Chemical bonding and electronic-structure in MAX phases as viewed by X-ray spectroscopy and density functional theory

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• 作者：Martin Magnuson^a ; ^{Martin.Magnuson@liu.se} ; Maurizio Mattesini^b ; ^c
• 关键词：Nanolaminates ; Chemical bonding ; X-ray emission spectroscopy ; Electronic Structure calculations ; Elastic and magnetic properties ; Seebeck measurements
• 刊名：Thin Solid Films
• 出版年：2017
• 出版时间：1 January 2017
• 年：2017
• 卷：621
• 期：Complete
• 页码：108-130
• 全文大小：3135 K
• 卷排序：621

文摘

This is a critical review of MAX-phase carbides and nitrides from an electronic-structure and chemical bonding perspective. This large group of nanolaminated materials is of great scientific and technological interest and exhibits a combination of metallic and ceramic features. These properties are related to the special crystal structure and bonding characteristics with alternating strong MC bonds in high-density MC slabs, and relatively weak MA bonds between the slabs. Here, we review the trend and relationship between the chemical bonding, conductivity, elastic and magnetic properties of the MAX phases in comparison to the parent binary MX compounds with the underlying electronic structure probed by polarized X-ray spectroscopy. Spectroscopic studies constitute important tests of the results of state-of-the-art electronic structure density functional theory that is extensively discussed and are generally consistent. By replacing the elements on the M, A, or X-sites in the crystal structure, the corresponding changes in the conductivity, elasticity, magnetism and other material properties make it possible to tailor the characteristics of this class of materials by controlling the strengths of their chemical bonds.