A superlattice interface and S-scheme heterojunction for ultrafast charge separation and transfer in photocatalytic H<sub>2</sub> evolution.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39511168.
- Also identified by DOI 10.1038/s41467-024-53951-6 and PMC identifier 11543929.
- Licence recorded as CC BY-NC-ND.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
The rapid recombination of photoinduced charge carriers in semiconductors fundamentally limits their application in photocatalysis. Herein, we report that a superlattice interface and S-scheme heterojunction based on Mn<sub>0.5</sub>Cd<sub>0.5</sub>S nanorods can significantly promote ultrafast charge separation and transfer. Specifically, the axially distributed zinc blende/wurtzite superlattice interfaces in Mn<sub>0.5</sub>Cd<sub>0.5</sub>S nanorods can redistribute photoinduced charge carriers more effectively when boosted by homogeneous internal electric fields and promotes bulk separation. Accordingly, S-scheme heterojunctions between the Mn<sub>0.5</sub>Cd<sub>0.5</sub>S nanorods and MnWO<sub>4</sub> nanoparticles can further accelerate the surface separation of charge carriers via a heterogeneous internal electric field. Subsequent capture of the photoelectrons by adsorbed H<sub>2</sub>O is as fast as several picoseconds which results in a photocatalytic H<sub>2</sub> evolution rate of 54.4 mmol·g<sup>-1</sup>·h<sup>-1</sup> without any cocatalyst under simulated solar irradiation. The yields are increased by a factor of ~5 times relative to control samples and an apparent quantum efficiency of 63.1% at 420 nm is measured. This work provides a protocol for designing synergistic interface structure for efficient photocatalysis.