Tunable Water Adhesion on Titanium Oxide Surfaces with Different Surface Structures

被引:37
|
作者
Ou, Junfei [1 ]
Hu, Weihua [1 ]
Li, Changquan [1 ]
Wang, Ying [2 ]
Xue, Mingshan [1 ]
Wang, Fajun [1 ]
Li, Wen [1 ]
机构
[1] Nanchang Hangkong Univ, Sch Mat Sci & Engn, Nanchang 330063, Peoples R China
[2] Jiangsu Key Lab Solar Cell Mat & Technol, Changzhou 213164, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
dynamic wetting; sliding angle; contact angle hysteresis; surface structures; titanium oxide; hydrothermal treatment; SUPERHYDROPHOBIC SURFACES; HYDROPHOBIC SURFACES; DEPOSITION; FILMS; SLIPPERY; DROPLETS; FORCE;
D O I
10.1021/am301946t
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Tunable water adhesion with high static contact angle (SCA) on titanium oxide surfaces was achieved by a two-step process: first, titanium oxide surfaces with different structures were obtained by immersion the titanium alloy substrates into H2O-H2O2-HF solution at 140 degrees C for different time of 30, 60, and 120 min; then, low-surface-energy molecules of 1H, 1H, 21-1, 2H-perfluorooctyltrichlorosilane (PFOTS) were deposited thereon. SCA for all so-fabricated samples were higher than 150 degrees and sliding angle (SA) for different immersion time of 30 min, 60 min, and 120 min is 180 degrees, 31+2 degrees, and 8+1 degrees, respectively. To analyze the correlation between the surface structures and the dynamic wetting behaviors, we adopted, three contact modes (i.e., Wenzel, Cassie impregnating, and Cassie modes). The analyses showed that the surface adhesion was influenced greatly by water/solid interfacial interaction and could be artificially tuned between Wenzel state with high adhesion to Cassie state with low adhesion through the design of appropriate microstructures.
引用
收藏
页码:5737 / 5741
页数:5
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