M. A. Hadi1,a), S. H. Naqib1
, S.-R. G. Christopoulos,2 A. Chroneos2,3,b), and A. K. M. A. Islam1,4
1Department of Physics, University of Rajshahi, Rajshahi-6205, Bangladesh
2
Faculty of Engineering, Environment and Computing, Coventry University, Priory Street, Coventry CV1 5FB, UK
3Department of Materials, Imperial College, London SW7 2AZ, UK
4
International Islamic University Chittagong, 154/A College Road, Chittagong 4203, Bangladesh
Abstract
In the present study we employed density functional theory calculations to investigate the mechanical
behavior, bonding nature and defect processes of the new ordered MAX phase Mo2ScAlC2. The
mechanical stability of the compound is verified with its single crystal elastic constants. The new
phase Mo2ScAlC2 is anticipated to be prone to shear along the crystallographic b and c axes, when a
rational force is applied to the crystallographic a axis. The compressibility along the 001 direction
under uniaxial stress is expected to be easier in Mo2ScAlC2. Additionally, the volume deformation
should be easier in Mo2ScAlC2 than the isostructural Mo2TiAlC2. Mo2ScAlC2 is predicted to behave
in a brittle manner. Due to its higher Debye temperature, Mo2ScAlC2 is expected to be thermally more
conductive than Mo2TiAlC2. The cross-slip pining procedure should be significantly easier in
Mo2ScAlC2 as compared to Mo2TiAlC2. The new ordered MAX phase Mo2ScAlC2 has a mixed
character of strong covalent and metallic bonding with limited ionic nature. Both Mo–C and Mo–Al
bonds are expected to be more covalent in Mo2ScAlC2 than those of Mo2TiAlC2. The level of
covalency of Sc–C bond is somewhat low compared to a similar bond Ti–C in Mo2ScAlC2. Due to its
reduced hardness Mo2ScAlC2, it should be softer and more easily machinable compared to
Mo2TiAlC2. Fermi surface topology of the new compound is formed mainly due to the low-dispersive
Mo 4d-like bands. The intrinsic defect processes reveal that the level of radiation tolerance in
Mo2ScAlC2 is not as high as in other MAX phases such as Ti3AlC2.
https://arxiv.org/ftp/arxiv/papers/1702/1702.03048.pdf
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