TY - GEN
A1 - Wirth, Jonas
A1 - Kirsch, Harald
A1 - Wlosczyk, Sebastian
A1 - Tong, Yujin
A1 - Saalfrank, Peter
A1 - Kramer Campen, Richard
T1 - Characterization of water dissociation on α-Al2O3(1102)
BT - theory and experiment
N2 - The interaction of water with α-alumina (i.e. α-Al2O3) surfaces is important in a variety of applications and a useful model for the interaction of water with environmentally abundant aluminosilicate phases. Despite its significance, studies of water interaction with α-Al2O3 surfaces other than the (0001) are extremely limited. Here we characterize the interaction of water (D2O) with a well defined α-Al2O3(1[1 with combining macron]02) surface in UHV both experimentally, using temperature programmed desorption and surface-specific vibrational spectroscopy, and theoretically, using periodic-slab density functional theory calculations. This combined approach makes it possible to demonstrate that water adsorption occurs only at a single well defined surface site (the so-called 1–4 configuration) and that at this site the barrier between the molecularly and dissociatively adsorbed forms is very low: 0.06 eV. A subset of OD stretch vibrations are parallel to this dissociation coordinate, and thus would be expected to be shifted to low frequencies relative to an uncoupled harmonic oscillator. To quantify this effect we solve the vibrational Schrödinger equation along the dissociation coordinate and find fundamental frequencies red-shifted by more than 1500 cm−1. Within the context of this model, at moderate temperatures, we further find that some fraction of surface deuterons are likely delocalized: dissociatively and molecularly absorbed states are no longer distinguishable.
T3 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 320
Y1 - 2016
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-394497
SP - 14822
EP - 14832
ER -
TY - GEN
A1 - Ehlert, Christopher
A1 - Holzweber, Markus
A1 - Lippitz, Andreas
A1 - Unger, Wolfgang E. S.
A1 - Saalfrank, Peter
T1 - A detailed assignment of NEXAFS resonances of imidazolium based ionic liquids
N2 - In Near Edge X-Ray Absorption Fine Structure (NEXAFS) spectroscopy X-Ray photons are used to excite tightly bound core electrons to low-lying unoccupied orbitals of the system. This technique offers insight into the electronic structure of the system as well as useful structural information. In this work, we apply NEXAFS to two kinds of imidazolium based ionic liquids ([CnC1im]+[NTf2]- and [C4C1im]+[I]-). A combination of measurements and quantum chemical calculations of C K and N K NEXAFS resonances is presented. The simulations, based on the transition potential density functional theory method (TP-DFT), reproduce all characteristic features observed by the experiment. Furthermore, a detailed assignment of resonance features to excitation centers (carbon or nitrogen atoms) leads to a consistent interpretation of the spectra.
T3 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 315
KW - ray absorption-spectroscopy
KW - fine-structure
KW - spectra
KW - simulations
KW - molecules
KW - dynamics
KW - graphene
KW - surface
KW - salts
Y1 - 2016
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-394417
SP - 8654
EP - 8661
ER -