Time–space conversion spectral analysis for the nanosecond fluorescent processes of organic–inorganic compounds
Source abstract
Abstract
Time-resolved spectral measurements were conducted by using a continuous-wave laser and a CCD-based spectrometer. A spinning polygon mirror swung both the excitation laser beam and fluorescent rays, in the process of which a temporal change in the fluorescent spectrum was converted to a spatial distribution. The temporal resolution could be adjusted in the nano- and micro-second ranges by changing the rotation rate of the mirror. In comparison with the conventional pulsed-laser spectrometry, a higher sensitivity is attainable due to the slow features of the devices, i.e., continuous excitation by the laser and a long exposure time (1 s) of the CCD. The usefulness and reliability of the constructed system were demonstrated by spectral measurements of an organic–inorganic hybrid phosphor, which exhibited both a rapid fluorescent decay of organic ligands and a long-lasting afterglow of metal ions.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Spectroscopy and Laser Applications · Photochemistry and Electron Transfer Studies · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Electronics and Informatics, Ryukoku University , Seta, Otsu 520-2194, Japan
References (29)
Show source-provided references
1. Appl. Phys. Lett. · 2007 · 90 · 14350110.1063/1.2718503 ↗
2. Opt. Express · 2015 · 23 · 2552310.1364/oe.23.025523 ↗
3. Shionoya · 1999
4. Opt. Express · 2009 · 17 · 588510.1364/oe.17.005885 ↗
5. Opt. Mater. Express · 2018 · 8 · 67610.1364/ome.8.000676 ↗
6. Adv. Mater. · 2009 · 21 · 50910.1002/adma.200801635 ↗
7. Inorg. Chem. · 2010 · 49 · 930010.1021/ic100974e ↗
8. Sci. Rep. · 2016 · 6 · 2445810.1038/srep24458 ↗
9. J. Opt. Soc. Am. · 1964 · 54 · 121110.1364/josa.54.001211 ↗
10. Polym. J. · 2015 · 47 · 19510.1038/pj.2014.88 ↗
11. Opt. Lett. · 2004 · 29 · 47710.1364/ol.29.000477 ↗
12. Opt. Lett. · 2010 · 35 · 52010.1364/ol.35.000520 ↗
13. Opt. Lett. · 2011 · 36 · 190210.1364/ol.36.001902 ↗
14. Photochem. Photobiol. Sci. · 2017 · 16 · 68310.1039/c7pp00007c ↗
15. Appl. Opt. · 1968 · 7 · 215510.1364/ao.7.002155 ↗
16. Annu. Rev. Phys. Chem. · 1994 · 45 · 59310.1146/annurev.pc.45.100194.003113 ↗
17. Optica · 2016 · 3 · 8210.1364/optica.3.000082 ↗
18. Appl. Spectrosc. · 2010 · 64 · 93010.1366/000370210792081127 ↗
19. Biomed. Opt. Express · 2012 · 3 · 152110.1364/boe.3.001521 ↗
20. Opt. Express · 2013 · 21 · 656110.1364/oe.21.006561 ↗
21. Appl. Spectrosc. · 2016 · 70 · 64510.1177/0003702816631302 ↗
22. Opt. Express · 2017 · 25 · 1110310.1364/oe.25.011103 ↗
23. OSA Continuum · 2019 · 2 · 172610.1364/osac.2.001726 ↗
24. Opt. Express · 2014 · 22 · 2020510.1364/oe.22.020205 ↗
25. Opt. Lett. · 2015 · 40 · 480310.1364/ol.40.004803 ↗
26. Opt. Lett. · 2016 · 41 · 432810.1364/ol.41.004328 ↗
27. Appl. Opt. · 2001 · 40 · 672510.1364/ao.40.006725 ↗
28. Opt. Lett. · 2007 · 32 · 165610.1364/ol.32.001656 ↗
29. Vib. Spectrosc. · 2017 · 91 · 16310.1016/j.vibspec.2016.07.007 ↗