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Revision 3219 by gezelter, Thu Sep 6 15:58:45 2007 UTC vs.
Revision 3220 by chuckv, Thu Sep 6 19:15:14 2007 UTC

# Line 24 | Line 24 | groups.\cite{HartlandG.V._jp0276092,Hodak:2000rb,Hartl
24  
25   Much of the experimental work on this subject has been carried out in
26   the Hartland and von~Plessen
27 < groups.\cite{HartlandG.V._jp0276092,Hodak:2000rb,Hartland:2003yf,HuM._jp020581+,plech:195423}
27 > groups.\cite{HartlandG.V._jp0276092,Hodak:2000rb,Hartland:2003yf,HuM._jp020581+,Petrova:2007qy,plech:195423}
28   They have [BRIEF SURVEY OF THE EXPERIMENTAL WORK]
29  
30  
# Line 32 | Line 32 | nanoparticles,\cite{} we observed that the cooling rat
32   surroundings, the large surface area to volume ratio makes the heat
33   transfer to the surrounding solvent also a relatively rapid process.
34   In our recent simulation study of the laser excitation of gold
35 < nanoparticles,\cite{} we observed that the cooling rate for these
35 > nanoparticles,\cite{VardemanC.F._jp051575r} we observed that the cooling rate for these
36   particles (10$^{11}$-10$^{12}$ K/s) is in excess of the cooling rate
37   required for glass formation in bulk metallic alloys.  Given this
38   fact, it may be possible to use laser excitation to melt, alloy and
# Line 46 | Line 46 | another.\cite{XXX} Experimentally, however Ag-Cu alloy
46   dynamics.\cite{Vardeman-II:2001jn} The Hume-Rothery rules suggest that
47   alloys composed of Copper and Silver should be miscible in the solid
48   state, because their lattice constants are within 15\% of each
49 < another.\cite{XXX} Experimentally, however Ag-Cu alloys are a
49 > another.\cite{kittel} Experimentally, however Ag-Cu alloys are a
50   well-known exception to this rule and are only miscible in the liquid
51   state given equilibrium conditions. Below the eutectic temperature of
52   779 $^\circ$C and composition (60.1\% Ag, 39.9\% Cu), the
# Line 54 | Line 54 | of +6~kJ/mole.\cite{Ma:2005zt} Non-equilibrium solid s
54   $\alpha$ and $\beta$ phases, respectively. This behavior is due to a
55   positive heat of mixing in both the solid and liquid phases. For the
56   one-to-one composition fcc solid solution, $\Delta H$ is on the order
57 < of +6~kJ/mole.\cite{Ma:2005zt} Non-equilibrium solid solutions may be
57 > of +6~kJ/mole.\cite{Ma:2005fk} Non-equilibrium solid solutions may be
58   formed by undercooling, and under these conditions, a
59   compositionally-disordered $\gamma$ fcc phase can be formed.
60  
# Line 116 | Line 116 | infinite time limit.\cite{Kob} However, diffusion in n
116   displacement that is linear in time (at long times). Glassy materials
117   deviate significantly from this linear behavior at intermediate times,
118   entering a sub-linear regime with a return to linear behavior in the
119 < infinite time limit.\cite{Kob} However, diffusion in nanoparticles
119 > infinite time limit.\cite{Kob:1999fk} However, diffusion in nanoparticles
120   differs significantly from the bulk in that atoms are confined to a
121   roughly spherical volume and cannot explore any region larger than the
122   particle radius ($R$). In these confined geometries, $\langle r^2(t)
123 < \rangle$ approaches a limiting value of $3R^2/40$.\cite{CHUCK}  This limits the
123 > \rangle$ approaches a limiting value of $3R^2/40$.\cite{ShibataT._ja026764r}  This limits the
124   utility of dynamical measures of glass formation when studying
125   nanoparticles.
126  
# Line 133 | Line 133 | in liquid and solid solutions.\cite{FrenkelXXX}
133   et al.}  defined an orientational bond order parameter that is
134   sensitive to icosahedral ordering.\cite{Steinhardt:1983mo} This bond
135   order parameter can therefore be used to characterize glass formation
136 < in liquid and solid solutions.\cite{FrenkelXXX}
136 > in liquid and solid solutions.\cite{wolde:9932}
137  
138   Theoretical molecular dynamics studies have been performed on the
139   formation of amorphous single component nanoclusters of either

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