Half or full core hole in density functional theory X-ray absorption spectrum calculations of water?

We analyze the performance of two different core-hole potentials in the theoretical modeling of XAS of ice, liquid and gas phase water; the use of a full core-hole (FCH) in the calculations, as suggested by Hetenyi et al. [B. Hetenyi, F. De Angelis, P. Giamozzi and R. Car, J. Chem. Phys., 2004, 120(18), 8632], gives poor agreement with experiment in terms of intensity distribution as well as transition energies, while the half core hole (HCH) potential, in the case of water, provides a better compromise between initial and final state effects, leading to good agreement with the experimental data.

[1]  Comment on "Energetics of Hydrogen Bond Network Rearrangements in Liquid Water" , 2005, Science.

[2]  H. Ogasawara,et al.  The interpretation of X-ray absorption spectra of water and ice , 2002 .

[3]  A. Becke,et al.  Density-functional exchange-energy approximation with correct asymptotic behavior. , 1988, Physical review. A, General physics.

[4]  Richard J. Saykally,et al.  Energetics of Hydrogen Bond Network Rearrangements in Liquid Water , 2004, Science.

[5]  P. Wernet,et al.  X-ray Raman Spectroscopy at the Oxygen K Edge of Water and Ice: Implications on Local Structure Models , 2002 .

[6]  Mathieu Taillefumier,et al.  X-ray absorption near-edge structure calculations with the pseudopotentials: Application to the K edge in diamond and α-quartz , 2002 .

[7]  Anders Nilsson,et al.  X-ray absorption spectra of water within a plane-wave Car-Parrinello molecular dynamics framework. , 2004, The Journal of chemical physics.

[8]  D. C. Edwards,et al.  Direct evidence of orbital mixing between water and solvated transition-metal ions: An oxygen 1s XAS and DFT study of aqueous systems , 2003 .

[9]  J. C. Slater Statistical Exchange-Correlation in the Self-Consistent Field , 1972 .

[10]  L. Pettersson,et al.  Functional dependence of core-excitation energies. , 2004, The Journal of chemical physics.

[11]  N. Mårtensson,et al.  Initial and final state rules in X-ray spectroscopies of adsorbates , 1995 .

[12]  L. Pettersson,et al.  Effective core potential parameters for first‐ and second‐row atoms , 1987 .

[13]  P. Feulner,et al.  Photon stimulated desorption of neutral hydrogen atoms from condensed water and ammonia by resonant O1s and N1s excitation: search for the signature of ultrafast bond breaking , 2000 .

[14]  P. Wernet,et al.  The Structure of the First Coordination Shell in Liquid Water , 2004, Science.

[15]  P. Wernet,et al.  Surface structure of thin ice films , 2004 .

[16]  H. Ågren,et al.  Separate state vs. transition state Kohn-Sham calculations of X-ray photoelectron binding energies and chemical shifts , 1999 .

[17]  Eric L. Shirley,et al.  AB INITIO INCLUSION OF ELECTRON-HOLE ATTRACTION : APPLICATION TO X-RAY ABSORPTION AND RESONANT INELASTIC X-RAY SCATTERING , 1998 .

[18]  H. Ågren,et al.  Detailed study of pyridine at the C 1s and N 1s ionization thresholds: The influence of the vibrational fine structure , 2001 .

[19]  Car,et al.  Unified approach for molecular dynamics and density-functional theory. , 1985, Physical review letters.

[20]  Hans Ågren,et al.  Calculations of near-edge x-ray-absorption spectra of gas-phase and chemisorbed molecules by means of density-functional and transition-potential theory , 1998 .

[21]  C. C. Chen,et al.  Ordering of hydrogen bonds in high-pressure low-temperature H2O. , 2005, Physical review letters.

[22]  J. Perdew,et al.  Erratum: Density-functional approximation for the correlation energy of the inhomogeneous electron gas , 1986, Physical review. B, Condensed matter.

[23]  J. C. Slater,et al.  Self-Consistent-Field X α Cluster Method for Polyatomic Molecules and Solids , 1972 .

[24]  U. V. Barth,et al.  Dynamical effects in X-ray spectra and the final-state rule , 1982 .

[25]  Roberto Car,et al.  Calculation of near-edge x-ray-absorption fine structure at finite temperatures: spectral signatures of hydrogen bond breaking in liquid water. , 2004, The Journal of chemical physics.