OH emission from warm and dense gas in the Orion Bar PDR

As part of a far-infrared (FIR) spectral scan with Herschel/PACS, we present the first detection of the hydroxyl radical (OH) towards the Orion Bar photodissociation region (PDR). Five OH rotational Lambda-doublets involving energy levels out to E_u/k~511 K have been detected (at ~65, ~79, ~84, ~119 and ~163um). The total intensity of the OH lines is I(OH)~5x10^-4 erg s^-1 cm^-2 sr^-1. The observed emission of rotationally excited OH lines is extended and correlates well with the high-J CO and CH^+ J=3-2 line emission (but apparently not with water vapour), pointing towards a common origin. Nonlocal, non-LTE radiative transfer models including excitation by the ambient FIR radiation field suggest that OH arises in a small filling factor component of warm (Tk~160-220 K) and dense (n_H~10^{6-7} cm^-3) gas with source-averaged OH column densities of ~10^15 cm^-2. High density and temperature photochemical models predict such enhanced OH columns at low depths (A_V<1) and small spatial scales (~10^15 cm), where OH formation is driven by gas-phase endothermic reactions of atomic oxygen with molecular hydrogen. We interpret the extended OH emission as coming from unresolved structures exposed to far-ultraviolet (FUV) radiation near the Bar edge (photoevaporating clumps or filaments) and not from the lower density "interclump" medium. Photodissociation leads to OH/H2O abundance ratios (>1) much higher than those expected in equally warm regions without enhanced FUV radiation fields.Comment: Accepted for publication in A&A Letters. Figure B.2. is bitmapped to lower resolutio

Molecular excitation in the Interstellar Medium: recent advances in collisional, radiative and chemical processes

We review the different excitation processes in the interstellar mediumComment: Accepted in Chem. Re

First ultraviolet absorption band of methane: An ab initio study

Contains fulltext : 34782.pdf (publisher's version ) (Open Access)Quantum mechanical calculations of the cross sections for photodissociation of CH4 and CD4 in the 1t(2)-> 3s band are presented. The potential energy surfaces for the three states correlating with the 1 T-1(2) state at tetrahedral geometries are calculated. The elements of the (3x3) matrix representing the electronic Hamiltonian in the diabatic basis are expanded in powers of nuclear coordinates, up to the second order. The expansion coefficients are based on accurate multireference configuration interaction calculations. The electronically nonadiabatic dynamics is treated with the multiconfiguration time-dependent Hartree approach. All nine internal degrees of methane are included in the quantum dynamics simulations. The calculated cross section agrees well with experiment. Semiclassical calculations using the reflection principle suggest that the peaks in the spectrum correspond to the three adiabatic electronic states correlating with the 1 T-1(2) state at T-d geometries. However, the non-Born-Oppenheimer terms in the Hamiltonian have a strong effect on the positions of the peaks in the absorption spectrum. The results of semiclassical calculations, which neglect these terms, are therefore quite different from the accurate quantum results and experiment. (c) 2007 American Institute of Physics

Degeneracy in discrete variable representations: General considerations and application to the multiconfigurational time-dependent Hartree approach

van Harrevelt R, Manthe U. Degeneracy in discrete variable representations: General considerations and application to the multiconfigurational time-dependent Hartree approach. Journal of Chemical Physics. 2004;121(12):5623-5628.Problems appear in discrete variable representations (DVRs) based on general basis sets when the coordinate matrix has degenerate eigenvalues. Then the DVR is not uniquely defined. This paper shows that this problem can be caused by symmetry. Taking the symmetry into account when constructing the DVR solves the problem. The symmetry effect can be particularly important for the time-dependent DVR used in multiconfigurational time-dependent Hartree calculations employing the correlation DVR (CDVR) approach. Problems reported previously for the initial-state selected treatment of the H+H-2 reaction can be attributed to this symmetry effect. They can be solved by using a symmetry-adapted approach to construct the time-dependent DVR. Thus, the present paper shows that the CDVR scheme can be employed also in initial-state selected scattering calculations if the symmetry of the system is properly taken into account in the construction of the time-dependent DVR. (C) 2004 American Institute of Physics

Multidimensional time-dependent discrete variable representations in multiconfiguration Hartree calculations

van Harrevelt R, Manthe U. Multidimensional time-dependent discrete variable representations in multiconfiguration Hartree calculations. JOURNAL OF CHEMICAL PHYSICS. 2005;123(6): 64106.In the multiconfiguration time-dependent Hartree (MCTDH) approach, the wave function is expanded in time-dependent basis functions, called single-particle functions, to increase the efficiency of the wave-packet propagation. The correlation discrete variable representation (CDVR) approach, which is based on a time-dependent discrete variable representation (DVR), can be employed to evaluate matrix elements of the potential energy. The efficiency of the MCTDH method can be further enhanced by using multidimensional single-particle functions. However, up to now the CDVR approach could not be used in MCTDH calculations employing multidimensional single-particle functions, since this would require a general multidimensional non-direct-product DVR scheme. Recently, Dawes and Carrington presented a practical scheme to implement general non-direct-product multidimensional DVRs [R. Dawes and T. Carrington, Jr., J. Chem. Phys. 121, 726 (2004)]. The present work utilizes their scheme in the MCTDH/CDVR approach. The accuracy is tested using the photodissociation of NOCl as example. The results show that the CDVR scheme based on multidimensional time-dependent DVRs allows for an accurate evaluation of the potential in MCTDH calculations with multidimensional single-particle functions. (C) 2005 American Institute of Physics

Off-normal incidence dissociative sticking of H2 on Cu(100) studied using six-dimensional quantum calculations

van Harrevelt R, Manthe U. Off-normal incidence dissociative sticking of H2 on Cu(100) studied using six-dimensional quantum calculations. Journal of Chemical Physics. 2005;123(12): 124706

An accurate analytic representation of the water pair potential

Contains fulltext : 75521.pdf (publisher's version ) (Open Access)16 p

Multiconfigurational time-dependent Hartree calculations for dissociative adsorption of H2 on Cu(100)

van Harrevelt R, Manthe U. Multiconfigurational time-dependent Hartree calculations for dissociative adsorption of H2 on Cu(100). Journal of Chemical Physics. 2004;121(8):3829-3835.The efficiency of the multiconfigurational time-dependent Hartree (MCTDH) method for calculating the initial-state selected dissociation probability of H-2(v=0,j=0) on Cu(100) is investigated. The MCTDH method is shown to be significantly more efficient than standard wave packet methods. A large number of single-particle functions is required to converge the initial-state selected reaction probability for dissociative adsorption. Employing multidimensional coordinates in the MCTDH ansatz (mode combination) is found to be crucial for the efficiency of these MCTDH calculations. Perspectives towards the application of the MCTDH approach to study dissociative adsorption of polyatomic molecules on surfaces are discussed. (C) 2004 American Institute of Physics

Single rotational product propensity in the photodissociation of HOD

Theoretical Chemistr