Affiliation:
1. Center for Specialty Chemicals Korea Research Institute of Chemical Technology (KRICT) Ulsan 44412 Republic of Korea
2. Department of Polymer Science and Engineering Pusan National University Busan 46241 Republic of Korea
3. Department of Materials Science and Engineering Seoul National University (SNU) Seoul 08826 Republic of Korea
Abstract
AbstractLight‐driven 3D printing is gaining significant attention for its unparalleled build speed and high‐resolution in additive manufacturing. However, extending vat photopolymerization to multifunctional, photoresponsive materials poses challenges, such as light attenuation and interference between the photocatalysts (PCs) and photoactive moieties. This study introduces novel visible‐light‐driven acrylic resins that enable rapid, high‐resolution photoactive 3D printing. The synergistic combination of a cyanine‐based PC, borate, and iodonium coinitiators (HNu 254) achieves an excellent printing rate and feature resolution under low‐intensity, red light exposure. The incorporation of novel hexaarylbiimidazole (HABI) crosslinkers allows for spatially‐resolved photoactivation upon exposure to violet/blue light. Furthermore, a photobleaching mechanism inhibited by HNu 254 during the photopolymerization process results in the production of optically‐clear 3D printed objects. Real‐time Fourier transform infrared spectroscopy validates the rapid photopolymerization of the HABI‐containing acrylic resin, whereas mechanistic evaluations reveal the underlying dynamics that are responsible for the rapid photopolymerization rate, wavelength‐orthogonal photoactivation, and observed photobleaching phenomenon. Ultimately, this visible‐light‐based printing method demonstrates: (i) rapid printing rate of 22.5 mm h−1, (ii) excellent feature resolution (≈20 µm), and (iii) production of optically clear object with self‐healing capability and spatially controlled cleavage. This study serves as a roadmap for developing next‐generation “smart” 3D printing technologies.
Cited by
4 articles.
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