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Light-induced states and Autler-Townes splitting of laser-coupled states are common features in the photoionization spectra of laser-dressed atoms. The entangled light-matter character of metastable Autler-Townes multiplets, which makes them autoionizing polaritons, however, is still largely unexplored. We employ attosecond transient-absorption spectroscopy in argon to study the formation of polariton multiplets between the 3s^{-1}4p and several light-induced states. We measure a controllable stabilization of the polaritons against ionization, in excellent agreement with ab initio theory. Using an extension of the Jaynes-Cummings model to autoionizing states, we show that this stabilization is due to the destructive interference between the Auger decay and the radiative ionization of the polaritonic components. These results give new insights into the optical control of electronic structure in the continuum and unlock the door to applications of radiative stabilization in metastable polyelectronic systems.
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This corrects the article DOI: 10.1103/PhysRevLett.115.133001.
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Ultrafast processes in matter, such as the electron emission after light absorption, can now be studied using ultrashort light pulses of attosecond duration (10-18 seconds) in the extreme ultraviolet spectral range. The lack of spectral resolution due to the use of short light pulses has raised issues in the interpretation of the experimental results and the comparison with theoretical calculations. We determine photoionization time delays in neon atoms over a 40-electron volt energy range with an interferometric technique combining high temporal and spectral resolution. We spectrally disentangle direct ionization from ionization with shake-up, in which a second electron is left in an excited state, and obtain excellent agreement with theoretical calculations, thereby solving a puzzle raised by 7-year-old measurements.
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Spin-orbit mediated phonon relaxation in a two-dimensional quantum dot is investigated using different confining potentials. Elliptical harmonic oscillator and cylindrical well results are compared to each other in the case of a two-electron GaAs quantum dot subjected to a tilted magnetic field. The lowest energy set of two-body singlet and triplet states are calculated including spin-orbit and magnetic effects. These are used to calculate the phonon induced transition rate from the excited triplet to the ground state singlet for magnetic fields up to where the states cross. The roll of the cubic Dresselhaus effect, which is found to be much more important than previously assumed, and the positioning of 'spin hot-spots' are discussed and relaxation rates for a few different systems are exhibited.
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Larvicidal oils can be used to control immature Aedes aegypti and other pestiferous mosquitoes. To test whether oil-based larvicides also act as oviposition deterrents, indoor and semi-field trials were conducted at the Navy Entomology Center of Excellence in Jacksonville, FL. In both studies, treatment cages consisted of oviposition cups lined with seed germination paper as an oviposition substrate and filled with 1-wk-old southern live oak ( Quercus virginiana) leaf litter-infused water. Treatment cages consisted of 2 cups treated with CocoBear™ Mosquito Larvicidal Oil, while 2 cups were untreated. Control cages contained oviposition cups with only oak leaf litter-infused water. Gravid Ae. aegypti were released into cages and allowed to oviposit for 24 h, after which eggs were counted. The number of eggs deposited in treatment and control cages was not significantly different (indoor P = 0.0865; outdoor P = 0.9765). However, the number of eggs deposited in untreated cups was significantly greater than that deposited in treated cups within treatment cages (indoor P < 0.0001; outdoor P = 0.0050). These results suggest that the presence of the larvicidal oil CocoBear may cause gravid female Ae. aegypti to seek alternative oviposition sites.
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Aedes , Inseticidas , Óleo Mineral , Controle de Mosquitos , Oviposição/efeitos dos fármacos , Aedes/fisiologia , Animais , LarvaRESUMO
Electron dynamics induced by resonant absorption of light is of fundamental importance in nature and has been the subject of countless studies in many scientific areas. Above the ionization threshold of atomic or molecular systems, the presence of discrete states leads to autoionization, which is an interference between two quantum paths: direct ionization and excitation of the discrete state coupled to the continuum. Traditionally studied with synchrotron radiation, the probability for autoionization exhibits a universal Fano intensity profile as a function of excitation energy. However, without additional phase information, the full temporal dynamics cannot be recovered. Here we use tunable attosecond pulses combined with weak infrared radiation in an interferometric setup to measure not only the intensity but also the phase variation of the photoionization amplitude across an autoionization resonance in argon. The phase variation can be used as a fingerprint of the interactions between the discrete state and the ionization continua, indicating a new route towards monitoring electron correlations in time.
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We present measurements of single-photon ionization time delays between the outermost valence electrons of argon and neon using a coincidence detection technique that allows for the simultaneous measurement of both species under identical conditions. The analysis of the measured traces reveals energy-dependent time delays of a few tens of attoseconds with high energy resolution. In contrast to photoelectrons ejected through tunneling, single-photon ionization can be well described in the framework of Wigner time delays. Accordingly, the overall trend of our data is reproduced by recent Wigner time delay calculations. However, besides the general trend we observe resonance features occurring at specific photon energies. These features have been qualitatively reproduced and identified by a calculation using the multiconfigurational Hartree-Fock method, including the influence of doubly excited states and ionization thresholds.
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Wireworms are a common soil-dwelling pest of maize, Zea mays L., in the midwestern United States. Wireworms are a problematic group to control and study due to the difficulty involved in identification. The objectives of this study are to identify this species complex of wireworms by using molecular diagnostic techniques and to reconstruct a phylogeny of economically important wireworm species. The cytochrome oxidase I gene of mitochondrial DNA was sequenced from > 300 individuals. The species analyzed include all economically important members of the genus Melanotus Eschscholtz as well as Conoderus lividus (De Geer). The species that are indistinguishable in the larval stage were successfully separated using nucleotide p-distances, and sequence data were then used in phylogenetic analyses. The data presented here represent an initial phylogenetic hypothesis concerning economically important wireworms. Our results indicate that the molecular phylogeny of the mitochondrial cytochrome oxidase subunit I gene provides a fast and accurate method of separating wireworm species. By increasing the ease and accuracy of identification, we hope to facilitate further investigations into their biology and control.
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Besouros/genética , Filogenia , Animais , Besouros/enzimologia , DNA/genética , Complexo IV da Cadeia de Transporte de Elétrons/genética , Variação Genética , Meio-Oeste dos Estados Unidos , Zea mays/parasitologiaRESUMO
Term energies for dielectronic-recombination Rydberg resonances below 0.07 eV are determined for Sc18+ with absolute accuracies below 0.0002 eV by electron collision spectroscopy in an ion storage ring, using the twin-electron-beam technique and a cryogenic photocathode. The lithiumlike 2s_{1/2}-2p_{3/2} transition energy for Z=21 is determined to 4.6 ppm, less than 1% of the few-body effects on radiative corrections. Features from the hyperfine structure of the 2s state could be resolved in the dielectronic-recombination spectrum.
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Long standing problems in the comparison of very accurate hyperfine-shift measurements to theory were partly overcome by precise measurements on few-electron highly charged ions. Still the agreement between theory and experiment is unsatisfactory. In this Letter, we present a radically new way of precisely measuring hyperfine shifts, and demonstrate its effectiveness in the case of the hyperfine shift of 4s1/2 and 4p1/2 in 207Pb53+. It is based on the precise detection of dielectronic resonances that occur in electron-ion recombination at very low energy. This allows us to determine the hyperfine constant to around 0.6 meV accuracy which is on the order of 10%.
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We solve a long standing problem with relativistic calculations done with the widely used multiconfiguration Dirac-Fock method. We show, using relativistic many-body perturbation theory (RMBPT), how, even for relatively high-Z, relaxation or correlation causes the nonrelativistic limit of states of different total angular momentum but identical orbital angular momentum to have different energies. We show that only large scale calculations that include all single excitations, even those obeying Brillouin's theorem, have the correct limit. We reproduce very accurately recent high-precision measurements in F-like Ar, and turn then to a precise test of QED. We obtain the correct nonrelativistic limit not only for fine structure but also for level energies and show that RMBPT calculations are not immune to this problem.
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In an electron-ion recombination study with Pb53+ dielectronic recombination resonances are found for as low as approximately 10(-3)-10(-4) eV relative energy. The resonances have been calculated by relativistic many-body perturbation theory and through comparison with experiment the Pb53+(4p(1/2)-4s(1/2)) energy splitting of approximately 118 eV is determined with an accuracy comparable to the position of the first few resonances, i.e., approximately 10(-3) eV. Such a precision provides a test of QED in a many-body environment at a level which can still not be reached in calculations.
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Radiative recombination (inverse photoionization) is believed to be well understood since the beginning of quantum mechanics. Still, modern experiments consistently reveal excess recombination rates at very low electron-ion center-of-mass energies. In a detailed study on recombination of F6+ and C6+ ions with magnetically guided electrons we explored the yet unexplained rate enhancement, its dependence on the magnetic field B, the electron density n(e), and the beam temperatures T( perpendicular) and T( ||). The excess scales as T(-1/2)( perpendicular) and, surprisingly, as T(-1/2)( ||), increases strongly with B, and is insensitive to n(e). This puts strong constraints on explanations of the enhancement.
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A strong emission of characteristic M x rays is observed, without an M vacancy initially present, when slow highly charged ions (Ta(q+), q = 39--48) capture a single electron in single collisions with rare gas atoms (He). This is explained by the formation of bound doubly excited states through electron correlation. An elaborate theoretical treatment shows that bound doubly excited states are mixed with states where a Rydberg electron is bound in the core of a highly charged ion. It is striking that this occurs with a large probability (close to unity), and one needs to assume that higher Rydberg states are populated than predicted by the overbarrier model in order to explain the experimental results.