Energy landscape view of phase transitions and slow dynamics in thermotropic liquid crystals

被引:18
作者
Chakrabarti, Dwaipayan [1 ]
Bagchi, Biman [1 ]
机构
[1] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
关键词
inherent structure;
D O I
10.1073/pnas.0508355103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Thermotropic liquid crystals are known to display rich phase behavior on temperature variation. Although the nematic phase is orientationally ordered but translationally disordered, a smectic phase is characterized by the appearance of a partial translational order in addition to a further increase in orientational order. In an attempt to understand the interplay between orientational and translational order in the mesophases that thermotropic liquid crystals typically exhibit upon cooling from the high-temperature isotropic phase, we investigate the potential energy landscapes of a family of model liquid crystalline systems. The configurations of the system corresponding to the local potential energy minima, known as the inherent structures, are determined from computer simulations across the mesophases. We find that the depth of the potential energy minima explored by the system along an isochor grows through the nematic phase as temperature drops in contrast to its insensitivity to temperature in the isotropic and smectic phases. The onset of the growth of the orientational order in the parent phase is found to induce a translational order, resulting in a smectic-like layer in the underlying inherent structures; the inherent structures, surprisingly, never seem to sustain orientational order alone if the parent nematic phase is sandwiched between the high-temperature isotropic phase and the low-temperature smectic phase. The Arrhenius temperature dependence of the orientational relaxation time breaks down near the isotropic-nematic transition. We find that this breakdown occurs at a temperature below which the system explores increasingly deeper potential energy minima.
引用
收藏
页码:7217 / 7221
页数:5
相关论文
共 24 条
[1]   Effects of elongation on the phase behavior of the Gay-Berne fluid [J].
Brown, JT ;
Allen, MP ;
del Rio, EM ;
de Miguel, E .
PHYSICAL REVIEW E, 1998, 57 (06) :6685-6699
[2]   Dynamics in supercooled liquids and in the isotropic phase of liquid crystals: A comparison [J].
Cang, H ;
Li, J ;
Novikov, VN ;
Fayer, MD .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (20) :9303-9311
[3]   Universal power law in the orientational relaxation in thermotropic liquid crystals [J].
Chakrabarti, D ;
Jose, PP ;
Chakrabarty, S ;
Bagchi, B .
PHYSICAL REVIEW LETTERS, 2005, 95 (19)
[4]  
Chandrasekhar S., 1992, Liquid Crystals, V2nd ed.
[5]  
de Gennes P.-G., 1993, PHYS LIQUID CRYSTALS
[6]   The global phase diagram of the Gay-Berne model [J].
de Miguel, E ;
Vega, C .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (13) :6313-6322
[7]   ANALOGY BETWEEN SUPERCONDUCTORS AND SMECTICS-A [J].
DEGENNES, PG .
SOLID STATE COMMUNICATIONS, 1972, 10 (09) :753-&
[8]   Effect of the attractive interactions on the phase behavior of the Gay-Berne liquid crystal model [J].
deMiguel, E ;
delRio, EM ;
Brown, JT ;
Allen, MP .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (10) :4234-4249
[9]   MODIFICATION OF THE OVERLAP POTENTIAL TO MIMIC A LINEAR SITE-SITE POTENTIAL [J].
GAY, JG ;
BERNE, BJ .
JOURNAL OF CHEMICAL PHYSICS, 1981, 74 (06) :3316-3319
[10]   Comparison of the ultrafast to slow time scale dynamics of three liquid crystals in the isotropic phase [J].
Gottke, SD ;
Cang, H ;
Bagchi, B ;
Fayer, MD .
JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (14) :6339-6347