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# Line 43 | Line 43 | Fig.~\ref{LCFig:SMCP}).
43   \begin{figure}
44   \centering
45   \includegraphics[width=\linewidth]{smcp.eps}
46 < \caption[]
47 < {}
46 > \caption[SmCP Phase Packing] {Four possible SmCP phase packings that
47 > are characterized by the relative tilt direction(A and S refer an
48 > anticlinic tilt or a synclinic ) and the polarization orientation (A
49 > and F represent antiferroelectric or ferroelectric polar order).}
50   \label{LCFig:SMCP}
51   \end{figure}
52  
# Line 181 | Line 183 | ratio between \textit{end-to-end} well depth $\epsilon
183   \begin{figure}
184   \centering
185   \includegraphics[width=\linewidth]{banana.eps}
186 < \caption[]{} \label{LCFig:BananaMolecule}
186 > \caption[Schematic representation of a typical banana shaped
187 > molecule]{Schematic representation of a typical banana shaped
188 > molecule.} \label{LCFig:BananaMolecule}
189   \end{figure}
190  
187 %\begin{figure}
188 %\centering
189 %\includegraphics[width=\linewidth]{bananGB.eps}
190 %\caption[]{} \label{LCFigure:BananaGB}
191 %\end{figure}
192
191   \begin{figure}
192   \centering
193   \includegraphics[width=\linewidth]{gb_scheme.eps}
194 < \caption[]{Schematic diagram showing definitions of the orientation
195 < vectors for a pair of Gay-Berne molecules}
196 < \label{LCFigure:GBScheme}
194 > \caption[Schematic diagram showing definitions of the orientation
195 > vectors for a pair of Gay-Berne molecules]{Schematic diagram showing
196 > definitions of the orientation vectors for a pair of Gay-Berne
197 > molecules} \label{LCFigure:GBScheme}
198   \end{figure}
199  
200   To account for the permanent dipolar interactions, there should be
# Line 271 | Line 270 | scatting\cite{Blum1971}. Latterly, expansion of the or
270   As a useful set of correlation functions to describe
271   position-orientation correlation, rotation invariants were first
272   applied in a spherical symmetric system to study x-ray and light
273 < scatting\cite{Blum1971}. Latterly, expansion of the orientation pair
273 > scatting\cite{Blum1972}. Latterly, expansion of the orientation pair
274   correlation in terms of rotation invariant for molecules of
275   arbitrary shape was introduce by Stone\cite{Stone1978} and adopted
276 < by other researchers in liquid crystal studies\cite{Berardi2000}.
276 > by other researchers in liquid crystal studies\cite{Berardi2003}.
277  
278   \begin{eqnarray}
279   S_{22}^{220} (r) & = & \frac{1}{{4\sqrt 5 }} \left< \delta (r -
# Line 292 | Line 291 | S_{00}^{221} (r) =  - \frac{{\sqrt 3 }}{{\sqrt {10} }}
291   \end{equation}
292  
293   \section{Results and Conclusion}
295 \label{sec:results and conclusion}
296
294   To investigate the molecular organization behavior due to different
295   dipolar orientation and position with respect to the center of the
296   molecule,

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