| 831 |
|
error of splitting method in terms of commutator of the |
| 832 |
|
operators(\ref{introEquation:exponentialOperator}) associated with |
| 833 |
|
the sub-flow. For operators $hX$ and $hY$ which are associate to |
| 834 |
< |
$\varphi_1(t)$ and $\varphi_2(t$ respectively , we have |
| 834 |
> |
$\varphi_1(t)$ and $\varphi_2(t)$ respectively , we have |
| 835 |
|
\begin{equation} |
| 836 |
|
\exp (hX + hY) = \exp (hZ) |
| 837 |
|
\end{equation} |
| 846 |
|
\] |
| 847 |
|
Applying Baker-Campbell-Hausdorff formula to Sprang splitting, we |
| 848 |
|
can obtain |
| 849 |
< |
\begin{eqnarray*} |
| 849 |
> |
\begin{equation} |
| 850 |
|
\exp (h X/2)\exp (h Y)\exp (h X/2) & = & \exp (h X + h Y + h^2 |
| 851 |
|
[X,Y]/4 + h^2 [Y,X]/4 \\ & & \mbox{} + h^2 [X,X]/8 + h^2 [Y,Y]/8 \\ |
| 852 |
|
& & \mbox{} + h^3 [Y,[Y,X]]/12 - h^3 [X,[X,Y]]/24 & & \mbox{} + |
| 853 |
|
\ldots ) |
| 854 |
< |
\end{eqnarray*} |
| 854 |
> |
\end{equation} |
| 855 |
|
Since \[ [X,Y] + [Y,X] = 0\] and \[ [X,X] = 0\], the dominant local |
| 856 |
|
error of Spring splitting is proportional to $h^3$. The same |
| 857 |
|
procedure can be applied to general splitting, of the form |
| 892 |
|
simulations. For instance, instantaneous temperature of an |
| 893 |
|
Hamiltonian system of $N$ particle can be measured by |
| 894 |
|
\[ |
| 895 |
< |
T(t) = \sum\limits_{i = 1}^N {\frac{{m_i v_i^2 }}{{fk_B }}} |
| 895 |
> |
T = \sum\limits_{i = 1}^N {\frac{{m_i v_i^2 }}{{fk_B }}} |
| 896 |
|
\] |
| 897 |
|
where $m_i$ and $v_i$ are the mass and velocity of $i$th particle |
| 898 |
|
respectively, $f$ is the number of degrees of freedom, and $k_B$ is |
| 913 |
|
These three individual steps will be covered in the following |
| 914 |
|
sections. Sec.~\ref{introSec:initialSystemSettings} deals with the |
| 915 |
|
initialization of a simulation. Sec.~\ref{introSec:production} will |
| 916 |
< |
discusses issues in production run, including the force evaluation |
| 917 |
< |
and the numerical integration schemes of the equations of motion . |
| 918 |
< |
Sec.~\ref{introSection:Analysis} provides the theoretical tools for |
| 919 |
< |
trajectory analysis. |
| 916 |
> |
discusses issues in production run. Sec.~\ref{introSection:Analysis} |
| 917 |
> |
provides the theoretical tools for trajectory analysis. |
| 918 |
|
|
| 919 |
|
\subsection{\label{introSec:initialSystemSettings}Initialization} |
| 920 |
|
|
| 984 |
|
|
| 985 |
|
\subsection{\label{introSection:production}Production} |
| 986 |
|
|
| 987 |
< |
\subsubsection{\label{introSec:forceCalculation}The Force Calculation} |
| 987 |
> |
Production run is the most important steps of the simulation, in |
| 988 |
> |
which the equilibrated structure is used as a starting point and the |
| 989 |
> |
motions of the molecules are collected for later analysis. In order |
| 990 |
> |
to capture the macroscopic properties of the system, the molecular |
| 991 |
> |
dynamics simulation must be performed in correct and efficient way. |
| 992 |
> |
|
| 993 |
> |
The most expensive part of a molecular dynamics simulation is the |
| 994 |
> |
calculation of non-bonded forces, such as van der Waals force and |
| 995 |
> |
Coulombic forces \textit{etc}. For a system of $N$ particles, the |
| 996 |
> |
complexity of the algorithm for pair-wise interactions is $O(N^2 )$, |
| 997 |
> |
which making large simulations prohibitive in the absence of any |
| 998 |
> |
computation saving techniques. |
| 999 |
|
|
| 1000 |
< |
\subsubsection{\label{introSection:integrationSchemes} Integration |
| 1001 |
< |
Schemes} |
| 1000 |
> |
A natural approach to avoid system size issue is to represent the |
| 1001 |
> |
bulk behavior by a finite number of the particles. However, this |
| 1002 |
> |
approach will suffer from the surface effect. To offset this, |
| 1003 |
> |
\textit{Periodic boundary condition} is developed to simulate bulk |
| 1004 |
> |
properties with a relatively small number of particles. In this |
| 1005 |
> |
method, the simulation box is replicated throughout space to form an |
| 1006 |
> |
infinite lattice. During the simulation, when a particle moves in |
| 1007 |
> |
the primary cell, its image in other cells move in exactly the same |
| 1008 |
> |
direction with exactly the same orientation. Thus, as a particle |
| 1009 |
> |
leaves the primary cell, one of its images will enter through the |
| 1010 |
> |
opposite face. |
| 1011 |
> |
%\begin{figure} |
| 1012 |
> |
%\centering |
| 1013 |
> |
%\includegraphics[width=\linewidth]{pbcFig.eps} |
| 1014 |
> |
%\caption[An illustration of periodic boundary conditions]{A 2-D |
| 1015 |
> |
%illustration of periodic boundary conditions. As one particle leaves |
| 1016 |
> |
%the right of the simulation box, an image of it enters the left.} |
| 1017 |
> |
%\label{introFig:pbc} |
| 1018 |
> |
%\end{figure} |
| 1019 |
> |
|
| 1020 |
> |
%cutoff and minimum image convention |
| 1021 |
> |
Another important technique to improve the efficiency of force |
| 1022 |
> |
evaluation is to apply cutoff where particles farther than a |
| 1023 |
> |
predetermined distance, are not included in the calculation |
| 1024 |
> |
\cite{Frenkel1996}. The use of a cutoff radius will cause a |
| 1025 |
> |
discontinuity in the potential energy curve |
| 1026 |
> |
(Fig.~\ref{introFig:shiftPot}). Fortunately, one can shift the |
| 1027 |
> |
potential to ensure the potential curve go smoothly to zero at the |
| 1028 |
> |
cutoff radius. Cutoff strategy works pretty well for Lennard-Jones |
| 1029 |
> |
interaction because of its short range nature. However, simply |
| 1030 |
> |
truncating the electrostatic interaction with the use of cutoff has |
| 1031 |
> |
been shown to lead to severe artifacts in simulations. Ewald |
| 1032 |
> |
summation, in which the slowly conditionally convergent Coulomb |
| 1033 |
> |
potential is transformed into direct and reciprocal sums with rapid |
| 1034 |
> |
and absolute convergence, has proved to minimize the periodicity |
| 1035 |
> |
artifacts in liquid simulations. Taking the advantages of the fast |
| 1036 |
> |
Fourier transform (FFT) for calculating discrete Fourier transforms, |
| 1037 |
> |
the particle mesh-based methods are accelerated from $O(N^{3/2})$ to |
| 1038 |
> |
$O(N logN)$. An alternative approach is \emph{fast multipole |
| 1039 |
> |
method}, which treats Coulombic interaction exactly at short range, |
| 1040 |
> |
and approximate the potential at long range through multipolar |
| 1041 |
> |
expansion. In spite of their wide acceptances at the molecular |
| 1042 |
> |
simulation community, these two methods are hard to be implemented |
| 1043 |
> |
correctly and efficiently. Instead, we use a damped and |
| 1044 |
> |
charge-neutralized Coulomb potential method developed by Wolf and |
| 1045 |
> |
his coworkers. The shifted Coulomb potential for particle $i$ and |
| 1046 |
> |
particle $j$ at distance $r_{rj}$ is given by: |
| 1047 |
> |
\begin{equation} |
| 1048 |
> |
V(r_{ij})= \frac{q_i q_j \textrm{erfc}(\alpha |
| 1049 |
> |
r_{ij})}{r_{ij}}-\lim_{r_{ij}\rightarrow |
| 1050 |
> |
R_\textrm{c}}\left\{\frac{q_iq_j \textrm{erfc}(\alpha |
| 1051 |
> |
r_{ij})}{r_{ij}}\right\}. \label{introEquation:shiftedCoulomb} |
| 1052 |
> |
\end{equation} |
| 1053 |
> |
where $\alpha$ is the convergence parameter. Due to the lack of |
| 1054 |
> |
inherent periodicity and rapid convergence,this method is extremely |
| 1055 |
> |
efficient and easy to implement. |
| 1056 |
> |
%\begin{figure} |
| 1057 |
> |
%\centering |
| 1058 |
> |
%\includegraphics[width=\linewidth]{pbcFig.eps} |
| 1059 |
> |
%\caption[An illustration of shifted Coulomb potential]{An illustration of shifted Coulomb potential.} |
| 1060 |
> |
%\label{introFigure:shiftedCoulomb} |
| 1061 |
> |
%\end{figure} |
| 1062 |
|
|
| 1063 |
+ |
%multiple time step |
| 1064 |
+ |
|
| 1065 |
|
\subsection{\label{introSection:Analysis} Analysis} |
| 1066 |
|
|
| 1067 |
|
Recently, advanced visualization technique are widely applied to |
| 1076 |
|
|
| 1077 |
|
\subsubsection{\label{introSection:thermodynamicsProperties}Thermodynamics Properties} |
| 1078 |
|
|
| 1079 |
+ |
Thermodynamics properties, which can be expressed in terms of some |
| 1080 |
+ |
function of the coordinates and momenta of all particles in the |
| 1081 |
+ |
system, can be directly computed from molecular dynamics. The usual |
| 1082 |
+ |
way to measure the pressure is based on virial theorem of Clausius |
| 1083 |
+ |
which states that the virial is equal to $-3Nk_BT$. For a system |
| 1084 |
+ |
with forces between particles, the total virial, $W$, contains the |
| 1085 |
+ |
contribution from external pressure and interaction between the |
| 1086 |
+ |
particles: |
| 1087 |
+ |
\[ |
| 1088 |
+ |
W = - 3PV + \left\langle {\sum\limits_{i < j} {r{}_{ij} \cdot |
| 1089 |
+ |
f_{ij} } } \right\rangle |
| 1090 |
+ |
\] |
| 1091 |
+ |
where $f_{ij}$ is the force between particle $i$ and $j$ at a |
| 1092 |
+ |
distance $r_{ij}$. Thus, the expression for the pressure is given |
| 1093 |
+ |
by: |
| 1094 |
+ |
\begin{equation} |
| 1095 |
+ |
P = \frac{{Nk_B T}}{V} - \frac{1}{{3V}}\left\langle {\sum\limits_{i |
| 1096 |
+ |
< j} {r{}_{ij} \cdot f_{ij} } } \right\rangle |
| 1097 |
+ |
\end{equation} |
| 1098 |
+ |
|
| 1099 |
|
\subsubsection{\label{introSection:structuralProperties}Structural Properties} |
| 1100 |
|
|
| 1101 |
|
Structural Properties of a simple fluid can be described by a set of |
| 1102 |
|
distribution functions. Among these functions,\emph{pair |
| 1103 |
|
distribution function}, also known as \emph{radial distribution |
| 1104 |
< |
function}, are of most fundamental importance to liquid-state |
| 1105 |
< |
theory. Pair distribution function can be gathered by Fourier |
| 1106 |
< |
transforming raw data from a series of neutron diffraction |
| 1107 |
< |
experiments and integrating over the surface factor \cite{Powles73}. |
| 1108 |
< |
The experiment result can serve as a criterion to justify the |
| 1109 |
< |
correctness of the theory. Moreover, various equilibrium |
| 1110 |
< |
thermodynamic and structural properties can also be expressed in |
| 1111 |
< |
terms of radial distribution function \cite{allen87:csl}. |
| 1104 |
> |
function}, is of most fundamental importance to liquid-state theory. |
| 1105 |
> |
Pair distribution function can be gathered by Fourier transforming |
| 1106 |
> |
raw data from a series of neutron diffraction experiments and |
| 1107 |
> |
integrating over the surface factor \cite{Powles73}. The experiment |
| 1108 |
> |
result can serve as a criterion to justify the correctness of the |
| 1109 |
> |
theory. Moreover, various equilibrium thermodynamic and structural |
| 1110 |
> |
properties can also be expressed in terms of radial distribution |
| 1111 |
> |
function \cite{allen87:csl}. |
| 1112 |
|
|
| 1113 |
|
A pair distribution functions $g(r)$ gives the probability that a |
| 1114 |
|
particle $i$ will be located at a distance $r$ from a another |
| 1150 |
|
function is called \emph{auto correlation function}. One example of |
| 1151 |
|
auto correlation function is velocity auto-correlation function |
| 1152 |
|
which is directly related to transport properties of molecular |
| 1153 |
< |
liquids. Another example is the calculation of the IR spectrum |
| 1154 |
< |
through a Fourier transform of the dipole autocorrelation function. |
| 1153 |
> |
liquids: |
| 1154 |
> |
\[ |
| 1155 |
> |
D = \frac{1}{3}\int\limits_0^\infty {\left\langle {v(t) \cdot v(0)} |
| 1156 |
> |
\right\rangle } dt |
| 1157 |
> |
\] |
| 1158 |
> |
where $D$ is diffusion constant. Unlike velocity autocorrelation |
| 1159 |
> |
function which is averaging over time origins and over all the |
| 1160 |
> |
atoms, dipole autocorrelation are calculated for the entire system. |
| 1161 |
> |
The dipole autocorrelation function is given by: |
| 1162 |
> |
\[ |
| 1163 |
> |
c_{dipole} = \left\langle {u_{tot} (t) \cdot u_{tot} (t)} |
| 1164 |
> |
\right\rangle |
| 1165 |
> |
\] |
| 1166 |
> |
Here $u_{tot}$ is the net dipole of the entire system and is given |
| 1167 |
> |
by |
| 1168 |
> |
\[ |
| 1169 |
> |
u_{tot} (t) = \sum\limits_i {u_i (t)} |
| 1170 |
> |
\] |
| 1171 |
> |
In principle, many time correlation functions can be related with |
| 1172 |
> |
Fourier transforms of the infrared, Raman, and inelastic neutron |
| 1173 |
> |
scattering spectra of molecular liquids. In practice, one can |
| 1174 |
> |
extract the IR spectrum from the intensity of dipole fluctuation at |
| 1175 |
> |
each frequency using the following relationship: |
| 1176 |
> |
\[ |
| 1177 |
> |
\hat c_{dipole} (v) = \int_{ - \infty }^\infty {c_{dipole} (t)e^{ - |
| 1178 |
> |
i2\pi vt} dt} |
| 1179 |
> |
\] |
| 1180 |
|
|
| 1181 |
|
\section{\label{introSection:rigidBody}Dynamics of Rigid Bodies} |
| 1182 |
|
|
| 1238 |
|
where $I_{ii}$ is the diagonal element of the inertia tensor. This |
| 1239 |
|
constrained Hamiltonian equation subjects to a holonomic constraint, |
| 1240 |
|
\begin{equation} |
| 1241 |
< |
Q^T Q = 1$, \label{introEquation:orthogonalConstraint} |
| 1241 |
> |
Q^T Q = 1, \label{introEquation:orthogonalConstraint} |
| 1242 |
|
\end{equation} |
| 1243 |
|
which is used to ensure rotation matrix's orthogonality. |
| 1244 |
|
Differentiating \ref{introEquation:orthogonalConstraint} and using |
