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New Strategy to Achieve Laser Direct Writing of Polymers: Fabrication of the Color-Changing Microcapsule with a Core–Shell Structure

机译:实现聚合物激光直接写入的新策略:用芯壳结构制造变色微胶囊

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This paper proposed an efficient and environmentally friendly strategy to prepare a new color-changing microcapsule with a core–shell structure for laser direct writing of polymers, and only the physical melt blending of polymers was employed. The laser absorber (SnO_(2)) and the easily carbonized polymer (PC) were designed as the “core” and the “shell” of the microcapsule, respectively. The microcapsules were in situ formed during melt blending. Scanning electron microscopy, transmission electron microscopy, and energy-dispersive spectrometry confirmed the successful preparation of SnO_(2)/PC microcapsules with a core–shell structure. Their average diameter was 2.2 μm, and the “shell” thickness was 0.21–0.24 μm. As expected, these SnO_(2)/PC microcapsules endowed polymers with an outstanding performance of near-infrared (NIR) laser direct writing. Raman spectroscopy and X-ray photoelectron spectroscopy indicated that the color change was ascribed to the polymer carbonization because of the instantaneous high temperature caused by the SnO_(2) absorption of NIR laser energy. Optical microscopy observed a thick carbonization layer of 234 μm. Moreover, Raman depth imaging revealed the carbonization distribution, confirming that the amorphous carbon produced by the carbonization of the PC “shell” is the key factor of SnO_(2)/PC microcapsules to provide polymers an outstanding performance of laser direct writing. This color-changing microcapsule has no selectivity to polymers because of providing a black color source (the carbonization of PC) itself, ensuring the high contrast and precision of patterns or texts after laser direct writing for all general-purpose polymers. We believe that this novel strategy to achieve laser direct writing of polymers will have broad application prospects.
机译:本文提出了一种高效且环保的策略,用于制备新的变形微胶囊,其具有用于激光直接写入聚合物的激光直接写入的核心 - 壳结构,并且仅采用聚合物的物理熔融混合。激光吸收剂(SnO_(2))和易碳化聚合物(PC)分别设计为微胶囊的“核心”和“壳”。在熔融共混期间形成微胶囊原位。扫描电子显微镜,透射电子显微镜和能量分散光谱法证实了具有核壳结构的SnO_(2)/ PC微胶囊的成功制备。它们的平均直径为2.2μm,“壳”厚度为0.21-0.24μm。如预期的那样,这些SnO_(2)/ PC微胶囊赋予了具有近红外(NIR)激光直接写入的优异性能的聚合物。拉曼光谱和X射线光电子能谱表明,由于瞬时高温引起的NIR激光能量引起的瞬时高温,颜色变化归因于聚合物碳化。光学显微镜观察到厚的碳化层234μm。此外,拉曼深度成像揭示了碳化分布,确认通过PC“壳”碳化产生的非晶碳是SnO_(2)/ PC微胶囊的关键因素,以提供聚合物的激光直接写入的出色性能。由于提供黑色源(PC的碳化)本身,这种变色的微胶囊没有选择性,因为提供了所有通用聚合物激光直接写入后的图案或文本的高对比度和精度。我们认为,这种实现激光直接写入聚合物的新型战略将具有广泛的应用前景。

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