Systematic study of chemical bonding states of lithium binary compounds from Li K-L emission spectra obtained by a VUV spectrometer mounted on a scanning electron microscope.

IF 1.9
Takanori Murano, Shogo Koshiya
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引用次数: 0

Abstract

The Li K-L emission spectra of lithium metal and its binary compounds (Li3N, Li2O and LiF) were measured by using a soft X-ray emission spectrometer, which was equipped with a newly developed high-efficiency diffraction grating (JS35BC) and attached to an electron probe microanalyzer. The new grating enables the observation of the entire intensity profile of both Li K-L and Mg L2,3-M emission spectra. The systematic energy shift of the Li K-L spectra to the lower energy side with an increasing electronegativity (or the ionization tendency) of elements of N, O and F bonded with the Li atom was clearly detected. This shift was reproduced by theoretical calculations and was assigned mainly due to the change of the binding energy of the valence band of those materials. The main peak and its distinct shoulder structure observed in Li K-L spectrum of LiF were assigned as 2p dominated and 2s + 2p mixed states, respectively, from the comparison with theoretical calculations.

利用安装在扫描电子显微镜上的VUV光谱仪获得的Li K-L发射光谱,系统地研究了锂二元化合物的化学键态。
采用新型高效衍射光栅(JS35BC)和电子探针微量分析仪(EPMA)连接的软x射线发射光谱仪(SXES)测量了金属锂及其二元化合物(Li3N、Li2O和LiF)的Li K-L发射光谱。该光栅能够观测Li K-L和Mg L2,3-M发射光谱的整个强度分布。随着与Li原子成键的N、O和F元素电负性(或电离倾向)的增加,Li K-L光谱的系统能量向低能量侧转移。理论计算再现了这一变化,主要是由于这些材料的价带结合能的变化。通过与理论计算的比较,将LiF的Li K-L光谱中观测到的主峰及其明显的肩状结构分别归为2p主导态和2s + 2p混合态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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