The anharmonic features of the short-time dynamics of fluids: The time evolution and mixing of instantaneous normal modes

被引:29
作者
David, EF [1 ]
Stratt, RM [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
关键词
D O I
10.1063/1.476690
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Despite the obvious role of sharply varying repulsive forces in determining the structure of most liquids, for short periods of time, motion in liquids looks remarkably harmonic. That is, there seem to be well-defined collective, but independent, harmonic modes governing the ultrafast dynamics launched from any given liquid configuration. Because liquids are not truly harmonic, however, these modes cannot last forever. In particular, "instantaneous" modes of this sort eventually have to give way to new instantaneous modes-ones more appropriate to whatever new configuration the liquid has evolved into. In this paper we investigate just this process of mode evolution. By concentrating on solely the highest frequency modes, it is possible to formulate analytical models for both the modes and the anharmonic interactions that affect them. We can therefore begin to understand the mechanisms by which modes change in time and the kinds of time scales on which the specific anharmonic processes occur in liquids. What we find is that there are several rather distinct signatures of anharmonicity: we see first that the anharmonicity within a mode itself continually causes the mode frequency to fluctuate. More sporadically, we find that two different but nearly resonant modes will sometimes interact strongly enough with one another to cause a temporary-though not a permanent-mixing between the modes. Of course, both of these processes are, in some sense, breakdowns of instantaneous-normal-mode theory, but neither of them affects the basic identity and existence of instantaneous modes. The eventual destruction-of the modes turns out to be an even less frequent event precipitated by an even stronger mixing between a mode and the motion of surrounding atoms. It is precisely this longer time scale that may mark the first point at which diffusive motion plays an essential role in liquid dynamics. (C) 1998 American Institute of Physics.
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页码:1375 / 1390
页数:16
相关论文
共 58 条
[1]   EXTENSIONS TO THE INSTANTANEOUS NORMAL MODE ANALYSIS OF CLUSTER DYNAMICS - DIFFUSION CONSTANTS AND THE ROLE OF ROTATIONS IN CLUSTERS [J].
ADAMS, JE ;
STRATT, RM .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (03) :1632-1640
[2]  
Allen M.P., 1987, COMPUTER SIMULATION
[3]   The role of localization in glasses and supercooled liquids [J].
Bembenek, SD ;
Laird, BB .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (13) :5199-5208
[4]   INSTANTANEOUS NORMAL-MODES AND THE GLASS-TRANSITION [J].
BEMBENEK, SD ;
LAIRD, BB .
PHYSICAL REVIEW LETTERS, 1995, 74 (06) :936-939
[5]   COLLECTIVE VIBRATIONAL DYNAMICS OF SIMPLE LIQUIDS [J].
BUCHNER, M ;
DORFMULLER, T .
JOURNAL OF MOLECULAR LIQUIDS, 1995, 65-6 :157-168
[6]   THE SHORT-TIME DYNAMICS OF MOLECULAR LIQUIDS - INSTANTANEOUS-NORMAL-MODE THEORY [J].
BUCHNER, M ;
LADANYI, BM ;
STRATT, RM .
JOURNAL OF CHEMICAL PHYSICS, 1992, 97 (11) :8522-8535
[7]  
BUCHNER M, UNPUB
[8]   INSTANTANEOUS NORMAL-MODE ANALYSIS OF LIQUID WATER [J].
CHO, M ;
FLEMING, GR ;
SAITO, S ;
OHMINE, I ;
STRATT, RM .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (09) :6672-6683
[9]   The integrated photon echo and solvation dynamics [J].
Cho, MH ;
Yu, JY ;
Joo, TH ;
Nagasawa, Y ;
Passino, SA ;
Fleming, GR .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (29) :11944-11953
[10]   Absorption line shapes and solvation dynamics of CH3I in supercritical Ar [J].
Egorov, SA ;
Stephens, MD ;
Skinner, JL .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (24) :10485-10491