Many-Body Contributions in Water Nanoclusters

被引:4
|
作者
Abella, David [1 ,2 ]
Franzese, Giancarlo [2 ,3 ]
Hernandez-Rojas, Javier [4 ,5 ]
机构
[1] UIB, CSIC, IFISC, Palma De Mallorca 07122, Spain
[2] Univ Barcelona, Dept Fis Mat Condensada, Seccio Fis Estadist & Interdisciplinaria, Barcelona 08028, Spain
[3] Univ Barcelona, Inst Nanociencia & Nanotecnol, Barcelona 08028, Spain
[4] Univ La Laguna, Dept Fis, Tenerife 38205, Spain
[5] Univ La Laguna, IUdEA, Tenerife 38205, Spain
关键词
water; many-body; coordination shell; molecular dynamics; interaction radius; dipole interaction; POTENTIAL-ENERGY SURFACE; MOLECULAR-DYNAMICS; 1ST PRINCIPLES; GLOBAL MINIMA; CLUSTERS (H2O)(N); BINDING-ENERGIES; LIQUID WATER; MODEL; N-LESS-THAN-OR-EQUAL-TO-21; OPTIMIZATION;
D O I
10.1021/acsnano.2c06077
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Many-body interactions in water are known to be important but difficult to treat in atomistic models and often are included only as a correction. Polarizable models treat them explicitly, with long-range many-body potentials, within their classical approximation. However, their calculation is computationally expensive. Here, we evaluate how relevant the contributions to the many-body interaction associated with different coordination shells are. We calculate the global energy minimum, and the corresponding configuration, for nanoclusters of up to 20 water molecules. We find that including the first coordination shell, i.e., the five-body term of the central molecule, is enough to approximate within 5% the global energy minimum and its structure. We show that this result is valid for three different polarizable models, the Dang-Chang, the MB-pol, and the Kozack-Jordan potentials. This result suggests a strategy to develop many-body potentials for water that are reliable and, at the same time, computationally efficient.
引用
收藏
页码:1959 / 1964
页数:6
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