自立石墨烯的泵浦探针X射线光电子能谱

IF 1.9 Q3 PHYSICS, CONDENSED MATTER
R. Costantini, Dario Marchiani, M. Betti, C. Mariani, Samuel Jeong, Yoshikazu Ito, A. Morgante, M. Dell’Angela
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引用次数: 1

摘要

通过高分辨率X射线光电子能谱(XPS)研究的C1s核水平中sp3键组分的出现,在约60at.%H的吸收下对独立的纳米多孔石墨烯进行氢化。在2.4eV的光激发下,通过XPS研究了完全无负载的石墨烯。在1.6mJ/cm2的激光注量下,观察到石墨烯的部分不可逆脱氢,这可能归因于局部温度升高或H-to-C拉伸模式的光诱导软化。C1s核心能级的能量偏移和峰值加宽的亚ns动力学揭示了两个不同的衰变常数:分别为210ps和130ps,前者与光电压动力学有关,后者与在与同步加速器时间分辨率相当的时间尺度上的热加热有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pump-Probe X-ray Photoemission Spectroscopy of Free-Standing Graphane
Free-standing nanoporous graphene was hydrogenated at about 60 at.% H uptake, as determined by the emerging of the sp3 bonding component in the C 1s core level investigated by high-resolution X-ray photoelectron spectroscopy (XPS). Fully unsupported graphane was investigated by XPS under optical excitation at 2.4 eV. At a laser fluence of 1.6 mJ/cm2, a partial irreversible dehydrogenation of the graphane was observed, which could be attributed either to the local temperature increase or to a photo-induced softening of the H-to-C stretching mode. The sub-ns dynamics of the energy shift and peak broadening of the C 1s core level revealed two different decay constants: 210 ps and 130 ps, respectively, the former associated with photovoltage dynamics and the latter with thermal heating on a time scale comparable with the synchrotron temporal resolution.
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来源期刊
Condensed Matter
Condensed Matter PHYSICS, CONDENSED MATTER-
CiteScore
2.90
自引率
11.80%
发文量
58
审稿时长
10 weeks
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