动态交联两性凝胶的可重构和正交刚度结构图案化

SmartMat Pub Date : 2024-01-02 DOI:10.1002/smm2.1255
Chen Yang, Weizhong Zheng, Chujun Ni, Ye Li, Di Chen, Tao Xie, Qiao Zhao
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引用次数: 0

摘要

对聚合物材料的多样化特性和表面结构进行图案化,对于挖掘其在生物、光学和电子学领域的潜力具有重要意义。然而,以可重新配置的方式实现硬度和微结构的可图案化仍然具有挑战性。在这里,我们制备了通过动态二硫键交联的两性凝胶,这种凝胶可以通过不相溶的水或液体石蜡可逆地膨胀。在石蜡形态下,由于氢键致密,材料显示出 130 兆帕的高模量。而被水溶胀后,由于氢键被破坏,模量下降了两个数量级。通过溶剂的区域化溶胀,可以创建良好的、可重写的软/硬机械模式。另一方面,通过二硫交联的动态交换,可以进行机械光刻,从而制造出复杂的宏观几何形状和微观结构。可重新配置的硬度-结构图案可以正交操作,这将在传统水凝胶和有机凝胶之外创造更多的应用机会。
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Reconfigurable and orthogonal stiffness‐structure patterning of dynamically crosslinked amphigels
Patterning diversified properties and surface structure of polymer materials are of great importance toward their potential in biology, optics, and electronics. However, achieving both the patternability of stiffness and microstructure in a reconfigurable manner remains challenging. Here, we prepare amphigels crosslinked by dynamic disulfide bonds, which can be reversibly swollen by immiscible water or liquid paraffin. In the paraffingel form, the materials exhibited a high modulus of 130 MPa due to densified hydrogen bonds. Whereas swollen by water, the modulus fell over two orders of magnitude owing to the destruction of the hydrogen bonds. Via regionalized swelling of the solvents, well‐controlled and rewritable soft/stiff mechanical patterns can be created. On the other hand, the dynamic exchange of the disulfide crosslinking enables mechanophoto patterning to fabricate sophisticated macrogeometries and microstructures. The reconfigurable stiffness‐structure patterning can be manipulated orthogonally, which will create more application opportunities beyond conventional hydrogels and organogels.
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