| Literature DB >> 25035485 |
Benjamin Erk1, Rebecca Boll2, Sebastian Trippel3, Denis Anielski2, Lutz Foucar4, Benedikt Rudek5, Sascha W Epp6, Ryan Coffee7, Sebastian Carron7, Sebastian Schorb7, Ken R Ferguson7, Michele Swiggers7, John D Bozek7, Marc Simon8, Tatiana Marchenko8, Jochen Küpper9, Ilme Schlichting4, Joachim Ullrich10, Christoph Bostedt7, Daniel Rolles11, Artem Rudenko12.
Abstract
Studies of charge transfer are often hampered by difficulties in determining the charge localization at a given time. Here, we used ultrashort x-ray free-electron laser pulses to image charge rearrangement dynamics within gas-phase iodomethane molecules during dissociation induced by a synchronized near-infrared (NIR) laser pulse. Inner-shell photoionization creates positive charge, which is initially localized on the iodine atom. We map the electron transfer between the methyl and iodine fragments as a function of their interatomic separation set by the NIR-x-ray delay. We observe signatures of electron transfer for distances up to 20 angstroms and show that a realistic estimate of its effective spatial range can be obtained from a classical over-the-barrier model. The presented technique is applicable for spatiotemporal imaging of charge transfer dynamics in a wide range of molecular systems.Entities:
Year: 2014 PMID: 25035485 DOI: 10.1126/science.1253607
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728