Interruption of Hydrogen Bonding Networks of Water in Carbon Nanotubes Due to Strong Hydration Shell Formation

被引:9
|
作者
Oya, Yoshifumi [1 ]
Hata, Kenji [2 ]
Ohba, Tomonori [1 ]
机构
[1] Chiba Univ, Grad Sch Sci, Inage Ku, 1-33 Yayoi, Chiba 2638522, Japan
[2] Natl Inst Adv Ind Sci & Technol, Nanotube Res Ctr, 1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
基金
日本学术振兴会;
关键词
CAPACITANCE; DESALINATION; DENSITY; SIMULATIONS; NANOPORES; INSIGHTS; LIQUID; IONS; NA+; K+;
D O I
10.1021/acs.langmuir.7b01712
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present the structures of NaCl aqueous solution in carbon nanotubes with diameters of 1, 2, and 3 nm based on an analysis performed using X-ray diffraction and canonical ensemble Monte Carlo simulations. Anomalously longer nearest-neighbor distances were observed in the electrolyte for the 1-nm-diameter carbon nanotubes; in contrast, in the 2 and 3 nm carbon nanotubes, the nearest-neighbor distances were shorter than those in the bulk electrolyte. We also observed similar properties for water in carbon nanotubes, which was expected because the main component of the electrolyte was water. However, the nearest-neighbor distances of the electrolyte were longer than those of water in all of the carbon nanotubes; the difference was especially pronounced in the 2-nm-diameter carbon nanotubes. Thus, small numbers of ions affected the entire structure of the electrolyte in the nanopores of the carbon nanotubes. The formation of strong hydration shells between ions and water molecules considerably interrupted the hydrogen bonding between water molecules in the nanopores of the carbon nanotubes. The hydration shell had a diameter of approximately 1 nm, and hydration shells were thus adopted for the nanopores of the 2-nm-diameter carbon nanotubes, providing an explanation for the large difference in the nearest-neighbor distances between the electrolyte and water in these nanopores.
引用
收藏
页码:11120 / 11125
页数:6
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