TY - JOUR A1 - Tetenoire, Auguste A1 - Ehlert, Christopher A1 - Juaristi, Joseba Iñaki A1 - Saalfrank, Peter A1 - Alducin, Maite T1 - Why ultrafast photoinduced CO desorption dominates over oxidation on Ru(0001) JF - The journal of physical chemistry letters N2 - CO oxidation on Ru(0001) is a long-standing example of a reaction that, being thermally forbidden in ultrahigh vacuum, can be activated by femtosecond laser pulses. In spite of its relevance, the precise dynamics of the photoinduced oxidation process as well as the reasons behind the dominant role of the competing CO photodesorption remain unclear. Here we use ab initio molecular dynamics with electronic friction that account for the highly excited and nonequilibrated system created by the laser to investigate both reactions. Our simulations successfully reproduce the main experimental findings: the existence of photoinduced oxidation and desorption, the large desorption to oxidation branching ratio, and the changes in the O K-edge X-ray absorption spectra attributed to the initial stage of the oxidation process. Now, we are able to monitor in detail the ultrafast CO desorption and CO oxidation occurring in the highly excited system and to disentangle what causes the unexpected inertness to the otherwise energetically favored oxidation. Y1 - 2022 U6 - https://doi.org/10.1021/acs.jpclett.2c02327 SN - 1948-7185 VL - 13 IS - 36 SP - 8516 EP - 8521 PB - American Chemical Society CY - Washington, DC ER - TY - JOUR A1 - Scholz, Robert A1 - Lindner, Steven A1 - Loncaric, Ivor A1 - Tremblay, Jean Christophe A1 - Juaristi, J. A1 - Alducin, Maite A1 - Saalfrank, Peter T1 - Vibrational response and motion of carbon monoxide on Cu(100) driven by femtosecond laser pulses: Molecular dynamics with electronic friction JF - Physical review : B, Condensed matter and materials physics N2 - Carbon monoxide on copper surfaces continues to be a fascinating, rich microlab for many questions evolving in surface science. Recently, hot-electron mediated, femtosecond-laser pulse induced dynamics of CO molecules on Cu(100) were the focus of experiments [Inoue et al., Phys. Rev. Lett. 117, 186101 (2016)] and theory [Novko et al., Phys. Rev. Lett. 122, 016806 (2019)], unraveling details of the vibrational nonequilibrium dynamics on ultrashort (subpicoseconds) timescales. In the present work, full-dimensional time-resolved hot-electron driven dynamics are studied by molecular dynamics with electronic friction (MDEF). Dissipation is included by a friction term in a Langevin equation which describes the coupling of molecular degrees of freedom to electron-hole pairs in the copper surface, calculated from gradient-corrected density functional theory (DFT) via a local density friction approximation (LDFA). Relaxation due to surface phonons is included by a generalized Langevin oscillator model. The hot-electron induced excitation is described via a time-dependent electronic temperature, the latter derived from an improved two-temperature model. Our parameter-free simulations on a precomputed potential energy surface allow for excellent statistics, and the observed trends are confirmed by on-the-fly ab initio molecular dynamics with electronic friction (AIMDEF) calculations. By computing time-resolved frequency maps for selected molecular vibrations, instantaneous frequencies, probability distributions, and correlation functions, we gain microscopic insight into hot-electron driven dynamics and we can relate the time evolution of vibrational internal CO stretch-mode frequencies to measured data, notably an observed redshift. Quantitatively, the latter is found to be larger in MDEF than in experiment and possible reasons are discussed for this observation. In our model, in addition we observe the excitation and time evolution of large-amplitude low-frequency modes, lateral CO surface diffusion, and molecular desorption. Effects of surface atom motion and of the laser fluence are also discussed. Y1 - 2019 U6 - https://doi.org/10.1103/PhysRevB.100.245431 SN - 2469-9950 SN - 2469-9969 VL - 100 IS - 24 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Juaristi, J. I. A1 - Alducin, Maite A1 - Saalfrank, Peter T1 - Femtosecond laser induced desorption of H-2, D-2, and HD from Ru(0001) BT - dynamical promotion and suppression studied with ab initio molecular dynamics with electronic friction JF - Physical review : B, Condensed matter and materials physics N2 - We perform ab initio molecular dynamics simulations to study the femtosecond laser induced desorption of H-2, D-2, and HD from a H: D-saturated Ru(0001) surface. To this aim we have extended the ab initio molecular dynamics with electronic friction (AIMDEF) scheme to include a random force that is a function of a timedependent electronic temperature. The latter characterizes the action of the ultrashort laser pulse according to a two temperature model. This allows us to perform multidimensional, hot-electron driven reaction dynamics and investigate the dependence of the desorption yields on the relative H: D isotope concentration on the surface. Our AIMDEF simulations show that the desorption process takes place in the presence of a heated adsorbate system that clearly influences the desorption dynamics. The heating of the adsorbate system is more (less) pronounced the larger is the concentration of the lighter (heavier) isotope. As a result, we conclude that the presence of H on the surface favors the desorption of molecules, whereas the presence of D hampers it, in agreement with previous experimental observations in which the phenomenon of "dynamical promotion" of a surface reaction had been postulated. Y1 - 2017 U6 - https://doi.org/10.1103/PhysRevB.95.125439 SN - 2469-9950 SN - 2469-9969 VL - 95 IS - 12 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Loncaric, Ivor A1 - Alducin, Maite A1 - Saalfrank, Peter A1 - Inaki Juaristi, J. T1 - Femtosecond laser pulse induced desorption: A molecular dynamics simulation JF - Nature climate change N2 - In recent simulations of femtosecond laser induced desorption of molecular oxygen from the Ag(110) surface, it has been shown that depending on the properties (depth and electronic environment) of the well in which 02 is adsorbed, the desorption can be either induced dominantly by hot electrons or via excitations of phonons. In this work we explore whether the ratios between the desorption yields from different adsorption wells can be tuned by changing initial surface temperature and laser pulse properties. We show that the initial surface temperature is an important parameter, and that by using low initial surface temperatures the electronically mediated process can be favored. In contrast, laser properties seem to have only a modest influence on the results. (C) 2016 Elsevier B.V. All rights reserved. KW - Laser induced desorption KW - Molecular dynamics with friction KW - Local density friction approximation KW - Generalized Langevin oscillator model Y1 - 2016 U6 - https://doi.org/10.1016/j.nimb.2016.02.051 SN - 0168-583X SN - 1872-9584 VL - 382 SP - 114 EP - 118 PB - Elsevier CY - Amsterdam ER - TY - JOUR A1 - Loncaric, Ivor A1 - Alducin, Maite A1 - Saalfrank, Peter A1 - Juaristi, J. I. T1 - Femtosecond-laser-driven molecular dynamics on surfaces: Photodesorption of molecular oxygen from Ag(110) JF - Physical review : B, Condensed matter and materials physics N2 - We simulate the femtosecond-laser-induced desorption dynamics of a diatomic molecule from a metal surface by including the effect of the electron and phonon excitations created by the laser pulse. Following previous models, the laser-induced surface excitation is treated through the two temperature model, while the multidimensional dynamics of the molecule is described by a classical Langevin equation, in which the friction and random forces account for the action of the heated electrons. In this work we propose the additional use of the generalized Langevin oscillator model to also include the effect of the energy exchange between the molecule and the heated surface lattice in the desorption dynamics. The model is applied to study the laser-induced desorption of O-2 from the Ag(110) surface, making use of a six-dimensional potential energy surface calculated within density functional theory. Our results reveal the importance of the phonon mediated process and show that, depending on the value of the electronic density in the surroundings of the molecule adsorption site, its inclusion can significantly enhance or reduce the desorption probabilities. Y1 - 2016 U6 - https://doi.org/10.1103/PhysRevB.93.014301 SN - 1098-0121 SN - 1550-235X VL - 93 PB - American Physical Society CY - College Park ER - TY - JOUR A1 - Saalfrank, Peter A1 - Juaristi, J. I. A1 - Alducin, Maite A1 - Blanco-Rey, Maria A1 - Muino, R. Diez T1 - Vibrational lifetimes of hydrogen on lead films : an ab initio molecular dynamics with electronic friction (AIMDEF) study JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr N2 - Using density functional theory and Ab Initio Molecular Dynamics with Electronic Friction (AIMDEF), we study the adsorption and dissipative vibrational dynamics of hydrogen atoms chemisorbed on free-standing lead films of increasing thickness. Lead films are known for their oscillatory behaviour of certain properties with increasing thickness, e.g., energy and electron spill-out change in discontinuous manner, due to quantum size effects [G. Materzanini, P. Saalfrank, and P.J.D. Lindan, Phys. Rev. B 63, 235405 (2001)]. Here, we demonstrate that oscillatory features arise also for hydrogen when chemisorbed on lead films. Besides stationary properties of the adsorbate, we concentrate on finite vibrational lifetimes of H-surface vibrations. As shown by AIMDEF, the damping via vibration-electron hole pair coupling dominates clearly over the vibration-phonon channel, in particular for high-frequency modes. Vibrational relaxation times are a characteristic function of layer thickness due to the oscillating behaviour of the embedding surface electronic density. Implications derived from AIMDEF for frictional many-atom dynamics, and physisorbed species will also be given. (C) 2014 AIP Publishing LLC. Y1 - 2014 U6 - https://doi.org/10.1063/1.4903309 SN - 0021-9606 SN - 1089-7690 VL - 141 IS - 23 PB - American Institute of Physics CY - Melville ER -