Photo-driven electron transfer from FAPbBr 3 perovskites nanocrystals to photodeactivatable 4-(phenylazo) benzoic acid
Formamidinium lead bromide (FAPbBr 3 ) perovskite nanocrystals (NCs) are promising materials due to their narrow band emission and high photoluminescence (PL) quantum yield. In the present work, oleyl amine functionalized FAPbBr 3 NCs were synthesized. These NCs were then attached to 4-(phenylazo)be...
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Veröffentlicht in: | New journal of chemistry 2024-06, Vol.48 (23), p.10636-10645 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Formamidinium lead bromide (FAPbBr
3
) perovskite nanocrystals (NCs) are promising materials due to their narrow band emission and high photoluminescence (PL) quantum yield. In the present work, oleyl amine functionalized FAPbBr
3
NCs were synthesized. These NCs were then attached to 4-(phenylazo)benzoic acid (PABA) to form a fluorescent photodeactivatable FAPbBr
3
NCs-PABA dyad. Ultraviolet (UV) irradiation caused
trans–cis
isomerization of PABA that reverted to the
trans
-isomer upon storage in the dark after 40 min. Upon UV irradiation of the FAPbBr
3
NCs-PABA dyad, PABA was converted from the
trans
isomer to the
cis
isomer. Strong PL quenching of FAPbBr
3
NCs was observed due to photoexcited charge transfer from the conduction band of NCs to the LUMO of the
cis
-isomer of PABA. The decrease in the PL intensity of NCs also manifested as a decrease in the PL lifetime. The positions of band edges, estimated by cyclic voltammetry, suggested that the electron transfer from photoexcited FAPbBr
3
NCs to the
cis
-isomer of PABA was responsible for the PL quenching of FAPbBr
3
NCs. The photoinduced reversible
trans–cis
isomerization of PABA accompanied by the strong PL quenching of FAPbBr
3
NCs in the FAPbBr
3
NCs-PABA dyad, due to photoexcited electron transfer from NCs to PABA in the dyad, could help in the design of photo-driven fluorescent probes with high-contrast due to the narrow emission band of FAPbBr
3
NCs. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/D4NJ02009J |