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      Temperature and energy effects on secondary electron emission from SiC ceramics induced by Xe 17+ ions

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          Abstract

          Secondary electron emission yield from the surface of SiC ceramics induced by Xe 17+ ions has been measured as a function of target temperature and incident energy. In the temperature range of 463–659 K, the total yield gradually decreases with increasing target temperature. The decrease is about 57% for 3.2 MeV Xe 17+ impact, and about 62% for 4.0 MeV Xe 17+ impact, which is much larger than the decrease observed previously for ion impact at low charged states. The yield dependence on the temperature is discussed in terms of work function, because both kinetic electron emission and potential electron emission are influenced by work function. In addition, our experimental data show that the total electron yield gradually increases with the kinetic energy of projectile, when the target is at a constant temperature higher than room temperature. This result can be explained by electronic stopping power which plays an important role in kinetic electron emission.

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          Electron emission from clean metal surfaces induced by low-energy light ions

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            Electron emission from slow hollow atoms at a clean metal surface.

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              Ultrafast electronic response of graphene to a strong and localized electric field

              The way conduction electrons respond to ultrafast external perturbations in low dimensional materials is at the core of the design of future devices for (opto)electronics, photodetection and spintronics. Highly charged ions provide a tool for probing the electronic response of solids to extremely strong electric fields localized down to nanometre-sized areas. With ion transmission times in the order of femtoseconds, we can directly probe the local electronic dynamics of an ultrathin foil on this timescale. Here we report on the ability of freestanding single layer graphene to provide tens of electrons for charge neutralization of a slow highly charged ion within a few femtoseconds. With values higher than 1012 A cm−2, the resulting local current density in graphene exceeds previously measured breakdown currents by three orders of magnitude. Surprisingly, the passing ion does not tear nanometre-sized holes into the single layer graphene. We use time-dependent density functional theory to gain insight into the multielectron dynamics.
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                Author and article information

                Contributors
                zhfxu@mail.xjtu.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                25 July 2017
                25 July 2017
                2017
                : 7
                : 6482
                Affiliations
                [1 ]ISNI 0000 0001 0599 1243, GRID grid.43169.39, Institute of Science and Technology for Laser and Particle Beams, , Xi’an Jiaotong University, ; Xi’an, 710049 China
                [2 ]ISNI 0000 0001 0599 1243, GRID grid.43169.39, School of Science, , Xi’an Jiaotong University, ; Xi’an, 710049 China
                [3 ]ISNI 0000000119573309, GRID grid.9227.e, Institute of Modern Physics, , Chinese Academy of Science, ; Lanzhou, 730000 China
                [4 ]ISNI 0000 0004 1765 5556, GRID grid.459947.2, Ion Beam and Optical Physical Laboratory, , Xianyang Normal University, ; Xianyang, 712000 China
                Author information
                http://orcid.org/0000-0002-7932-3050
                Article
                6891
                10.1038/s41598-017-06891-9
                5526893
                28743901
                e7e85df9-253b-42ce-8450-b34cc67153ea
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 4 April 2017
                : 19 June 2017
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