Watching electrons move in real time
At its most basic level, understanding chemistry means understanding what electrons are doing. Research published in The Journal of Chemical Physics not only maps the movement of electrons in real time but also observes a concerted electron and proton transfer that is quite different from any previously known phase transitions in the model crystal, ammonium sulfate. By extending X-ray powder diffraction into the femtosecond realm, the researchers were able to map the relocation of charges in the ammonium sulfate crystal after they were displaced by photoexcitation.
"Our prototype experiment produces a sort of 'molecular movie' of the atoms in action," says author Michael Woerner of the Max-Born-Institut für Nichtlineare Optik und Kurzzeitspektroskopie in Germany. "The time and spatial resolution is now at atomic time and length scales, respectively."
Electron positions were mapped by observing the diffraction of X-ray pulses lasting tens of femtoseconds (quadrillionth of a second). Positions of protons and other nuclei were deduced from the locations of regions of high electron density. Within the crystal, the excited electrons transferred from the sulfate groups to a tight channel within crystal matrix. This channel was stabilized by the transfer of protons from adjacent ammonium groups into the channel. This transfer mechanism had not been previously observed or proposed, and the researchers had expected to see much smaller displacements.
According to Woerner, the technique should be applicable to structural studies of materials ranging from biomolecules to high-temperature superconductors. "We expect that the technique will be applied to many interesting material systems." He says. "In principle, femtosecond X-ray powder diffraction can be applied to any crystalline form of matter. Only the complexity of crystals and the presence of heavy elements, which reduces the penetration depth of X-rays, set some constraints."
Original publication: Michael Woerner et al.; "Concerted electron and proton transfer in ionic crystals mapped by femtosecond x-ray powder diffraction"; J. Chem. Phys. 2010
Most read news
Topics
Organizations
Other news from the department science
Get the analytics and lab tech industry in your inbox
By submitting this form you agree that LUMITOS AG will send you the newsletter(s) selected above by email. Your data will not be passed on to third parties. Your data will be stored and processed in accordance with our data protection regulations. LUMITOS may contact you by email for the purpose of advertising or market and opinion surveys. You can revoke your consent at any time without giving reasons to LUMITOS AG, Ernst-Augustin-Str. 2, 12489 Berlin, Germany or by e-mail at revoke@lumitos.com with effect for the future. In addition, each email contains a link to unsubscribe from the corresponding newsletter.
Most read news
More news from our other portals
Last viewed contents
Paper-based biodegradable and eco-friendly sensor for sensing the food status - Eco-friendly and biodegradable electronics that is fitting the worldwide ‘Green New Deal’ trend, big contribution is expected not only in daily life but food industry
The ‘selenosome’: The choreography which governs recoding - Cryo-electron microscopy visualizes cellular structures
Simulations Suggest Graphene Can Stretch to Be a Tunable Ion Filter
ISO recognition for Quality Management Systems at Malvern Instruments US headquarters
Analytica 2020: The leading guide to the smart laboratory - The focus on digital transformation is being further expanded
How fatal biofilms form
Easy printing of biosensors made of graphene - Cost-effective roll-to-roll production
multi N/C | TOC analysers | Analytik Jena
Fluoreye - an On-Deck Module for Fluorescence Detection | Fluorescence detection systems | Hamilton
Response Biomedical Achieves Superior Performance Targets With Rapid Flu A Test Development - Development Program Initiated for RAMP Test Specific to H5N1 Strain
How to switch liver cancer cell growth from 2-D to 3-D structures