Nanoscale Interfacial Engineering for Flexible Barrier Films

被引:11
作者
Cai, Can [1 ]
Dauskardt, Reinhold H. [1 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
关键词
Thin film adhesion; fracture mechanics; interfacial nanostructures; nanosphere lithography; barrier film; UV degradation; BRITTLE-MATRIX COMPOSITES; ORGANIC SOLAR-CELLS; NANOSPHERE LITHOGRAPHY; PERMEATION; MONOLAYERS; SURFACES; LIFETIME; FRACTURE; CRACKING;
D O I
10.1021/acs.nanolett.5b02597
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Alternating layers of organic and oxide thin films used as diffusion barriers in emerging flexible device technologies are vulnerable to degradation under the influence of mechanical stresses, temperature cycling, photo degradation, and chemically active environmental species. Delamination of the internal organic to oxide interfaces often limits the operational lifetime of the barrier system. We demonstrate a method for increasing the adhesion of organic and oxide thin films by generating nanostructures at the interface. We show that the adhesion of an acrylate to silicon oxide model system can be increased by up to an order of magnitude (from similar to 2 J/m(2) to 24 J/m(2)). By altering the diameter and depth of the patterns in the model systems, the adhesion energy can be changed, and the delamination pathway can be controlled. In addition, we show that a patterned interface maintains a higher adhesion than its planar counterpart for all durations of UV-A and UV-B exposure.
引用
收藏
页码:6751 / 6755
页数:5
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