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Promoting Photocatalytic Hydrogen Evolution Activity of Graphitic Carbon Nitride with Hole-Transfer Agents

dc.contributor.authorIndra A.; Beltrán-Suito R.; Müller M.; Sivasankaran R.P.; Schwarze M.; Acharjya A.; Pradhan B.; Hofkens J.; Brückner A.; Thomas A.; Menezes P.W.; Driess M.
dc.date.accessioned2025-05-23T11:26:48Z
dc.description.abstractVisible light-driven photocatalytic reduction of protons to H2 is considered a promising way of solar-to-chemical energy conversion. Effective transfer of the photogenerated electrons and holes to the surface of the photocatalyst by minimizing their recombination is essential for achieving a high photocatalytic activity. In general, a sacrificial electron donor is used as a hole scavenger to remove photogenerated holes from the valence band for the continuation of the photocatalytic hydrogen (H2) evolution process. Here, for the first time, the hole-transfer dynamics from Pt-loaded sol−gel-prepared graphitic carbon nitride (Pt-sg-CN) photocatalyst were investigated using different adsorbed hole acceptors along with a sacrificial agent (ascorbic acid). A significant increment (4.84 times) in H2 production was achieved by employing phenothiazine (PTZ) as the hole acceptor with continuous H2 production for 3 days. A detailed charge-transfer dynamic of the photocatalytic process in the presence of the hole acceptors was examined by time-resolved photoluminescence and in situ electron paramagnetic resonance studies. © 2020 The Authors. ChemSusChem published by Wiley-VCH GmbH
dc.identifier.doihttps://doi.org/10.1002/cssc.202002500
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/10719
dc.relation.ispartofseriesChemSusChem
dc.titlePromoting Photocatalytic Hydrogen Evolution Activity of Graphitic Carbon Nitride with Hole-Transfer Agents

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