Signatures of quantum phase transitions and excited state quantum phase transitions in the vibrational bending dynamics of triatomic molecules

被引:63
作者
Larese, Danielle [1 ]
Perez-Bernal, Francisco [2 ]
Iachello, Francesco [3 ]
机构
[1] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[2] Univ Huelva, Fac CC Experiment, Dept Fis Aplicada, Huelva 21071, Spain
[3] Yale Univ, Ctr Theoret Phys, New Haven, CT 06511 USA
关键词
Algebraic methods; Quantum phase transition; Quantum monodromy; POTENTIAL-ENERGY SURFACE; INFRARED-EMISSION-SPECTRUM; HIGH-RESOLUTION ANALYSIS; PURE ROTATIONAL SPECTRA; INTERACTING-BOSON MODEL; CLASSICAL LIMIT; ELECTRONIC-STATE; WATER MOLECULE; GROUND-STATE; REGION;
D O I
10.1016/j.molstruc.2013.08.020
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
Signatures of quantum phase transitions (QPTs) and excited state quantum phase transitions (ESQPTs) in the bending motion of eight XYZ triatomic molecules (HCN, HNC, NiCN; CaOH, CaOD, MgOH, MgOD and OCS), the large-amplitude bending degree of freedom of a tetratomic molecule (HNCS), and four symmetric XY2 triatomic molecules (H2O,D2O,H2S,H2Se) are investigated in an attempt to understand their dependence on the composition of the molecular species. It is shown that the isomerizing HCN/HNC system leads to quasi-linearity, that the water molecule H2O displays a dramatic effect at E-x similar to 11,000 cm(-1) with clear indication of an ESQPT at about vibrational quantum number upsilon(b) = 8, and that the heavy water molecule D2O is expected to undergo an ESQPT at upsilon(b) = 10. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:310 / 327
页数:18
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