Picosecond pump–probe and polarization techniques in supersonic molecular beams: Measurement of ultrafast vibrational-rotational dephasing and coherence

In the last few years, the time-resolved dynamics of collisionless intramolecular vibrational-energy redistribution (IVR) [1] has been probed [2] using picosecond excitation and fluorescence detection. By this method new information on IVR, coherence and photochemical changes (e.g., trans-cis isomerization) has been obtained. [2,3] However, in a number of cases the (early time) primary step following picosecond excitation could not be resolved simply because the time resolution was limited to ~50ps

Direct picosecond time resolution of unimolecular reactions initiated by local mode excitation

The concept of local mode (LM) states [1] in large molecules raises the possibilty of inducing chemical reactions from a well-defined initial state (bond-selective chemistry). The results of linewidth and energy measurements in gases, [2(a)] and low temperature solids, [2(b)] however, indicate that the relaxation times for such high energy (> 15000 cm^-1) states can be extremely short, < 1ps. Because of the lack of direct time-resolved measurements, the following fundamental questions have not been unequivocally answered: What are the homogeneous linewidths of LM states and what are the rates of energy relaxation or reaction out of these states? Over the past five years we have made several attempts to observe the picosecond dynamics of LM states. Due to the inherent difficulties associated with making these measurements, such as the very small oscillator strength (σ < 10^-23 cm^2), an extremely sensitive probing technique becomes imperative

Topology and Evolution of Technology Innovation Networks

The web of relations linking technological innovation can be fairly described in terms of patent citations. The resulting patent citation network provides a picture of the large-scale organization of innovations and its time evolution. Here we study the patterns of change of patents registered by the US Patent and Trademark Office (USPTO). We show that the scaling behavior exhibited by this network is consistent with a preferential attachment mechanism together with a Weibull-shaped aging term. Such attachment kernel is shared by scientific citation networks, thus indicating an universal type of mechanism linking ideas and designs and their evolution. The implications for evolutionary theory of innovation are discussed.Comment: 6 pages, 5 figures, submitted to Physical Review

Real-time clocking of bimolecular reactions: Application to H+CO_2

An experimental methodology is described for the real-time clocking of elementary bimolecular reactions, i.e., timing the process of formation and decay of the collision complex. The method takes advantage of the propinquity of the potential reagents in a binary van der Waals (vdW) ``precursor'' molecule. An ultrashort pump laser pulse initiates the reaction, establishing the zero-of-time (e.g., by photodissociating one of the component molecules in the vdW precursor, liberating a ``hot'' atom that attacks the nearby coreagent). A second ultrashort, suitably tuned, variably delayed probe laser pulse detects either the intermediate complex or the newly born product. From an analysis of this temporal data as a function of pump and probe wavelengths, the real-time dynamics of such a ``van der Waals-impacted bimolecular (VIB)'' reaction can be determined. Chosen as a demonstration example is the VIB reaction H+CO2-->HOCO[double-dagger]-->HO+CO, using the HI·CO2 vdW precursor. The pump laser wavelength was varied over the range 231–263 nm; the probe laser detected OH in two different quantum states. The measured rates of formation and decay of the HOCO[double-dagger] complex are characterized by time constants tau1 and tau2; tau2 spanned the range 0.4–4.7 ps, varying with the available energy. The dynamics of the HOCO[double-dagger] decay are discussed

Evidence for a diffusion-controlled mechanism for fluorescence blinking of colloidal quantum dots

Fluorescence blinking in nanocrystal quantum dots is known to exhibit power-law dynamics, and several different mechanisms have been proposed to explain this behavior. We have extended the measurement of quantum-dot blinking by characterizing fluctuations in the fluorescence of single dots over time scales from microseconds to seconds. The power spectral density of these fluctuations indicates a change in the power-law statistics that occurs at a time scale of several milliseconds, providing an important constraint on possible mechanisms for the blinking. In particular, the observations are consistent with the predictions of models wherein blinking is controlled by diffusion of the energies of electron or hole trap states

Efeito da brusone sobre a produção de grãos de linhagens de trigo da população ITMI.

Editores técnicos: Joseani Mesquita Antunes, Ana Lídia Variani Bonato, Márcia Barrocas Moreira Pimentel

Tipos de lesiones de Piricularia en trigo.

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Exploration of a periodic GLOF in Halji, West Nepal using modeling and remote sensing

Abstract HKT-ISTP 2013 B