Surface adhesion of back-illuminated ultrafast laser-treated polymers

D. Kallepalli, Alan T. K. Godfrey, Jesse Ratté, A. Staudte, Chunmei Zhang, P. Corkum
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Abstract

We report a decreased surface wettability when polymer films on a glass substrate are treated by ultra-fast laser pulses in a back-illumination geometry. We propose that back-illumination through the substrate confines chemical changes beneath the surface of polymer films, leaving the surface blistered but chemically intact. To confirm this hypothesis, we measure the phase contrast of the polymer when observed with a focused ion beam. We observe a void at the polymer-quartz interface that results from the expansion of an ultrafast laser-induced plasma. A modified polymer layer surrounds the void, but otherwise the film seems unmodified. We also use X-ray photoelectron spectroscopy to confirm that there is no chemical change to the surface. When patterned with partially overlapping blisters, our polymer surface shows increased hydrophobicity. The increased hydrophobicity of back-illuminated surfaces can only result from the morphological change. This contrasts with the combined chemical and morphological changes of the polymer surface caused by a front-illumination geometry.
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背照超快激光处理聚合物的表面附着力
我们报告了当在玻璃基板上的聚合物薄膜在背光几何中被超快激光脉冲处理时,表面润湿性降低。我们建议通过衬底的反向照明限制聚合物薄膜表面下的化学变化,使表面起泡,但化学完整。为了证实这一假设,我们测量了用聚焦离子束观察聚合物时的相位差。我们在聚合物-石英界面上观察到一个空洞,这是由超快激光诱导等离子体膨胀引起的。一层修饰的聚合物层包围着空隙,但除此之外,薄膜似乎没有修饰。我们还使用x射线光电子能谱来确认表面没有化学变化。当图案与部分重叠的水泡,我们的聚合物表面显示出增加的疏水性。背照表面疏水性的增加只能由形态变化引起。这与由前照射几何形状引起的聚合物表面的化学和形态变化形成对比。
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