Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage
Here, we report a new photosensitive metal–organic framework (MOF) that was constructed via the modification of UiO-66-NH<sub>2</sub> with diarylethene molecules (DAE, 4-(5-Methoxy-1,2-dimethyl-1H-indol-3-yl)-3-(2,5-dimethylthiophen-3-yl)-4-furan-2,5-dione). The material that was obtaine...
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MDPI AG
2021-11-01
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author | Vera V. Butova Olga A. Burachevskaya Vitaly A. Podshibyakin Evgenii N. Shepelenko Andrei A. Tereshchenko Svetlana O. Shapovalova Oleg I. Il’in Vladimir A. Bren’ Alexander V. Soldatov |
author_facet | Vera V. Butova Olga A. Burachevskaya Vitaly A. Podshibyakin Evgenii N. Shepelenko Andrei A. Tereshchenko Svetlana O. Shapovalova Oleg I. Il’in Vladimir A. Bren’ Alexander V. Soldatov |
author_sort | Vera V. Butova |
collection | DOAJ |
description | Here, we report a new photosensitive metal–organic framework (MOF) that was constructed via the modification of UiO-66-NH<sub>2</sub> with diarylethene molecules (DAE, 4-(5-Methoxy-1,2-dimethyl-1H-indol-3-yl)-3-(2,5-dimethylthiophen-3-yl)-4-furan-2,5-dione). The material that was obtained was a highly crystalline porous compound. The photoresponse of the modified MOF was observed via UV–Vis and IR spectroscopy. Most of the DAE molecules inside of the UiO-66-pores had an open conformation after synthesis. However, the equilibrium was able to be shifted further toward an open conformation using visible light irradiation with a wavelength of 520 nm. Conversely, UV-light with a wavelength of 450 nm initiated the transformation of the photoresponsive moieties inside of the pores to a closed modification. We have shown that this transformation could be used to stimulate hydrogen adsorption–desorption processes. Specifically, visible light irradiation increased the H<sub>2</sub> capacity of modified MOF, while UV-light decreased it. A similar hybrid material with DAE moieties in the UiO-66 scaffold was applied for hydrogen storage for the first time. Additionally, the obtained results are promising for smart H<sub>2</sub> storage that is able to be managed via light stimuli. |
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language | English |
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series | Polymers |
spelling | doaj.art-e25a132926d247fcabd451e47c05e8ba2023-11-23T01:11:09ZengMDPI AGPolymers2073-43602021-11-011322405210.3390/polym13224052Photoswitchable Zirconium MOF for Light-Driven Hydrogen StorageVera V. Butova0Olga A. Burachevskaya1Vitaly A. Podshibyakin2Evgenii N. Shepelenko3Andrei A. Tereshchenko4Svetlana O. Shapovalova5Oleg I. Il’in6Vladimir A. Bren’7Alexander V. Soldatov8The Smart Materials Research Institute, Southern Federal University, Sladkova 178/24, 344090 Rostov-on-Don, RussiaThe Smart Materials Research Institute, Southern Federal University, Sladkova 178/24, 344090 Rostov-on-Don, RussiaInstitute of Physical and Organic Chemistry, Southern Federal University, 344090 Rostov-on-Don, RussiaFederal Research Center the Southern Scientific Center of the Russian Academy of Sciences, 344006 Rostov-on-Don, RussiaThe Smart Materials Research Institute, Southern Federal University, Sladkova 178/24, 344090 Rostov-on-Don, RussiaThe Smart Materials Research Institute, Southern Federal University, Sladkova 178/24, 344090 Rostov-on-Don, RussiaInstitute of Nanotechnologies, Electronics and Equipment Engineering, Southern Federal University, Shevchenko 2, 347922 Taganrog, RussiaInstitute of Physical and Organic Chemistry, Southern Federal University, 344090 Rostov-on-Don, RussiaThe Smart Materials Research Institute, Southern Federal University, Sladkova 178/24, 344090 Rostov-on-Don, RussiaHere, we report a new photosensitive metal–organic framework (MOF) that was constructed via the modification of UiO-66-NH<sub>2</sub> with diarylethene molecules (DAE, 4-(5-Methoxy-1,2-dimethyl-1H-indol-3-yl)-3-(2,5-dimethylthiophen-3-yl)-4-furan-2,5-dione). The material that was obtained was a highly crystalline porous compound. The photoresponse of the modified MOF was observed via UV–Vis and IR spectroscopy. Most of the DAE molecules inside of the UiO-66-pores had an open conformation after synthesis. However, the equilibrium was able to be shifted further toward an open conformation using visible light irradiation with a wavelength of 520 nm. Conversely, UV-light with a wavelength of 450 nm initiated the transformation of the photoresponsive moieties inside of the pores to a closed modification. We have shown that this transformation could be used to stimulate hydrogen adsorption–desorption processes. Specifically, visible light irradiation increased the H<sub>2</sub> capacity of modified MOF, while UV-light decreased it. A similar hybrid material with DAE moieties in the UiO-66 scaffold was applied for hydrogen storage for the first time. Additionally, the obtained results are promising for smart H<sub>2</sub> storage that is able to be managed via light stimuli.https://www.mdpi.com/2073-4360/13/22/4052UiO-66smart materialdiaryletheneUiO-66-NH<sub>2</sub>photochromismactivation |
spellingShingle | Vera V. Butova Olga A. Burachevskaya Vitaly A. Podshibyakin Evgenii N. Shepelenko Andrei A. Tereshchenko Svetlana O. Shapovalova Oleg I. Il’in Vladimir A. Bren’ Alexander V. Soldatov Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage Polymers UiO-66 smart material diarylethene UiO-66-NH<sub>2</sub> photochromism activation |
title | Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage |
title_full | Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage |
title_fullStr | Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage |
title_full_unstemmed | Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage |
title_short | Photoswitchable Zirconium MOF for Light-Driven Hydrogen Storage |
title_sort | photoswitchable zirconium mof for light driven hydrogen storage |
topic | UiO-66 smart material diarylethene UiO-66-NH<sub>2</sub> photochromism activation |
url | https://www.mdpi.com/2073-4360/13/22/4052 |
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