Biomedical subjects

A C Luntz

Publications and source records attributed to A C Luntz.

7 recordsLinked to original sources

PubMed2006

High translational energy release in H2 (D2) associative desorption from H (D) chemisorbed on C(0001).

Highly energetic translational energy distributions are reported for hydrogen and deuterium molecules desorbing associatively from the atomic chemisorption states on highly oriented pyrolytic graphite (HOPG). Laser assisted associative desorption is used to measure the time of flight of molecules desorbing from a hydrogen (deuterium) saturated HOPG surface produced by atomic exposure from a thermal atom source at around 2100 K. The translational energy distributions normal to the surface are very broad, from approximately 0.5 to approximately 3 eV, with a peak at approximately 1.3 eV. The highest translational energy measured is close to the theoretically predicted barrier height. The angular distribution of the desorbing molecules is sharply peaked along the surface normal and is consistent with thermal broadening contributing to energy release parallel to the surface. All results are in qualitative agreement with recent density functional theory calculations suggesting a lowest energy para-type dimer recombination path.

Journal Article↗

PubMed2006

Femtosecond laser induced associative desorption of H2 from Ru(0001): comparison of "first principles" theory with experiment.

A three dimensional model based on molecular dynamics with electronic frictions is developed to describe the femtosecond laser induced associative desorption of H2 from Ru(0001)(1 x 1)H. Two molecular coordinates (internuclear separation d and center of mass distance to surface z) and a single phonon coordinate are included in the dynamics. Both the potential energy surface and the electronic friction tensor are calculated by density functional theory so that there are no adjustable parameters in the comparison of this model with the wide range of experiments available for this system. This "first principles" dynamic model gives results in semiquantitative agreement with all experimental results; nonlinear fluence dependence of the yield, isotope effect, two pulse correlation, and energy partitioning. The good agreement of theory with experiment supports a description of this surface femtochemistry in terms of thermalized hot electron induced chemistry with coupling to nuclear coordinates through electronic frictions. By comparing the dynamics with the analytical one dimensional frictional model used previously to fit the experiments for this system, we show that the success of the one dimensional model is based on the rapid intermixing of the z and d coordinates as the H-H climbs out of the adsorption well. However, projecting the three dimensional dynamics onto one dimension introduces a fluence (adsorbate temperature) dependent "entropic" barrier in addition to the potential barrier for the chemistry. This implies that some caution must be used in interpreting activation energies obtained in fitting experiments to the one dimensional model.

Journal Article↗

PubMed2006

Theoretical evidence for nonadiabatic vibrational deexcitation in H2(D2) state-to-state scattering from Cu(100).

Dynamical calculations are presented for electronically nonadiabatic vibrational deexcitation of H2 and D2 in scattering from Cu(111). Both the potential energy surface and the nonadiabatic coupling strength were obtained from density functional calculations. The theoretically predicted magnitude of the deexcitation and its dependence on incident energy and isotope are all in agreement with state-to-state scattering experiments [on Cu(100)], and this gives indirect evidence for a nonadiabatic mechanism of the observed deexcitation. Direct evidence could be obtained by measuring the chemicurrent associated with the deexcitation, and its properties have been predicted.

Journal Article↗

PubMed2005

How adiabatic is activated adsorption/associative desorption?

Using density-functional theory we calculate friction coefficients describing the damping of nuclear motion into electron-hole pair excitation for the two best-known examples of activated adsorption: H2 dissociation on a Cu(111) surface and N2 dissociation on a Ru(0001) surface. In both cases, the frictions increase dramatically along the reaction path towards the transition state and can be an order of magnitude larger there than typical in the molecularly adsorbed state. In addition, the frictions for N2/Ru(0001) are typically an order of magnitude larger than for H2/Cu(111). We rationalize these trends in terms of the electron structure as the systems proceed to dissociation along the reaction paths. Combining these friction coefficients with the potential-energy surface in quasiclassical dynamics allows first-principles studies of the importance of the breakdown in the Born-Oppenheimer approximation in describing the chemistry. We find that nonadiabatic effects are minimal for the H2/Cu(111) system, but are quite important for N2/Ru(0001).

Journal Article↗

PubMed2005

Influence of surface morphology on D2 desorption kinetics from amorphous solid water.

The influence of surface morphology/porosity on the desorption kinetics of weakly bound species was investigated by depositing D2 on amorphous solid water (ASW) films grown by low temperature vapor deposition under various conditions and with differing thermal histories. A broad distribution of binding energies of the D2 monolayer on nonporous and porous ASW was measured experimentally and correlated by theoretical calculations to differences in the degree of coordination of the adsorbed H2 (D2) to H2O molecules in the ASW depending on the nature of the adsorption site, i.e., surface valleys vs surface peaks in a nanoscale rough film surface. For porous films, the effect of porosity on the desorption kinetics was observed to be a reduction in the desorption rate with film thickness and a change in peak shape. This can be partly explained by fast diffusion into the ASW pore structure via a simple one-dimensional diffusion model and by a change in binding energy statistics with increasing total effective surface area. Furthermore, the D2 desorption kinetics on thermally annealed ASW films were investigated. The main effect was seen to be a reduction in porosity and in the number of highly coordinated binding sites with anneal temperature due to ASW restructuring and pore collapse. These results contribute to the understanding of desorption from porous materials and to the development of correct models for desorption from and catalytic processes on dust grain surfaces in the interstellar medium.

Journal Article↗

PubMed2003

Importance of surface morphology in interstellar H2 formation.

Detailed laboratory experiments on the formation of HD from atom recombination on amorphous solid water films show that this process is extremely efficient in a temperature range of 8 to 20 kelvin, temperatures relevant for H2 formation on dust grain surfaces in the interstellar medium (ISM). The fate of the 4.5 electron volt recombination energy is highly dependent on film morphology. These results suggest that grain morphology, rather than the detailed chemical nature of the grain surface, is most important in determining the energy content of the H2 as it is released from the grain into the ISM.

Astronomical Phenomena↗

PubMed2003

Chemistry. Toward vibrational mode control in catalysis.

Vibrational excitations of specific bonds in molecules have been used to enhance the reactivity of the molecules in direct gas-phase reactions. In his Perspective, Luntz highlights a report by Beck et al., who show that such vibrational control may also be possible for catalytic reactions at a surface. The authors demonstrate that differently excited deuterated methane molecules have different dissociation probabilities on a nickel surface, even though the energies of the different molecules are similar.

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