Journal
INORGANIC CHEMISTRY COMMUNICATIONS
Volume 125, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.inoche.2020.108394
Keywords
Layered double hydroxide; Photoluminescence; Terbium; CO2
Categories
Funding
- Japan Society for the Promotion of Science (JSPS) [18K05269]
- Grants-in-Aid for Scientific Research [18K05269] Funding Source: KAKEN
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Terbium-substituted layered double hydroxides (NO3-LDH) were synthesized using a hydrothermal method, which showed green photoluminescence as CO3-LDH under a CO2 gas flow containing water vapor. The fluorescence intensity of CO3-LDH increased with CO2 absorption time and concentration, with a greater bandgap compared to NO3-LDH.
Terbium-substituted layered double hydroxides with NO3 in the interlayer (NO3-LDH) were synthesized using a hydrothermal method. The synthesized NO3-LDH reacted with CO2 at 30 degrees C under a CO2 gas flow containing water vapor to produce CO2-absorbed LDH (CO3-LDH). Fluorescent spectroscopy clarified that the intensity of the excitation and emission spectra of the CO3-LDH increased with increasing CO2 absorption time and CO2 concentration under the CO2 gas flow. The CO3-LDH exhibited green photoluminescence owing to the transition of D-5(4) -> F-7(J) (J = 3, 4, 5, 6), which was excited by UV-light irradiation at 353 nm. The bandgap of the CO3-LDH was greater than that of the NO3-LDH, which caused an increase of the intensity of the excitation and emission spectra of the CO3-LDH. It was clarified that the NO3-LDH is capable of capturing CO2 as a carbonate species under water vapor, and resultant CO3-LDH emitted green photoluminescence.
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