paul trap. Using a tunable, narrow-bandwidth, continuous wave (cw) laser system for the ionization process, we have succeeded in producing Mg⁺ and Ca⁺ ions at rates controlled by the atomic beam flux, the laser intensity, and the laser frequency detuning from resonance. We have observed that with a proper choice of control parameters, it is rather easy to load a specific number of ions into a string. This observation has direct applications in quantum optics and quantum computation experiments. Furthermore, resonant photo-ionization loading facilitates the formation of large isotope-pure Coulomb crystals. Received: 21 December 1999 / Published online: 11 May 2000     

Fluorescence and Judd-Ofelt analysis of Nd ions in oxyfluoride glass ceramics containing CaF2 nanocrystals

Judd-Ofelt analyses of Nd³⁺ ions in the oxyfluoride glasses and glass ceramics containing CaF₂ nanocrystals are performed to evaluate the intensity parameters Ω_2,4,6, spontaneous emission probability, radiative lifetime, quantum efficiency, as well as stimulated emission cross-section. The influences of Nd³⁺-doping level and heating temperature on these parameters for the ⁴F_3/2→⁴I_J (J=9/2, 11/2, and 13/2) transitions are systematically discussed. The decrease of intensity parameter Ω₂ evidences the incorporation of Nd³⁺ ions into CaF₂ nanocrystals after crystallization. With increasing of Nd³⁺-doping level, the measured lifetime and quantum efficiency gradually decrease, while the stimulated emission cross-section keeps almost unchanged. For 1.0 mol% Nd³⁺-doped sample, both the emission intensity and the measured lifetime enhance with increasing of heating temperature up to 650 °C. The results indicate that the investigated glass ceramics are potentially applicable as the 1.06 um laser host.     

Superradiant laser: First-order phase transition and non-stationary regime

We solve the superradiant laser model in two limiting cases. First the stationary low-pumping regime is considered where a first-order phase transition in the semiclassical solution occurs. This discontinuity is smeared out in the quantum regime. Second, we solve the model in the non-stationary regime where we find a temporally periodic solution. For a certain parameter range well-separated pulses may occur. Received: 19 June 1998 / Accepted: 19 October 1998     

Temporal coherent control induced by wave packet interferences in one and two photon atomic transitions

The interaction of a sequence of two identical ultrashort laser pulses with an atomic system results in quantum interferences as in Ramsey fringes experiments. These interferences allow achievement of temporal coherent control of the excitation probability. We present the results of a temporal coherent control experiment on two different atomic systems: one-photon absorption in K (4s-4p) and two-photon absorption in Cs (6s-7d). In K, the quantum interferences between the two excitation paths associated with the laser pulses are revealed through rapid oscillations of the excitation probability as a function of the time delay between the two pulses. These oscillations take place at the transition frequency (period T = 2.56 fs). The interferences are modulated by beats (at about 580 fs) resulting from the doublet structure of the excited state (4p (² P _1/2 , ² P _3/2 )). Three complementary interpretations of this experiment are presented: in terms of beats of quantum interferences, of variation in the spectrum intensity, and of wave packet interferences. Whenever the two laser pulses are temporally overlapped, optical interferences are superimposed on to the quantum interferences. The distinction between these two types of interference is clearly revealed in the two-photon excitation scheme performed on Cs (6s-7d (² D _3/2 , ² D _5/2 )) because quantum interferences occur at twice the frequency of the optical interferences. Received: 30 December 1997 / Revised: 28 February 1998 / Accepted: 4 March 1998     

Diode laser spectrometer at 493 nm for single trapped Ba+ ions

+ ions. Frequency doubling of a 100 mW diode laser at 986 nm results in up to 60 mW output power at 493 nm in a bandwidth of less than 60 kHz with respect to the cavity used for locking. Reference frequencies of 18 spectral lines of Te₂ near the 493 nm resonance of Ba⁺ have been measured using modulation transfer spectroscopy. The fluorescence excitation spectrum of a single Ba⁺ ion, measured with this laser, exhibits well-resolved dark resonances, which confirms the versatility of the system for quantum optical experiments. Received: 12 June 1998     

Linearly-polarized Tm-doped double-clad fiber laser

We report a linearly polarized Tm doped fiber laser. The fiber laser was set up by using a piece of polarization maintaining Tm doped double clad fiber of 5 m length as gain medium and a polarization beam splitter as a polarization selector. The fiber laser was pumped by a fiber pigtailed laser diode working at 790 nm with a maximum output power of 90 W. The linearly polarized Tm laser operated at wavelength around 2030 nm. A maximum output power up to 21.9 W was achieved when the pump power was 63.27 W with a threshold of 11.92 W, a slope efficiency of about 43.7%, and a polarization extinction ratio of 92.7% (11.37 dB). In addition to the blue fluorescence, we also observed the violet fluorescence under high pump power level. The up-conversion fluorescence was considered to be attributed to the ¹ G ₄ → ³ H ₆, and ¹ D ₂ → ³ F ₄ transitions of Tm ions, respectively.