Photochromic property of ternary transition metal oxide nanocomposite prepared with co-solvated deep eutectic mixtures
The application of deep eutectic solvents (DES) in the synthesis of photochromic transition metal oxide (TMO)-based nanocomposites is gaining attention in recent years. In this study, DES-based on choline chloride and ethylene glycol (1:2) was prepared with the addition of different volume of water...
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Published in: | Research on chemical intermediates Vol. 47; no. 9; pp. 3807 - 3823 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Dordrecht
Springer Netherlands
01-09-2021
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | The application of deep eutectic solvents (DES) in the synthesis of photochromic transition metal oxide (TMO)-based nanocomposites is gaining attention in recent years. In this study, DES-based on choline chloride and ethylene glycol (1:2) was prepared with the addition of different volume of water as co-solvent for the dissolution and preparation of ternary TMO nanocomposites at different temperatures. TGA showed a corresponding increase in weight loss as the volume of the co-solvent increases with a 10–22% loss in mass of the nanocomposites at > 432 °C. SEM images revealed an aggregated and clustered particle distribution, while the TEM revealed an uneven polyhedral-like shaped morphology. The nanocomposites exhibited fast photochromic response by a change from pale-yellow to light blue coloration after 5 s of irradiation with UV-light. The intensity of the coloration deepens after 180 s of irradiation due to the excitation of electrons from the valence band to the conduction band of the metallic systems via a synergistic electronic transition. The variable oxidation states of the individual metal oxides and their redox property inspired the fast fading in a dark oxygenated environment after 30 min, thus, rendering the material suitable for application in smart windows/glasses and color display devices. |
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ISSN: | 0922-6168 1568-5675 |
DOI: | 10.1007/s11164-021-04497-5 |