{"title":"Upconversion enabled optical limiting behaviour in Y2O3: Yb, Er nanophosphors under 532 nm and 1064 nm laser excitation","authors":"J. Kawya, T.C. Sabari Girisun","doi":"10.1016/j.jlumin.2024.120903","DOIUrl":null,"url":null,"abstract":"<div><div>Y<sub>2</sub>O<sub>3</sub>: Yb, Er nanophosphors were synthesized by sol-gel approach and preliminary characterization confirms the existence of lanthanide dopants and the host material in the appropriate ratio with nanosphere-like morphology. Linear absorption displays visible and NIR absorption regions due to the sub-bandgap states involved in f-f transitions of Er- Yb ions. PL study shows more intense red emissions than blue and green emissions due to the combination of energy transfer and cross-relaxation process in Er ions. Wavelength-dependent nonlinear optical response of Y<sub>2</sub>O<sub>3</sub>: Yb, Er was examined by adapting the intensity-dependent Z-scan technique (open aperture) using nano pulsed Nd: YAG laser. Remarkably Y<sub>2</sub>O<sub>3</sub>: Yb, Er nanophosphors show reverse saturable absorption ascribed due to the two-photon absorption and two/three-photon absorption at 532 nm and 1064 nm respectively. The nonlinear absorption coefficient reliant on the intensity of the laser unambiguously demonstrates the presence of a sequential multi-photon absorption process. The results from the Z-scan experiment demonstrate the influence of the sub-bandgap energy states of the Y<sub>2</sub>O<sub>3</sub> matrix due to the Yb and Er dopants in the excited state absorption behaviour. Upconversion integrated optical limiting of Y<sub>2</sub>O<sub>3</sub>: Yb, Er nanophosphors provide a potential origin for designing high-performance broadband solid-state optical limiters for laser protection devices.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"277 ","pages":"Article 120903"},"PeriodicalIF":3.3000,"publicationDate":"2024-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231324004678","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
Y2O3: Yb, Er nanophosphors were synthesized by sol-gel approach and preliminary characterization confirms the existence of lanthanide dopants and the host material in the appropriate ratio with nanosphere-like morphology. Linear absorption displays visible and NIR absorption regions due to the sub-bandgap states involved in f-f transitions of Er- Yb ions. PL study shows more intense red emissions than blue and green emissions due to the combination of energy transfer and cross-relaxation process in Er ions. Wavelength-dependent nonlinear optical response of Y2O3: Yb, Er was examined by adapting the intensity-dependent Z-scan technique (open aperture) using nano pulsed Nd: YAG laser. Remarkably Y2O3: Yb, Er nanophosphors show reverse saturable absorption ascribed due to the two-photon absorption and two/three-photon absorption at 532 nm and 1064 nm respectively. The nonlinear absorption coefficient reliant on the intensity of the laser unambiguously demonstrates the presence of a sequential multi-photon absorption process. The results from the Z-scan experiment demonstrate the influence of the sub-bandgap energy states of the Y2O3 matrix due to the Yb and Er dopants in the excited state absorption behaviour. Upconversion integrated optical limiting of Y2O3: Yb, Er nanophosphors provide a potential origin for designing high-performance broadband solid-state optical limiters for laser protection devices.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.