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S-Scheme Interface Between K-C 3 N 4 and FePS 3 Fosters Photocatalytic H 2 Evolution.

Authors :
Bootz P
Frank K
Eichhorn J
Döblinger M
Bagaria T
Nickel B
Feldmann J
Debnath B
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 Nov 27; Vol. 16 (47), pp. 65610-65619. Date of Electronic Publication: 2024 Nov 18.
Publication Year :
2024

Abstract

In photocatalysis, photogenerated charge separation is pivotal and can be achieved through various mechanisms. Building heterojunctions is a promising method to enhance charge separation, where effective contact and charge exchange between heterojunction components remains challenging. Mostly used synthesis processes for making heterostructures require high temperatures, difficult processes, or expensive materials. Herein, a heterojunction of potassium intercalated graphitic carbon nitride (K-CN) and nanoflakes of iron phosphor trisulfide (FPS) is designed via a simple mechanical grinding process to boost the hydrogen evolution by a factor of more than 25 compared to pure K-CN. This significant improvement is rarely reached by other combinations of two semiconductors without cocatalysts, such as platinum. It can be attributed to the band alignment and band bending of an S-scheme that is validated via optical and X-ray photoelectron spectroscopy. As a consequence, strong quenching of the photoluminescence and significant H <subscript>2</subscript> evolution occur for this unique heterojunction. Furthermore, the excellent durability of the designed photocatalytic heterostructure is confirmed by monitoring the catalysts' H <subscript>2</subscript> -evolution rate and crystal structure after 72 h under light illumination. This study opens up promising and simple pathways for constructing efficient S-scheme heterojunctions for photocatalytic water-splitting.

Details

Language :
English
ISSN :
1944-8252
Volume :
16
Issue :
47
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
39552308
Full Text :
https://doi.org/10.1021/acsami.4c15236