Author Topic: Computing surface energies  (Read 508 times)

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Offline Weckman

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Computing surface energies
« on: November 24, 2021, 22:20 »
I would like to study the stability of different surface orientations of wurtzite/zinc blende materials which exhibit asymmetric surfaces for certain lattice orientations and therefore would like to use the periodic surface model (electrode) to compute the relative stabilities of these surfaces.

I do not yet have the full licence in my disposal, so I ran some test calculations on my desktop for Au(111) surface. However, when I compute the total energy of surfaces with varying thickness, in some instances I get negative surface energies.

For example, when using surfaces with 6 and 8 layers of gold, medium basis set and SG15 pseudo, I get energies
6   -22519.98379
7   -26273.25555
8   -30026.51107
Making a linear fit gives a slope of -3751.264 eV, close to that of a bulk calculation (-3753.231 eV). However, the intercept is negative and so is the surface energy.

If I use a HGH pseudo, I get a positive surface energies that vary depending on the basis set used.

What I would like to know:
Is this a correct approach to take and are the results some kind of an artifact resulting from a thin surface model or am I making a fundamental error somewhere or how should I approach the issue? In the original paper ("First-principles Green’s-function method for surface calculations: A pseudopotential localized basis set approach") the authors discuss developing the procedure for SG15 pseudos. However, QuantumATK allows me to set from a variety of different pseudos. Is the Green's function method suitable for all the available pseudos and basis sets?

- Weckman

Offline Anders Blom

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Re: Computing surface energies
« Reply #1 on: February 1, 2022, 22:53 »