Hydrogen production by photocatalytic water splitting is one of the most promising sustainable routes to store solar energy in the form of chemical bonds. To obtain significant H2 evolution rates (HERs) a variety of defective TiO2 catalysts were synthesized by means of procedures generally requiring highly energy-consuming treatments, e.g. hydrogenation. Even if a complete understanding of the relationship between defects, electronic structure and catalytic active sites is far from being achieved, the band gap narrowing and Ti3+-self-doping have been considered essential to date. In most reports a metal co-catalyst (commonly Pt) and a sacrificial electron donor (such as methanol) are used to improve HERs. Here we report the synthesis of TiO2/C bulk heterostructures, obtained from a hybrid TiO2-based gel by simple heat treatments at 400 °C under different atmospheres. The electronic structure and properties of the grey or black gel-derived powders are deeply inspected by a combination of classical and less conventional techniques, in order to identify the origin of their photoresponsivity. The defective sites of these heterostructures, namely oxygen vacancies, graphitic carbon and unpaired electrons localized on the C matrix, result in a remarkable visible light activity in spite of the lack of band gap narrowing or Ti3+-self doping. The materials provide HER values ranging from about 0.15 to 0.40 mmol h-1 gcat-1, under both UV- and visible-light irradiation, employing glycerol as sacrificial agent and without any co-catalyst.

Photocatalytic hydrogen evolution by co-catalyst-free TiO2/C bulk heterostructures synthesized under mild conditions / Imparato, C.; Iervolino, G.; Fantauzzi, M.; Koral, C.; Macyk, W.; Kobielusz, M.; D'Errico, G.; Rea, I.; Di Girolamo, R.; De Stefano, L.; Andreone, A.; Vaiano, V.; Rossi, A.; Aronne, A.. - In: RSC ADVANCES. - ISSN 2046-2069. - 10:21(2020), pp. 12519-12534. [10.1039/d0ra01322f]

Photocatalytic hydrogen evolution by co-catalyst-free TiO2/C bulk heterostructures synthesized under mild conditions

Imparato C.;Koral C.;D'Errico G.;Rea I.;Di Girolamo R.;Andreone A.;Aronne A.
2020

Abstract

Hydrogen production by photocatalytic water splitting is one of the most promising sustainable routes to store solar energy in the form of chemical bonds. To obtain significant H2 evolution rates (HERs) a variety of defective TiO2 catalysts were synthesized by means of procedures generally requiring highly energy-consuming treatments, e.g. hydrogenation. Even if a complete understanding of the relationship between defects, electronic structure and catalytic active sites is far from being achieved, the band gap narrowing and Ti3+-self-doping have been considered essential to date. In most reports a metal co-catalyst (commonly Pt) and a sacrificial electron donor (such as methanol) are used to improve HERs. Here we report the synthesis of TiO2/C bulk heterostructures, obtained from a hybrid TiO2-based gel by simple heat treatments at 400 °C under different atmospheres. The electronic structure and properties of the grey or black gel-derived powders are deeply inspected by a combination of classical and less conventional techniques, in order to identify the origin of their photoresponsivity. The defective sites of these heterostructures, namely oxygen vacancies, graphitic carbon and unpaired electrons localized on the C matrix, result in a remarkable visible light activity in spite of the lack of band gap narrowing or Ti3+-self doping. The materials provide HER values ranging from about 0.15 to 0.40 mmol h-1 gcat-1, under both UV- and visible-light irradiation, employing glycerol as sacrificial agent and without any co-catalyst.
2020
Photocatalytic hydrogen evolution by co-catalyst-free TiO2/C bulk heterostructures synthesized under mild conditions / Imparato, C.; Iervolino, G.; Fantauzzi, M.; Koral, C.; Macyk, W.; Kobielusz, M.; D'Errico, G.; Rea, I.; Di Girolamo, R.; De Stefano, L.; Andreone, A.; Vaiano, V.; Rossi, A.; Aronne, A.. - In: RSC ADVANCES. - ISSN 2046-2069. - 10:21(2020), pp. 12519-12534. [10.1039/d0ra01322f]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/812644
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