International Journal of Molecular Sciences (Nov 2022)

The Effect of Femtosecond Laser Irradiation and Plasmon Field on the Degree of Conversion of a UDMA-TEGDMA Copolymer Nanocomposite Doped with Gold Nanorods

  • Attila Bonyár,
  • Melinda Szalóki,
  • Alexandra Borók,
  • István Rigó,
  • Judit Kámán,
  • Shereen Zangana,
  • Miklós Veres,
  • Péter Rácz,
  • Márk Aladi,
  • Miklós Ákos Kedves,
  • Ágnes Szokol,
  • Péter Petrik,
  • Zsolt Fogarassy,
  • Kolos Molnár,
  • Mária Csete,
  • András Szenes,
  • Emese Tóth,
  • Dávid Vas,
  • István Papp,
  • Gábor Galbács,
  • László P. Csernai,
  • Tamás S. Biró,
  • Norbert Kroó,
  • NAPLIFE Collaboration

DOI
https://doi.org/10.3390/ijms232113575
Journal volume & issue
Vol. 23, no. 21
p. 13575

Abstract

Read online

In this work, the effects of femtosecond laser irradiation and doping with plasmonic gold nanorods on the degree of conversion (DC) of a urethane dimethacrylate (UDMA)–triethylene glycol dimethacrylate (TEGDMA) nanocomposite were investigated. The UDMA-TEGDMA photopolymer was prepared in a 3:1 weight ratio and doped with dodecanethiol- (DDT) capped gold nanorods of 25 × 75 or 25 × 85 nm nominal diameter and length. It was found that the presence of the gold nanorods alone (without direct plasmonic excitation) can increase the DC of the photopolymer by 6–15%. This increase was found to be similar to what could be achieved with a control heat treatment of 30 min at 180 °C. It was also shown that femtosecond laser impulses (795 nm, 5 mJ pulse energy, 50 fs pulse length, 2.83 Jcm−2 fluence), applied after the photopolymerization under a standard dental curing lamp, can cause a 2–7% increase in the DC of undoped samples, even after thermal pre-treatment. The best DC values (12–15% increase) were obtained with combined nanorod doping and subsequent laser irradiation close to the plasmon resonance peak of the nanorods (760–800 nm), which proves that the excited plasmon field can directly facilitate double bond breakage (without thermoplasmonic effects due to the short pulse length) and increase the crosslink density independently from the initial photopolymerization process.

Keywords