A Li K-edge XANES study of salts and minerals

Journal of Synchrotron Radiation
Cedrick O'ShaughnessyDaniel R Neuville

Abstract

The first comprehensive Li K-edge XANES study of a varied suite of Li-bearing minerals is presented. Drastic changes in the bonding environment for lithium are demonstrated and this can be monitored using the position and intensity of the main Li K-absorption edge. The complex silicates confirm the assignment of the absorption edge to be a convolution of triply degenerate p-like states as previously proposed for simple lithium compounds. The Li K-edge position depends on the electronegativity of the element to which it is bound. The intensity of the first peak varies depending on the existence of a 2p electron and can be used to evaluate the degree of ionicity of the bond. The presence of a 2p electron results in a weak first-peak intensity. The maximum intensity of the absorption edge shifts to lower energy with increasing SiO2 content for the lithium aluminosilicate minerals. The bond length distortion of the lithium aluminosilicates decreases with increasing SiO2 content, thus increased distortion leads to an increase in edge energy which measures lithium's electron affinity.

References

Jan 15, 1991·Physical Review. B, Condensed Matter·M KasraiJ M Chen
Aug 30, 2005·Ultramicroscopy·Nan Jiang, John C H Spence
Mar 11, 2009·Journal of Physics. Condensed Matter : an Institute of Physics Journal·W OlovssonC Ambrosch-Draxl

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Citations

Feb 11, 2021·Journal of Synchrotron Radiation·Masanari Nagasaka
Sep 29, 2020·Journal of the American Chemical Society·Chenji HuLiwei Chen
Sep 17, 2021·ACS Applied Materials & Interfaces·Subhayan RoychoudhuryWanli Yang

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