Water nanostructure formation on oxide probed in situ by optical resonances

被引:13
|
作者
Yin, Yin [1 ]
Wang, Jiawei [1 ,2 ]
Wang, Xiaoxia [1 ]
Li, Shilong [1 ]
Jorgensen, Matthew R. [1 ]
Ren, Junfeng [3 ]
Meng, Sheng [4 ,5 ]
Ma, Libo [1 ]
Schmidt, Oliver G. [1 ,2 ,6 ,7 ]
机构
[1] Leibniz IFW Dresden, Inst Integrat Nanosci, Helmholtzstr 20, D-01069 Dresden, Germany
[2] Tech Univ Chemnitz, Mat Syst Nanoelect, Reichenhainer Str 70, D-09107 Chemnitz, Germany
[3] Shandong Normal Univ, Sch Phys & Elect, Jinan 250014, Shandong, Peoples R China
[4] Chinese Acad Sci, Beijing Natl Lab Condensed Matter Phys, Beijing 100190, Peoples R China
[5] Chinese Acad Sci, Inst Phys, Beijing 100190, Peoples R China
[6] TU Chemnitz, Res Ctr Mat Architectures & Integrat Nanomembrane, Rosenbergstr 6, D-09126 Chemnitz, Germany
[7] Tech Univ Dresden, Fac Phys, Nanophys, D-01062 Dresden, Germany
关键词
LABEL-FREE; ADSORPTION; HYDROGEN; ICE; INTERFACES; FILMS;
D O I
10.1126/sciadv.aax6973
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
The dynamic characterization of water multilayers on oxide surfaces is hard to achieve by currently available techniques. Despite this, there is an increasing interest in the evolution of water nanostructures on oxides to fully understand the complex dynamics of ice nucleation and growth in natural and artificial environments. Here, we report the in situ detection of the dynamic evolution of nanoscale water layers on an amorphous oxide surface probed by optical resonances. In the water nanolayer growth process, we find an initial nanocluster morphology that turns into a planar layer beyond a critical thickness. In the reverse process, the planar water film converts to nanoclusters, accompanied by a transition from a planar amorphous layer to crystalline nanoclusters. Our results are explained by a simple thermodynamic model as well as kinetic considerations. Our work represents an approach to reveal the nanostructure and dynamics at the water-oxide interface using resonant light probing.
引用
收藏
页数:6
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