Category:Density mixing: Difference between revisions

Theory

In each iteration of a DFT cycle, we start from a given charge density ${\displaystyle \rho_{in}}$ and obtain the corresponding Kohn-Sham Hamiltonian and its eigenstates (wavefunctions). From the occupied states, we can compute a new charge density ${\displaystyle \rho_{out}}$, so that conceptionally we need to solve a multidimensional fixed-point problem. In the case of magnetism and MetaGGAs, the problem becomes even more complex, because in addition also the magnetization density and the kinetic-energy density are relevant.

To solve this problem, we use nonlinear solvers that work with the input vector ${\displaystyle \rho_{in}}$ and the residual ${\displaystyle R = \rho_{out} - \rho_{in}}$. In these methods a subspace is built from the input vectors and the optimal solution within this subspace is obtained. The most efficient solutions are the Broyden^[1] and the Pulay^[2] mixing scheme. In the former method, an approximate of the Jacobian matrix is iteratively improved to find the optimal solution. In the latter method, the input vectors are combined assuming linearity to minimize the residual.

The implementation in VASP is based on the work of Johnson^[3]. Kresse and Furthmüller^[4] extended on it and demonstrated that the Broyden and Pulay scheme transform into each other for certain choices of weights for the previous iterations. They also introduced an efficient metric putting additional weight on the long-range components of the density (small ${\displaystyle \mathbf G}$ vectors) resulting in a more robust convergence. Furthermore, a preconditioning can improve the choice of the input density for the next iteration and we use a Kerker preconditioning^[5] in VASP.

How to

Improve the convergence

For most simple DFT calculations the default choice of the convergence parameters is quite well suited to converge the calculation. As a first step, we suggest to visualize your structure or examine the output for warnings to check for very close atoms. This can occasionally happen during a relaxation if a too large ionic step is performed. If the structure is correct, we recommend to increase the number of steps NELM and only if that doesn't work starting to tweak the parameters AMIX or BMIX; preferably the latter.

Magnetic calculations

For magnetic materials not only the charge density, but also the magnetization density needs to converge. Converge magnetic calculations

MetaGGAs

For the density mixing schemes to work reliably, the charge density mixer must be aware of all quantities that affect the total energy during the self-consistency cycle. For a standard DFT functional, this is solely the charge density. In case of meta-GGAs, however, the total energy depends on the kinetic energy density as well.

In many cases the density mixing scheme works well enough without passing the kinetic energy density through the mixer, which is why LMIXTAU=.FALSE., per default. However, when the selfconsistency cycle fails to converge for one of the density-mixing algorithms (for instance, IALGO=38 or 48), one may set LMIXTAU=.TRUE. to have VASP pass the kinetic energy density through the mixer as well. This sometimes helps to cure convergence problems in the selfconsistency cycle.

References