A charge-driven molecular water pump

被引:276
作者
Gong, Xiaojing
Li, Jingyuan
Lu, Hangjun
Wan, Rongzheng
Li, Jichen
Hu, Jun
Fang, Haiping
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China
[3] Zhejiang Univ, Dept Phys, Hangzhou 310027, Peoples R China
[4] Zhejiang Normal Univ, Dept Phys, Jinhua 321004, Peoples R China
[5] Univ Manchester, Dept Phys & Astron, Manchester M60 1QD, Lancs, England
[6] Shanghai Jiao Tong Univ, Coll Life Sci & Technol, Bio X Life Sci Res Ctr, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1038/nnano.2007.320
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Understanding and controlling the transport of water across nanochannels is of great importance for designing novel molecular devices, machines and sensors and has wide applications(1-9), including the desalination of seawater(5). Nanopumps driven by electric or magnetic fields can transport ions(10,11) and magnetic quanta(12), but water is charge- neutral and has no magnetic moment. On the basis of molecular dynamics simulations, we propose a design for a molecular water pump. The design uses a combination of charges positioned adjacent to a nanopore and is inspired by the structure of channels in the cellular membrane that conduct water in and out of the cell (aquaporins). The remarkable pumping ability is attributed to the charge dipole- induced ordering of water confined in the nanochannels(13,14), where water can be easily driven by external fields in a concerted fashion. These findings may provide possibilities for developing water transport devices that function without osmotic pressure or a hydrostatic pressure gradient.
引用
收藏
页码:709 / 712
页数:4
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