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RESEARCH PRODUCT
Divergent Adsorption-Dependent Luminescence of Amino-Functionalized Lanthanide Metal-Organic Frameworks for Highly Sensitive NO2 Sensors
José Sánchez CostaEstefania Fernandez-bartolomeRoberta PoloniBess VlaisavljevichJuan Cabanillas-gonzalezElena Guerrero-sanvicenteReinhold WannemacherJavier Castells-gilChen SunCarlos Martí-gastaldoArturo GamonalA. Lorenzo Marianosubject
LanthanideIonsPhotoluminescenceLuminescenceChemistryLigandAb initioMetal organic frameworks02 engineering and technology[CHIM.MATE]Chemical Sciences/Material chemistryMolecules010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryLigands01 natural sciences0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryAdsorptionGeneral Materials ScienceMetal-organic frameworkPhysical and Theoretical ChemistryIsostructural0210 nano-technologyLuminescencedescription
International audience; A novel gas sensing mechanism exploiting lanthanide luminescence modulation upon NO2 adsorption is demonstrated here. Two isostructural lanthanide-based metal–organic frameworks (MOFs) are used, including an amino group as the sensitive recognition center for NO2 molecules. The transfer of energy from the organic ligands to Ln is strongly dependent on the presence of NO2, resulting in an unprecedented photoluminescent sensing scheme. Thereby, NO2 exposition triggers either a reversible enhancement or a decrease in the luminescence intensity, depending on the lanthanide ion (Eu or Tb). Our experimental studies combined with density functional theory and complete active space self-consistent field calculations provide an understanding of the nature and effects of NO2 interactions within the MOFs and the signal transduction mechanism.
year | journal | country | edition | language |
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2020-03-20 |