阳离子聚合
材料科学
链式转移
聚合
丙烯酸酯
高分子化学
光致聚合物
单体
木筏
固化(化学)
可逆加成-断裂链转移聚合
自由基聚合
聚合物
3D打印
混合材料
纳米技术
预聚物
光诱导电子转移
作者
Chongyang Yang,Xiaofeng Pan,Zhihan Yuan,Xiangqiang Pan,Jiajia Li,Jian Zhu
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-11-10
卷期号:58 (22): 12264-12270
标识
DOI:10.1021/acs.macromol.5c02907
摘要
The integration of mechanical adaptability and functional versatility in 3D-printed materials remains a central challenge in additive manufacturing. Here, we introduce a photoinduced 3D printing strategy that couples reversible addition–fragmentation chain transfer (RAFT) polymerization with cationic ring-opening polymerization (CROP) in a single resin. Using a dual-functional monomer, 3,4-epoxycyclohexylmethyl acrylate (ECMA), and a bis(4- tert -butylphenyl)iodonium hexafluorophosphate/2-isopropylthioxanthone (Iod/ITX) photoinitiating system, orthogonal polymerizations are triggered under 405 nm light to generate dual-cross-linking networks. The resulting materials exhibit unprecedented mechanical tunability, with Young’s moduli spanning from 8.4 MPa to 2.26 GPa, by varying monomer ratios, RAFT agent content, and postcuring conditions. RAFT-mediated chain ends enable postprinting welding and surface functionalization, while spatial control of radical versus cationic curing yields objects with coexisting soft and rigid domains. This hybrid platform establishes a versatile design principle for mechanically adaptive and multifunctional 3D-printed materials with broad potential in soft robotics, biomimetics, and responsive devices.
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