X-Git-Url: https://hackdaworld.org/gitweb/?a=blobdiff_plain;f=posic%2Fthesis%2Fbasics.tex;h=0e62f52459d15319738bdc7228cdec2b75c41e07;hb=308fce67d5c701822d5cb2d960a056644498cd03;hp=e71ece7c97ab9817da7a4ae3a583d90c9dbd5cff;hpb=5b013258b564a15f580b0b4275067c44da4e15ce;p=lectures%2Flatex.git diff --git a/posic/thesis/basics.tex b/posic/thesis/basics.tex index e71ece7..0e62f52 100644 --- a/posic/thesis/basics.tex +++ b/posic/thesis/basics.tex @@ -321,9 +321,9 @@ The answer to this question, whether the charge density completely characterizes Considering a system with a nondegenerate ground state, there is obviously only one ground-state charge density $n_0(\vec{r})$ that corresponds to a given potential $V(\vec{r})$. In 1964, Hohenberg and Kohn showed the opposite and far less obvious result~\cite{hohenberg64}. -Employing no more than the Rayleigh-Ritz minimal principle it is concluded by {\em reductio ad absurdum} that for a nondegenerate ground state the same charge density cannot be generated by different potentials. +Employing no more than the Rayleigh-Ritz minimal principle, it is concluded by {\em reductio ad absurdum} that for a nondegenerate ground state the same charge density cannot be generated by different potentials. Thus, the charge density of the ground state $n_0(\vec{r})$ uniquely determines the potential $V(\vec{r})$ and, consequently, the full Hamiltonian and ground-state energy $E_0$. -In mathematical terms the full many-electron ground state is a unique functional of the charge density. +In mathematical terms, the full many-electron ground state is a unique functional of the charge density. In particular, $E$ is a functional $E[n(\vec{r})]$ of $n(\vec{r})$. The ground-state charge density $n_0(\vec{r})$ minimizes the energy functional $E[n(\vec{r})]$, its value corresponding to the ground-state energy $E_0$, which enables the formulation of a minimal principle in terms of the charge density~\cite{hohenberg64,levy82} @@ -386,12 +386,12 @@ The KS equations may be considered the formal exactification of the Hartree theo In addition to the Hartree-Fock (HF) method, KS theory includes the difference of the kinetic energy of interacting and non-interacting electrons as well as the remaining contributions to the correlation energy that are not part of the HF correlation. The self-consistent KS equations \eqref{eq:basics:kse1}, \eqref{eq:basics:kse2} and \eqref{eq:basics:kse3} are non-linear partial differential equations, which may be solved numerically by an iterative process. -Starting from a first approximation for $n(\vec{r})$ the effective potential $V_{\text{eff}}(\vec{r})$ can be constructed followed by determining the one-electron orbitals $\Phi_i(\vec{r})$, which solve the single-particle Schr\"odinger equation for the respective potential. +Starting from a first approximation for $n(\vec{r})$, the effective potential $V_{\text{eff}}(\vec{r})$ can be constructed followed by determining the one-electron orbitals $\Phi_i(\vec{r})$, which solve the single-particle Schr\"odinger equation for the respective potential. The $\Phi_i(\vec{r})$ are used to obtain a new expression for $n(\vec{r})$. These steps are repeated until the initial and new density are equal or reasonably converged. Again, it is worth to note that the KS equations are formally exact. -Assuming exact functionals $E_{\text{xc}}[n(\vec{r})]$ and potentials $V_{\text{xc}}(\vec{r})$ all many-body effects are included. +Assuming exact functionals $E_{\text{xc}}[n(\vec{r})]$ and potentials $V_{\text{xc}}(\vec{r})$, all many-body effects are included. Clearly, this directs attention to the functional, which now contains the costs involved with the many-electron problem. \subsection{Approximations for exchange and correlation} @@ -400,7 +400,7 @@ Clearly, this directs attention to the functional, which now contains the costs As discussed above, the HK and KS formulations are exact and so far no approximations except the adiabatic approximation entered the theory. However, to make concrete use of the theory, effective approximations for the exchange and correlation energy functional $E_{\text{xc}}[n(\vec{r})]$ are required. -Most simple and at the same time remarkably useful is the approximation of $E_{\text{xc}}[n(\vec{r})]$ by a function of the local density~\cite{kohn65} +Most simple and at the same time remarkably useful, is the approximation of $E_{\text{xc}}[n(\vec{r})]$ by a function of the local density~\cite{kohn65}, \begin{equation} E^{\text{LDA}}_{\text{xc}}[n(\vec{r})]=\int\epsilon_{\text{xc}}(n(\vec{r}))n(\vec{r}) d\vec{r} \text{ ,} @@ -428,13 +428,13 @@ This is called the generalized-gradient approximation (GGA), which expresses the E^{\text{GGA}}_{\text{xc}}[n(\vec{r})]=\int\epsilon_{\text{xc}}(n(\vec{r}),|\nabla n(\vec{r})|)n(\vec{r}) d\vec{r} \text{ .} \end{equation} -These functionals constitute the simplest extensions of LDA for inhomogeneous systems. -At modest computational costs gradient-corrected functionals very often yield much better results than the LDA with respect to cohesive and binding energies. +This functional constitutes the simplest extension of the LDA for inhomogeneous systems. +At modest computational costs, gradient-corrected functionals very often yield much better results than the LDA with respect to cohesive and binding energies. \subsection{Plane-wave basis set} Finally, a set of basis functions is required to represent the one-electron KS wave functions. -With respect to the numerical treatment it is favorable to approximate the wave functions by linear combinations of a finite number of such basis functions. +With respect to the numerical treatment, it is favorable to approximate the wave functions by linear combinations of a finite number of such basis functions. Convergence of the basis set, i.e.\ convergence of the wave functions with respect to the amount of basis functions, is most crucial for the accuracy of the numerical calculations. Two classes of basis sets, the plane-wave and local basis sets, exist. @@ -448,7 +448,7 @@ Another approach is to represent the KS wave functions by plane waves. In fact, the employed \textsc{vasp} software is solving the KS equations within a plane-wave (PW) basis set. The idea is based on the Bloch theorem~\cite{bloch29}, which states that in a periodic crystal each electronic wave function $\Phi_i(\vec{r})$ can be written as the product of a wave-like envelope function $\exp(i\vec{kr})$ and a function that has the same periodicity as the lattice. The latter one can be expressed by a Fourier series, i.e.\ a discrete set of plane waves whose wave vectors just correspond to reciprocal lattice vectors $\vec{G}$ of the crystal. -Thus, the one-electron wave function $\Phi_i(\vec{r})$ associated with the wave vector $\vec{k}$ can be expanded in terms of a discrete PW basis set +Thus, the one-electron wave function $\Phi_i(\vec{r})$ associated with the wave vector $\vec{k}$ can be expanded in terms of a discrete PW basis set: \begin{equation} \Phi_i(\vec{r})=\sum_{\vec{G} %, |\vec{G}+\vec{k}|