First-principles interatomic potentials for transition-metal aluminides: Theory and trends across the<mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline"><mml:mn>3</mml:mn><mml:mi>d</mml:mi></mml:math>series

Abstract

In this paper the first-principles generalized pseudopotential theory (GPT) of transition-metal interatomic potentials [J. A. Moriarty, Phys. Rev. B 38, 3199 (1988)] is extended to $\mathrm{AB}$ binary compounds and alloys. For general transition-metal (TM) systems, the GPT total-energy functional involves a volume term, central-force pair potentials, and angular-force multi-ion potentials, which are both volume $(\ensuremath{\Omega})$ and concentration $(x)$ dependent and include all $sp,$ $sp\ensuremath{-}d,$ and $d\ensuremath{-}d$ interactions within local density-functional quantum mechanics. The formalism is developed here in detail for intermetallic systems where $A$ is a simple metal and $B$ is a transition metal and applied to the prominent special case of the transition-metal aluminides ${\mathrm{TM}}_{x}{\mathrm{Al}}_{1\ensuremath{-}x},$ where $sp\ensuremath{-}d$ hybridization is especially important. Emphasis is given to the aluminum-rich $3d$ binary systems for $x&lt;0.30,$ which appear to be well described at the pair-potential level without angular forces and for which the present GPT potentials can be used directly in atomistic simulations. Volume terms and pair potentials for all of the $3d$ aluminides have been calculated and their behavior with atomic number, $\ensuremath{\Omega},$ and $x$ is elaborated through illustrative applications to the cohesive and structural trends across the $3d$ series. More extensive applications to the Co-Al and Ni-Al phase diagrams will be given elsewhere.