Sebastiano Arcidiacono
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Sebastiano Arcidiacono has a total of 11 co-authors. Here are the top co-authors by number of shared publications:
- Anna Lucia Pellegrino
Department of Chemical Sciences, University of Catania, v.le A. Doria 6, 95125 Catania, Italy
1 shared publication - Cristina Maria Belfiore
Department of Biological Geological and Environmental Sciences, University of Catania, Catania, Italy
1 shared publication - Eleonora La Greca
Department of Chemical Sciences, University of Catania, v.le A. Doria 6, 95125 Catania, Italy
1 shared publication - Giuliana Impellizzeri
CNR-IMM, Via Santa Sofia 64, 95123 Catania, Italy
1 shared publication - Leonarda Francesca Liotta
Institute for the Study of Nanostructured Materials (ISMN), National Research Council (CNR), Via Ugo La Malfa 153, 90146 Palermo, Italy
1 shared publication - Marco Viccaro
Dipartimento di Scienze Biologiche, Geologiche e Ambientali, Università degli Studi di Catania, Catania, Italy
1 shared publication
Latest Publications
- Open Access
Nb2O5/g-C3N4 Composite Photocatalysts Supported on Etna-Derived Aluminosilicate for Solar H2 Production
In this work, Etna ash-derived photocatalysts were investigated for the first time for solar H2 production. Volcanic ash, commonly treated as a special waste in eastern Sicily (Italy), was modified through chemical treatment followed by microwave-assisted crystallization, avoiding the conventional high-temperature thermal route. The obtained material was tested both as a bare photocatalyst and as a support for a Nb2O5/graphitic carbon nitride composite prepared by a hydrothermal method. The Etna-derived photocatalyst exhibited a solar H2 production rate (by TEOA photoreforming) of 920 μmol/gcat∙h. Upon incorporation of the Nb-based composite, the H2 evolution rate increased by about 2.5 times, reaching 2370.5 μmol/gcat∙h, demonstrating a strong synergistic effect. Notably, the developed materials largely outperformed commercial TiO2 P25 (25 μmol/gcat∙h). The enhanced photocatalytic activity was attributed to the tailored modifications of Etna ash, which increased porosity and promoted aluminosilicate framework reorganization, favoring an optimal distribution of the photocatalytically active TiO2 and iron oxide phases. The obtained Nb oxide/carbon nitride supported on modified Etna ash also showed a remarkable stability after six consecutive runs of solar photocatalytic H2 production. This work demonstrates a sustainable strategy for converting volcanic waste into efficient multifunctional photocatalysts while minimizing the use of critical raw materials.
Open AccessNb2O5/g-C3N4 Composite Photocatalysts Supported on Etna-Derived Aluminosilicate for Solar H2 Production
In this work, Etna ash-derived photocatalysts were investigated for the first time for solar H2 production. Volcanic ash, commonly treated as a special waste in eastern Sicily (Italy), was modified through chemical treatment followed by microwave-assisted crystallization, avoiding the conventional high-temperature thermal route. The obtained material was tested both as a bare photocatalyst and as a support for a Nb2O5/graphitic carbon nitride composite prepared by a hydrothermal method. The Etna-derived photocatalyst exhibited a solar H2 production rate (by TEOA photoreforming) of 920 μmol/gcat∙h. Upon incorporation of the Nb-based composite, the H2 evolution rate increased by about 2.5 times, reaching 2370.5 μmol/gcat∙h, demonstrating a strong synergistic effect. Notably, the developed materials largely outperformed commercial TiO2 P25 (25 μmol/gcat∙h). The enhanced photocatalytic activity was attributed to the tailored modifications of Etna ash, which increased porosity and promoted aluminosilicate framework reorganization, favoring an optimal distribution of the photocatalytically active TiO2 and iron oxide phases. The obtained Nb oxide/carbon nitride supported on modified Etna ash also showed a remarkable stability after six consecutive runs of solar photocatalytic H2 production. This work demonstrates a sustainable strategy for converting volcanic waste into efficient multifunctional photocatalysts while minimizing the use of critical raw materials.