Herein, the integration of SnO2 nanoparticles with two Zn(II) porphyrins – Zn(II) 5,10,15,20-tetraphenylporphyrin (ZnTPP) and its perfluorinated counterpart, Zn(II) 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin (ZnTPPF20) – was investigated for the sensing of gaseous acetone at 120 °C, adopting three Zn-porphyrin/SnO2 weight ratios (1:4, 1:32, and 1:64). For the first time, we were able to provide evidence of the correlation between the materials’ conductivity and these nanocomposites’ sensing performances, obtaining optimal results with a 1:32 ratio for ZnTPPF20/SnO2 and showcasing a remarkable detection limit of 200 ppb together with a boosted sensing signal with respect to bare SnO2. To delve deeper, the combination of experimental data with density functional theory calculations unveiled an electron-donating behavior of both porphyrins when interacting with tin dioxide semiconductor, especially for the non-fluorinated one. The study suggested that the interplay between electrons injected, from the porphyrins’ highest occupied molecular orbital to SnO2 conduction band, and the latter’s available electronic states has a dramatic impact to boost the chemiresistive sensing. Indeed, we highlighted that the key lies in preventing the full saturation of SnO2 electronic states concomitantly increasing the materials’ conductivity: in this respect, the best compromise turned out to be the perfluorinated porphyrin. A further corroboration of our findings was obtained by illuminating the sensors during measurements with a LED light. Actually, we demonstrated that it does not have any impact on improving the sensing behavior, most probably due to the electronic oversaturation and scattering caused by LED excitation in porphyrins. Lastly, the most effective hybrids (1:32 ratio) were physicochemically characterized, confirming the physisorption of the macrocycles onto SnO2 surface. In conclusion, herein, we underscored the feasibility of customizing porphyrin chemistry and porphyrin-to-SnO2 ratio to enhance the gaseous sensing of bare metal oxides, providing valuable insights for the engineering of highly performing light-free chemiresistors.

How the interplay between SnO2 and Zn(II) porphyrins impacts on the electronic features of gaseous acetone chemiresistors / F. Tessore, E. Pargoletti, G. DI CARLO, C. Albanese, R. Soave, M. Italo Trioni, F. Marelli, G. Cappelletti. - In: ACS APPLIED MATERIALS & INTERFACES. - ISSN 1944-8252. - 16:31(2024), pp. 41086-41098. [10.1021/acsami.4c05478]

How the interplay between SnO2 and Zn(II) porphyrins impacts on the electronic features of gaseous acetone chemiresistors

F. Tessore
Primo
;
E. Pargoletti
Secondo
;
G. DI CARLO;C. Albanese;G. Cappelletti
Ultimo
2024

Abstract

Herein, the integration of SnO2 nanoparticles with two Zn(II) porphyrins – Zn(II) 5,10,15,20-tetraphenylporphyrin (ZnTPP) and its perfluorinated counterpart, Zn(II) 5,10,15,20-tetrakis(pentafluorophenyl)porphyrin (ZnTPPF20) – was investigated for the sensing of gaseous acetone at 120 °C, adopting three Zn-porphyrin/SnO2 weight ratios (1:4, 1:32, and 1:64). For the first time, we were able to provide evidence of the correlation between the materials’ conductivity and these nanocomposites’ sensing performances, obtaining optimal results with a 1:32 ratio for ZnTPPF20/SnO2 and showcasing a remarkable detection limit of 200 ppb together with a boosted sensing signal with respect to bare SnO2. To delve deeper, the combination of experimental data with density functional theory calculations unveiled an electron-donating behavior of both porphyrins when interacting with tin dioxide semiconductor, especially for the non-fluorinated one. The study suggested that the interplay between electrons injected, from the porphyrins’ highest occupied molecular orbital to SnO2 conduction band, and the latter’s available electronic states has a dramatic impact to boost the chemiresistive sensing. Indeed, we highlighted that the key lies in preventing the full saturation of SnO2 electronic states concomitantly increasing the materials’ conductivity: in this respect, the best compromise turned out to be the perfluorinated porphyrin. A further corroboration of our findings was obtained by illuminating the sensors during measurements with a LED light. Actually, we demonstrated that it does not have any impact on improving the sensing behavior, most probably due to the electronic oversaturation and scattering caused by LED excitation in porphyrins. Lastly, the most effective hybrids (1:32 ratio) were physicochemically characterized, confirming the physisorption of the macrocycles onto SnO2 surface. In conclusion, herein, we underscored the feasibility of customizing porphyrin chemistry and porphyrin-to-SnO2 ratio to enhance the gaseous sensing of bare metal oxides, providing valuable insights for the engineering of highly performing light-free chemiresistors.
Settore CHIM/02 - Chimica Fisica
Settore CHIM/01 - Chimica Analitica
Settore CHIM/03 - Chimica Generale e Inorganica
Settore CHEM-02/A - Chimica fisica
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2024
25-lug-2024
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1080888
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