Laser-induced electron tunneling and diffraction.

Science

National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, Canada, K1A 0R6.

Published: June 2008

Molecular structure is usually determined by measuring the diffraction pattern the molecule impresses on x-rays or electrons. We used a laser field to extract electrons from the molecule itself, accelerate them, and in some cases force them to recollide with and diffract from the parent ion, all within a fraction of a laser period. Here, we show that the momentum distribution of the extracted electron carries the fingerprint of the highest occupied molecular orbital, whereas the elastically scattered electrons reveal the position of the nuclear components of the molecule. Thus, in one comprehensive technology, the photoelectrons give detailed information about the electronic orbital and the position of the nuclei.

Download full-text PDF

Source
http://dx.doi.org/10.1126/science.1157980DOI Listing

Publication Analysis

Top Keywords

laser-induced electron
4
electron tunneling
4
tunneling diffraction
4
diffraction molecular
4
molecular structure
4
structure determined
4
determined measuring
4
measuring diffraction
4
diffraction pattern
4
pattern molecule
4

Similar Publications

The coupling effect of gamma-ray radiation and 532 nm nanosecond laser radiation on optical coatings and substrates was investigated. Fused silica and S-BSL7 glass with 532 nm high reflectivity (HR) coatings were irradiated using Co gamma-ray source at a dose rate of 1 Gy/s for a total dose of 1-500 kGy. After irradiation, the samples were subjected to raster scan testing using a laser with a pulse width of approximately 8.

View Article and Find Full Text PDF

In this work, laser-induced graphene from kraft paper (kraft paper-LIG) was employed for the nonenzymatic electrochemical sensing of dopamine (DA). We reported the fabrication and characterization of a disposable, cost-effective, kraft-based electrochemical dopamine sensor with the sensing electrode consisting of laser-induced graphene derived from kraft paper. Kraft paper-LIG was formed by the femtosecond laser modification of kraft paper into a three-dimensional (3D) graphene arrangement.

View Article and Find Full Text PDF

Synthetic antioxidants are often introduced to biodiesel to increase its oxidative stability, and -butyl hydroquinone (TBHQ) has been selected due to its high efficiency for this purpose. The monitoring of antioxidants in biodiesel therefore provides information on the oxidative stability of biodiesels. Herein, a laser-induced graphene (LIG) electrode is introduced as a new sensor for detecting -butyl hydroquinone (TBHQ) in biodiesel samples.

View Article and Find Full Text PDF

Nanosecond Nanothermometry in an Electron Microscope.

Nano Lett

January 2025

University Paris-Saclay, CNRS, Laboratoire de Physique des Solides, Orsay 91405, France.

Thermal transport in nanostructures plays a critical role in modern technologies. As devices shrink, techniques that can measure thermal properties at nanometer and nanosecond scales are increasingly needed to capture transient, out-of-equilibrium phenomena. We present a novel pump-probe photon-electron method within a scanning transmission electron microscope (STEM) to map temperature dynamics with unprecedented spatial and temporal resolutions.

View Article and Find Full Text PDF

In this study, we investigated in detail the regulation mechanism of electron transfer under laser-induced breakdown (LIB) on weak O-D stimulated Raman scattering (SRS) in DMSO-DO solutions. Significantly, the Raman activity of O-D vibrations was greatly enhanced by two orders of magnitude due to electron transfer in DMSO molecules. Density functional theory (DFT) calculations showed that the O-D Raman activity was significantly enhanced in the DMSO-DO dimer compared to the DO dimer.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!