Role of Thin Film Adhesion on Capillary Peeling

被引:11
|
作者
Ma, Jingcheng [2 ]
Kim, Jin Myung [1 ]
Hoque, Muhammad Jahidul [2 ]
Thompson, Kamila J. [3 ]
Nam, SungWoo [4 ,5 ]
Cahill, David G. [4 ,5 ]
Miljkovic, Nenad [2 ,5 ,6 ,7 ]
机构
[1] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Mech Sci & Engn, Urbana, IL 61801 USA
[3] Ohio State Univ, Dept Elect & Comp Engn, Columbus, OH 43210 USA
[4] Univ Illinois, Dept Mech Sci & Engn, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[5] Univ Illinois, Mat Res Lab, Urbana, IL 61801 USA
[6] Univ Illinois, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[7] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Fukuoka 8190395, Japan
关键词
thin film; peeling; capillary; adhesion; surface energy; 2D materials; SURFACE-ENERGY; TENSION; LAYER;
D O I
10.1021/acs.nanolett.1c03494
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The capillary force can peel off a substrate-attached film if the adhesion energy (G(w)) is low. Capillary peeling has been used as a convenient, rapid, and nondestructive method for fabricating free-standing thin films. However, the critical value of G(w), which leads to the transition between peeling and sticking, remains largely unknown. As a result, capillary peeling remains empirical and applicable to a limited set of materials. Here, we investigate the critical value of G(w) and experimentally show the critical adhesion (G(w,c)) to scale with the water-film interfacial energy (approximate to 0.7 gamma(fw)), which corresponds well with our theoretical prediction of (Gw, c) =gamma(fw). Based on the critical adhesion, we propose quantitative thermodynamic guidelines for designing thin film interfaces that enable successful capillary peeling. The outcomes of this work present a powerful technique for thin film transfer and advanced nanofabrication in flexible photovoltaics, battery materials, biosensing, translational medicine, and stretchable bioelectronics.
引用
收藏
页码:9983 / 9989
页数:7
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