Next: 4.6 Supercell calculations Up: 4. Implementation Previous: 4.4 Algorithms and practicalities   Contents

Subsections

# 4.5 Pseudopotentials

The inclusion of core electrons poses special problems in QMC calculations distinct from those encountered in other electronic structure methods. The differing timescale (or equivalently distance scale) on which the electrons move compared with valence electrons requires the use of special modified sampling schemes or the use of very small timesteps which reduce the efficiency of the simulation. Large ionic and kinetic energies in the core regions are a further problem. Although accurate wavefunctions may be constructed for low atoms,4.7 for high atoms accurate wavefunctions have yet to be designed and obtained.

These two difficulties conspire to focus computational effort on the core electrons, forcing attention away from the chemically interacting and physically interesting valence and bonding regions. Fortunately for many properties of interest, and for many materials, the core remains almost independent of its environment and may be substituted by a pseudopotential with negligible loss of accuracy.4.8 This replacement serves to reduce the effective of the atoms that must be dealt with. The -dependence in the scaling of QMC calculations is then determined by the number of valence electrons that must be included in order to obtain satisfactory results.

## 4.5.1 Non-local pseudopotentials

Pseudopotentials are used routinely in DFT and quantum chemical applications and consequently there exists a large literature and continued research effort on the subject. [54,55,56,57,58,59,60,61] Improvements to the pseudopotential approximation are not an aim of this work: accurate potentials exist for carbon and silicon, the main atomic species used. The pseudopotentials user were generated within LDA-DFT. Evaluation of the pseudopotentials requires techniques particular to QMC, and these are described in the remainder of the section.

The pseudopotentials modify the many-body Hamiltonian, replacing the electron-ion coulomb terms with

 (4.34)

where signifies the electron-ion dependent terms of ion , and and are respectively a long-ranged local potential and a short-ranged non-local potential. The two potentials are chosen within a pseudopotential construction scheme to accurately model the valence electrons. At long-range, typically of order 2-3 a.u., the local potential returns to the Coulomb tail.

The non-local potentials are written in terms of several short-ranged angular momentum dependent potentials. The operator is given by these potentials multiplied by the appropriate projection operators, written as integrals over the angular interval :

 (4.35)

The local component of the pseudopotential may be directly evaluated during a Monte Carlo simulation. In supercell simulations, Ewald's method (see section 4.6.1) is required to deal with the long-range of the potential, but this this not a significant complication. In VMC, the non-local potentials must be projected onto the trial function which requires statistical evaluation of the projection operators.

### 4.5.1.1 Evaluation of the non-local energy

Evaluation of the non-local projection operators, and hence the non-local energy cannot be performed analytically. For general correlated wavefunctions, the projection operators depend on all inter-particle distances and are therefore not amenable to analytic or numerical integration. Fahy [38,26] developed an exact scheme for evaluating the non-local energy in VMC and first applied the technique in simulations of bulk carbon and silicon in the diamond structure. This scheme is now used almost exclusively, approximate evaluation methods having been discarded due to insufficient accuracy.

In the Fahy scheme, evaluation of is performed stochastically during a VMC simulation. The projection is written in terms of ratios of the trial function,

 (4.36)

where the sum runs over all electrons at distances from the ion. The orientation of the coordinate system (which is arbitrary) is chosen for each electron so that the vector lies along the -direction, thus eliminating the -dependence of the integrals. [26]

The angular integral over is performed stochastically during the simulation. Optimised integration grids have been developed to exactly integrate functions of up to a certain angular momentum. [62] The variance of the estimator for the non-local energy is chosen to optimise the balance of work spent evaluating the non-local pseudopotential with the work performing other parts of the simulation. The grids are very efficient, and in calculations on bulk silicon and carbon, taking multiple samples of a grid was always found to be less efficient than using a single larger grid. This result is expected to be general; the integrals are effectively of low dimensionality and grid-based integration methods should converge more rapidly than Monte Carlo methods. In practice, 6-12 points give sufficient accuracy for first and second row elements, [26,63] where the character of the wavefunctions is dominated by and angular-momenta. 6 point grids are sufficient to exactly integrate momenta, and 12 points grids, momenta.

### 4.5.1.2 The locality approximation

The non-locality of accurate pseudopotentials is a significant problem in DMC calculations. An explicit form for the many-body wavefunction is not available in DMC and it has been shown (e.g. Ref. [64]) that the matrix elements of the non-local operator for imaginary time diffusion are negative. This creates a sign problem similar to the sign problem of fermion DMC. This problem has been avoided by replacing the non-local potential operator by an approximate local potential determined by evaluating the full non-local operator on the trial wavefunction, as in VMC. [65,66] This approximation has been shown to converge quadratically to the exact energy as the trial wavefunction improves. [63] In practice this approximation is very good and is not overly sensitive to details of the trial function. The locality approximation'' results in a non-variational DMC energy.

## 4.5.2 Core polarisation potentials

Core polarisation potentials (CPPs) are a refinement of pseudopotential theory particularly designed for use in many-body calculations. The pseudopotentials most commonly used in many-body calculations are derived from mean field calculations. This represents an approximation at some level, and to consistently achieve an accuracy better than eV on atomic energy levels, some many-body effects must be incorporated into the pseudopotential.

Direct methods of generating pseudopotentials within QMC have met with little success due to the difficulties in performing accurate all-electron calculations of sufficient statistical accuracy. [67]. Methods based on configuration interaction calculations and quasiparticle calculations have met with most success. [60,68,69,70]

The accuracy of pseudopotentials may be increased by taking into account the polarisability of the core, which is one of the most important effects excluded by a conventional rigid core approach. It is has been shown that this incorporates the leading terms of core relaxation'', the change that a core undergoes in different chemical environments (Ref. [71] and references within). The formulation of CPPs considers the polarisation of the atomic core by the valence electrons, within a point-dipole picture. To avoid divergences in the potential, the effect fields experienced by valence electrons are truncated close to the core. By parameterising the truncation, the correct binding energies of valence electrons is ensured. The scheme includes some of the core-core, core-valence and valence-valence correlation effects of an all-electron, many-body calculation. [71,68]

The many-body Hamiltonian is initially modified to include additional CPP terms resulting from the polarisation induced electric fields[68]

 (4.37)

where is the core polarisability, and the sums run over all ions, , and electrons. The terms are due to ion-ion, ion-ion-electron, electron-ion and electron-electron-ion interactions respectively. The electron dependent terms are further parameterised, by means of a cutoff function, removing the divergences:
 (4.38)

where is a rescaled coordinate. The Hamiltonian terms become
 (4.39)

where is the projection operator for angular momentum , and the and are parameters obtained during construction of the CPP.[68]

These terms may be directly evaluated within VMC and DMC. The non-local projection operator, , is evaluated at the same time as non-local component of the full pseudopotential, avoiding costly evaluations of the many-body wavefunction.

Sample data comparing DMC results for the ionisation potentials of a Ti atom for different pseudopotentials [61] is given in Table 4.1.

Table 4.1: Ionisation potentials of Ti for several pseudopotentials computed using DMC. Energies are in eV and statistical error bars are given in brackets. Experimental data from [72]. Rel-TM denotes a relativistic pseudopotential constructed in the Troullier-Martins scheme, [58] HF and HF+CPP denote a bare HF pseudopotential and an HF pseudopotential with core-polarisation potential terms respectively. [68] The pseudopotentials were generated in the configuration suggested by G. B. Bachelet et al.[56] Data courtesy Y. Lee [61]
 IP Expt Rel-TM HF HF+CPP 1st 6.82 6.862(15) 6.693(13) 6.767(16) 2nd 13.58 12.347(8) 12.218(8) 13.639(9) 3rd 27.48 27.666(4) 28.288(4) 28.413(5) 4th 43.24 44.336(0) 44.774(0) 46.228(0)

Next: 4.6 Supercell calculations Up: 4. Implementation Previous: 4.4 Algorithms and practicalities   Contents