| 1. |
- Anderson, Emma K., 1986-, et al.
(author)
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Fragmentation of and electron detachment from hot copper and silver dimer anions : A comparison
- 2023
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In: Physical Review A: covering atomic, molecular, and optical physics and quantum information. - 2469-9926 .- 2469-9934. ; 107:6
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Journal article (peer-reviewed)abstract
- We measured the spontaneous decays of internally hot copper and silver dimer anions, and , stored in one of the two ion-beam storage rings of the Double Electrostatic Ion Ring Experiment (DESIREE) at Stockholm University. A coincidence detection technique was utilized enabling essentially background-free measurements of -> Cu + Cu- and -> Ag + Ag- fragmentation rates. Furthermore, the total rates of neutral decay products (monomers and dimers) were measured and the relative contributions of fragmentation and electron emission ( -> Cu2 + e- and -> Ag2 + e-) were deduced as functions of storage time. Fragmentation is completely dominant at early times. However, after about 20 ms of storage, electron emission is observed and becomes the leading decay path after 100 ms for both dimer anions. The branching ratios between fragmentation and electron emission (vibrationally assisted autodetachment processes) are very nearly the same for and Ag-2 throughout the present storage cycle of 10 seconds. This is surprising considering the difference between the electron affinities of the neutral dimers, Cu2 and Ag2, and the difference between the and the dissociation energies.
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| 2. |
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| 3. |
- Eklund, Gustav, 1990-, et al.
(author)
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Experimental lifetime of the a1Δ electronically excited state of CH−
- 2022
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In: Physical Review Research. - : American Physical Society (APS). - 2643-1564. ; 4:1
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Journal article (peer-reviewed)abstract
- By repeatedly probing the a1Δ excited state and the X3Σ− ground-state populations in a beam of CH− ions stored in a cryogenic ion-beam storage ring for 100 s, we extract an intrinsic lifetime of 14.9±0.5 s for this excited state. This is far longer than all earlier experimental and theoretical results, exposing large difficulties in measuring and calculating slow decays and the need for benchmark quality experiments.
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| 4. |
- Eklund, Gustav, 1990-
(author)
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Experiments on mutual neutralization using storage rings with merged ion beams
- 2020
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Doctoral thesis (other academic/artistic)abstract
- This thesis presents work on merged-beams experiments using the DESIREE facility, which consists of two electrostatic ion-storage rings operated at cryogenic temperatures of about 13 K. The two storage rings have a common straight section, where oppositely charged ions can interact at sub-eV collision energies. The work consists of development of the experimental method, tools for data analysis, and simulations for interpretation of the experimental results. This development has led to the first results from merged-beams experiments at DESIREE. The experiments are performed on mutual neutralization, a collision process where an electron is transferred from a negatively charged ion to a positively charged ion, resulting in two neutral products. This reaction is investigated for three systems: Li+ with D−, Na+ with D−, and Mg+ with D−. The reactions studied are of astrophysical interest, in particular for modeling of stellar atmospheres. The detection of the reaction products is done by using a position- and time-sensitive detector, and from this information it is possible to determine the quantum states involved in the reaction. The branching fractions of the reaction channels are measured and compared to theoretical modeling.
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| 7. |
- Kristiansson, Moa K., 1989-, et al.
(author)
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High-precision electron affinity of oxygen
- 2022
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In: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 13:1
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Journal article (peer-reviewed)abstract
- Negative ions are important in many areas of science and technology, e.g., in interstellar chemistry, for accelerator-based radionuclide dating, and in anti-matter research. They are unique quantum systems where electron-correlation effects govern their properties. Atomic anions are loosely bound systems, which with very few exceptions lack optically allowed transitions. This limits prospects for high-resolution spectroscopy, and related negative-ion detection methods. Here, we present a method to measure negative ion binding energies with an order of magnitude higher precision than what has been possible before. By laser-manipulation of quantum-state populations, we are able to strongly reduce the background from photodetachment of excited states using a cryogenic electrostatic ion-beam storage ring where keV ion beams can circulate for up to hours. The method is applicable to negative ions in general and here we report an electron affinity of 1.461 112 972(87) eV for O-16. High-precision measurements are useful to find isotopic shifts and electron correlation. Here the authors measure electron affinity and hyperfine splitting of atomic oxygen with higher precision than previous studies.
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| 8. |
- Navarro-Navarrete, José E., 1988-, et al.
(author)
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High-resolution measurement of the electron affinity of cesium
- 2024
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In: PHYSICAL REVIEW A. - : American Physical Society. - 2469-9926 .- 2469-9934. ; 109:2
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Journal article (peer-reviewed)abstract
- Negative ions are unique quantum systems where electron correlation plays a decisive role in determining their properties. The lack of optically allowed transitions prevents traditional optical spectroscopy and the electron affinity is, therefore, for most elements, the only atomic quantity that can be determined with high accuracy. In this work, we present a high-precision experimental determination of the electron affinity of cesium. A collinear laser-ion beam apparatus was used to investigate the partial photodetachment cross section for the cesium anion, leaving the neutral atom in the 6p 2P3/2 excited state. A resonance ionization scheme was used to obtain final-state selectivity, which enabled the investigation of a sharp onset of the cross section associated with a Wigner s-wave threshold behavior. The electron affinity was determined to be 0.471 598 3(38) eV.
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| 9. |
- Poline, Mathias, et al.
(author)
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Mutual neutralisation of O+ with O− : investigation of the role of metastable ions in a combined experimental and theoretical study
- 2021
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In: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 23:43, s. 24607-24616
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Journal article (peer-reviewed)abstract
- The mutual neutralisation of O+ with O− has been studied in a double ion-beam storage ring with combined merged-beams, imaging and timing techniques. Branching ratios were measured at the collision energies of 55, 75 and 170 (± 15) meV, and found to be in good agreement with previous single-pass merged-beams experimental results at 7 meV collision energy. Several previously unidentified spectral features were found to correspond to mutual neutralisation channels of the first metastable state of the cation (O+(2Do), τ ≈ 3.6 hours), while no contributions from the second metastable state (O+(2Po), τ ≈ 5 seconds) were observed. Theoretical calculations were performed using the multi-channel Landau–Zener model combined with the anion centered asymptotic method, and gave good agreement with several experimentally observed channels, but could not describe well observed contributions from the O+(2Do) metastable state as well as channels involving the O(3s 5So) state.
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| 10. |
- Schmidt-May, Alice F., 1988-, et al.
(author)
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Observation of an isotope effect in state-selective mutual neutralization of lithium with hydrogen
- 2023
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In: Physical Review A: covering atomic, molecular, and optical physics and quantum information. - : American Physical Society. - 2469-9926 .- 2469-9934. ; 108:4
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Journal article (peer-reviewed)abstract
- We report on mutual neutralization measurements between 7Li+ and 1H- at effective center-of-mass collision energies in the range of 100 to 350 meV. We find that final states of lithium with principal quantum number n = 3 dominate with 3s separated from the unresolved 3p and 3d states. We measure the 3s branching fraction to be 0.665(12) at 100(16) meV and no significant dependence on collision energy is observed in the studied range. Comparing to previous results on mutual neutralization between 7Li+ and 2H- [G. Eklund et al., Phys. Rev. A 102, 012823 (2020)], we find that 7Li+ collisions with 1H- result in a significantly higher 3s branching fraction than collisions with 2H-. The difference is 0.087(14). The 3s branching fraction of 7Li+ + 1H- and the determined isotope difference are in agreement with results from extended full quantum calculations based on the same input data and numerical method as in Croft et al. [H. Croft, A. S. Dickinson, and F. X. Gadea, J. Phys. B 32, 81 (1999)]. These calculations reveal strong Stueckelberg oscillations of the 3s branching fraction for both isotopes.
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