AI Article Synopsis

  • The study explored how the lasing abilities of Thioflavin T and Thioflavin X dyes change based on solvent viscosity and DNA structure (natural, fragmented, and aggregated).
  • Key findings showed that the dye's lasing thresholds and photostability are influenced by the solvation shell, dipole moment organization driven by DNA, and molecular diffusion in the excitation area.
  • By manipulating DNA-related factors like magnesium salts, heating, and sonication, researchers significantly reduced the thresholds for amplified spontaneous emission in dye-doped DNA films, paving the way for better optical materials for solid-state lasers.

Article Abstract

The lasing characteristics of Thioflavin T (ThT) and Thioflavin X (ThX) dyes were investigated in solvents with increasing viscosity: water, ethanol, butanol, ethylene glycol, and glycerol and three forms of DNA (double-helix natural, fragmented, and aggregated). The results identified that lasing thresholds and photostability depend on three critical factors: the solvation shell surrounding dye molecules, the organization of their dipole moments, which is driven by the DNA structure, and the molecules diffusion coefficient in the excitation focal spot. The research highlights that dye doped to DNA accumulated in binding sites fosters long-range dye orientation, facilitating a marked reduction of lasing thresholds in the liquid phase as well as amplified spontaneous emission (ASE) thresholds in the solid state. Leveraging insights from lasing characteristics obtained in liquid, ASE in the solid state was optimized in a controlled way by changing the parameters influencing the DNA structure, i.e., magnesium salt addition, heating, and sonication. The modifications led to a large decrease in the ASE thresholds in the dye-doped DNA films. It was shown that the examination of lasing in cavities can be useful for preparing optical materials with improved architectures and functionalities for solid-state lasers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10749465PMC
http://dx.doi.org/10.1021/acsaom.3c00264DOI Listing

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