From d02fc9175bf382d3fede6800f667cda3de7528b3 Mon Sep 17 00:00:00 2001 From: hackbard Date: Mon, 26 Sep 2011 22:37:04 +0200 Subject: [PATCH] commas --- posic/thesis/basics.tex | 8 ++++---- 1 file changed, 4 insertions(+), 4 deletions(-) diff --git a/posic/thesis/basics.tex b/posic/thesis/basics.tex index e71ece7..8d57d43 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} -- 2.20.1