材料科学
聚合物
自愈水凝胶
共价键
光致聚合物
原子转移自由基聚合
水溶液
复合数
固化(化学)
紫外线固化
胶粘剂
聚合
化学工程
自由基聚合
单体
高分子化学
纳米技术
复合材料
化学
有机化学
工程类
图层(电子)
作者
Ge Yan,Mengjie Zhou,Jun Zhang,Wenjie Zhang,Yanjie He,Xiaoguang Qiao,Ge Shi,Xinchang Pang
出处
期刊:Small
[Wiley]
日期:2025-05-03
卷期号:21 (24): e2411688-e2411688
被引量:4
标识
DOI:10.1002/smll.202411688
摘要
Abstract Photocurable 3D printing (SLA or DLP) materials have garnered considerable attention due to their remarkable efficiency and precision in manufacturing. However, the presence of covalent crosslinking makes the recycling and reuse of printed materials extremely challenging. Here a novel approach to covalent crosslinker‐free photo‐curing 3D printing (via DLP) of liquid metal (LM) composite hydrogels is reported, leveraging surface‐initiated photoinduced atom radical transfer polymerization (SI ‐photo ATRP). The pre‐synthesized PHEA‐Br macroinitiators are grafted onto the surfaces of LM nanoparticles (LMNPs) by mechanical sonication, stabilizing the LMNPs within the resin solution while simultaneously generating active sites for SI ‐photo ATRP. During the SI ‐photo ATRP process, polymer chains of sufficient length form hydrogen bonds with multiple LMNPs, effectively transforming the LMNPs into crosslinking points. By integrating the aqueous photoATRP system catalyzed by carbon dots, LM@polymer composite hydrogel with complex structures are successfully established through DLP technology. The versatility of the 3D printed hydrogel is investigated by employing HEA, OEGA 480, and AAm as the monomers in resin solution, respectively. Notably, all the LM@polymer composite hydrogels can be degraded in aqueous NaOH solution. Furthermore, LM@polymer‐based networks exhibit self‐repairing capabilities, serve as underwater adhesives, and conduct electricity. This work offers new insights into designing 3D printing materials and sustainable photocurable technology.
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