Continuously broken ergodicity

被引:102
作者
Mauro, John C.
Gupta, Prabhat K.
Loucks, Roger J.
机构
[1] Corning Inc, Div Sci & Technol, Corning, NY 14831 USA
[2] Ohio State Univ, Dept Mat Sci & Engn, Columbus, OH 43210 USA
[3] Alfred Univ, Dept Phys & Astron, Alfred, NY 14802 USA
关键词
D O I
10.1063/1.2731774
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
A system that is initially ergodic can become nonergodic, i.e., display "broken ergodicity," if the relaxation time scale of the system becomes longer than the observation time over which properties are measured. The phenomenon of broken ergodicity is of vital importance to the study of many condensed matter systems. While previous modeling efforts have focused on systems with a sudden, discontinuous loss of ergodicity, they cannot be applied to study a gradual transition between ergodic and nonergodic behavior. This transition range, where the observation time scale is comparable to that of the structural relaxation process, is especially pertinent for the study of glass transition range behavior, as ergodicity breaking is an inherently continuous process for normal laboratory glass formation. In this paper, we present a general statistical mechanical framework for modeling systems with continuously broken ergodicity. Our approach enables the direct computation of entropy loss upon ergodicity breaking, accounting for actual transition rates between microstates and observation over a specified time interval. In contrast to previous modeling efforts for discontinuously broken ergodicity, we make no assumptions about phase space partitioning or confinement. We present a hierarchical master equation technique for implementing our approach and apply it to two simple one-dimensional landscapes. Finally, we demonstrate the compliance of our approach with the second and third laws of thermodynamics. (C) 2007 American Institute of Physics.
引用
收藏
页数:11
相关论文
共 56 条
[1]   ON TEMPERATURE DEPENDENCE OF COOPERATIVE RELAXATION PROPERTIES IN GLASS-FORMING LIQUIDS [J].
ADAM, G ;
GIBBS, JH .
JOURNAL OF CHEMICAL PHYSICS, 1965, 43 (01) :139-&
[2]  
[Anonymous], 2021, METASTABLE LIQUIDS
[3]   Democratic particle motion for metabasin transitions in simple glass formers [J].
Appignanesi, GA ;
Fris, JAR ;
Montani, RA ;
Kob, W .
PHYSICAL REVIEW LETTERS, 2006, 96 (05)
[4]   Information entropy production in non-Markovian systems [J].
Bag, BC .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (09) :4988-4990
[5]   MAGNETIC-PROPERTIES OF A MODEL SPIN-GLASS AND THE FAILURE OF LINEAR RESPONSE THEORY [J].
BANTILAN, FT ;
PALMER, RG .
JOURNAL OF PHYSICS F-METAL PHYSICS, 1981, 11 (01) :261-266
[6]   Weak ergodicity breaking in the continuous-time random walk [J].
Bel, G ;
Barkai, E .
PHYSICAL REVIEW LETTERS, 2005, 94 (24)
[7]   Occupation times and ergodicity breaking in biased continuous time random walks [J].
Bel, G ;
Barkai, E .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2005, 17 (49) :S4287-S4304
[8]  
Callen H. B., 1985, THERMODYNAMICS INTRO, DOI 10.1119/1.19071
[9]   A new method to compute the configurational entropy in glassy systems [J].
Coluzzi, B ;
Crisanti, A ;
Marinari, E ;
Ritort, F ;
Rocco, A .
EUROPEAN PHYSICAL JOURNAL B, 2003, 32 (04) :495-502
[10]   Entropy production and phase space volume contraction [J].
Daems, D ;
Nicolis, G .
PHYSICAL REVIEW E, 1999, 59 (04) :4000-4006