First‐order Raman scattering of the MAX phases Ta₄AlC₃, Nb₄AlC₃, Ti₄AlN₃, and Ta₂AlC

Herein, we report on the Raman spectra of the following ternary hexagonal carbides and nitrides (MAX phases): Ta 4 AlC 3 , Ta 2 AlC and Ti 4 AlN 3 . We also present the Raman‐active modes of α‐ and β‐Ta 4 AlC 3 , Nb 4 AlC 3 and Ti 4 AlN 3 , – also referred to as the 413 MAX phases – as predicted from first principles calculations using density functional theory. We compare the obtained experimental and calculated results with previous studies on Ta 2 AlC and Ti 4 AlN 3 . The vibrational behavior associated with the Raman‐active modes for the 413 phases has been identified for the first time. In general, the agreement is good between theory and experiment. The experimental and calculated results indicate that the modes at low wavenumbers ‐ dominated by the Al atoms ‐ are a weak function of chemistry and the differences in energy can be traced to variations in the reduced mass. The modes at higher wavenumbers are dominated by the C and N atoms and show a strong dependence on the unit cell chemistry, with the Ta–C bond being stiffer than the Nb–C bond, which is in turn stiffer than Ti–N.