We report the synthesis of bell-shaped Bi/Bi13S18Br2 metal/semiconductor heterostructures as a photocatalyst based on nontoxic and Earth-abundant elements. Their unique morphology arises from a multistep growth process, involving (1) the nucleation of Bi13S18Br2 nanorods, (2) the reduction of a metallic-Bi domain on their surface induced by N,N-didodecylmethylamine, and (3) the heterostructure accretion by a localized reaction at the Bi/Bi13S18Br2 interface promoted by Ostwald ripening. These heterostructures display remarkable stability in polar solvents, remaining almost unaffected by prolonged exposure to isopropanol and water, and exhibit high photocatalytic efficiency for the degradation of organic dyes (i.e., Rhodamine B and Methylene Blue) under visible-light irradiation, with good recyclability. Additionally, preliminary tests demonstrate CO2 reduction capabilities, which make these heterostructures promising for both the photocatalytic degradation of pollutants and photoelectrochemical CO2 conversion. The straightforward synthesis process and the use of nontoxic and Earth-abundant elements offer significant potential for sustainable energy conversion technologies.

Synthesis, Growth Mechanism, and Photocatalytic Properties of Metallic-Bi/Bi13S18Br2 Nano-Bell Heterostructures / Cabona, Anna; Toso, Stefano; Griesi, Andrea; Rizzo, Martina; Ferri, Michele; Rusch, Pascal; Divitini, Giorgio; Pérez-Prieto, Julia; Galian, Raquel E.; Kriegel, Ilka; Manna, Liberato. - In: ACS MATERIALS LETTERS. - ISSN 2639-4979. - 7:5(2025), pp. 1707-1716. [10.1021/acsmaterialslett.5c00043]

Synthesis, Growth Mechanism, and Photocatalytic Properties of Metallic-Bi/Bi13S18Br2 Nano-Bell Heterostructures

Cabona, Anna;Rizzo, Martina;Ferri, Michele;Kriegel, Ilka;
2025

Abstract

We report the synthesis of bell-shaped Bi/Bi13S18Br2 metal/semiconductor heterostructures as a photocatalyst based on nontoxic and Earth-abundant elements. Their unique morphology arises from a multistep growth process, involving (1) the nucleation of Bi13S18Br2 nanorods, (2) the reduction of a metallic-Bi domain on their surface induced by N,N-didodecylmethylamine, and (3) the heterostructure accretion by a localized reaction at the Bi/Bi13S18Br2 interface promoted by Ostwald ripening. These heterostructures display remarkable stability in polar solvents, remaining almost unaffected by prolonged exposure to isopropanol and water, and exhibit high photocatalytic efficiency for the degradation of organic dyes (i.e., Rhodamine B and Methylene Blue) under visible-light irradiation, with good recyclability. Additionally, preliminary tests demonstrate CO2 reduction capabilities, which make these heterostructures promising for both the photocatalytic degradation of pollutants and photoelectrochemical CO2 conversion. The straightforward synthesis process and the use of nontoxic and Earth-abundant elements offer significant potential for sustainable energy conversion technologies.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11583/2999893