Direct observation of anisotropic growth of water films on minerals driven by defects and surface tension

被引:41
作者
Yalcin, Sibel Ebru [1 ,2 ]
Legg, Benjamin A. [3 ,4 ]
Yesilbas, Merve [5 ,6 ]
Malvankar, Nikhil S. [1 ,2 ]
Boily, Jean-Francois [1 ,2 ]
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06511 USA
[2] Yale Univ, Microbial Sci Inst, West Haven, CT 06516 USA
[3] Pacific Northwest Natl Lab, Phys Sci Div, Richland, WA 99352 USA
[4] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
[5] Umea Univ, Dept Chem, SE-90187 Umea, Sweden
[6] SETI Inst, Carl Sagan Ctr, Mountain View, CA 94043 USA
基金
瑞典研究理事会; 美国国家科学基金会;
关键词
CLOUD CONDENSATION; FORCE; ADSORPTION; GIBBSITE; MODEL; FIELD; AFM;
D O I
10.1126/sciadv.aaz9708
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Knowledge of the occurrences of water films on minerals is critical for global biogeochemical and atmospheric processes, including element cycling and ice nucleation. The underlying mechanisms controlling water film growth are, however, misunderstood. Using infrared nanospectroscopy, amplitude-modulated atomic force microscopy, and molecular simulations, we show how water films grow from water vapor on hydrophilic mineral nanoparticles. We imaged films with up to four water layers that grow anisotropically over a single face. Growth usually begins from the near edges of a face where defects preferentially capture water vapor. Thicker films produced by condensation cooling completely engulf nanoparticles and form thicker menisci over defects. The high surface tension of water smooths film surfaces and produces films of inhomogeneous thickness. Nanoscale topography and film surface energy thereby control anisotropic distributions and thicknesses of water films on hydrophilic mineral nanoparticles.
引用
收藏
页数:9
相关论文
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