Hugh F. Wilson

Contributed by David Bowler

Reposted from Atomistic Computer Simulations with permission

*Computer Physics Communications*2015, 197, 1Contributed by David Bowler

Reposted from Atomistic Computer Simulations with permission

*Ab initio*thermodynamics is both extremely challenging and extremely important. The challenge arises from the need to sample an energy distribution sufficiently well to converge calculations; the importance comes from the insight that we can gain into experimentally inaccessible situations (I have several colleagues who work on iron in the Earth’s core which is not readily accessible experimentally). A new paper[1] suggests an approach to

*ab initio*thermodynamics that will be extremely helpful for certain calculations (and potentially useful for general calculations). I have written about calculations on liquid iron in Section 4.6 of the book, and on general approaches to thermodynamics in Chapter 6.

When finding average values of variables at finite temperature, we have to sample over a set of micro-states which are distributed according to a potential energy, U1(r) , with a Boltzmann factor that depends on the potential giving the probability of each state. The standard approach to this is to use either MD or Monte Carlo (MC) to sample the potential energy surface, possibly using a weighting scheme to speed up convergence. This tends to be quite expensive when using

*ab initio*methods where a long MD run may be required.
The key insight of the new method is that we can perform the same averaging using a set of micro-states that are distributed according to a different potential energy, U0(r) , with the Boltzmann factor now accounting for the distribution of each state relative to the new potential,U1(r)−U0(r) . If the new potential is significantly cheaper than the first, then we can perform a long sampling run using this potential, and draw the micro-states from this distribution, reducing significantly the number of expensive calculations that need to be performed.

This paper presents a careful analysis of the effect of the accuracy of the cheap method (here taken to be a classical potential, ideally fitted to some

*ab initio*MD) and its effect on the sampling. While the method is efficient for standard averages, it is outstanding for thermodynamic integration, where it can reduce the number of simulations by an order of magnitude or more. It is clear that it’s been developed in this context - where the absolute free energy is required. In the context of*ab initio*thermodynamics, this is a significant step forward.