https://scholars.lib.ntu.edu.tw/handle/123456789/369571
標題: | Assessment of density functional approximations for the hemibonded structure of the water dimer radical cation | 作者: | JENG-DA CHAI | 公開日期: | 2012 | 卷: | 14 | 期: | 30 | 起(迄)頁: | 10705-10712 | 來源出版物: | Physical Chemistry Chemical Physics | 摘要: | Due to the severe self-interaction errors associated with some density functional approximations, conventional density functionals often fail to dissociate the hemibonded structure of the water dimer radical cation (H 2O) 2 + into the correct fragments: H 2O and H 2O +. Consequently, the binding energy of the hemibonded structure (H 2O) 2 + is not well-defined. For a comprehensive comparison of different functionals for this system, we propose three criteria: (i) the binding energies, (ii) the relative energies between the conformers of the water dimer radical cation, and (iii) the dissociation curves predicted by different functionals. The long-range corrected (LC) double-hybrid functional, ωB97X-2(LP) [J.-D. Chai and M. Head-Gordon, J. Chem. Phys., 2009, 131, 174105], is shown to perform reasonably well based on these three criteria. Reasons that LC hybrid functionals generally work better than conventional density functionals for hemibonded systems are also explained in this work. © 2012 the Owner Societies. |
URI: | http://scholars.lib.ntu.edu.tw/handle/123456789/369571 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863917801&doi=10.1039%2fc2cp41116d&partnerID=40&md5=2e0808be6f40f058e151941982f032f5 |
ISSN: | 14639076 | DOI: | 10.1039/c2cp41116d |
顯示於: | 物理學系 |
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