Issue 26, 2021

An investigation of broadband optical nonlinear absorption and transient nonlinear refraction in a fluorenone-based compound

Abstract

A novel fluorenone derivative, FO52, is designed and synthesized. The fluorenone group is introduced to provide the central π-conjugated system in the molecule and triphenylamine is substituted at both sides. Intramolecular Charge Transfer (ICT) from the terminal groups to the molecular center is confirmed via DFT calculations. Ultrafast optical nonlinearities are investigated via Z-scan and transient absorption spectroscopy (TAS) studies with a 190 fs laser. Reverse saturable absorption, two-photon induced excited-state absorption, and pure two-photon absorption are observed at 532 nm, 650 nm, and 800 nm, respectively. The different mechanisms at these wavelengths are discussed and interpreted with assistance from the results from TAS. Furthermore, strong excited-state refraction and ultrafast negative refraction from the bound electron response are resolved and discussed in phase object pump probe (POPP) experiments. The results suggest that the ICT-enhanced optical nonlinearities provide FO52 with strong optical limiting capabilities at visible wavelengths and ultrafast refraction with tiny attenuation in the near infrared region. The combination of these properties in one compound could be attractive for applications like laser protection and low-loss all-optical switching.

Graphical abstract: An investigation of broadband optical nonlinear absorption and transient nonlinear refraction in a fluorenone-based compound

Supplementary files

Article information

Article type
Paper
Submitted
10 Feb 2021
Accepted
31 Mar 2021
First published
29 Apr 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 15952-15958

An investigation of broadband optical nonlinear absorption and transient nonlinear refraction in a fluorenone-based compound

X. Wu, J. Xiao, Y. Han, J. Xu, W. Zhou, Y. Li, Y. Fang, Y. Chen, Q. Wu and Y. Song, RSC Adv., 2021, 11, 15952 DOI: 10.1039/D1RA01134K

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