Anharmonicity of inner-OH stretching modes in hydrous phyllosilicates:: assessment from first-principles frozen-phonon calculations

被引:56
作者
Balan, Etienne [1 ]
Lazzeri, Michele
Delattre, Simon
Meheut, Merlin
Refson, Keith
Winkler, Bjoern
机构
[1] Univ Paris 06, Inst Mineral & Phys Milieux Condenses, F-75015 Paris, France
[2] Univ Paris 07, CNRS, Inst Mineral & Phys Milieux Condenses IMPMC, UMR 7590, F-75252 Paris, France
[3] Rutherford Appleton Lab, Oxford OX11 0QX, England
[4] Univ Frankfurt, Inst Geowissensch, D-60438 Mainz, Germany
[5] CEREGE, Europole Mediterraneen Arbois, IRD UMR 161, F-13545 Aix En Provence, France
关键词
OH bond; anharmonicity; infrared; raman; ab initio;
D O I
10.1007/s00269-007-0176-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The theoretical anharmonicity of the inner-OH stretching modes of kaolinite and lizardite is determined using a frozen-phonon approach. The anharmonicity parameter, defined as the difference between half the first overtone frequency and the frequency of the fundamental transition, is -95 and -92 cm(-1) for kaolinite and lizardite, respectively. These values are consistent with the experimental measurements. The very good agreement usually observed between harmonic calculations of vibrational frequencies at the density functional theory (DFT) level, using the generalized gradient approximation (GGA), and experimental positions of vibrational bands results from the fortuitous, but almost exact, cancelation of two types of errors. One is related to the GGA approximation and the other to the neglect of anharmonicity.
引用
收藏
页码:621 / 625
页数:5
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