Pseudopotential

<h2 id="atomic-physics">Atomic physics</h2>
The pseudopotential is an attempt to replace the complicated effects of the motion of the <a href="/facts/Core_electron/LQuGLKcG">core</a> (i.e. non-<a href="/facts/Valence_electron/mXPA15VP">valence</a>) <a href="/facts/Electrons/L0KBo5cW">electrons</a> of an <a href="/facts/Atom/FoQ4kGN5">atom</a> and its nucleus with an effective <a href="/facts/Potential/8Fcbtnt9">potential</a>, or pseudopotential, so that the <a href="/facts/Schr%25C3%25B6dinger_equation/3csgSIWF">Schrödinger equation</a> contains a modified effective potential term instead of the <a href="/facts/Coulomb%2527s_law/V0lR5NKv">Coulombic</a> potential term for core electrons normally found in the Schrödinger equation.
The pseudopotential is an effective potential constructed to replace the atomic all-electron potential (full-potential) such that core states are eliminated and the valence electrons are described by pseudo-wavefunctions with significantly fewer nodes. This allows the pseudo-wavefunctions to be described with far fewer <a href="/facts/Fourier_series/s3fsxPAT">Fourier modes</a>, thus making <a href="/facts/Basis_set_(chemistry)/rQCPt3yl">plane-wave basis sets</a> practical to use. In this approach usually only the chemically active valence electrons are dealt with explicitly, while the core electrons are 'frozen', being considered together with the nuclei as rigid non-polarizable ion cores. It is possible to self-consistently update the pseudopotential with the chemical environment that it is embedded in, having the effect of relaxing the frozen core approximation, although this is rarely done. In codes using local basis functions, like Gaussian, often effective core potentials are used that only freeze the core electrons. 
First-principles pseudopotentials are derived from an atomic reference state, requiring that the pseudo- and all-electron valence eigenstates have the same energies and amplitude (and thus density) outside a chosen core cut-off radius 
 
 
 
 
 r
 
 c
 
 
 
 
 {\displaystyle r_{c}}
 
.
Pseudopotentials with larger cut-off radius are said to be softer, that is more rapidly convergent, but at the same time less transferable, that is less accurate to reproduce realistic features in different environments.
Motivation:

<ol><li>Reduction of basis set size</li>
<li>Reduction of number of electrons</li>
<li>Inclusion of relativistic and other effects</li></ol>
Approximations:

<ol><li>One-electron picture.</li>
<li>The small-core approximation assumes that there is no significant overlap between core and valence wave-function. Nonlinear core corrections<a class="footnote-ref" id="fnref:2" href="#fn:2">2</a> or "semicore" electron inclusion<a class="footnote-ref" id="fnref:3" href="#fn:3">3</a> deal with situations where overlap is non-negligible.</li></ol>
Early applications of pseudopotentials to atoms and solids based on attempts to fit atomic spectra achieved only limited success. Solid-state pseudopotentials achieved their present popularity largely because of the successful fits by Walter Harrison to the nearly free electron Fermi surface of aluminum (1958) and by <a href="/facts/James_Charles_Phillips/cHP64QyE">James C. Phillips</a> to the covalent energy gaps of silicon and germanium (1958). Phillips and coworkers (notably <a href="/facts/Marvin_L._Cohen/Ad7pTaRh">Marvin L. Cohen</a> and coworkers) later extended this work to many other semiconductors, in what they called "semiempirical pseudopotentials".<a class="footnote-ref" id="fnref:4" href="#fn:4">4</a>

<h3>Norm-conserving pseudopotential</h3>
Norm-conserving and ultrasoft are the two most common forms of pseudopotential used in modern <a href="/facts/Basis_set_(chemistry)/rQCPt3yl">plane-wave</a> <a href="/facts/Quantum_chemistry_computer_programs/WpF4uoKD">electronic structure codes</a>. They allow a basis-set with a significantly lower cut-off (the frequency of the highest Fourier mode) to be used to describe the electron wavefunctions and so allow proper numerical convergence with reasonable computing resources. An alternative would be to augment the basis set around nuclei with atomic-like functions, as is done in <a href="/facts/Linearized_augmented-plane-wave_method/36CgpWU9">LAPW</a>. Norm-conserving pseudopotential was first proposed by Hamann, Schlüter, and Chiang (HSC) in 1979.<a class="footnote-ref" id="fnref:5" href="#fn:5">5</a> The original HSC norm-conserving pseudopotential takes the following form:

V
                ^
              
            
          
          
            
              ps
            
          
        
        (
        r
        )
        =
        
          ∑
          
            l
          
        
        
          ∑
          
            m
          
        
        
          |
        
        
          Y
          
            l
            m
          
        
        ⟩
        
          V
          
            l
            m
          
        
        (
        r
        )
        ⟨
        
          Y
          
            l
            m
          
        
        
          |
        
      
    
    {\displaystyle {\hat {V}}_{\textit {ps}}(r)=\sum _{l}\sum _{m}|Y_{lm}\rangle V_{lm}(r)\langle Y_{lm}|}

where 
 
 
 
 
 |
 
 
 Y
 
 l
 m
 
 
 ⟩
 
 
 {\displaystyle |Y_{lm}\rangle }
 
 projects a one-particle wavefunction, such as one Kohn-Sham orbital, to the angular momentum labeled by 
 
 
 
 {
 l
 ,
 m
 }
 
 
 {\displaystyle \{l,m\}}
 
. 
 
 
 
 
 V
 
 l
 m
 
 
 (
 r
 )
 
 
 {\displaystyle V_{lm}(r)}
 
 is the pseudopotential that acts on the projected component. Different angular momentum states then feel different potentials, thus the HSC norm-conserving pseudopotential is non-local, in contrast to local pseudopotential which acts on all one-particle wave-functions in the same way.
Norm-conserving pseudopotentials are constructed to enforce two conditions.
1. Inside the cut-off radius 
 
 
 
 
 r
 
 c
 
 
 
 
 {\displaystyle r_{c}}
 
, the <a href="/facts/Normalizable_wave_function/KgM5ykjY">norm</a> of each pseudo-wavefunction be identical to its corresponding all-electron wavefunction:<a class="footnote-ref" id="fnref:6" href="#fn:6">6</a>

∫
 
 r
 <
 
 r
 
 c
 
 
 
 
 d
 
 r
 
 3
 
 
 
 ϕ
 
 
 R
 
 ,
 i
 
 
 (
 
 
 
 r
 →
 
 
 
 )
 
 ϕ
 
 
 R
 
 ,
 j
 
 
 (
 
 
 
 r
 →
 
 
 
 )
 =
 
 ∫
 
 r
 <
 
 r
 
 c
 
 
 
 
 d
 
 r
 
 3
 
 
 
 
 
 
 ϕ
 ~
 
 
 
 
 
 R
 
 ,
 i
 
 
 (
 
 
 
 r
 →
 
 
 
 )
 
 
 
 
 ϕ
 ~
 
 
 
 
 
 R
 
 ,
 j
 
 
 (
 
 
 
 r
 →
 
 
 
 )
 
 
 {\displaystyle \int _{r<r_{c}}dr^{3}\phi _{\mathbf {R} ,i}({\vec {r}})\phi _{\mathbf {R} ,j}({\vec {r}})=\int _{r<r_{c}}dr^{3}{\tilde {\phi }}_{\mathbf {R} ,i}({\vec {r}}){\tilde {\phi }}_{\mathbf {R} ,j}({\vec {r}})}
 
,
where 
 
 
 
 
 ϕ
 
 
 R
 
 ,
 i
 
 
 
 
 {\displaystyle \phi _{\mathbf {R} ,i}}
 
 and 
 
 
 
 
 
 
 
 ϕ
 ~
 
 
 
 
 
 R
 
 ,
 i
 
 
 
 
 {\displaystyle {\tilde {\phi }}_{\mathbf {R} ,i}}
 
 are the all-electron and pseudo reference states for the pseudopotential on atom 
 
 
 
 
 R
 
 
 
 {\displaystyle \mathbf {R} }
 
.
2. All-electron and pseudo wavefunctions are identical outside cut-off radius 
 
 
 
 
 r
 
 c
 
 
 
 
 {\displaystyle r_{c}}
 
.

<h3>Ultrasoft pseudopotentials</h3>
Ultrasoft pseudopotentials relax the norm-conserving constraint to reduce the necessary basis-set size further at the expense of introducing a generalized eigenvalue problem.<a class="footnote-ref" id="fnref:7" href="#fn:7">7</a> With a non-zero difference in norms we can now define:

q
 
 
 R
 
 ,
 i
 j
 
 
 =
 ⟨
 
 ϕ
 
 
 R
 
 ,
 i
 
 
 
 |
 
 
 ϕ
 
 
 R
 
 ,
 j
 
 
 ⟩
 −
 ⟨
 
 
 
 
 ϕ
 ~
 
 
 
 
 
 R
 
 ,
 i
 
 
 
 |
 
 
 
 
 
 ϕ
 ~
 
 
 
 
 
 R
 
 ,
 j
 
 
 ⟩
 
 
 {\displaystyle q_{\mathbf {R} ,ij}=\langle \phi _{\mathbf {R} ,i}|\phi _{\mathbf {R} ,j}\rangle -\langle {\tilde {\phi }}_{\mathbf {R} ,i}|{\tilde {\phi }}_{\mathbf {R} ,j}\rangle }
 
,
and so a normalised eigenstate of the pseudo Hamiltonian now obeys the generalized equation

H
 ^
 
 
 
 
 |
 
 
 Ψ
 
 i
 
 
 ⟩
 =
 
 ϵ
 
 i
 
 
 
 
 
 S
 ^
 
 
 
 
 |
 
 
 Ψ
 
 i
 
 
 ⟩
 
 
 {\displaystyle {\hat {H}}|\Psi _{i}\rangle =\epsilon _{i}{\hat {S}}|\Psi _{i}\rangle }
 
,
where the operator 
 
 
 
 
 
 
 S
 ^
 
 
 
 
 
 {\displaystyle {\hat {S}}}
 
 is defined as

S
 ^
 
 
 
 =
 1
 +
 
 ∑
 
 
 R
 
 ,
 i
 ,
 j
 
 
 
 |
 
 
 p
 
 
 R
 
 ,
 i
 
 
 ⟩
 
 q
 
 
 R
 
 ,
 i
 j
 
 
 ⟨
 
 p
 
 
 R
 
 ,
 j
 
 
 
 |
 
 
 
 {\displaystyle {\hat {S}}=1+\sum _{\mathbf {R} ,i,j}|p_{\mathbf {R} ,i}\rangle q_{\mathbf {R} ,ij}\langle p_{\mathbf {R} ,j}|}
 
,
where 
 
 
 
 
 p
 
 
 R
 
 ,
 i
 
 
 
 
 {\displaystyle p_{\mathbf {R} ,i}}
 
 are projectors that form a <a href="/facts/Dual_basis/3S14kq2A">dual basis</a> with the pseudo reference states inside the cut-off radius, and are zero outside:

⟨
 
 p
 
 
 R
 
 ,
 i
 
 
 
 |
 
 
 
 
 
 ϕ
 ~
 
 
 
 
 
 R
 
 ,
 j
 
 
 
 ⟩
 
 r
 <
 
 r
 
 c
 
 
 
 
 =
 
 δ
 
 i
 ,
 j
 
 
 
 
 {\displaystyle \langle p_{\mathbf {R} ,i}|{\tilde {\phi }}_{\mathbf {R} ,j}\rangle _{r<r_{c}}=\delta _{i,j}}
 
.
A related technique<a class="footnote-ref" id="fnref:8" href="#fn:8">8</a> is the <a href="/facts/Projector_augmented_wave_method/GYQzDTf7">projector augmented wave (PAW) method</a>.

<h2 id="fermi-pseudopotential">Fermi pseudopotential</h2>
<a href="/facts/Enrico_Fermi/cmYcY15H">Enrico Fermi</a> introduced a pseudopotential, 
 
 
 
 V
 
 
 {\displaystyle V}
 
, to describe the scattering of a free neutron by a nucleus.<a class="footnote-ref" id="fnref:9" href="#fn:9">9</a> The scattering is assumed to be <a href="/facts/Partial_wave_analysis/laen1JEx">s-wave</a> scattering, and therefore spherically symmetric. Therefore, the potential is given as a function of radius, 
 
 
 
 r
 
 
 {\displaystyle r}
 
:

V
 (
 r
 )
 =
 
 
 
 2
 π
 
 ℏ
 
 2
 
 
 
 m
 
 
 b
 
 δ
 (
 r
 )
 
 
 {\displaystyle V(r)={\frac {2\pi \hbar ^{2}}{m}}b\,\delta (r)}
 
,
where 
 
 
 
 ℏ
 
 
 {\displaystyle \hbar }
 
 is the <a href="/facts/Planck_constant/qGHAe3qq">Planck constant</a> divided by 
 
 
 
 2
 π
 
 
 {\displaystyle 2\pi }
 
, 
 
 
 
 m
 
 
 {\displaystyle m}
 
 is the <a href="/facts/Mass/HHdc8XmF">mass</a>, 
 
 
 
 δ
 (
 r
 )
 
 
 {\displaystyle \delta (r)}
 
 is the <a href="/facts/Dirac_delta_function/V8PjRP8T">Dirac delta function</a>, 
 
 
 
 b
 
 
 {\displaystyle b}
 
 is the bound coherent neutron <a href="/facts/Scattering_length/6GlNnu6D">scattering length</a>, and 
 
 
 
 r
 =
 0
 
 
 {\displaystyle r=0}
 
 the <a href="/facts/Center_of_mass/n4Lr9GAz">center of mass</a> of the <a href="/facts/Atomic_nucleus/orpIm5Xl">nucleus</a>.<a class="footnote-ref" id="fnref:10" href="#fn:10">10</a> The Fourier transform of this 
 
 
 
 δ
 
 
 {\displaystyle \delta }
 
-function leads to the constant <a href="/facts/Atomic_form_factor/EgA8KPE4">neutron form factor</a>.

<h2 id="phillips-pseudopotential">Phillips pseudopotential</h2>
<a href="/facts/James_Charles_Phillips/cHP64QyE">James Charles Phillips</a> developed a simplified pseudopotential while at <a href="/facts/Bell_Labs/fKP5Gk0H">Bell Labs</a> useful for describing silicon and germanium.<a class="footnote-ref" id="fnref:11" href="#fn:11">11</a>

<h2 id="see-also">See also</h2>
<ul><li><a href="/facts/Density_functional_theory/wwz4Gqdg">Density functional theory</a></li>
<li><a href="/facts/Projector_augmented_wave_method/GYQzDTf7">Projector augmented wave method</a></li>
<li><a href="/facts/Marvin_L._Cohen/Ad7pTaRh">Marvin L. Cohen</a></li>
<li><a href="/facts/Alex_Zunger/18MwYCK3">Alex Zunger</a></li></ul>

<h2 id="pseudopotential-libraries">Pseudopotential libraries</h2>
<ul><li><a href="https://pseudopotentiallibrary.org/">Pseudopotential Library</a> : A community website for pseudopotentials/effective core potentials developed for high accuracy correlated many-body methods such as quantum Monte Carlo and quantum chemistry</li>
<li><a href="http://www.nnin.org/nnin_comp_psp_vault.html">NNIN Virtual Vault for Pseudopotentials</a> : This webpage maintained by the <a href="http://www.nnin.org/nnin_compsim.html">NNIN/C</a> provides a searchable database of pseudopotentials for density functional codes as well as links to pseudopotential generators, converters, and other online databases.</li>
<li><a href="http://www.physics.rutgers.edu/~dhv/uspp/">Vanderbilt Ultra-Soft Pseudopotential Site</a> : Website of <a href="/facts/David_Vanderbilt/H7Kxq1e5">David Vanderbilt</a> with links to codes that implement ultrasoft pseudopotentials and libraries of generated pseudopotentials.</li>
<li><a href="https://www.physics.rutgers.edu/gbrv/">GBRV pseudopotential site</a> : This site hosts the GBRV pseudopotential library</li>
<li><a href="https://www.pseudo-dojo.org">PseudoDojo</a> : This site collates tested pseudo potentials sorted by type, accuracy, and efficiency, shows information on convergence of various tested properties and provides download options.</li>
<li><a href="https://www.materialscloud.org/discover/sssp/table/">SSSP</a> : Standard Solid State Pseudopotentials</li></ul>
<h2 id="further-reading">Further reading</h2>
<ul><li><a href="/facts/Hans_Hellmann/9dSIWSMc">Hellmann, Hans</a> (1935), <a href="https://archive.today/20130223111650/http://jcp.aip.org/resource/1/jcpsa6/v3/i1/p61_s1">"A New Approximation Method in the Problem of Many Electrons"</a>, Journal of Chemical Physics, vol. 3, no. 1, Karpow-Institute for Physical Chemistry, Moscow, p. 61, <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/1935JChPh...3...61H">1935JChPh...3...61H</a>, <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1063%2F1.1749559">10.1063/1.1749559</a>, <a href="/facts/ISSN_(identifier)/DPAflDvU">ISSN</a> <a href="https://search.worldcat.org/issn/0021-9606">0021-9606</a>, archived from <a href="http://jcp.aip.org/resource/1/jcpsa6/v3/i1/p61_s1">the original</a> on 2013-02-23</li>
<li>Hellmann, H.; Kassatotschkin, W. (1936), <a href="https://archive.today/20130223083105/http://jcp.aip.org/resource/1/jcpsa6/v4/i5/p324_s2">"Metallic Binding According to the Combined Approximation Procedure"</a>, Journal of Chemical Physics, vol. 4, no. 5, Karpow-Institute for Physical Chemistry, Moscow, p. 324, <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/1936JChPh...4..324H">1936JChPh...4..324H</a>, <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1063%2F1.1749851">10.1063/1.1749851</a>, <a href="/facts/ISSN_(identifier)/DPAflDvU">ISSN</a> <a href="https://search.worldcat.org/issn/0021-9606">0021-9606</a>, archived from <a href="http://jcp.aip.org/resource/1/jcpsa6/v4/i5/p324_s2">the original</a> on 2013-02-23</li>
<li>Harrison, Walter Ashley (1966), Pseudopotentials in the theory of metals, Frontiers in Physics, University of Virginia</li>
<li>Brust, David (1968), Alder, Berni (ed.), "The Pseudopotential Method and the Single-Particle Electronic Excitation Spectra of Crystals", Methods in Computational Physics, vol. 8, New York: Academic Press, pp. 33–61, <a href="/facts/ISSN_(identifier)/DPAflDvU">ISSN</a> <a href="https://search.worldcat.org/issn/0076-6860">0076-6860</a></li>
<li><a href="/facts/Volker_Heine/jhf2Ipl3">Heine, Volker</a> (1970), "The Pseudopotential Concept", Solid State Physics, Solid State Physics, vol. 24, Academic Press, pp. 1–36, <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2FS0081-1947%2808%2960069-7">10.1016/S0081-1947(08)60069-7</a>, <a href="/facts/ISBN_(identifier)/15AdSPa9">ISBN</a> 9780126077247</li>
<li>Pickett, Warren E. (April 1989), "Pseudopotential methods in condensed matter applications", Computer Physics Reports, vol. 9, no. 3, pp. 115–197, <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/1989CoPhR...9..115P">1989CoPhR...9..115P</a>, <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2F0167-7977%2889%2990002-6">10.1016/0167-7977(89)90002-6</a></li>
<li>Hamann, D. R. (2013), "Optimized norm-conserving Vanderbilt pseudopotentials", Physical Review B, vol. 88, no. 8, p. 085117, <a href="/facts/ArXiv_(identifier)/H6EtgnBe">arXiv</a>:<a href="https://arxiv.org/abs/1306.4707">1306.4707</a>, <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/2013PhRvB..88h5117H">2013PhRvB..88h5117H</a>, <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1103%2FPhysRevB.88.085117">10.1103/PhysRevB.88.085117</a>, <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:119232272">119232272</a></li>
<li>Lejaeghere, K.; Bihlmayer, G.; Bjorkman, T.; Blaha, P.; Blugel, S.; Blum, V.; Caliste, D.; Castelli, I. E.; Clark, S. J.; Dal Corso, A.; de Gironcoli, S.; Deutsch, T.; Dewhurst, J. K.; Di Marco, I.; Draxl, C.; Du ak, M.; Eriksson, O.; Flores-Livas, J. A.; Garrity, K. F.; Genovese, L.; Giannozzi, P.; Giantomassi, M.; Goedecker, S.; Gonze, X.; Granas, O.; Gross, E. K. U.; Gulans, A.; Gygi, F.; Hamann, D. R.; Hasnip, P. J.; Holzwarth, N. A. W.; Iu an, D.; Jochym, D. B.; Jollet, F.; Jones, D.; Kresse, G.; Koepernik, K.; Kucukbenli, E.; Kvashnin, Y. O.; Locht, I. L. M.; Lubeck, S.; Marsman, M.; Marzari, N.; Nitzsche, U.; Nordstrom, L.; Ozaki, T.; Paulatto, L.; Pickard, C. J.; Poelmans, W.; Probert, M. I. J.; Refson, K.; Richter, M.; Rignanese, G.-M.; Saha, S.; Scheffler, M.; Schlipf, M.; Schwarz, K.; Sharma, S.; Tavazza, F.; Thunstrom, P.; Tkatchenko, A.; Torrent, M.; Vanderbilt, D.; van Setten, M. J.; Van Speybroeck, V.; Wills, J. M.; Yates, J. R.; Zhang, G.-X.; Cottenier, S. (2016), "Reproducibility in density functional theory calculations of solids", Science, 351 (6280): aad3000, <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/2016Sci...351.....L">2016Sci...351.....L</a>, <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1126%2Fscience.aad3000">10.1126/science.aad3000</a>, <a href="/facts/Hdl_(identifier)/rdebSxmC">hdl</a>:<a href="https://hdl.handle.net/1854%2FLU-7191263">1854/LU-7191263</a>, <a href="/facts/ISSN_(identifier)/DPAflDvU">ISSN</a> <a href="https://search.worldcat.org/issn/0036-8075">0036-8075</a>, <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/27013736">27013736</a></li>
<li>Bosoni, Emanuele; Beal, Louis; Bercx, Marnik; Blaha, Peter; Blügel, Stefan; Bröder, Jens; Callsen, Martin; Cottenier, Stefaan; Degomme, Augustin; Dikan, Vladimir; Eimre, Kristjan; Flage-Larsen, Espen; Fornari, Marco; Garcia, Alberto; Genovese, Luigi; Giantomassi, Matteo; Huber, Sebastiaan P.; Janssen, Henning; Kastlunger, Georg; Krack, Matthias; Kresse, Georg; Kühne, Thomas D.; Lejaeghere, Kurt; Madsen, Georg K. H.; Marsman, Martijn; Marzari, Nicola; Michalicek, Gregor; Mirhosseini, Hossein; Müller, Tiziano M. A.; Petretto, Guido; Pickard, Chris J.; Poncé, Samuel; Rignanese, Gian-Marco; Rubel, Oleg; Ruh, Thomas; Sluydts, Michael; Vanpoucke, Danny E. P.; Vijay, Sudarshan; Wolloch, Michael; Wortmann, Daniel; Yakutovich, Aliaksandr V.; Yu, Jusong; Zadoks, Austin; Zhu, Bonan; Pizzi, Giovanni (January 2024). "How to verify the precision of density-functional-theory implementations via reproducible and universal workflows". Nature Reviews Physics. 6 (1): 45–58. <a href="/facts/ArXiv_(identifier)/H6EtgnBe">arXiv</a>:<a href="https://arxiv.org/abs/2305.17274">2305.17274</a>. <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/2024NatRP...6...45B">2024NatRP...6...45B</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2Fs42254-023-00655-3">10.1038/s42254-023-00655-3</a>.</li></ul>

<h2 id="references">References</h2>

<ol>
<li id="fn:1">Schwerdtfeger, P. (August 2011), "The Pseudopotential Approximation in Electronic Structure Theory", ChemPhysChem, 12 (17): 3143–3155, doi:10.1002/cphc.201100387, PMID 21809427 <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></li>
<li id="fn:2">Louie, Steven G.; Froyen, Sverre; Cohen, Marvin L. (August 1982), "Nonlinear ionic pseudopotentials in spin-density-functional calculations", Physical Review B, 26 (4): 1738–1742, Bibcode:1982PhRvB..26.1738L, doi:10.1103/PhysRevB.26.1738 <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></li>
<li id="fn:3">Reis, Carlos L.; Pacheco, J. M.; Martins, José Luís (October 2003), "First-principles norm-conserving pseudopotential with explicit incorporation of semicore states", Physical Review B, vol. 68, no. 15, American Physical Society, p. 155111, Bibcode:2003PhRvB..68o5111R, doi:10.1103/PhysRevB.68.155111 <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></li>
<li id="fn:4">M. L. Cohen, J. R. Chelikowsky, "Electronic Structure and Optical Spectra of Semiconductors", (Springer Verlag, Berlin 1988) <a href="#fnref:4" class="footnote-back-ref">↩</a></li>
<li id="fn:5">Hamann, D. R.; Schlüter, M.; Chiang, C. (1979-11-12). "Norm-Conserving Pseudopotentials". Physical Review Letters. 43 (20): 1494–1497. Bibcode:1979PhRvL..43.1494H. doi:10.1103/PhysRevLett.43.1494. <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></li>
<li id="fn:6">Bachelet, G. B.; Hamann, D. R.; Schlüter, M. (October 1982), "Pseudopotentials that work: From H to Pu", Physical Review B, vol. 26, no. 8, American Physical Society, pp. 4199–4228, Bibcode:1982PhRvB..26.4199B, doi:10.1103/PhysRevB.26.4199 <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></li>
<li id="fn:7">Vanderbilt, David (April 1990), "Soft self-consistent pseudopotentials in a generalized eigenvalue formalism", Physical Review B, vol. 41, no. 11, American Physical Society, pp. 7892–7895, Bibcode:1990PhRvB..41.7892V, doi:10.1103/PhysRevB.41.7892, PMID 9993096 <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></li>
<li id="fn:8">Kresse, G.; Joubert, D. (1999). "From ultrasoft pseudopotentials to the projector augmented-wave method". Physical Review B. 59 (3): 1758–1775. Bibcode:1999PhRvB..59.1758K. doi:10.1103/PhysRevB.59.1758. <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:8" class="footnote-back-ref">↩</a></li>
<li id="fn:9">E. Fermi (July 1936), "Motion of neutrons in hydrogenous substances", Ricerca Scientifica, 7: 13–52 <a href="#fnref:9" class="footnote-back-ref">↩</a></li>
<li id="fn:10">Squires, Introduction to the Theory of Thermal Neutron Scattering, Dover Publications (1996) ISBN 0-486-69447-X <a href="/wiki/ISBN_(identifier)" target="_blank">/wiki/ISBN_(identifier)</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></li>
<li id="fn:11">J. C. Phillips (November 1958), "Energy-Band Interpolation Scheme Based on a Pseudopotential", Physical Review, 112 (3): 685–695, Bibcode:1958PhRv..112..685P, doi:10.1103/PhysRev.112.685 <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:11" class="footnote-back-ref">↩</a></li>
</ol>

Pseudopotential open-in-new

Pseudopotential