Michael GatchellPostdoktor
Om mig
Forskare vid Stockholms universitet och Leopold-Franzens-Universität Innsbruck. Mina forskningsområden inkluderar experimentiella studier av atomära och molekylära kluster; kollisioner mellan atomer, joner och molekyler; samt teoretistka undersökningar av dessa processer med kvantkemi och molekyldynamiksimuleringar.
Publikationer
I urval från Stockholms universitets publikationsdatabas
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Survival of polycyclic aromatic hydrocarbon knockout fragments in the interstellar medium
2021. Michael Gatchell (et al.). Nature Communications 12 (1)
ArtikelLäs mer om Survival of polycyclic aromatic hydrocarbon knockout fragments in the interstellar mediumLaboratory studies play a crucial role in understanding the chemical nature of the interstellar medium (ISM), but the disconnect between experimental timescales and the timescales of reactions in space can make a direct comparison between observations, laboratory, and model results difficult. Here we study the survival of reactive fragments of the polycyclic aromatic hydrocarbon (PAH) coronene, where individual C atoms have been knocked out of the molecules in hard collisions with He atoms at stellar wind and supernova shockwave velocities. Ionic fragments are stored in the DESIREE cryogenic ion-beam storage ring where we investigate their decay for up to one second. After 10 ms the initially hot stored ions have cooled enough so that spontaneous dissociation no longer takes place at a measurable rate; a majority of the fragments remain intact and will continue to do so indefinitely in isolation. Our findings show that defective PAHs formed in energetic collisions with heavy particles may survive at thermal equilibrium in the interstellar medium indefinitely, and could play an important role in the chemistry in there, due to their increased reactivity compared to intact or photo-fragmented PAHs. Ion storage rings allow reactions to be studied over orders of magnitude in time, bridging the gap between typical experimental and astronomical timescales. Here the authors observe that polycyclic aromatic hydrocarbon fragments produced upon collision with He atoms at velocities typical of stellar winds and supernova shockwaves remain intact up to second timescales, thus may play an important role in interstellar chemistry.
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Splashing of Large Helium Nanodroplets upon Surface Collisions
2021. Paul Martini (et al.). Physical Review Letters 127 (26)
ArtikelLäs mer om Splashing of Large Helium Nanodroplets upon Surface CollisionsIn the present work we observe that helium nanodroplets colliding with surfaces can exhibit splashing in a way that is analogous to classical liquids. We use transmission electron microscopy and mass spectrometry to demonstrate that neutral and ionic dopants embedded in the droplets are efficiently backscattered in such events. High abundances of weakly bound He-tagged ions of both polarities indicate a gentle extraction mechanism of these ions from the droplets upon collision with a solid surface. This backscattering process is observed for dopant particles with masses up to 400 kilodaltons, indicating an unexpected mechanism that effectively lowers deposition rates of nanoparticles formed in helium droplets.
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Multiply Charged Helium Droplet Anions
2021. Felix Laimer (et al.). Chemistry - A European Journal 27 (25), 7283-7287
ArtikelLäs mer om Multiply Charged Helium Droplet AnionsThe detection of multiply charged helium droplet anions is reported for the first time. By ionizing droplets of superfluid helium with low energy electrons (up to 25 eV), it was possible to produce droplets containing up to five negative charges, which remain intact on the timescale of the experiment. The appearance sizes for different charge states are determined and are found to be orders of magnitude larger than for the equivalent cationic droplets, starting at 4 million He atoms for dianions. Droplets with He*(-) as charge carriers show signs of being metastable, but this effect is quenched by the pickup of water molecules.
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Roadmap on dynamics of molecules and clusters in the gas phase
2021. Henning Zettergren (et al.). European Physical Journal D 75 (5)
ArtikelLäs mer om Roadmap on dynamics of molecules and clusters in the gas phaseThis roadmap article highlights recent advances, challenges and future prospects in studies of the dynamics of molecules and clusters in the gas phase. It comprises nineteen contributions by scientists with leading expertise in complementary experimental and theoretical techniques to probe the dynamics on timescales spanning twenty order of magnitudes, from attoseconds to minutes and beyond, and for systems ranging in complexity from the smallest (diatomic) molecules to clusters and nanoparticles. Combining some of these techniques opens up new avenues to unravel hitherto unexplored reaction pathways and mechanisms, and to establish their significance in, e.g. radiotherapy and radiation damage on the nanoscale, astrophysics, astrochemistry and atmospheric science.
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Solvation of ions in helium
2020. Tomás González-Lezana (et al.). International reviews in physical chemistry (Print) 39 (4), 465-516
ArtikelLäs mer om Solvation of ions in heliumWe review the solvation of atomic, molecular or cluster ions in HNDs. After briefly discussing the properties of snowballs in bulk helium we consider experimental conditions for the efficient synthesis of charged, doped HNDs. We show that the cluster ions observed in conventional mass spectrometers originate from fission of highly charged HNDs. The ionization threshold of HNDs doped with alkalis reveals the minimum cluster size required for full immersion. The abundance distributions of HeNX +/- ions frequently reveal local anomalies or magic numbers. We demonstrate that the abundance is approximately proportional to the evaporation energy. Observed and calculated magic numbers will be compiled, including data for ions solvated in molecular hydrogen. Alternative methods to forming HeNX+ that do not employ HNDs will be summarized. Electronic excitation spectra of C-60(+) and polycyclic aromatic hydrocarbon ions reveal the properties of the helium adsorption layer in quantitative detail. Next we discuss theoretical efforts to describe the interaction between ions and helium. We close with summarizing the size dependence of physical quantities computed for atomic alkali and alkaline earth cations in helium, such as binding energy, superfluid fraction, structural order, radial density profiles, and the existence of first and higher solvation shells.
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Isotope enrichment in neon clusters grown in helium nanodroplets
2020. Lukas Tiefenthaler (et al.). Journal of Chemical Physics 153 (16)
ArtikelLäs mer om Isotope enrichment in neon clusters grown in helium nanodropletsNeon cluster ions Ne-s(+) grown in pre-ionized, mass-to-charge selected helium nanodroplets (HNDs) reveal a strong enrichment of the heavy isotope Ne-22 that depends on cluster size s and the experimental conditions. For small sizes, the enrichment is much larger than previously reported for bare neon clusters grown in nozzle expansions and subsequently ionized. The enrichment is traced to the massive evaporation of neon atoms in a collision cell that is used to strip helium from the HNDs. We derive a relation between the enrichment of Ne-22 in the cluster ion and its corresponding depletion factor F in the vapor phase. The value thus found for F is in excellent agreement with a theoretical expression that relates isotopic fractionation in two-phase equilibria of atomic gases to the Debye temperature. Furthermore, the difference in zero-point energies between the two isotopes computed from F agrees reasonably well with theoretical studies of neon cluster ions that include nuclear quantum effects in the harmonic approximation. Another fitting parameter provides an estimate for the size s(i) of the precursor of the observed Ne-s(+). The value is in satisfactory agreement with the size estimated by modeling the growth of Ne-s(+) and with lower and upper limits deduced from other experimental data. On the other hand, neon clusters grown in neutral HNDs that are subsequently ionized by electron bombardment exhibit no statistically significant isotope enrichment at all. The finding suggests that the extent of ionization-induced dissociation of clusters embedded in HNDs is considerably smaller than that for bare clusters.
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Radiative cooling of carbon cluster anions C-2n+1(-) (n=3-5)
2020. Mark H. Stockett (et al.). European Physical Journal D 74 (7)
ArtikelLäs mer om Radiative cooling of carbon cluster anions C-2n+1(-) (n=3-5)Radiative cooling of carbon cluster anions C-2n+1(-)(n = 3-5) is investigated using the cryogenic electrostatic ion storage ring DESIREE. Two different strategies are applied to infer infrared emission on slow (milliseconds to seconds) and ultraslow (seconds to minutes) timescales. Initial cooling of the ions over the millisecond timescale is probed indirectly by monitoring the decay in the yield of spontaneous neutralization by thermionic emission. The observed cooling rates are consistent with a statistical model of thermionic electron emission in competition with infrared photon emission due to vibrational de-excitation. Slower cooling over the seconds to minutes timescale associated with infrared emission from low-frequency vibrational modes is probed using time-dependent action spectroscopy. For C(9)(-)and C-11(-), cooling is evidenced by the time-evolution of the yield of photo-induced neutralization following resonant excitation of electronic transitions near the detachment threshold. The cross-section for resonant photo-excitation is at least two orders of magnitude greater than for direct photodetachment. In contrast, C(7)(-)lacks electronic transitions near the detachment threshold.
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C-60(+) as a diffuse interstellar band carrier; a spectroscopic story in 6 acts
2020. H. Linnartz (et al.). Journal of Molecular Spectroscopy 367
ArtikelLäs mer om C-60(+) as a diffuse interstellar band carrier; a spectroscopic story in 6 actsIn 2019 it was exactly 100 years ago that the first two DIBs, diffuse interstellar bands, were discovered by Mary Lea Heger. Today some 500 + DIBs are known. In numerous observational, modelling and laboratory studies, efforts have been made to identify the carriers of these absorption features that are observed in the light of reddened stars crossing diffuse and translucent clouds. Despite several claims over the years that specific DIBs could be assigned to specific species, not one of these withstood dedicated follow-up studies. An exception is C-60(+). In 2015, Campbell et al. showed that two strong bands, recorded in the laboratory around 960 nm, coincided precisely with known DIBs and in follow-up studies three more matches between C-60(+) transitions and new observational DIB studies were claimed. Over the last four years the evidence for C-60(+) as the first identified DIB carrier - including new laboratory data and Hubble Space Telescope observations - has been accumulating, but not all open issues have been solved yet. This article summarizes 6 spectroscopic achievements that sequentially contributed to what seems to become the first DIB story with a happy end.
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Mixed cationic clusters of nitrogen and hydrogen
2020. P. Martini (et al.). Journal of Chemical Physics 152 (1)
ArtikelLäs mer om Mixed cationic clusters of nitrogen and hydrogenThe addition of small impurities, such as a single proton charge carrier, in noble gas clusters has recently been shown to have considerable effects on their geometries and stabilities. Here, we report on a mass spectrometric study of cationic clusters of N-2 molecules and the effects that adding hydrogen, in the form of D-2, has on the systems. Protonated nitrogen clusters formed by the breakup of D-2 are shown to have similar behaviors as protonated rare gas clusters. For larger systems consisting of different mixtures of intact N-2 and D-2, different molecular species are found to be interchangeable sometimes with regard to magic numbers. This is especially true for the (N2)n(D-2)(m)D+ systems with n + m = 17, which is particularly abundant for all measured combinations of n and m.
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Protonated and Cationic Helium Clusters
2020. Linnea Lundberg (et al.). Molecules 25 (5)
ArtikelLäs mer om Protonated and Cationic Helium ClustersProtonated rare gas clusters have previously been shown to display markably different structures compared to their pure, cationic counterparts. Here, we have performed high-resolution mass spectrometry measurements of protonated and pristine clusters of He containing up to 50 atoms. We identify notable differences between the magic numbers present in the two types of clusters, but in contrast to heavier rare gas clusters, neither the protonated nor pure clusters exhibit signs of icosahedral symmetries. These findings are discussed in light of results from heavier rare gases and previous theoretical work on protonated helium.
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Highly Charged Droplets of Superfluid Helium
2019. Felix Laimer (et al.). Physical Review Letters 123 (16)
ArtikelLäs mer om Highly Charged Droplets of Superfluid HeliumWe report on the production and study of stable, highly charged droplets of superfluid helium. Using a novel experimental setup we produce neutral beams of liquid helium nanodroplets containing millions of atoms or more that can be ionized by electron impact, mass-per-charge selected, and ionized a second time before being analyzed. Droplets containing up to 55 net positive charges are identified and the appearance sizes of multiply charge droplets are determined as a function of the charge state. We show that the droplets are stable on the millisecond timescale of the experiment and decay through the loss of small charged clusters, not through symmetric Coulomb explosions.
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Atomic Gold Ions Clustered with Noble Gases
2019. Paul Martini (et al.). Journal of Physical Chemistry A 123 (44), 9505-9513
ArtikelLäs mer om Atomic Gold Ions Clustered with Noble GasesHigh-resolution mass spectra of helium droplets doped with gold and ionized by electrons reveal HenAu+ cluster ions. Additional doping with heavy noble gases results in NenAu+, ArnAu+, KrnAu+, and XenAu+ cluster ions. The high stability predicted for covalently bonded Ar2Au+, Kr2Au+, and Xe2Au+ is reflected in their relatively high abundance. Surprisingly, the abundance of Ne2Au+, which is predicted to have zero covalent bonding character and no enhanced stability, features a local maximum, too. The predicted size and structure of complete solvation shells surrounding ions with essentially nondirectional bonding depends primarily on the ratio sigma* of the ion-ligand versus the ligand-ligand distance. For Au+ solvated in helium and neon, the ratio sigma* is slightly below 1, favoring icosahedral packing in agreement with a maximum observed in the corresponding abundance distributions at n = 12. HenAu+ appears to adopt two additional solvation shells of I-h symmetry, containing 20 and 12 atoms, respectively. For ArnAu+, with sigma* approximate to 0.67, one would expect a solvation shell of octahedral symmetry, in agreement with an enhanced ion abundance at n = 6. Another anomaly in the ion abundance at Ar9Au+ matches a local maximum in its computed dissociation energy.
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Considerable matrix shift in the electronic transitions of helium-solvated cesium dimer cation Cs2He+n
2019. Lorenz Kranabetter (et al.). Physical Chemistry, Chemical Physics - PCCP 21 (45), 25362-25368
ArtikelLäs mer om Considerable matrix shift in the electronic transitions of helium-solvated cesium dimer cation Cs2He+nWe investigate the photodissociation of helium-solvated cesium dimer cations using action spectroscopy and quantum chemical calculations. The spectrum of Cs2He+ shows three distinct absorption bands into both bound and dissociative states. Upon solvation with further helium atoms, considerable shifts of the absorption bands are observed, exceeding 0.1 eV (850 cm(-1)) already for Cs2He10+, along with significant broadening. The shifts are highly sensitive to the character of the excited state. Our calculations show that helium atoms adsorb on the ends of Cs-2(+). The shifts are particularly pronounced if the excited state orbitals extend to the area occupied by the helium atoms. In this case, Pauli repulsion leads to a deformation of the excited state orbitals, resulting in the observed blue shift of the transition. Since the position of the weakly bound helium atoms is ill defined, Pauli repulsion also explains the broadening.
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Protonated Clusters of Neon and Krypton
2019. Michael Gatchell (et al.). Journal of the American Society for Mass Spectrometry 30 (12), 2632-2636
ArtikelLäs mer om Protonated Clusters of Neon and KryptonWe present a study of cationic and protonated clusters of neon and krypton. Recent studies using argon have shown that protonated rare gas clusters can have very different magic sizes than pure, cationic clusters. Here, we find that neon behaves similarly to argon, but that the cationic krypton is more similar to its protonated counterparts than the lighter rare gases are, sharing many of the same magic numbers.
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Hydrogenated Gold Clusters from Helium Nanodroplets
2019. Linnea Lundberg (et al.). Journal of the American Society for Mass Spectrometry 30 (10), 1906-1913
ArtikelLäs mer om Hydrogenated Gold Clusters from Helium NanodropletsWe report the mass spectrometric detection of hydrogenated gold clusters ionized by electron transfer and proton transfer. The cations appear after the pickup of hydrogen molecules and gold atoms by helium nanodroplets (HNDs) near zero K and subsequent exposure to electron impact. We focus on the size distributions of the gold cluster cations and their hydrogen content, the electron energy dependence of the ion yield, patterns of hydrogenated gold cluster cation stability, and the presence of magic clusters. Ab initio molecular orbital calculations were performed to provide insight into ionization energies and proton affinities of gold clusters as well as into molecular hydrogen affinities of the ionized and protonated gold cluster cations.
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Spectroscopy of corannulene cations in helium nanodroplets
2019. Michael Gatchell (et al.). Faraday discussions (Online) 217, 276-289
ArtikelLäs mer om Spectroscopy of corannulene cations in helium nanodropletsHelium tagging in action spectroscopy is an efficient method for measuring the absorption spectra of complex molecular ions with minimal perturbations to the gas phase spectra. We have used superfluid helium nanodroplets doped with corannulene to prepare cations of these molecules complexed with different numbers of He atoms. In total we identify 13 different absorption bands from corannulene cations between 5500 angstrom and 6000 angstrom. The He atoms cause a small, chemically induced redshift of the band positions of the corannulene ion. By studying this effect as a function of the number of solvating atoms we are able to identify the formation of solvation structures that are not visible in the mass spectrum. The solvation features detected using action spectroscopy agree very well with the results of atomistic modeling based on path-integral molecular dynamics simulations. By additionally doping our He droplets with D-2, we produce protonated corannulene ions. The absorption spectrum of these ions differs significantly from the case of the radical cations as the numerous narrow bands are replaced by a broad absorption feature that spans nearly 2000 angstrom in width.
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Large expert-curated database for benchmarking document similarity detection in biomedical literature search
2019. Michael Gatchell. Database
ArtikelLäs mer om Large expert-curated database for benchmarking document similarity detection in biomedical literature searchDocument recommendation systems for locating relevant literature have mostly relied on methods developed a decade ago. This is largely due to the lack of a large offline gold-standard benchmark of relevant documents that cover a variety of research fields such that newly developed literature search techniques can be compared, improved and translated into practice. To overcome this bottleneck, we have established the RElevant LIterature SearcH consortium consisting of more than 1500 scientists from 84 countries, who have collectively annotated the relevance of over 180 000 PubMed-listed articles with regard to their respective seed (input) article/s. The majority of annotations were contributed by highly experienced, original authors of the seed articles. The collected data cover 76% of all unique PubMed Medical Subject Headings descriptors. No systematic biases were observed across different experience levels, research fields or time spent on annotations. More importantly, annotations of the same document pairs contributed by different scientists were highly concordant. We further show that the three representative baseline methods used to generate recommended articles for evaluation (Okapi Best Matching 25, Term Frequency-Inverse Document Frequency and PubMed Related Articles) had similar overall performances. Additionally, we found that these methods each tend to produce distinct collections of recommended articles, suggesting that a hybrid method may be required to completely capture all relevant articles. The established database server located at https://relishdb.ict.griffith.edu.au is freely available for the downloading of annotation data and the blind testing of new methods. We expect that this benchmark will be useful for stimulating the development of new powerful techniques for title and title/abstract-based search engines for relevant articles in biomedical research.
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Magic sizes of cationic and protonated argon clusters
2018. Michael Gatchell (et al.). Physical Review A: covering atomic, molecular, and optical physics and quantum information 98 (2)
ArtikelLäs mer om Magic sizes of cationic and protonated argon clustersThere has long been a discrepancy between the size distributions of Ar-n(+) clusters measured by different groups regarding whether or not magic numbers appear at sizes corresponding to the closure of icosahedral (sub-) shells. We show that the previously observed magic cluster size distributions are likely the result of an unresolved ArnH+ component, i.e., from protonated argon clusters. We find that the proton impurity gives cluster geometries that are much closer to those for neutral rare-gas clusters, which are known to form icosahedral structures, than for the pure cationic clusters, explaining why the mass spectra from protonated argon clusters better matches these structural models. Our results thus show that even small impurities, e.g., a single proton, can significantly influence the properties of clusters.
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Lithium ions solvated in helium
2018. Monisha Rastogi (et al.). Physical Chemistry, Chemical Physics - PCCP 20 (40), 25569-25576
ArtikelLäs mer om Lithium ions solvated in heliumWe report on a combined experimental and theoretical study of Li+ ions solvated by up to 50 He atoms. The experiments show clear enhanced abundances associated with HenLi+ clusters where n = 2, 6, 8, and 14. We find that classical methods, e.g. basin-hopping (BH), give results that qualitatively agree with quantum mechanical methods such as path integral Monte Carlo, diffusion Monte Carlo and quantum free energy, regarding both energies and the solvation structures that are formed. The theory identifies particularly stable structures for n = 4, 6 and 8 which line up with some of the most abundant features in the experiments.
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DESIREE electrospray ion source test bench and setup for collision induced dissociation experiments
2018. Nathalie de Ruette (et al.). Review of Scientific Instruments 89 (7)
ArtikelLäs mer om DESIREE electrospray ion source test bench and setup for collision induced dissociation experimentsIn this paper, we give a detailed description of an electrospray ion source test bench and a single-pass setup for ion fragmentation studies at the Double ElectroStatic Ion Ring ExpEriment infrastructure at Stockholm University. This arrangement allows for collision-induced dissociation experiments at the center-of-mass energies between 10 eV and 1 keV. Charged fragments are analyzed with respect to their kinetic energies (masses) by means of an electrostatic energy analyzer with a wide angular acceptance and adjustable energy resolution.
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Complexes of gold and imidazole formed in helium nanodroplets
2018. Michael Gatchell (et al.). Physical Chemistry, Chemical Physics - PCCP 20 (11), 7739-7745
ArtikelLäs mer om Complexes of gold and imidazole formed in helium nanodropletsWe have studied complexes of gold atoms and imidazole (C3N2H4, abbreviated Im) produced in helium nanodroplets. Following the ionization of the doped droplets we detect a broad range of different Au(m)Im(n)(+) complexes, however we find that for specific values of m certain n are magic and thus particularly abundant. Our density functional theory calculations indicate that these abundant clusters sizes are partially the result of particularly stable complexes, e.g. AuIm(2)(+), and partially due to a transition in fragmentation patterns from the loss of neutral imidazole molecules for large systems to the loss of neutral gold atoms for smaller systems.
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The threshold displacement energy of buckminsterfullerene C-60 and formation of the endohedral defect fullerene He@C-59
2018. Mark H. Stockett (et al.). Carbon 139, 906-912
ArtikelLäs mer om The threshold displacement energy of buckminsterfullerene C-60 and formation of the endohedral defect fullerene He@C-59We have measured the threshold center-of-mass kinetic energy for knocking out a single carbon atom from C-60(-) in collisions with He. Combining this experimental result with classical molecular dynamics simulations, we determine a semi-empirical value of 24.1+0.5 eV for the threshold displacement energy, the energy needed to remove a single carbon atom from the C-60 cage. We report the first observation of an endohedral complex with an odd number of carbon atoms, He@C-59(-), and discuss its formation and decay mechanisms.
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Decays of excited silver-cluster anions Ag-n, n=4 to 7, in the Double ElectroStatic Ion Ring ExpEriment
2018. Emma K. Anderson (et al.). Physical Review A: covering atomic, molecular, and optical physics and quantum information 98 (2)
ArtikelLäs mer om Decays of excited silver-cluster anions Ag-n, n=4 to 7, in the Double ElectroStatic Ion Ring ExpErimentSpontaneous decays of small, hot silver-cluster anions Ag-n(-), n = 4-7, have been studied using one of the rings of the Double ElectroStatic Ion Ring ExpEriment (DESIREE). Observation of these decays over very long time scales is possible due to the very low residual gas pressure (similar to 10(-14)) and cryogenic (13 K) operation of DESIREE. The yield of neutral particles from stored beams of Ag-6(-) and Ag-2(-) anions were measured for 100 milliseconds and were found to follow single power-law behavior with millisecond time-scale exponential cutoffs. The Ag-4(-) and Ag-5(-) anions were stored for 60 s and the observed decays show two-component power-law behaviors. We present calculations of the rate constants for electron detachment from and fragmentation of Ag-4(-) and Ag-5(-). In these calculations, we assume that the internal energy distribution of the clusters are flat and with this we reproduce the early steep parts of the experimentally measured decay curves for Ag-4(-) and Ag-5(-) which extends to tens and hundreds of milliseconds, respectively. The fact that the calculations reproduce the early slopes of Ag-4(-) and Ag-5(-), which differ for the two cases, suggests that it is the changes in fragmentation rates with internal cluster energies of Ag-4(-) and Ag-5(-) rather than conditions in the ion source that determine this behavior. Comparisons with the measurements strongly suggest that the neutral particles detected in these time domains originate from Ag-4(-) -> Ag-3(-) + Ag and Ag-5(-) -> Ag-3(-) +Ag-2 fragmentation processes.
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DESIREE electrospray ion source test bench and setup for collision induced dissociation experiments
2018. Nathalie de Ruette (et al.). Review of Scientific Instruments 89 (7)
ArtikelLäs mer om DESIREE electrospray ion source test bench and setup for collision induced dissociation experimentsIn this paper, we give a detailed description of an electrospray ion source test bench and a single-pass setup for ion fragmentation studies at the Double ElectroStatic Ion Ring ExpEriment infrastructure at Stockholm University. This arrangement allows for collision-induced dissociation experiments at the center-of-mass energies between 10 eV and 1 keV. Charged fragments are analyzed with respect to their kinetic energies (masses) by means of an electrostatic energy analyzer with a wide angular acceptance and adjustable energy resolution.
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Ion collision-induced chemistry in pure and mixed loosely bound clusters of coronene and C-60 molecules
2018. Alicja Domaracka (et al.). Physical Chemistry, Chemical Physics - PCCP 20 (22), 15052-15060
ArtikelLäs mer om Ion collision-induced chemistry in pure and mixed loosely bound clusters of coronene and C-60 moleculesIonization, fragmentation and molecular growth have been studied in collisions of 22.5 keV He2+-or 3 keV Ar+-projectiles with pure loosely bound clusters of coronene (C24H12) molecules or with loosely bound mixed C-60-C24H12 clusters by using mass spectrometry. The heavier and slower Ar+ projectiles induce prompt knockout-fragmentation - C- and/or H-losses - from individual molecules and highly efficient secondary molecular growth reactions before the clusters disintegrate on picosecond timescales. The lighter and faster He2+ projectiles have a higher charge and the main reactions are then ionization by ions that are not penetrating the clusters. This leads mostly to cluster fragmentation without molecular growth. However, here penetrating collisions may also lead to molecular growth but to a much smaller extent than with 3 keV Ar+. Here we present fragmentation and molecular growth mass distributions with 1 mass unit resolution, which reveals that the same numbers of C- and H-atoms often participate in the formation and breaking of covalent bonds inside the clusters. We find that masses close to those with integer numbers of intact coronene molecules, or with integer numbers of both intact coronene and C-60 molecules, are formed where often one or several H-atoms are missing or have been added on. We also find that super-hydrogenated coronene is formed inside the clusters.
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The adsorption of helium atoms on small cationic gold clusters
2018. Marcelo Goulart (et al.). Physical Chemistry, Chemical Physics - PCCP 20 (14), 9554-9560
ArtikelLäs mer om The adsorption of helium atoms on small cationic gold clustersAdducts formed between small gold cluster cations and helium atoms are reported for the first time. These binary ions, Aun+Hem, were produced by electron ionization of helium nanodroplets doped with neutral gold clusters and were detected using mass spectrometry. For a given value of n, the distribution of ions as a function of the number of added helium atoms, m, has been recorded. Peaks with anomalously high intensities, corresponding to so-called magic number ions, are identified and interpreted in terms of the geometric structures of the underlying Au-n(+) ions. These features can be accounted for by planar structures for Au-n(+) ions with n <= 7, with the addition of helium having no significant effect on the structures of the underlying gold cluster ions. According to ion mobility studies and some theoretical predictions, a 3-D structure is expected for Au-8(+). However, the findings for Au-8(+) in this work are more consistent with a planar structure.
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Shock-driven formation of covalently bound carbon nanoparticles from ion collisions with clusters of C-60 fullerenes
2018. R. Delaunay (et al.). Carbon 129, 766-774
ArtikelLäs mer om Shock-driven formation of covalently bound carbon nanoparticles from ion collisions with clusters of C-60 fullerenesWe show that the energetic processing of C-60 clusters by slow atomic projectiles leads to ultrafast (< ps) formation of large covalent carbon nanoparticles containing a few hundreds of atoms. The underlying mechanism is found to be due to impulse-driven collisions between the projectile and the nuclei of the molecules. Experimental findings are well reproduced by classical molecular dynamics simulations. The cross sections for molecular growth processes forming covalent systems which contain more than 60 carbon atoms are about 5.10(-14) cm(2) representing more than 70% of the geometrical cross sections. This demonstrates the high efficiency of the underlying processes. The formed carbon nanoparticles contain both aromatic and aliphatic structures which have also been considered as dust components in space.
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The structure of coronene cluster ions inferred from H-2 uptake in the gas phase
2017. Marcelo Goulart (et al.). Physical Chemistry, Chemical Physics - PCCP 19 (41), 27968-27973
ArtikelLäs mer om The structure of coronene cluster ions inferred from H-2 uptake in the gas phaseMass spectra of helium nanodroplets doped with H-2 and coronene feature anomalies in the ion abundance that reveal anomalies in the energetics of adsorption sites. The coronene monomer ion strongly adsorbs up to n = 38 H-2 molecules indicating a commensurate solvation shell that preserves the D-6h symmetry of the substrate. No such feature is seen in the abundance of the coronene dimer through tetramer complexed with H-2; this observation rules out a vertical columnar structure. Instead we see evidence for a columnar structure in which adjacent coronenes are displaced in parallel, forming terraces that offer additional strong adsorption sites. The experimental value for the number of adsorption sites per terrace, approximately six, barely depends on the number of coronene molecules. The displacement estimated from this number exceeds the value reported in several theoretical studies of the bare, neutral coronene dimer.
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Rotationally Cold OH- Ions in the Cryogenic Electrostatic Ion-Beam Storage Ring DESIREE
2017. Henning T. Schmidt (et al.). Physical Review Letters 119 (7)
ArtikelLäs mer om Rotationally Cold OH- Ions in the Cryogenic Electrostatic Ion-Beam Storage Ring DESIREEWe apply near-threshold laser photodetachment to characterize the rotational quantum level distribution of OH- ions stored in the cryogenic ion-beam storage ring DESIREE at Stockholm University. We find that the stored ions relax to a rotational temperature of 13.4 +/- 0.2 K with 94.9 +/- 0.3% of the ions in the rotational ground state. This is consistent with the storage ring temperature of 13.5 +/- 0.5 K as measured with eight silicon diodes but in contrast to all earlier studies in cryogenic traps and rings where the rotational temperatures were always much higher than those of the storage devices at their lowest temperatures. Furthermore, we actively modify the rotational distribution through selective photodetachment to produce an OH- beam where 99.1 +/- 0.1% of approximately one million stored ions are in the J = 0 rotational ground state. We measure the intrinsic lifetime of the J = 1 rotational level to be 145 +/- 28 s.
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Ion-induced molecular growth in clusters of small hydrocarbon chains
2017. Michael Gatchell (et al.). Physical Chemistry, Chemical Physics - PCCP 19 (30), 19665-19672
ArtikelLäs mer om Ion-induced molecular growth in clusters of small hydrocarbon chainsWe report on studies of collisions between 3 keV Ar+ projectile ions and neutral targets of isolated 1,3-butadiene (C4H6) molecules and cold, loosely bound clusters of these molecules. We identify molecular growth processes within the molecular clusters that appears to be driven by knockout processes and that could result in the formation of (aromatic) ring structures. These types of reactions are not unique to specific projectile ions and target molecules, but will occur whenever atoms or ions with suitable masses and kinetic energies collide with aggregates of matter, such as carbonaceous grains in the interstellar medium or aerosol nanoparticles in the atmosphere.
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Knockout driven fragmentation of porphyrins
2017. Linda Giacomozzi (et al.). Physical Chemistry, Chemical Physics - PCCP 19 (30), 19750-19755
ArtikelLäs mer om Knockout driven fragmentation of porphyrinsWe have studied collisions between tetraphenylporphyrin cations and He or Ne at center-of-mass energies in the range 50-110 eV. The experimental results were interpreted in view of density functional theory calculations of dissociation energies and classical molecular dynamics simulations of how the molecules respond to the He/Ne impact. We demonstrate that prompt atom knockout strongly contributes to the total destruction cross sections. Such impulse driven processes typically yield highly reactive fragments and are expected to be important for collisions with any molecular system in this collision energy range, but have earlier been very difficult to isolate for biomolecules.
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Spontaneous decay of small copper-cluster anions Cu-n(-) (n=3-6), on long time scales
2017. K. Hansen (et al.). Physical Review A 95 (2)
ArtikelLäs mer om Spontaneous decay of small copper-cluster anions Cu-n(-) (n=3-6), on long time scalesWe have measured the spontaneous neutral particle emission from copper-cluster anions ( Cu-n(-), n = 3-6) stored at cryogenic temperatures in one of the electrostatic ion storage rings of the Double ElectroStatic Ion Ring ExpEriment facility at Stockholm University. The measured rate of emission from the stored Cu-3(-) ions follows a single power-law decay for about 1 ms but then decreases much more rapidly with time. The latter behavior may be due to a decrease in the density of available final states in Cu-3 as the excitation energies of the decaying ions approach the electron detachment threshold. The emissions from Cu-4(-), Cu-5(-), and Cu-6(-) are well described by sums of two power laws that are quenched by radiative cooling of the stored ions with characteristic times between a few and hundreds of milliseconds. We relate these two-component behaviors to populations of stored ions with higher and lower angular momenta. In a separate experiment, we studied the laser-induced decay of Cu-6(-) ions that were excited by 1.13- or 1.45-eV photons after 46 ms of storage.
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Knockout driven reactions in complex molecules and their clusters
2016. Michael Gatchell, Henning Zettergren. Journal of Physics B 49 (16)
ArtikelLäs mer om Knockout driven reactions in complex molecules and their clustersEnergetic ions lose some of their kinetic energy when interacting with electrons or nuclei in matter. Here, we discuss combined experimental and theoretical studies on such impulse driven reactions in polycyclic aromatic hydrocarbons (PAHs), fullerenes, and pure or mixed clusters of these molecules. These studies show that the nature of excitation is important for how complex molecular systems respond to ion/atom impact. Rutherford-like nuclear scattering processes may lead to prompt atom knockout and formation of highly reactive fragments, while heating of the molecular electron clouds in general lead to formation of more stable and less reactive fragments. In this topical review, we focus on recent studies of knockout driven reactions, and present new calculations of the angular dependent threshold (displacement) energies for such processes in PAHs. The so-formed fragments may efficiently form covalent bonds with neighboring molecules in clusters. These unique molecular growth processes may be important in astrophysical environments such as low velocity shock waves.
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A precedent of van-der-Waals interactions outmatching Coulomb explosion
2016. S. E. Huber (et al.). Carbon 109, 843-850
ArtikelLäs mer om A precedent of van-der-Waals interactions outmatching Coulomb explosionFullerenes (and clusters composed of them) yield a variety of promising structural, electronic, magnetic and chemical properties, governed by their specific electronic and geometric configuration. These systems have attracted many theoretical and experimental endeavors in order to describe, explain and predict their features. The conclusive description of some specific properties has remained a challenge though, such as a sound physicochemical description of the stability of multiply charged fullerene clusters, which we explore here. We show how simple models based on classical electrostatics allow one to understand the (fragmentation) dynamics of multiply ionized fullerene aggregates without the use of elaborate and time-consuming computational quantum chemical approaches. These models successfully explain why the fullerene pentamer is the smallest dicationic cluster experimentally observed, despite its thermodynamic instability. These predictions are of importance in various fields such as cluster physics, astrochemistry, electrochemistry and solid-state chemistry.
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Molecular Hole Punching
2016. Michael Gatchell (et al.).
Avhandling (Dok)Läs mer om Molecular Hole PunchingWhen molecules are excited by photons or energetic particles, they will cool through the emission of photons, electrons, or by fragmenting. Such processes are often thermal as they occur after the excitation energy has been redistributed across all degrees-of-freedom in the system. Collisions with atoms or ions may also lead to ultrafast fragmentation in Rutherford-like scattering processes, where one or several atoms can literally be knocked out of the molecule by the incoming projectile before the energy can be completely redistributed. The resulting fragmentation pathways can in such knockout processes be very different from those in thermal processes.
This thesis covers extensive studies of collisions between ions/atoms and isolated Polycyclic Aromatic Hydrocarbon (PAH) molecules, isolated fullerene molecules, or clusters of these. The high stabilities and distinct fragmentation channels make these types of molecules excellent test cases for characterizing knockout-driven fragmentation and the reactions that these processes can lead to. I will present experimental measurements for a wide range of energies and compare them with my own molecular dynamics simulations and quantum chemical calculations. In this thesis, I present an in-depth study of the role of knockout in the energetic processing of molecules and clusters. The competition between knockout and thermally driven fragmentation is discussed in detail.
Knockout-driven fragmentation is shown to result in exotic fragments that are far more reactive than the intact parent molecules or fragments from thermal processes. When such reactive species are formed within molecular clusters efficient molecular growth can take place on sub-picosecond timescales. The cluster environments are crucial here because they protect the newly formed molecules by absorbing excess energy. This is a possible pathway for the growth of large PAHs, fullerenes, and similar carbonaceous complexes found in, for instance, the interstellar medium.
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Failure of hydrogenation in protecting polycyclic aromatic hydrocarbons from fragmentation
2015. Michael Gatchell (et al.). Physical Review A. Atomic, Molecular, and Optical Physics 92 (5)
ArtikelLäs mer om Failure of hydrogenation in protecting polycyclic aromatic hydrocarbons from fragmentationA recent study of soft x-ray absorption in native and hydrogenated coronene cations, C24H12+m + m = 0-7, led to the conclusion that additional hydrogen atoms protect (interstellar) polycyclic aromatic hydrocarbon (PAH) molecules from fragmentation [Reitsma et al., Phys. Rev. Lett. 113, 053002 (2014)]. The present experiment with collisions between fast (30-200 eV) He atoms and pyrene (C16H10+m +, m = 0, 6, and 16) and simulations without reference to the excitation method suggests the opposite. We find that the absolute carbon-backbone fragmentation cross section does not decrease but increases with the degree of hydrogenation for pyrene molecules.
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Molecular growth inside polycyclic aromatic hydrocarbon clusters induced by ion collisions
2015. Delaunay Rudy (et al.). Journal of Physical Chemistry Letters 6 (9), 1536-1542
ArtikelLäs mer om Molecular growth inside polycyclic aromatic hydrocarbon clusters induced by ion collisionsThe present work combines experimental and theoretical studies of the collision between keV ion projectiles and clusters of pyrene, one of the simplest polycyclic aromatic hydrocarbons (PAHs). Intracluster growth processes induced by ion collisions lead to the formation of a wide range of new molecules with masses larger than that of the pyrene molecule. The efficiency of these processes is found to strongly depend on the mass and velocity of the incoming projectile. Classical molecular dynamics simulations of the entire collision process-from the ion impact (nuclear scattering) to the formation of new molecular species-reproduce the essential features of the measured molecular growth process and also yield estimates of the related absolute cross sections. More elaborate density functional tight binding calculations yield the same growth products as the classical simulations. The present results could be relevant to understand the physical chemistry of the PAH-rich upper atmosphere of Saturn’s moon Titan.
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Threshold Energies for Single-Carbon Knockout from Polycyclic Aromatic Hydrocarbons
2015. Mark H. Stockett (et al.). Journal of Physical Chemistry Letters 6 (22), 4504-4509
ArtikelLäs mer om Threshold Energies for Single-Carbon Knockout from Polycyclic Aromatic HydrocarbonsWe have measured absolute cross sections for ultrafast (femtosecond) single-carbon knockout from polycyclic aromatic hydrocarbon (PAR) cations as functions of He-PAR center-of-mass collision energy in the 10-200 eV range. Classical molecular dynamics (MD) simulations cover this range and extend up to 105 eV. The shapes of the knockout cross sections are well-described by a simple analytical expression yielding experimental and MD threshold energies of E-th(Exp) = 32.5 +/- 0.4 eV and E-th(MD) = 41.0 +/- 0.3 eV, respectively. These are the first measurements of knockout threshold energies for molecules isolated in vacuo. We further deduce semiempirical (SE) and MD displacement energies, i.e., the energy transfers to the PAH molecules at the threshold energies for knockout, of T-disp(SE) = 23.3 +/- 0.3 eV and T-disp(MD) = 27.0 +/- 0.3 eV. The semiempirical results compare favorably with measured displacement energies for graphene (T-disp = 23.6 eV).
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