33 |
|
%\doublespacing |
34 |
|
|
35 |
|
\begin{abstract} |
36 |
< |
The free energies of several ice polymorphs in the low pressure regime |
37 |
< |
were calculated using thermodynamic integration. These integrations |
38 |
< |
were done for most of the common water models. Ice-{\it i}, a |
39 |
< |
structure we recently observed to be stable in one of the single-point |
40 |
< |
water models, was determined to be the stable crystalline state (at 1 |
41 |
< |
atm) for {\it all} the water models investigated. Phase diagrams were |
36 |
> |
The absolute free energies of several ice polymorphs which are stable |
37 |
> |
at low pressures were calculated using thermodynamic integration to a |
38 |
> |
reference system (the Einstein crystal). These integrations were |
39 |
> |
performed for most of the common water models (SPC/E, TIP3P, TIP4P, |
40 |
> |
TIP5P, SSD/E, SSD/RF). Ice-{\it i}, a structure we recently observed |
41 |
> |
crystallizing at room temperature for one of the single-point water |
42 |
> |
models, was determined to be the stable crystalline state (at 1 atm) |
43 |
> |
for {\it all} the water models investigated. Phase diagrams were |
44 |
|
generated, and phase coexistence lines were determined for all of the |
45 |
< |
known low-pressure ice structures under all of the common water |
46 |
< |
models. Additionally, potential truncation was shown to have an |
47 |
< |
effect on the calculated free energies, and can result in altered free |
48 |
< |
energy landscapes. |
45 |
> |
known low-pressure ice structures under all of these water models. |
46 |
> |
Additionally, potential truncation was shown to have an effect on the |
47 |
> |
calculated free energies, and can result in altered free energy |
48 |
> |
landscapes. Structure factor predictions for the new crystal were |
49 |
> |
generated and we await experimental confirmation of the existence of |
50 |
> |
this new polymorph. |
51 |
|
\end{abstract} |
52 |
|
|
53 |
|
%\narrowtext |
58 |
|
|
59 |
|
\section{Introduction} |
60 |
|
|
57 |
– |
Computer simulations are a valuable tool for studying the phase |
58 |
– |
behavior of systems ranging from small or simple molecules to complex |
59 |
– |
biological species.\cite{Matsumoto02,Li96,Marrink01} Useful techniques |
60 |
– |
have been developed to investigate the thermodynamic properites of |
61 |
– |
model substances, providing both qualitative and quantitative |
62 |
– |
comparisons between simulations and |
63 |
– |
experiment.\cite{Widom63,Frenkel84} Investigation of these properties |
64 |
– |
leads to the development of new and more accurate models, leading to |
65 |
– |
better understanding and depiction of physical processes and intricate |
66 |
– |
molecular systems. |
67 |
– |
|
61 |
|
Water has proven to be a challenging substance to depict in |
62 |
|
simulations, and a variety of models have been developed to describe |
63 |
|
its behavior under varying simulation |
64 |
< |
conditions.\cite{Rahman75,Berendsen81,Jorgensen83,Bratko85,Berendsen87,Liu96,Berendsen98,Mahoney00,Fennell04} |
64 |
> |
conditions.\cite{Stillinger74,Rahman75,Berendsen81,Jorgensen83,Bratko85,Berendsen87,Caldwell95,Liu96,Berendsen98,Dill00,Mahoney00,Fennell04} |
65 |
|
These models have been used to investigate important physical |
66 |
< |
phenomena like phase transitions, molecule transport, and the |
66 |
> |
phenomena like phase transitions, transport properties, and the |
67 |
|
hydrophobic effect.\cite{Yamada02,Marrink94,Gallagher03} With the |
68 |
|
choice of models available, it is only natural to compare the models |
69 |
|
under interesting thermodynamic conditions in an attempt to clarify |
70 |
|
the limitations of each of the |
71 |
|
models.\cite{Jorgensen83,Jorgensen98b,Clancy94,Mahoney01} Two |
72 |
< |
important property to quantify are the Gibbs and Helmholtz free |
72 |
> |
important properties to quantify are the Gibbs and Helmholtz free |
73 |
|
energies, particularly for the solid forms of water. Difficulty in |
74 |
|
these types of studies typically arises from the assortment of |
75 |
|
possible crystalline polymorphs that water adopts over a wide range of |
77 |
|
of ice, and it is a challenging task to investigate the entire free |
78 |
|
energy landscape.\cite{Sanz04} Ideally, research is focused on the |
79 |
|
phases having the lowest free energy at a given state point, because |
80 |
< |
these phases will dictate the true transition temperatures and |
80 |
> |
these phases will dictate the relevant transition temperatures and |
81 |
|
pressures for the model. |
82 |
|
|
83 |
|
In this paper, standard reference state methods were applied to known |
84 |
|
crystalline water polymorphs in the low pressure regime. This work is |
85 |
< |
unique in the fact that one of the crystal lattices was arrived at |
86 |
< |
through crystallization of a computationally efficient water model |
87 |
< |
under constant pressure and temperature conditions. Crystallization |
88 |
< |
events are interesting in and of |
89 |
< |
themselves;\cite{Matsumoto02,Yamada02} however, the crystal structure |
90 |
< |
obtained in this case is different from any previously observed ice |
91 |
< |
polymorphs in experiment or simulation.\cite{Fennell04} We have named |
92 |
< |
this structure Ice-{\it i} to indicate its origin in computational |
93 |
< |
simulation. The unit cell (Fig. \ref{iceiCell}A) consists of eight |
94 |
< |
water molecules that stack in rows of interlocking water |
95 |
< |
tetramers. Proton ordering can be accomplished by orienting two of the |
96 |
< |
molecules so that both of their donated hydrogen bonds are internal to |
97 |
< |
their tetramer (Fig. \ref{protOrder}). As expected in an ice crystal |
98 |
< |
constructed of water tetramers, the hydrogen bonds are not as linear |
99 |
< |
as those observed in ice $I_h$, however the interlocking of these |
100 |
< |
subunits appears to provide significant stabilization to the overall |
85 |
> |
unique in that one of the crystal lattices was arrived at through |
86 |
> |
crystallization of a computationally efficient water model under |
87 |
> |
constant pressure and temperature conditions. Crystallization events |
88 |
> |
are interesting in and of themselves;\cite{Matsumoto02,Yamada02} |
89 |
> |
however, the crystal structure obtained in this case is different from |
90 |
> |
any previously observed ice polymorphs in experiment or |
91 |
> |
simulation.\cite{Fennell04} We have named this structure Ice-{\it i} |
92 |
> |
to indicate its origin in computational simulation. The unit cell |
93 |
> |
(Fig. \ref{iceiCell}A) consists of eight water molecules that stack in |
94 |
> |
rows of interlocking water tetramers. Proton ordering can be |
95 |
> |
accomplished by orienting two of the molecules so that both of their |
96 |
> |
donated hydrogen bonds are internal to their tetramer |
97 |
> |
(Fig. \ref{protOrder}). As expected in an ice crystal constructed of |
98 |
> |
water tetramers, the hydrogen bonds are not as linear as those |
99 |
> |
observed in ice $I_h$, however the interlocking of these subunits |
100 |
> |
appears to provide significant stabilization to the overall |
101 |
|
crystal. The arrangement of these tetramers results in surrounding |
102 |
|
open octagonal cavities that are typically greater than 6.3 \AA\ in |
103 |
|
diameter. This relatively open overall structure leads to crystals |
105 |
|
|
106 |
|
\begin{figure} |
107 |
|
\includegraphics[width=\linewidth]{unitCell.eps} |
108 |
< |
\caption{Unit cells for (A) Ice-{\it i} and (B) Ice-$i^\prime$, the |
109 |
< |
elongated variant of Ice-{\it i}. The spheres represent the |
108 |
> |
\caption{Unit cells for (A) Ice-{\it i} and (B) Ice-{\it i}$^\prime$, |
109 |
> |
the elongated variant of Ice-{\it i}. The spheres represent the |
110 |
|
center-of-mass locations of the water molecules. The $a$ to $c$ |
111 |
|
ratios for Ice-{\it i} and Ice-{\it i}$^\prime$ are given by |
112 |
|
$a:2.1214c$ and $a:1.7850c$ respectively.} |
124 |
|
|
125 |
|
Results from our previous study indicated that Ice-{\it i} is the |
126 |
|
minimum energy crystal structure for the single point water models we |
127 |
< |
investigated (for discussions on these single point dipole models, see |
128 |
< |
our previous work and related |
127 |
> |
had investigated (for discussions on these single point dipole models, |
128 |
> |
see our previous work and related |
129 |
|
articles).\cite{Fennell04,Liu96,Bratko85} Those results only |
130 |
|
considered energetic stabilization and neglected entropic |
131 |
< |
contributions to the overall free energy. To address this issue, the |
132 |
< |
absolute free energy of this crystal was calculated using |
131 |
> |
contributions to the overall free energy. To address this issue, we |
132 |
> |
have calculated the absolute free energy of this crystal using |
133 |
|
thermodynamic integration and compared to the free energies of cubic |
134 |
|
and hexagonal ice $I$ (the experimental low density ice polymorphs) |
135 |
|
and ice B (a higher density, but very stable crystal structure |
138 |
|
from which Ice-{\it i} was crystallized (SSD/E) in addition to several |
139 |
|
common water models (TIP3P, TIP4P, TIP5P, and SPC/E) and a reaction |
140 |
|
field parametrized single point dipole water model (SSD/RF). It should |
141 |
< |
be noted that a second version of Ice-{\it i} (Ice-$i^\prime$) was used |
142 |
< |
in calculations involving SPC/E, TIP4P, and TIP5P. The unit cell of |
143 |
< |
this crystal (Fig. \ref{iceiCell}B) is similar to the Ice-{\it i} unit |
144 |
< |
it is extended in the direction of the (001) face and compressed along |
145 |
< |
the other two faces. |
141 |
> |
be noted that a second version of Ice-{\it i} (Ice-{\it i}$^\prime$) |
142 |
> |
was used in calculations involving SPC/E, TIP4P, and TIP5P. The unit |
143 |
> |
cell of this crystal (Fig. \ref{iceiCell}B) is similar to the Ice-{\it |
144 |
> |
i} unit it is extended in the direction of the (001) face and |
145 |
> |
compressed along the other two faces. There is typically a small |
146 |
> |
distortion of proton ordered Ice-{\it i}$^\prime$ that converts the |
147 |
> |
normally square tetramer into a rhombus with alternating approximately |
148 |
> |
85 and 95 degree angles. The degree of this distortion is model |
149 |
> |
dependent and significant enough to split the tetramer diagonal |
150 |
> |
location peak in the radial distribution function. |
151 |
|
|
152 |
|
\section{Methods} |
153 |
|
|
166 |
|
crystals at 200 K using the TIP3P, TIP4P, TIP5P, SPC/E, SSD/RF, and |
167 |
|
SSD/E water models.\cite{Baez95a} Liquid state free energies at 300 |
168 |
|
and 400 K for all of these water models were also determined using |
169 |
< |
this same technique in order to determine melting points and generate |
170 |
< |
phase diagrams. All simulations were carried out at densities |
171 |
< |
resulting in a pressure of approximately 1 atm at their respective |
172 |
< |
temperatures. |
169 |
> |
this same technique in order to determine melting points and to |
170 |
> |
generate phase diagrams. All simulations were carried out at densities |
171 |
> |
which correspond to a pressure of approximately 1 atm at their |
172 |
> |
respective temperatures. |
173 |
|
|
174 |
< |
A single thermodynamic integration involves a sequence of simulations |
175 |
< |
over which the system of interest is converted into a reference system |
176 |
< |
for which the free energy is known analytically. This transformation |
177 |
< |
path is then integrated in order to determine the free energy |
178 |
< |
difference between the two states: |
174 |
> |
Thermodynamic integration involves a sequence of simulations during |
175 |
> |
which the system of interest is converted into a reference system for |
176 |
> |
which the free energy is known analytically. This transformation path |
177 |
> |
is then integrated in order to determine the free energy difference |
178 |
> |
between the two states: |
179 |
|
\begin{equation} |
180 |
|
\Delta A = \int_0^1\left\langle\frac{\partial V(\lambda |
181 |
|
)}{\partial\lambda}\right\rangle_\lambda d\lambda, |
237 |
|
literature.\cite{Hermens88,Quintana92,Mezei92,Baez95b} These methods |
238 |
|
typically differ in regard to the path taken for switching off the |
239 |
|
interaction potential to convert the system to an ideal gas of water |
240 |
< |
molecules. In this study, we apply of one of the most convenient |
241 |
< |
methods and integrate over the $\lambda^4$ path, where all interaction |
242 |
< |
parameters are scaled equally by this transformation parameter. This |
243 |
< |
method has been shown to be reversible and provide results in |
244 |
< |
excellent agreement with other established methods.\cite{Baez95b} |
240 |
> |
molecules. In this study, we applied of one of the most convenient |
241 |
> |
methods and integrated over the $\lambda^4$ path, where all |
242 |
> |
interaction parameters are scaled equally by this transformation |
243 |
> |
parameter. This method has been shown to be reversible and provide |
244 |
> |
results in excellent agreement with other established |
245 |
> |
methods.\cite{Baez95b} |
246 |
|
|
247 |
|
Charge, dipole, and Lennard-Jones interactions were modified by a |
248 |
|
cubic switching between 100\% and 85\% of the cutoff value (9 \AA |
255 |
|
simulations.\cite{Onsager36} For a series of the least computationally |
256 |
|
expensive models (SSD/E, SSD/RF, and TIP3P), simulations were |
257 |
|
performed with longer cutoffs of 12 and 15 \AA\ to compare with the 9 |
258 |
< |
\AA\ cutoff results. Finally, results from the use of an Ewald |
259 |
< |
summation were estimated for TIP3P and SPC/E by performing |
260 |
< |
calculations with Particle-Mesh Ewald (PME) in the TINKER molecular |
261 |
< |
mechanics software package.\cite{Tinker} The calculated energy |
262 |
< |
difference in the presence and absence of PME was applied to the |
263 |
< |
previous results in order to predict changes to the free energy |
264 |
< |
landscape. |
258 |
> |
\AA\ cutoff results. Finally, the effects of utilizing an Ewald |
259 |
> |
summation were estimated for TIP3P and SPC/E by performing single |
260 |
> |
configuration calculations with Particle-Mesh Ewald (PME) in the |
261 |
> |
TINKER molecular mechanics software package.\cite{Tinker} The |
262 |
> |
calculated energy difference in the presence and absence of PME was |
263 |
> |
applied to the previous results in order to predict changes to the |
264 |
> |
free energy landscape. |
265 |
|
|
266 |
|
\section{Results and discussion} |
267 |
|
|
268 |
< |
The free energy of proton ordered Ice-{\it i} was calculated and |
268 |
> |
The free energy of proton-ordered Ice-{\it i} was calculated and |
269 |
|
compared with the free energies of proton ordered variants of the |
270 |
|
experimentally observed low-density ice polymorphs, $I_h$ and $I_c$, |
271 |
|
as well as the higher density ice B, observed by B\`{a}ez and Clancy |
275 |
|
$I_h$, was investigated initially, but was found to be not as stable |
276 |
|
as proton disordered or antiferroelectric variants of ice $I_h$. The |
277 |
|
proton ordered variant of ice $I_h$ used here is a simple |
278 |
< |
antiferroelectric version that we divised, and it has an 8 molecule |
278 |
> |
antiferroelectric version that we devised, and it has an 8 molecule |
279 |
|
unit cell similar to other predicted antiferroelectric $I_h$ |
280 |
|
crystals.\cite{Davidson84} The crystals contained 648 or 1728 |
281 |
|
molecules for ice B, 1024 or 1280 molecules for ice $I_h$, 1000 |
285 |
|
|
286 |
|
\begin{table*} |
287 |
|
\begin{minipage}{\linewidth} |
289 |
– |
\renewcommand{\thefootnote}{\thempfootnote} |
288 |
|
\begin{center} |
289 |
+ |
|
290 |
|
\caption{Calculated free energies for several ice polymorphs with a |
291 |
|
variety of common water models. All calculations used a cutoff radius |
292 |
|
of 9 \AA\ and were performed at 200 K and $\sim$1 atm. Units are |
293 |
< |
kcal/mol. Calculated error of the final digits is in parentheses. *Ice |
294 |
< |
$I_c$ rapidly converts to a liquid at 200 K with the SSD/RF model.} |
295 |
< |
\begin{tabular}{ l c c c c } |
293 |
> |
kcal/mol. Calculated error of the final digits is in parentheses.} |
294 |
> |
|
295 |
> |
\begin{tabular}{lcccc} |
296 |
|
\hline |
297 |
|
Water Model & $I_h$ & $I_c$ & B & Ice-{\it i}\\ |
298 |
|
\hline |
299 |
|
TIP3P & -11.41(2) & -11.23(3) & -11.82(3) & -12.30(3)\\ |
300 |
|
TIP4P & -11.84(3) & -12.04(2) & -12.08(3) & -12.33(3)\\ |
301 |
|
TIP5P & -11.85(3) & -11.86(2) & -11.96(2) & -12.29(2)\\ |
302 |
< |
SPC/E & -12.67(2) & -12.96(2) & -13.25(3) & -13.55(2)\\ |
302 |
> |
SPC/E & -12.87(2) & -13.05(2) & -13.26(3) & -13.55(2)\\ |
303 |
|
SSD/E & -11.27(2) & -11.19(4) & -12.09(2) & -12.54(2)\\ |
304 |
< |
SSD/RF & -11.51(2) & NA* & -12.08(3) & -12.29(2)\\ |
304 |
> |
SSD/RF & -11.51(2) & -11.47(2) & -12.08(3) & -12.29(2)\\ |
305 |
|
\end{tabular} |
306 |
|
\label{freeEnergy} |
307 |
|
\end{center} |
310 |
|
|
311 |
|
The free energy values computed for the studied polymorphs indicate |
312 |
|
that Ice-{\it i} is the most stable state for all of the common water |
313 |
< |
models studied. With the free energy at these state points, the |
314 |
< |
Gibbs-Helmholtz equation was used to project to other state points and |
315 |
< |
to build phase diagrams. Figures |
313 |
> |
models studied. With the calculated free energy at these state points, |
314 |
> |
the Gibbs-Helmholtz equation was used to project to other state points |
315 |
> |
and to build phase diagrams. Figures |
316 |
|
\ref{tp3phasedia} and \ref{ssdrfphasedia} are example diagrams built |
317 |
|
from the free energy results. All other models have similar structure, |
318 |
< |
although the crossing points between the phases exist at slightly |
318 |
> |
although the crossing points between the phases move to slightly |
319 |
|
different temperatures and pressures. It is interesting to note that |
320 |
|
ice $I$ does not exist in either cubic or hexagonal form in any of the |
321 |
|
phase diagrams for any of the models. For purposes of this study, ice |
322 |
|
B is representative of the dense ice polymorphs. A recent study by |
323 |
|
Sanz {\it et al.} goes into detail on the phase diagrams for SPC/E and |
324 |
< |
TIP4P in the high pressure regime.\cite{Sanz04} |
324 |
> |
TIP4P at higher pressures than those studied here.\cite{Sanz04} |
325 |
|
|
326 |
|
\begin{figure} |
327 |
|
\includegraphics[width=\linewidth]{tp3PhaseDia.eps} |
346 |
|
|
347 |
|
\begin{table*} |
348 |
|
\begin{minipage}{\linewidth} |
350 |
– |
\renewcommand{\thefootnote}{\thempfootnote} |
349 |
|
\begin{center} |
350 |
+ |
|
351 |
|
\caption{Melting ($T_m$), boiling ($T_b$), and sublimation ($T_s$) |
352 |
|
temperatures at 1 atm for several common water models compared with |
353 |
|
experiment. The $T_m$ and $T_s$ values from simulation correspond to a |
354 |
|
transition between Ice-{\it i} (or Ice-{\it i}$^\prime$) and the |
355 |
|
liquid or gas state.} |
356 |
< |
\begin{tabular}{ l c c c c c c c } |
356 |
> |
|
357 |
> |
\begin{tabular}{lccccccc} |
358 |
|
\hline |
359 |
< |
Equilibria Point & TIP3P & TIP4P & TIP5P & SPC/E & SSD/E & SSD/RF & Exp.\\ |
359 |
> |
Equilibrium Point & TIP3P & TIP4P & TIP5P & SPC/E & SSD/E & SSD/RF & Exp.\\ |
360 |
|
\hline |
361 |
|
$T_m$ (K) & 269(4) & 266(5) & 271(4) & 296(3) & - & 278(4) & 273\\ |
362 |
|
$T_b$ (K) & 357(2) & 354(2) & 337(2) & 396(2) & - & 348(2) & 373\\ |
385 |
|
not exhibit a melting point at 1 atm, but it shows a sublimation point |
386 |
|
at 355 K. This is due to the significant stability of Ice-{\it i} over |
387 |
|
all other polymorphs for this particular model under these |
388 |
< |
conditions. While troubling, this behavior turned out to be |
389 |
< |
advantageous in that it facilitated the spontaneous crystallization of |
390 |
< |
Ice-{\it i}. These observations provide a warning that simulations of |
388 |
> |
conditions. While troubling, this behavior resulted in spontaneous |
389 |
> |
crystallization of Ice-{\it i} and led us to investigate this |
390 |
> |
structure. These observations provide a warning that simulations of |
391 |
|
SSD/E as a ``liquid'' near 300 K are actually metastable and run the |
392 |
< |
risk of spontaneous crystallization. However, this risk changes when |
392 |
> |
risk of spontaneous crystallization. However, this risk lessens when |
393 |
|
applying a longer cutoff. |
394 |
|
|
395 |
|
\begin{figure} |
396 |
|
\includegraphics[width=\linewidth]{cutoffChange.eps} |
397 |
|
\caption{Free energy as a function of cutoff radius for (A) SSD/E, (B) |
398 |
< |
TIP3P, and (C) SSD/RF. Data points omitted include SSD/E: $I_c$ 12 |
399 |
< |
\AA\, TIP3P: $I_c$ 12 \AA\ and B 12 \AA\, and SSD/RF: $I_c$ 9 |
400 |
< |
\AA . These crystals are unstable at 200 K and rapidly convert into |
401 |
< |
liquids. The connecting lines are qualitative visual aid.} |
398 |
> |
TIP3P, and (C) SSD/RF with a reaction field. Both SSD/E and TIP3P show |
399 |
> |
significant cutoff radius dependence of the free energy and appear to |
400 |
> |
converge when moving to cutoffs greater than 12 \AA. Use of a reaction |
401 |
> |
field with SSD/RF results in free energies that exhibit minimal cutoff |
402 |
> |
radius dependence.} |
403 |
|
\label{incCutoff} |
404 |
|
\end{figure} |
405 |
|
|
407 |
|
computationally efficient water models was done in order to evaluate |
408 |
|
the trend in free energy values when moving to systems that do not |
409 |
|
involve potential truncation. As seen in Fig. \ref{incCutoff}, the |
410 |
< |
free energy of all the ice polymorphs show a substantial dependence on |
411 |
< |
cutoff radius. In general, there is a narrowing of the free energy |
412 |
< |
differences while moving to greater cutoff radius. Interestingly, by |
413 |
< |
increasing the cutoff radius, the free energy gap was narrowed enough |
414 |
< |
in the SSD/E model that the liquid state is preferred under standard |
415 |
< |
simulation conditions (298 K and 1 atm). Thus, it is recommended that |
416 |
< |
simulations using this model choose interaction truncation radii |
417 |
< |
greater than 9 \AA\ . This narrowing trend is much more subtle in the |
418 |
< |
case of SSD/RF, indicating that the free energies calculated with a |
419 |
< |
reaction field present provide a more accurate picture of the free |
420 |
< |
energy landscape in the absence of potential truncation. |
410 |
> |
free energy of all the ice polymorphs for the SSD/E and TIP3P models |
411 |
> |
show a substantial dependence on cutoff radius. In general, there is a |
412 |
> |
narrowing of the free energy differences while moving to greater |
413 |
> |
cutoff radii. As the free energies for the polymorphs converge, the |
414 |
> |
stability advantage that Ice-{\it i} exhibits is reduced; however, it |
415 |
> |
remains the most stable polymorph for both of these models over the |
416 |
> |
depicted range for both models. This narrowing trend is not |
417 |
> |
significant in the case of SSD/RF, indicating that the free energies |
418 |
> |
calculated with a reaction field present provide, at minimal |
419 |
> |
computational cost, a more accurate picture of the free energy |
420 |
> |
landscape in the absence of potential truncation. Interestingly, |
421 |
> |
increasing the cutoff radius a mere 1.5 \AA\ with the SSD/E model |
422 |
> |
destabilizes the Ice-{\it i} polymorph enough that the liquid state is |
423 |
> |
preferred under standard simulation conditions (298 K and 1 |
424 |
> |
atm). Thus, it is recommended that simulations using this model choose |
425 |
> |
interaction truncation radii greater than 9 \AA. Considering this |
426 |
> |
stabilization provided by smaller cutoffs, it is not surprising that |
427 |
> |
crystallization into Ice-{\it i} was observed with SSD/E. The choice |
428 |
> |
of a 9 \AA\ cutoff in the previous simulations gives the Ice-{\it i} |
429 |
> |
polymorph a greater than 1 kcal/mol lower free energy than the ice |
430 |
> |
$I_\textrm{h}$ starting configurations. |
431 |
|
|
432 |
|
To further study the changes resulting to the inclusion of a |
433 |
|
long-range interaction correction, the effect of an Ewald summation |
434 |
|
was estimated by applying the potential energy difference do to its |
435 |
< |
inclusion in systems in the presence and absence of the |
436 |
< |
correction. This was accomplished by calculation of the potential |
437 |
< |
energy of identical crystals with and without PME using TINKER. The |
438 |
< |
free energies for the investigated polymorphs using the TIP3P and |
439 |
< |
SPC/E water models are shown in Table \ref{pmeShift}. The same trend |
440 |
< |
pointed out through increase of cutoff radius is observed in these PME |
441 |
< |
results. Ice-{\it i} is the preferred polymorph at ambient conditions |
442 |
< |
for both the TIP3P and SPC/E water models; however, the narrowing of |
443 |
< |
the free energy differences between the various solid forms is |
435 |
> |
inclusion in systems in the presence and absence of the correction. |
436 |
> |
This was accomplished by calculation of the potential energy of |
437 |
> |
identical crystals both with and without PME. The free energies for |
438 |
> |
the investigated polymorphs using the TIP3P and SPC/E water models are |
439 |
> |
shown in Table \ref{pmeShift}. The same trend pointed out through |
440 |
> |
increase of cutoff radius is observed in these PME results. Ice-{\it |
441 |
> |
i} is the preferred polymorph at ambient conditions for both the TIP3P |
442 |
> |
and SPC/E water models; however, the narrowing of the free energy |
443 |
> |
differences between the various solid forms with the SPC/E model is |
444 |
|
significant enough that it becomes less clear that it is the most |
445 |
< |
stable polymorph with the SPC/E model. The free energies of Ice-{\it |
446 |
< |
i} and ice B nearly overlap within error, with ice $I_c$ just outside |
447 |
< |
as well, indicating that Ice-{\it i} might be metastable with respect |
448 |
< |
to ice B and possibly ice $I_c$ with SPC/E. However, these results do |
449 |
< |
not significantly alter the finding that the Ice-{\it i} polymorph is |
450 |
< |
a stable crystal structure that should be considered when studying the |
445 |
> |
stable polymorph. The free energies of Ice-{\it i} and $I_\textrm{c}$ |
446 |
> |
overlap within error, while ice B and $I_\textrm{h}$ are just outside |
447 |
> |
at t slightly higher free energy. This indicates that with SPC/E, |
448 |
> |
Ice-{\it i} might be metastable with all the studied polymorphs, |
449 |
> |
particularly ice $I_\textrm{c}$. However, these results do not |
450 |
> |
significantly alter the finding that the Ice-{\it i} polymorph is a |
451 |
> |
stable crystal structure that should be considered when studying the |
452 |
|
phase behavior of water models. |
453 |
|
|
454 |
|
\begin{table*} |
455 |
|
\begin{minipage}{\linewidth} |
444 |
– |
\renewcommand{\thefootnote}{\thempfootnote} |
456 |
|
\begin{center} |
457 |
+ |
|
458 |
|
\caption{The free energy of the studied ice polymorphs after applying |
459 |
|
the energy difference attributed to the inclusion of the PME |
460 |
|
long-range interaction correction. Units are kcal/mol.} |
461 |
< |
\begin{tabular}{ l c c c c } |
461 |
> |
|
462 |
> |
\begin{tabular}{ccccc} |
463 |
|
\hline |
464 |
< |
\ \ Water Model \ \ & \ \ \ \ \ $I_h$ \ \ & \ \ \ \ \ $I_c$ \ \ & \ \quad \ \ \ \ B \ \ & \ \ \ \ \ Ice-{\it i} \ \ \\ |
464 |
> |
Water Model & $I_h$ & $I_c$ & B & Ice-{\it i} \\ |
465 |
|
\hline |
466 |
< |
TIP3P & -11.53(2) & -11.24(3) & -11.51(3) & -11.67(3)\\ |
467 |
< |
SPC/E & -12.77(2) & -12.92(2) & -12.96(3) & -13.02(2)\\ |
466 |
> |
TIP3P & -11.53(2) & -11.24(3) & -11.51(3) & -11.67(3) \\ |
467 |
> |
SPC/E & -12.97(2) & -13.00(2) & -12.96(3) & -13.02(2) \\ |
468 |
|
\end{tabular} |
469 |
|
\label{pmeShift} |
470 |
|
\end{center} |
474 |
|
\section{Conclusions} |
475 |
|
|
476 |
|
The free energy for proton ordered variants of hexagonal and cubic ice |
477 |
< |
$I$, ice B, and recently discovered Ice-{\it i} were calculated under |
478 |
< |
standard conditions for several common water models via thermodynamic |
479 |
< |
integration. All the water models studied show Ice-{\it i} to be the |
480 |
< |
minimum free energy crystal structure in the with a 9 \AA\ switching |
481 |
< |
function cutoff. Calculated melting and boiling points show |
482 |
< |
surprisingly good agreement with the experimental values; however, the |
483 |
< |
solid phase at 1 atm is Ice-{\it i}, not ice $I_h$. The effect of |
484 |
< |
interaction truncation was investigated through variation of the |
485 |
< |
cutoff radius, use of a reaction field parameterized model, and |
477 |
> |
$I$, ice B, and our recently discovered Ice-{\it i} structure were |
478 |
> |
calculated under standard conditions for several common water models |
479 |
> |
via thermodynamic integration. All the water models studied show |
480 |
> |
Ice-{\it i} to be the minimum free energy crystal structure with a 9 |
481 |
> |
\AA\ switching function cutoff. Calculated melting and boiling points |
482 |
> |
show surprisingly good agreement with the experimental values; |
483 |
> |
however, the solid phase at 1 atm is Ice-{\it i}, not ice $I_h$. The |
484 |
> |
effect of interaction truncation was investigated through variation of |
485 |
> |
the cutoff radius, use of a reaction field parameterized model, and |
486 |
|
estimation of the results in the presence of the Ewald |
487 |
|
summation. Interaction truncation has a significant effect on the |
488 |
|
computed free energy values, and may significantly alter the free |
490 |
|
these effects, these results show Ice-{\it i} to be an important ice |
491 |
|
polymorph that should be considered in simulation studies. |
492 |
|
|
493 |
< |
Due to this relative stability of Ice-{\it i} in all manner of |
494 |
< |
investigated simulation examples, the question arises as to possible |
493 |
> |
Due to this relative stability of Ice-{\it i} in all of the |
494 |
> |
investigated simulation conditions, the question arises as to possible |
495 |
|
experimental observation of this polymorph. The rather extensive past |
496 |
|
and current experimental investigation of water in the low pressure |
497 |
|
regime makes us hesitant to ascribe any relevance of this work outside |
503 |
|
deposition environments, and in clathrate structures involving small |
504 |
|
non-polar molecules. Figs. \ref{fig:gofr} and \ref{fig:sofq} contain |
505 |
|
our predictions for both the pair distribution function ($g_{OO}(r)$) |
506 |
< |
and the structure factor ($S(\vec{q})$ for ice $I_c$ and for ice-{\it |
507 |
< |
i} at a temperature of 77K. In a quick comparison of the predicted |
508 |
< |
S(q) for Ice-{\it i} and experimental studies of amorphous solid |
509 |
< |
water, it is possible that some of the ``spurious'' peaks that could |
510 |
< |
not be assigned in HDA could correspond to peaks labeled in this |
511 |
< |
S(q).\cite{Bizid87} It should be noted that there is typically poor |
512 |
< |
agreement on crystal densities between simulation and experiment, so |
513 |
< |
such peak comparisons should be made with caution. We will leave it |
501 |
< |
to our experimental colleagues to determine whether this ice polymorph |
502 |
< |
is named appropriately or if it should be promoted to Ice-0. |
506 |
> |
and the structure factor ($S(\vec{q})$ for ice $I_h$, $I_c$, and for |
507 |
> |
ice-{\it i} at a temperature of 77K. In studies of the high and low |
508 |
> |
density forms of amorphous ice, ``spurious'' diffraction peaks have |
509 |
> |
been observed experimentally.\cite{Bizid87} It is possible that a |
510 |
> |
variant of Ice-{\it i} could explain some of this behavior; however, |
511 |
> |
we will leave it to our experimental colleagues to make the final |
512 |
> |
determination on whether this ice polymorph is named appropriately |
513 |
> |
(i.e. with an imaginary number) or if it can be promoted to Ice-0. |
514 |
|
|
515 |
|
\begin{figure} |
516 |
|
\includegraphics[width=\linewidth]{iceGofr.eps} |
517 |
< |
\caption{Radial distribution functions of Ice-{\it i} and ice $I_c$ |
518 |
< |
calculated from from simulations of the SSD/RF water model at 77 K.} |
517 |
> |
\caption{Radial distribution functions of ice $I_h$, $I_c$, |
518 |
> |
Ice-{\it i}, and Ice-{\it i}$^\prime$ calculated from from simulations |
519 |
> |
of the SSD/RF water model at 77 K.} |
520 |
|
\label{fig:gofr} |
521 |
|
\end{figure} |
522 |
|
|
523 |
|
\begin{figure} |
524 |
|
\includegraphics[width=\linewidth]{sofq.eps} |
525 |
< |
\caption{Predicted structure factors for Ice-{\it i} and ice $I_c$ at |
526 |
< |
77 K. The raw structure factors have been convoluted with a gaussian |
527 |
< |
instrument function (0.075 \AA$^{-1}$ width) to compensate for the |
528 |
< |
trunction effects in our finite size simulations. The labeled peaks |
529 |
< |
compared favorably with ``spurious'' peaks observed in experimental |
518 |
< |
studies of amorphous solid water.\cite{Bizid87}} |
525 |
> |
\caption{Predicted structure factors for ice $I_h$, $I_c$, Ice-{\it i}, |
526 |
> |
and Ice-{\it i}$^\prime$ at 77 K. The raw structure factors have |
527 |
> |
been convoluted with a gaussian instrument function (0.075 \AA$^{-1}$ |
528 |
> |
width) to compensate for the trunction effects in our finite size |
529 |
> |
simulations.} |
530 |
|
\label{fig:sofq} |
531 |
|
\end{figure} |
532 |
|
|