First observation of a resonance ionization signal on242mAm fission isomers

The feasibility of a hyperfine spectroscopy on^242mAm fission isomers has been demonstrated at the low target production rate of 10/s. The experimental method employed is based on resonance ionization spectroscopy in a buffer gas cell with detection of the ionization process by means of the fission decay of the isomers. The resonance ionization has been performed in two steps, utilizing an excimer dye laser combination with a repetition rate of 300 Hz. The first resonant step proceeds through theJ=7/2 term at 21440.35 cm⁻¹, which has been excited with the tuncable dye laser beam of a wavelength of 466.28 nm, the second non-resonant step is achieved with the 351 nm radiation of the excimer laser itself, running with XeF. The frequency scan of the tuneable dye laser exhibits a broad resonance ionization signal, the width of which is most likely explained by the magnetic hyperfine interaction.     

Photon-echo detected nuclear quadrupole resonance spectroscopy

Rare-earth-ion-doped crystals (REICs) have played an important role in quantum information processing due to their excellent coherent properties. In order to obtain the information regarding the hyperfine structures of the rare-earth ions in REICs, optically detected nuclear magnetic resonance (NMR) and nuclear quadrupole resonance (NQR) techniques based on RF resonance and various optical detection methods are widely employed in previous works. Here we demonstrate a new method of NQR spectroscopy based on the photon-echo detection. The hyperfine spectra of the ground state (⁷F₀) and the optically-excited state (⁵D₀) of ¹⁵¹Eu³⁺ in Y₂SiO₅ at zero field are obtained. This method can determine the hyperfine splittings within the ground state and the optically-excited state and is shown to be robust against electrical noise. Our results provide an alternative way for optical detection of NMR and NQR with high signal-to-noise ratio.     

Thermal photoionization in resonance ionization spectroscopy

In Resonance Ionization Spectroscopy, neutral atoms are usually produced by thermal effects, using an oven or a hot surface at high temperature. The radiation from these thermal sources is intense enough to effectively contribute to the photoionization of atoms excited by laser pumping. We show that, for the most common experimental conditions, the ratio of thermal to laser photoionization can be higher than one for excited levels which lie as far as a few thousand cm^–1 below the ionization threshold. This result is obtained with the use of the analytic expression for the photoionization cross-section of a hydrogen-like atom. We suggest two applications of this thermal photoionization. Namely, the study of highly excited states and Quasi Resonance Ionization Spectrometry, using only one laser of low radiance.Commissariat à l'Energie Atomique, Centre d'Etudes Nucléaires de Fontenay-aux-Roses DERDCA/DCAEA/SEA, BP no 6, F-92265 Fontenay-aux-Roses Cedex, France (Visiting scientist at Ecole Polytechnique from Commissariat à l'Energie Atomique)Commissariat à l'Energie Atomique, Centre d'Etudes Nucléaires de Saclay, IRF/DPHG/PAS. Bât 462, F-91191 Gif-sur-Yvette Cedex, France     

Laser developments and resonance ionization spectroscopy at IGISOL

We present an overview of recent laser ion source developments at the IGISOL facility, Jyväskylä. Technological advances in the lasers have led to a considerable increase in second-harmonic laser power with the use of intra-cavity second-harmonic generation, as well as to narrow linewidth capability by applying an injection-locking technique to a Ti:sapphire laser. The use of a diffraction grating for frequency selection in a new laser resonator has dramatically improved the wide-range tunability of the laser system, resulting in an ideal tool for the development of new ionization schemes. The role of different laser bandwidths, laser intensity and environmental broadening mechanisms on the experimental width of the measured spectral line have been studied using bismuth, silver and nickel, in the gas cell and expanding gas jet. Applications of novel ion guide nozzle design has led to remarkably collimated gas jets which overcome the current limitations in the gas cell-based laser ion source trap (LIST) method. Detailed planning is under way to optimize the new laser laboratory and laser transport path in order to fully exploit the unique opportunities afforded by the new IGISOL-4 facility.     

Picosecond time-resolved nonresonant ionization detected IR spectroscopy on 7-azaindole dimer

The picosecond time-resolved IR spectrum of the 7-azaindole dimer has been measured by picosecond time-resolved nonresonant ionization detected IR spectroscopy. This new time-resolved technique was developed by combining nonresonant ionization detected IR (NID-IR) spectroscopy with tunable picosecond IR and UV lasers. The time-resolved NID-IR spectrum from 2 600 cm^-1 to 3 800 cm^-1 shows a drastic change from 1.5 ps to 11 ps time evolution. A mode-specific vibrational redistribution has been suggested. Received 14 May 2002 / Received in final form 11 June 2002 Published online 13 September 2002     

Optically detected resonance spectroscopy of interface fluctuation quantum dots

We have performed optically detected resonance (ODR) spectroscopy on modulation-doped GaAs/AlGaAs quantum wells of different widths in which lateral fluctuations of the well width were purposely introduced by growth interruption at the interfaces. These monolayer fluctuations form quantum dots for which confinement and Coulomb correlation energies are comparable. By monitoring resonant changes of the dot ensemble photoluminescence induced by far-infrared (FIR) radiation in a magnetic field, we have observed cyclotron resonance (CR) of free electrons in the widest wells, as well as internal transitions of mobile and localized charged excitons. The latter, which are forbidden by magnetic translational invariance, have previously not been observed. For the narrower wells the effects of non-parabolicity and carrier localization on the CR and CR-like transitions have to be included for a proper interpretation of the measurements.     

邻羟基苯腈的双色共振增强多光子电离光谱及Franck-Condon模拟

在自制直线式飞行时间质谱仪上进行了双色共振增强双光子电离实验,获得了振动分辨的邻羟基苯腈的共振增强多光子电离(resonance enhanced multiphoton ionization, REMPI)光谱,结合高精度密度泛函理论计算和Franck-Condon光谱模拟,详细分析了光谱特征,发现了大量基频、泛频和组合振动,并进行了光谱归属.大部分苯环的基频振动归属为环在平面内的畸变或平面内的摇摆,这与分子激发过程中苯环的扩张有关.理论和实验结果都表明, REMPI光谱的低频段信号强,背景低,谱带少,分辨率好.随着振动频率的增加,信号向相反的方向变化.这是由于低频段光谱主要来自于低频的基频振动、少量泛频的贡献.随着振动频率增加,泛频和各种模的组合振动逐渐增多,导致了高频区谱带稠密,分辨率变差.高阶振动和多模的组合振动通常有较低的Franck-Condon因子,因此信号随频率增大逐渐变弱,信噪比变差.     

Frequency tripling for resonance ionization spectroscopy (RIS) of Cd

1 =228.8 nm). Laser light with an average power of 2 mW was obtained after frequency tripling and was successfully used for RIS test measurements on cadmium with a time-of-flight mass spectrometer. The eight stable Cd isotopes could be identified unambiguously. Received: 6 October 1997     

基于激光共振电离质谱的钆奇宇称高激发态研究

钆同位素可作为生产医用同位素¹⁶¹Tb等的靶材,受限于高效光电离路径缺失等问题,目前仅能通过电磁方法生产,为实现钆的多步光电离,需要获取高激发态等光谱数据.基于国内自主研发的高分辨激光共振电离质谱,利用双色三步光电离方案,扫描了钆的36900～37700 cm^-1能区,首次获取了7条奇宇称高激发态能级,能级位置准确度可达±0.1 cm^-1,并根据角动量选择定则确定了可能的J值,同时发现了可用于质谱性能检验的单色光电离谱线.     

In-source resonance ionization spectroscopy of high lying energy levels in atomic uranium

In-source resonance ionization spectroscopy of uranium has been carried out as preparation for the analysis of low contaminations of nuclear material in environmental samples via laser mass spectrometry. Using three-step resonance ionization spectroscopy, 86 levels of odd parity in the energy range from 37,200–38,650 cm^???1 were studied, 51 of these levels were previously unknown. Suitable excitation schemes for analytic applications are discussed.     

Determination of90Sr in environmental samples with resonance ionization spectroscopy in collinear geometry

A new, fast technique for trace analysis of the radioactive isotopes⁸⁹Sr and⁹⁰Sr in environmental samples has been developed. Conventional mass separation is combined with resonance ionization spectroscopy in collinear geometry, which provides high selectivity and sensitivity. In addition, a chemical separation procedure for sample preparation has been developed. The described technique was used to determine the⁹⁰Sr content in 870 m³ air samples collected near Munich during and shortly after the Chernobyl reactor accident in April 1986. The content of⁹⁰Sr was measured to be 1.4 mBq per m³, corresponding to 1.6 × 10⁹ atoms of⁹⁰Sr per sample. This value is in good agreement with the results of radiochemical measurements.This publication comprises part of the Dissertations of J. Stenner and K. Zimmer     

Experimental Studies on Radiation Damages of CsI(Tl) Crystals

The results of experimental studies on eadiation damage of CsI(Tl) crystal were reported.There are radiation damage effects on CsI(Tl) crystal.Experimental studies on recovery of damaged CsI(Tl) crystals were made.It seems that after heating at 200℃ for 4 hours,the damaged crystals could be recovered completely.     

Photoelectrically detected magnetic resonance spectroscopy of the excited triplet states of point defects in silicon

Highly sensitive methods for the detection of the electron paramagnetic resonance (EPR) spectra based on the spin-dependent microwave photoconductivity were applied to investigate the structural defects in irradiated silicon. The parameters of the EPR spectra of the excited triplet states of radiation defects were determined and several models of the carbon related defects were supposed. Fiz. Tverd. Tela (St. Petersburg) 41, 774–777 (May 1999) Published in English in the original Russian journal. Reproduced here with stylistic changes by the Translation Editor.     

Effect of polarization spectroscopy in multitep excitation and ionization of atoms on ionization efficiency

In this peper, the seventeen real motion equation of atoms were shown for the first time inconsiderlng the polarization choices of laser lights. The importance of polarization spectrcoscopy in thedetermination of ionization yields of multi-step excitation and ionization of atoms (MSEIA) wasshown.     

Characterization of a dual-etalon Ti:sapphire laser via resonance ionization spectroscopy of stable copper isotopes

Resonance ionization spectroscopy (RIS) inside a buffer gas-filled ion guide is a very sensitive tool for a first determination of nuclear moments and charge radii of radioactive isotopes produced using the IGISOL technique. Currently employed pulsed Ti:sapphire laser systems have a typical laser linewidth of 5 GHz in the fundamental, which in many cases is the dominant line broadening effect. We present results of RIS on stable ^63,65Cu using a dual-etalon Ti:sapphire laser with a reduced linewidth of 1 GHz. Determination of hyperfine parameters of ⁶³Cu revealed discrepancies when compared to existing higher resolution data. A study of systematic uncertainties is underway using a homemade scanning Fabry-Pérot interferometer (FPI). A real-time recording of the mode structure of the multi-longitudinal mode Ti:sapphire laser during a scan of the 244.238 nm atomic ground state transition in parallel with the readout from the commercial wavemeter has identified sources of uncertainty.     

Validation and Correction for 208Tl Activity to Assay 232Th in Equilibrium with Its Daughters

Physics of Particles and Nuclei Letters - The natural radioactivity measurements and analysis of 232Th have been studied using γ-ray spectroscopy depending on its decay daughters in...     

In-source spectroscopy on astatine and radium for resonant laser ionization

At on-line isotope separator facilities, rare isotopes of radioactive elements such as astatine, radium or polonium are demanded for fundamental research on nuclear structure. These elements are generally suitable for a resonance ionization laser ion source, but more data on the atomic structure is necessary to develop efficient laser ionization schemes. Due to the missing stable reference isotopes spectroscopic investigation of the atomic structure can only be performed during on-line operation. At the Isotope Separator and ACcelerator (ISAC) facility at TRIUMF, the elements astatine and radium were investigated by in-source laser spectroscopy to optimize the laser ionization efficiency. For astatine, laser spectroscopy was performed to search for high lying bound states as well as for auto-ionizing resonances. This led to the identification of four new high lying bound states of odd parity, while no auto-ionizing resonances were observed in the investigated region. Furthermore, the feasibility and the impact of laser ionization on the yield of radium isotopes was investigated using an activated target after proton irradiation.     

Complex resonance and complex-frequency spectroscopy

The response of a medium to radiation with a complex frequency corresponding to an exponential time decrease in the radiation amplitude has been analyzed. The effect of complex resonance has been demonstrated when the real and imaginary parts of the complex radiation frequency approach the real and imaginary parts of the complex frequency of damping natural oscillations of medium oscillators. In resonance itself, the absolute value of the refractive index is divergent and radiation is completely reflected from the medium boundary. It has been shown that scanning of not only the real part, but also the imaginary part of the probe radiation frequency expands the capabilities of spectroscopy and makes it possible to, e.g., distinguish resonances even with coinciding (real) frequencies and close (of the same order of magnitude) widths.