| 1. |
- Zhaunerchyk, Vitali, et al.
(författare)
-
Using covariance mapping to investigate the dynamics of multi-photon ionization processes of Ne atoms exposed to X-FEL pulses
- 2013
-
Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 46:16, s. 164034-
-
Tidskriftsartikel (refereegranskat)abstract
- We report on a detailed investigation into the electron emission processes of Ne atoms exposed to intense femtosecond x-ray pulses, provided by the Linac Coherent Light Source Free Electron Laser (FEL) at Stanford. The covariance mapping technique is applied to analyse the data, and the capability of this approach to disentangle both linear and nonlinear correlation features which may be hidden on coincidence maps of the same data set is demonstrated. Different correction techniques which enable improvements on the quality of the spectral features extracted from the covariance maps are explored. Finally, a method for deriving characteristics of the x-ray FEL pulses based on covariance mapping in combination with model simulations is presented.
|
|
| 2. |
- Hamberg, Mathias, et al.
(författare)
-
Experimental Studies of (HCO+)-C-13 Recombining with Electrons at Energies between 2-50 000 meV
- 2014
-
Ingår i: Journal of Physical Chemistry A. - : American Chemical Society (ACS). - 1089-5639 .- 1520-5215. ; 118:31, s. 6034-6049
-
Tidskriftsartikel (refereegranskat)abstract
- An investigation into the dissociative recombination process for (HCO+)-C-13 using merged ion-electron beam methods has been performed at the heavy ion storage ring CRYRING, Stockholm, Sweden. We have measured the branching fractions of the different product channels at similar to 0 eV collision energy to be the following: CO + H 87 +/- 2%, OH + C 9 +/- 2%, and O + CH 4 +/- 2%. The formation of electronically excited CO in the dominant reaction channel has also been studied, and we report the following tentative branching fractions for the different CO product electronic states: CO(X (1)Sigma(+)) + H, 54 +/- 10%; CO(a (3)Pi) + H, 23 +/- 4%; and CO(a' (3)Sigma(+)) + H, 23 +/- 4%. The absolute cross section between similar to 2-50 000 meV was measured and showed resonance structures between 3 and 15 eV. The cross section was fitted in the energy range relevant to astrophysics, i.e., between 1 and 300 meV, and was found to follow the expression sigma = 1.3 +/- 0.3 X 10(-16) E-1.29 +/- 0.05 cm(2) and the corresponding thermal rate constant was determined to be k(T) = 2.0 +/- 0.4 X 10(-7)(T/300)(-0.79 +/- 0.05) cm(3) s(-1). Radioastronomical observations with the IRAM 30 m telescope of HCO+ toward the Red Rectangle yielded an upper column density limit of 4 X 10(11) cm(-2) of HCO+ at the 1 sigma level in that object, indicating that previous claims that the dissociative recombination of HCO+ plays an important role in the production of excited CO molecules emitting the observed Cameron bands in that object are not supported.
|
|
| 3. |
- Hamberg, Mathias, et al.
(författare)
-
Experimental studies of the dissociative recombination processes for the dimethyl ether ions CD3OCD2+ and (CD3)2OD
- 2010
-
Ingår i: Astronomy and Astrophysics. - : EDP Sciences. - 0004-6361 .- 1432-0746. ; 514, s. A83-
-
Tidskriftsartikel (refereegranskat)abstract
- Aims: Determination of branching fractions, cross sections and thermal rate coefficients for the dissociative recombination of CD3OCD2+ (0-0.3 eV) and (CD3)2OD+ (0-0.2 eV) at the low relative kinetic energies encountered in the interstellar medium. Methods: The measurements were carried out using merged electron and ion beams at the CRYRING storage ring, Stockholm, Sweden. Results: For (CD3)2OD+ we have experimentally determined the branching fraction for ejection of a single hydrogen atom in the DR process to be maximally 7% whereas 49% of the reactions involve the break up of the COC chain into two heavy fragments and 44% ruptures both C-O bonds. The DR of CD3OCD2+ is dominated by fragmentation of the COC chain into two heavy fragments. The measured thermal rate constants and cross sections are k(T) =1.7 ± 0.5 × 10−6(T/300)−0.77±0.01 cm3s−1, σ= 1.2 ± 0.4 × 10−15(Ecm[eV])−1.27 ± 0.01 cm2 and k(T) = 1.7 ± 0.6 × 10−6(T/300)−0.70±0.02 cm3s−1,σ= 1.7 ± 0.6 × 10−15(Ecm[eV])−1.20±0.02 cm2 for CD3OCD2+ and (CD3)2OD+, respectively.
|
|
| 4. |
- Vigren, Erik, et al.
(författare)
-
Dissociative Recombination of Protonated Formic Acid : Implications for Molecular Cloud and Cometary Chemistry
- 2010
-
Ingår i: Astrophysical Journal. - 0004-637X .- 1538-4357. ; 709:2, s. 1429-1434
-
Tidskriftsartikel (refereegranskat)abstract
- At the heavy ion storage ring CRYRING in Stockholm, Sweden, we have investigated the dissociative recombination of DCOOD2+ at low relative kinetic energies, from similar to 1 meV to 1 eV. The thermal rate coefficient has been found to follow the expression k(T) = 8.43 x 10(-7) (T/300)(-0.78) cm(3) s(-1) for electron temperatures, T, ranging from similar to 10 to similar to 1000 K. The branching fractions of the reaction have been studied at similar to 2 meV relative kinetic energy. It has been found that similar to 87% of the reactions involve breaking a bond between heavy atoms. In only 13% of the reactions do the heavy atoms remain in the same product fragment. This puts limits on the gas-phase production of formic acid, observed in both molecular clouds and cometary comae. Using the experimental results in chemical models of the dark cloud, TMC-1, and using the latest release of the UMIST Database for Astrochemistry improves the agreement with observations for the abundance of formic acid. Our results also strengthen the assumption that formic acid is a component of cometary ices.
|
|
| 5. |
- Vigren, Erik, et al.
(författare)
-
Dissociative Recombination of Protonated Propionitrile, CH3CH2CNH+ : Implications for Titan's Upper Atmosphere
- 2010
-
Ingår i: Astrophysical Journal. - 0004-637X .- 1538-4357. ; 722:1, s. 847-850
-
Tidskriftsartikel (refereegranskat)abstract
- The dissociative recombination of protonated propionitrile, CH3CH2CNH+, has been investigated at the heavy ion storage ring, CRYRING, at the Manne Siegbahn Laboratory, Stockholm University, Sweden. The thermal rate coefficient has been deduced to follow k(T) = (1.5 ± 0.2) × 10–6 (T/300)–0.76 ± 0.02 cm3 s–1 for electron temperatures ranging from ~10 to ~1000 K. Measurements of the branching fractions were performed at ~0 eV relative kinetic energy. It has been found that in 43% ± 2% of the reactions the four heavy atoms remain in the same product fragment. An equal portion of the reactions leads to products where one of the heavy atoms is split off from the other three and 14% ± 1% result in a breakup into two heavy fragments containing two heavy atoms each. We discuss the significance of the data to Titan's upper atmosphere.
|
|
| 6. |
- Vigren, Erik, et al.
(författare)
-
Dissociative recombination of the acetaldehyde cation, CH3CHO
- 2010
-
Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 12:37, s. 11670-11673
-
Tidskriftsartikel (refereegranskat)abstract
- The dissociative recombination of the acetaldehyde cation, CH3CHO+, has been investigated at the heavy ion storage ring CRYRING at the Manne Siegbahn Laboratory in Stockholm, Sweden. The dependence of the absolute cross section of the reaction on the relative kinetic energy has been determined and a thermal rate coefficient of k(T) = (1.5 +/- 0.2) x 10(-6) (T/300)(-0.70 +/- 0.02) cm(3) s(-1) has been deduced, which is valid for electron temperatures between similar to 10 and 1000 K. The branching fractions of the reaction were studied at similar to 0 eV relative kinetic energy and we found that breaking one of the bonds between two of the heavy atoms occurs in 72 +/- 2% of the reactions. In the remaining events the three heavy atoms stay in the same product fragment. While the branching fractions are fairly similar to the results from an earlier investigation into the dissociative recombination of the fully deuterated acetaldehyde cation, CD3CDO+, the thermal rate coefficient is somewhat larger for CH3CHO+. Astrochemical implications of the results are discussed.
|
|
| 7. |
- Salén, Peter, et al.
(författare)
-
Selectivity in fragmentation of N-methylacetamide after resonant K-shell excitation
- 2014
-
Ingår i: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry (RSC). - 1463-9076 .- 1463-9084. ; 16:29, s. 15231-15240
-
Tidskriftsartikel (refereegranskat)abstract
- The fragmentation pattern of the peptide model system, N-methylacetamide, is investigated using ion time-of-flight (TOF) spectroscopy after resonant K-shell excitation. Corresponding near-edge X-ray absorption fine structure (NEXAFS) spectra recorded at high resolution at the C1s, N1s and O1s edges are presented. Analysis of the ion TOF data reveals a multitude of fragmentation channels and dissociation pathways. Comparison between the excitation of six different resonances in the vicinity of the C1s, N1s and O1s edges suggests evidence for site-selective bond breaking. In particular the breaking of the peptide bond and the N-C-alpha bond show a clear correlation with resonant excitation at the N1s edge. Also, stronger tendencies towards site-selective bond breaking are found for the generation of single ions compared with ion pairs. Analysis of angular distributions of ions from breakage of the peptide bond yields a fragmentation time of <400 fs.
|
|
| 8. |
- Vigren, Erik, et al.
(författare)
-
Reassessment of the dissociative recombination of n2h+ at cryring
- 2012
-
Ingår i: Astrophysical Journal. - 0004-637X .- 1538-4357. ; 757:1, s. 34-
-
Tidskriftsartikel (refereegranskat)abstract
- The dissociative recombination (DR) of N2H+ has been reinvestigated at the heavy ion storage ring CRYRING at the Manne Siegbahn Laboratory in Stockholm, Sweden. Thermal rate coefficients for electron temperatures between 10 and 1000 K have been deduced. We show that electron recombination is expected to play an approximately equally important role as CO in the removal of N2H+ in dark interstellar clouds. We note that a deeper knowledge on the influence of the ions' rotational temperature in the DR of N2H+ would be helpful to set further constraints on the relative importance of the different destruction mechanisms for N2H+ in these environments. The branching fractions in the DR of N2H+ have been reinvestigated at similar to 0 eV relative kinetic energy, showing a strong dominance of the N-2 + H production channel (93(-2)(+4)%) with the rest leading to NH + N. These results are in good agreement with flowing afterglow experiments and in disagreement with an earlier measurement at CRYRING.
|
|
