A. Al-Khalili
Stockholm University
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Featured researches published by A. Al-Khalili.
Nature | 2003
Benjamin J. McCall; A. J. Huneycutt; Richard J. Saykally; T. R. Geballe; N. Djurić; G. H. Dunn; J. Semaniak; O. Novotny; A. Al-Khalili; A. Ehlerding; Fredrik Hellberg; S. Kalhori; A. Neau; Richard D. Thomas; F. Österdahl; Mats Larsson
The H3+ molecular ion plays a fundamental role in interstellar chemistry, as it initiates a network of chemical reactions that produce many molecules. In dense interstellar clouds, the H3+ abundance is understood using a simple chemical model, from which observations of H3+ yield valuable estimates of cloud path length, density and temperature. But observations of diffuse clouds have suggested that H3+ is considerably more abundant than expected from the chemical models. Models of diffuse clouds have, however, been hampered by the uncertain values of three key parameters: the rate of H3+ destruction by electrons (e-), the electron fraction, and the cosmic-ray ionization rate. Here we report a direct experimental measurement of the H3+ destruction rate under nearly interstellar conditions. We also report the observation of H3+ in a diffuse cloud (towards ζ Persei) where the electron fraction is already known. From these, we find that the cosmic-ray ionization rate along this line of sight is 40 times faster than previously assumed. If such a high cosmic-ray flux is ubiquitous in diffuse clouds, the discrepancy between chemical models and the previous observations of H3+ can be resolved.
Nature | 2003
Benjamin J. McCall; A. J. Huneycutt; Richard J. Saykally; T. R. Geballe; N. Djurić; G. H. Dunn; J. Semaniak; O. Novotny; A. Al-Khalili; A. Ehlerding; Fredrik Hellberg; S. Kalhori; A. Neau; Richard D. Thomas; F. Österdahl; Mats Larsson
The H3+ molecular ion plays a fundamental role in interstellar chemistry, as it initiates a network of chemical reactions that produce many molecules. In dense interstellar clouds, the H3+ abundance is understood using a simple chemical model, from which observations of H3+ yield valuable estimates of cloud path length, density and temperature. But observations of diffuse clouds have suggested that H3+ is considerably more abundant than expected from the chemical models. Models of diffuse clouds have, however, been hampered by the uncertain values of three key parameters: the rate of H3+ destruction by electrons (e-), the electron fraction, and the cosmic-ray ionization rate. Here we report a direct experimental measurement of the H3+ destruction rate under nearly interstellar conditions. We also report the observation of H3+ in a diffuse cloud (towards ζ Persei) where the electron fraction is already known. From these, we find that the cosmic-ray ionization rate along this line of sight is 40 times faster than previously assumed. If such a high cosmic-ray flux is ubiquitous in diffuse clouds, the discrepancy between chemical models and the previous observations of H3+ can be resolved.
Journal of Chemical Physics | 2001
R. Peverall; S. Rosén; J. R. Peterson; Mats Larsson; A. Al-Khalili; Ljiljana Vikor; J. Semaniak; Rolf Bobbenkamp; Arnaud Le Padellec; Ahilleas Nikolaou Maurellis; Wim J. van der Zande
We present experimental data on the dissociative recombination (DR) and the dissociative excitation (DE) of O2+ in its electronic and vibrational ground state using a heavy ion storage ring. The absolute DR cross section has been determined over an electron collision energy range from 1 meV to 3 eV. The thermal DR rate coefficient is derived; α(Te)=2.4×10−7(300/Te)0.70±0.01 cm3 s−1, for T>200 K. The threshold for DE was observed near its energetic threshold of 6.7 eV. The DE cross section curve has a maximum of 3×10−16 cm2 near 15 eV. We have determined the branching fractions to the different dissociation limits and present atomic quantum yields for the DR process between 0 to 300 meV collision energy. The quantum yield of O(1D) is found to be 1.17±0.05, largely independent of the electron energy. Arguments are presented that the branching fraction to O(3P)+O(1S) is negligible. The branching fraction to the O(1S)+O(1D) is smaller than 0.06 and varies strongly as a function of collision energy. The O(1S) ...
Journal of Physics B | 1999
A. Derkatch; A. Al-Khalili; L. Vikor; A. Neau; W. Shi; H. Danared; M. af Ugglas; Mats Larsson
Branching ratios in dissociative recombination of C2H2+ molecular ions with electrons were measured using the CRYRING heavy-ion storage ring. We have determined complete branching ratios for C2H2+ at collision energies between 0 and 7.4 meV. We found dissociative recombination of C2H2+ to be dominated by the two-body C2H+H and three-body C2+H+H channels, with branching ratios of 0.50±0.06 and 0.30±0.05, respectively. The branching to CH+CH was measured to be 0.13±0.01, whereas two other energetically allowed channels were found to be almost negligible.
The Astrophysical Journal | 2004
Wolf D. Geppert; A. Ehlerding; Fredrik Hellberg; J. Semaniak; Fabian Österdahl; M. Kaminska; A. Al-Khalili; V. Zhaunerchyk; Richard D. Thomas; M. af Ugglas; A. Källberg; Ansgar Simonsson; Mats Larsson
Branching ratios and absolute cross sections have been measured for the dissociative recombination of DCCCN+ and DCCCND+ using the CRYRING ion storage ring. In the case of DCCCN+ the dissociation y ...
Faraday Discussions | 2000
S. Rosén; A. Derkatch; J. Semaniak; A. Neau; A. Al-Khalili; A. Le Padellec; L. Vikor; Richard D. Thomas; H. Danared; M. af Ugglas; Mats Larsson
Dissociative recombination of vibrationally relaxed H2O+ ions with electrons has been studied in the heavy-ion storage ring CRYRING. Absolute cross-sections have been measured for collision energies between 0 eV and 30 eV. The energy dependence of the cross-section below 0.1 eV is found to be much steeper than the E-1 behaviour associated with the dominance of the direct recombination mechanism. Resonant structures found at 4 eV and 11 eV have been attributed to the electron capture to Rydberg states converging to electronically excited ionic states. Complete branching fractions for all dissociation channels have been measured at a collision energy of 0 eV. The dissociation process is dominated by three-body H + H + O breakup that occurs with a branching ratio of 0.71.
The Astrophysical Journal | 2005
H. Montaigne; Wolf D. Geppert; J. Semaniak; Fabian Österdahl; Fredrik Hellberg; Richard D. Thomas; M. af Ugglas; Helen Roberts; T. J. Millar; V. Zhaunerchyk; M. Kaminska; A. Al-Khalili; A. Källberg; Mats Larsson
Branching ratios and absolute cross sections have been measured for the dissociative recombination of HCS+ and OCS+ at the CRYRING ion storage ring. In the case of OCS+, the channel leading to CO + S (83%) dominates, whereas the other exoergic pathways leading to CS + O (14%) and C + SO (3%) are of lesser importance. In the case of HCS+, fracture of the C–S bond is predominant (81%), with the production of H + CS accounting for the remainder (19%). The cross section of the reaction could be fitted by the expressions σ = 1.41 × 10-15E(eV)-1.11 and 4.47 × 10-16E(eV)-1.14 cm2 for HCS+ and OCS+, respectively. The derived energy dependences of the thermal reaction rate coefficients can be fitted by k(T) = 9.7 × 10-7(T/300)-0.57 and 3.5 × 10-7(T/300)-0.62 cm3 s-1 for HCS+ and OCS+, respectively. We use these data to perform model calculations on the HCS+/CS abundance ratio in dark clouds and find that the models using the UMIST and Ohio State University databases have even more difficulty in accounting for the large observed ratio.
Journal of Chemical Physics | 2004
A. Al-Khalili; Richard D. Thomas; A. Ehlerding; Fredrik Hellberg; Wolf D. Geppert; V. Zhaunerchyk; M. af Ugglas; Mats Larsson; Einar Uggerud; J. Vedde; Christian Adlhart; J. Semaniak; M. Kaminska; R. A. Zubarev; F. Kjeldsen; Patrik U. Andersson; Fabian Österdahl; V. A. Bednarska; A. Paal
Dimethyl disulfide (DMDS) and N-methylacetamide are two first choice model systems that represent the disulfide bridge bonding and the peptide bonding in proteins. These molecules are therefore suitable for investigation of the mechanisms involved when proteins fragment under electron capture dissociation (ECD). The dissociative recombination cross sections for both protonated DMDS and protonated N-methylacetamide were determined at electron energies ranging from 0.001 to 0.3 eV. Also, the branching ratios at 0 eV center-of-mass collision energy were determined. The present results give support for the indirect mechanism of ECD, where free hydrogen atoms produced in the initial fragmentation step induce further decomposition. We suggest that both indirect and direct dissociations play a role in ECD.
Nuclear Instruments & Methods in Physics Research Section B-beam Interactions With Materials and Atoms | 1999
J. Lidberg; A. Al-Khalili; L. O. Norlin; P. Royen; Xavier Tordoir; Sven Mannervik
Abstract A laser probing technique for atomic lifetime measurements of metastable states using an ion storage ring is presented. The method benefits from the high spectral resolution of conventional fast ion beam laser spectroscopy, and is applicable to metastable systems in lowly charged ions with lifetimes in the 10 ms–1 s regime. Due to strong probing mechanisms, the technique can be applied to ion beams with low metastable fractions. A comprehensive description of the laser probing technique is given, with examples from recent experiments on singly charged calcium, strontium and xenon, and future prospects are discussed.
The Astrophysical Journal | 2004
Wolf D. Geppert; Fredrik Hellberg; A. Ehlerding; J. Semaniak; Fabian Österdahl; M. Kaminska; V. Zhaunerchyk; A. Al-Khalili; M. af Ugglas; Richard D. Thomas; A. Källberg; Mats Larsson
Branching ratios and absolute cross sections have been measured for the dissociative recombination of (SO2+)-O-18 using the CRYRING ion storage ring. The branching ratio of the (SO2+)-O-18 + e(-)-->(SO)-O-18+O-18 channel amounts to 61%, while the three-body breakup (SO2+)-O-18 + e(-)-->S+2(18)O accounts for the remaining 39% of the total reaction. The cross section of the reaction could be fitted by the expression sigma=(1.2+/-0.4)x10(-15) E-0.96+/-0.02 cm(2), which leads to a thermal reaction rate of k(T)=(4.6+/-0.2)x10(-7)(T/300 K)(-0.52+/-0.02) cm(3) mol(-1) s(-1).