Department of Mechanical Engineering, Masdar Institute, Khalifa University of Science and Technology, P. O. Box 127788, Abu Dhabi, United Arab Emirates.
Department of Materials Science and Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.
Soft Matter. 2021 Aug 5;17(30):7188-7195. doi: 10.1039/d1sm00483b.
3D printing complex architectures of responsive-hydratable polymers are enabled by stereolithography via photopolymerization. Yet, insufficient crosslinking leads to compromised structural integrity of the photopolymerized samples, which affects the functionality and reliability of hydrogel devices significantly. Here we investigate how curing parameters and ink formulation affect 3D printed PEGDA samples by using a combination of microfabrication, structural characterization, and reactive coarse-grained molecular dynamics simulation. Our findings show that the degree of curing exhibits a graded profile from confocal Raman spectroscopy and submicron pores from atomic force microscopy, both of which are also observed in our molecular simulations. Moreover, with environmental scanning electron microscopy, we probe the microscopic swelling and bending dynamics of 3D printed hydratable PEGDA structures as well as their structural integrity. Our in-depth characterization results reveal how hydrogel elasticity and irreversible densification due to pore formation highly depends on the exposure time, light intensity and the associated degree of crosslinking. This work provides new molecular insights into processing-structure relation in stereolithography 3D printing.
立体光刻通过光聚合使响应性水凝胶聚合物的复杂结构得以 3D 打印。然而,交联不足会导致光聚合样品的结构完整性受损,从而显著影响水凝胶器件的功能和可靠性。在这里,我们通过微制造、结构表征和反应粗粒分子动力学模拟的组合,研究了固化参数和墨水配方如何影响 3D 打印的 PEGDA 样品。我们的研究结果表明,固化程度从共焦拉曼光谱和原子力显微镜的亚微米孔中呈现出分级分布,这在我们的分子模拟中也得到了观察。此外,我们还通过环境扫描电子显微镜研究了 3D 打印可水合的 PEGDA 结构的微观溶胀和弯曲动力学及其结构完整性。我们的深入表征结果揭示了水凝胶弹性和由于孔形成导致的不可逆致密化如何高度依赖于曝光时间、光强和相关交联程度。这项工作为立体光刻 3D 打印中的加工-结构关系提供了新的分子见解。