Rational design of a carbon/potassium poly(heptazine imide) heterojunction for enhanced photocatalytic H2 and H2O2 evolution

We present the rational design of carbon/potassium poly(heptazine imide) (KPHI) heterostructures via one-step salt-melt assisted condensation for efficient photocatalysis. Hybridizing KPHI with an adenine-derived carbonaceous material (Ad-carbon) displayed an outstanding photocatalytic H evolution a...

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Detalles Bibliográficos
Autores: Pelicano, Christian Mark, Li, Jiaxin, Cabrero-Antonino, María, Silva, Ingrid F., Peng, Lu, Tarakina, Nadezda V., Navalón, Sergio, García Gómez, Hermenegildo, Antonietti, Markus
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/352203
Acceso en línea:http://hdl.handle.net/10261/352203
Access Level:acceso abierto
Descripción
Sumario:We present the rational design of carbon/potassium poly(heptazine imide) (KPHI) heterostructures via one-step salt-melt assisted condensation for efficient photocatalysis. Hybridizing KPHI with an adenine-derived carbonaceous material (Ad-carbon) displayed an outstanding photocatalytic H evolution activity (738 μmol h g; with 3 wt% Pt as the cocatalyst) and photocatalytic HO production (3.94 mmol h g). We establish that the Ad-carbon simultaneously operates as an electron acceptor and a photosensitizer based on structural, optical and photo(electro)chemical characterization. Building an intimate heterojunction between the Ad-carbon and KPHI induced spatial charge separation and prolonged the carrier lifetime. From electrocatalysis, we confirmed that coupling Ad-carbon with KPHI enhanced the surface reaction kinetics towards H evolution and O reduction reactions. Moreover, visual evidence of superior charge transport in the hybrid photocatalyst is revealed through the photodeposition of smaller Pt nanoparticles (∼7 nm) with uniform distribution on the carbon regions, which also accounts for the increased catalytic activity.