4.8 Article

Ultrafast Visible-Light-Induced ATRP in Aqueous Media with Carbon Quantum Dots as the Catalyst and Its Application for 3D Printing

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 22, Pages 9817-9826

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c02303

Keywords

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Funding

  1. National Natural Science Foundation of China [51973201, U1804128, 52173209]
  2. 111 Project [D18023]
  3. Key Scientific Research Projects of Colleges and Universities in Henan Province [22ZX001]
  4. National Science Foundation for Young Scientists of China [22105179]
  5. National Key R&D Program of China [2017YFB0307600]
  6. China Postdoctoral Science Foundation [2020M682317]
  7. Scientific & Technological Research Projects in Henan Province [222102520009]

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Carbon quantum dots were introduced into ATRP in aqueous media, leading to the development of an ultrafast visible-light-induced polymerization system that enabled efficient 3D printing of hydrogels with excellent optical properties.
Photoinduced atom transfer radical polymerization (ATRP) has been proved to be a versatile technique for polymer network formation. However, the slow polymerization rates of typical ATRP limited its application in the field of additive manufacturing (3D printing). In this work, we introduced carbon quantum dots (CQDs) for the first time to the ATRP in aqueous media and developed an ultrafast visible-light-induced polymerization system. After optimization, the polymerization could achieve a high monomer conversion (>90%) within 1 min, and the polydispersity index (PDI) of the polymer was lower than 1.25. This system was then applied as the first example of ATRP for the 3D printing of hydrogel through digital light processing (DLP), and the printed object exhibited good dimensional accuracy. Additionally, the excellent and stable optical properties of CQDs also provided interesting photoluminescence capabilities to the printed objects. We deduce this ATRP mediated 3D printing process would provide a new platform for the preparation of functional and stimuli-responsive hydrogel materials.

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