Axial and radial random lasing in a biopolymer based liquid core ring resonator

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Mitty George , I. Hubert Joe , M. Kailasnath
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引用次数: 0

Abstract

Tunable random lasing from a liquid core cylindrical microcavity by transversely pumping a silica capillary filled with a BSA (Bovine Serum Albumin)-Rhodamine B (RhB) composite biopolymer solution is reported. The binding of RhB to discrete sites of BSA mediates the structural arrangement of lasing species, influencing the stimulated emission and tunability. The UV–Vis, Photoluminescence (PL), FTIR spectroscopy and molecular docking studies were used to analyze the dye binding with BSA. Laser emission was collected from the surface as well as the end of the capillary upon transverse pumping along its length. The optical feedback from the cavity effects of the cylindrical microstructure enhances the random lasing modes. Lasing threshold and red shift in the emission were found to be tunable with BSA concentrations. The surface emissions were characterized by sharp and distinct lasing peaks at low thresholds in contrast to the relatively broad end emissions requiring a four-fold pump pulse energy at a BSA concentration of 0.6 g/ml. This difference in lasing threshold is in agreement with the Power Fourier Transform (PFT) analysis of the surface and end emissions. The cavity path lengths corresponding to the surface and end emissions were analyzed and the shorter path length for surface emissions favours the formation of coherent loops of photons and a lower lasing threshold. The coexistence of surface and end emissions with entirely different characteristics from the capillary and its tunability opens up new avenues in the development of biomaterial-based integrated light sources for sensing, display technology and encryption.
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
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.
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