光致聚合物
无定形固体
聚合物
材料科学
纳米技术
背景(考古学)
化学
复合材料
聚合
有机化学
地质学
古生物学
作者
Mojtaba Ahmadi,Katharina Ehrmann,Thomas Koch,Robert Liska,Jürgen Stampfl
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2024-03-28
卷期号:124 (7): 3978-4020
被引量:2
标识
DOI:10.1021/acs.chemrev.3c00570
摘要
Photopolymers have been optimized as protective and decorative coating materials for decades. However, with the rise of additive manufacturing technologies, vat photopolymerization has unlocked the use of photopolymers for three-dimensional objects with new material requirements. Thus, the originally highly cross-linked, amorphous architecture of photopolymers cannot match the expectations for modern materials anymore, revealing the largely unanswered question of how diverse properties can be achieved in photopolymers. Herein, we review how microstructural features in soft matter materials should be designed and implemented to obtain high performance materials. We then translate these findings into chemical design suggestions for enhanced printable photopolymers. Based on this analysis, we have found microstructural heterogenization to be the most powerful tool to tune photopolymer performance. By combining the chemical toolbox for photopolymerization and the analytical toolbox for microstructural characterization, we examine current strategies for physical heterogenization (fillers, inkjet printing) and chemical heterogenization (semicrystalline polymers, block copolymers, interpenetrating networks, photopolymerization induced phase separation) of photopolymers and put them into a material scientific context to develop a roadmap for improving and diversifying photopolymers' performance.
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