Pump-probe Mass Spectrometry Research Articles

Nonadiabatic Photodissociation and Dehydrogenation Dynamics of n-Butyl Bromide Following p-Rydberg Excitation.

Femtosecond time-resolved mass spectrometry, correlation mapping, and density functional theory calculations are employed to reveal the mechanism of C═C and C≡C formation (and related H2 production) following excitation to the p-Rydberg states of n-butyl bromide. Ultrafast pump-probe mass spectrometry shows that nonadiabatic relaxation operates as a multistep process reaching an intermediate state within ∼500 fs followed by relaxation to a final state within 10 ps of photoexcitation. Absorption of three ultraviolet photons accesses the dense p-Rydberg state manifold, which is further excited by the probe beam for C─C bond dissociation and dehydrogenation reactions. Rapid internal conversion deactivates the dehydrogenation pathways, while activating carbon backbone dissociation pathways. Thus, unsaturated carbon fragments decay with the lifetime of p-Rydberg (∼500 fs), matching the growth recorded in saturated hydrocarbon fragments. The saturated hydrocarbon signals subsequently decay on the picosecond time scale as the molecule relaxes below the Rydberg states and into halogen release channels.

Tuning the ultrafast photodissociation dynamics of CH3Br on ultrathin MgO films by reducing the layer thickness to the 2D limit

The femtosecond-laser induced photodissociation of CH3Br adsorbed at sub-monolayer coverage on a solid surface was investigated by time-resolved pump-probe mass spectrometry. To tune the interaction of the CH3Br molecules with the substrate, an Mo(100) surface was covered with ultrathin insulating MgO layers of variable thickness. By gradually decreasing the magnesia layer thickness to the 2D limit the photodissociation dynamics observed by detection of the methyl fragment indicates an energetic lowering of the relevant methyl bromide excited states due to the increasing spatial proximity of the metallic support. Potential orientational effects of the methyl bromide adsorption geometry are also considered.

Dynamics of solvation and desolvation of rubidium attached to He nanodroplets.

The real-time dynamics of photoexcited and photoionized rubidium (Rb) atoms attached to helium (He) nanodroplets is studied by femtosecond pump-probe mass spectrometry. While excited Rb atoms in the perturbed 6p-state (Rb*) desorb off the He droplets, Rb(+) photoions tend to sink into the droplet interior when created near the droplet surface. The transition from Rb(+) solvation to full Rb* desorption is found to occur at a delay time τ ∼ 600 fs for Rb* in the 6pΣ-state and τ ∼ 1200 fs for the 6pΠ-state. Rb(+)He ions are found to be created by directly exciting bound Rb*He exciplex states as well as by populating bound Rb(+)He-states in a photoassociative ionization process.

ChemInform Abstract: Ultrathin Magnesia Films as Support for Molecules and Metal Clusters: Tuning Reactivity by Thickness and Composition

AbstractReview: 107 refs.

Femtosecond‐laser photoemission and photodesorption from magnesia supported gold clusters

AbstractNanosize gold clusters were grown by thermal evaporation on ultrathin magnesia films on Mo(100) and investigated by femtosecond (fs)‐laser photoemission spectroscopy. The surface work function in this system was found to increase with increasing nominal gold coverage. Methyl bromide (CH3Br) molecules adsorb molecularly on the magnesia surface as well as on the gold clusters. At sub‐monolayer coverage the CH3Br molecules were, however, considerably stronger bound to the gold particles than to the magnesia surface as revealed by temperature programmed desorption spectroscopy. To investigate the photoreaction dynamics of the adsorbate molecules fs‐laser pump–probe mass spectrometry was applied. In this new approach the methyl fragment appearance was monitored after photoexcitation of the adsorbed CH3Br with fs time resolution. The transient methyl data revealed that the CH3Br dissociation and subsequent methyl desorption proceeded in less than one picosecond. Most interestingly, a part of the transient signal could be unambiguously assigned to the dynamics of methyl desorption from the gold clusters. The appearance of this signal at about 270 fs after photoexcitation illustrates the massive distortion of the CH3Br electronic level structure due to the strong interaction with the gold clusters compared to the bare magnesia surface. magnified image

Ultrathin magnesia films as support for molecules and metal clusters: Tuning reactivity by thickness and composition

AbstractUltrathin metal oxide films have attracted considerable interest in recent years as versatile substrate for the design of nanocatalytic model systems. In particular, it has been proposed theoretically and confirmed experimentally that the electronic structure of adsorbates can be influenced by the layer thickness and the stoichiometry, i.e., the type and number of defects, of the oxide film. This has important consequences on the chemical reactivity of the oxide surface itself and of oxide supported metal clusters. It also opens new possibilities to influence and to control chemical reactions occurring at the surface of these systems. The present feature focuses on very recent experiments that illustrate the effects of a proper adjustment of layer thickness and composition of ultrathin MgO(100) films on chemical transformations. On the magnesia surface itself, the photodissociation dynamics of methyl iodide molecules is investigated via femtosecond‐laser pump–probe mass spectrometry. Furthermore, the catalytic oxidation of carbon monoxide at mass‐selected Au20 clusters deposited on magnesia is explored through temperature programmed reaction measurements. In the latter case, detailed first principles calculations are able to correlate the experimentally observed reactivity with structural dimensionality changes that are induced by the changing thickness and composition of the magnesia support. magnified image

Femtosecond time-resolved photophysics and photodissociation dynamics of 1-iodonaphthalene

The ultrafast relaxation of 1-iodonaphthalene, with particular attention to the dissociation channels, has been studied by time-resolved femtosecond pump-probe mass spectrometry following excitation at 267 and 317 nm. The measured transients for the parent ion and the isobaric fragments, iodine and naphthyl radical, show complex decay profiles with up to four lifetimes in the femto-picosecond time scales. The transients are interpreted as the result of parallel relaxation of the simultaneously excited n sigma* and pi pi* states of the molecule. While the former leads to dissociation in about 400 fs, the latter converts to lower energy pi pi* singlet states at an ultrafast rate (24 fs) followed by intersystem crossing to nearby pi pi* triplet states.

Femtosecond real-time probing of transition state dynamics in a surface photoreaction: Methyl desorption from CH3I on MgO(100)

A novel experimental approach to the investigation of surface adsorbate reaction dynamics is presented. The direct time-resolved monitoring of the surface reaction transition state and product formation dynamics were accomplished via pump-probe mass spectrometry. As an example, methyl iodide molecules adsorbed at submonolayer coverage on an ultrathin magnesia film on Mo(100) were photoexcited to the A-band by ultrafast laser pulse irradiation. Employing time-delayed multiphoton ionization the dynamics of the dissociative methyl iodide transition state and of the emerging methyl photoproduct could be detected with femtosecond resolution. The reaction times deduced from the temporal evolution of the methyl ion mass signal indicate a strong interaction of the methyl fragment with the substrate surface prior to desorption.