Loading…
Sustainable photocatalytic hydrogen peroxide production over octonary high-entropy oxide
The direct utilization of solar energy for the artificial photosynthesis of hydrogen peroxide (H 2 O 2 ) provides a reliable approach for producing this high-value green oxidant. Here we report on the utility of high-entropy oxide (HEO) semiconductor as an all-in-one photocatalyst for visible light-...
Saved in:
Published in: | Nature communications 2024-11, Vol.15 (1), p.9505-15, Article 9505 |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The direct utilization of solar energy for the artificial photosynthesis of hydrogen peroxide (H
2
O
2
) provides a reliable approach for producing this high-value green oxidant. Here we report on the utility of high-entropy oxide (HEO) semiconductor as an all-in-one photocatalyst for visible light-driven H
2
O
2
production directly from H
2
O and atmospheric O
2
without the need of any additional cocatalysts or sacrificial agents. This high-entropy photocatalyst contains eight earth-abundant metal elements (Ti/V/Cr/Nb/Mo/W/Al/Cu) homogeneously arranged within a single rutile phase, and the intrinsic chemical complexity along with the presence of a high density of oxygen vacancies endow high-entropy photocatalyst with distinct broadband light harvesting capability. An efficient H
2
O
2
production rate with an apparent quantum yield of 38.8% at 550 nm can be achieved. The high-entropy photocatalyst can be readily assembled into floating artificial leaves for sustained on-site production of H
2
O
2
from open water resources under natural sunlight irradiation.
An “all-in-one” high-entropy semiconductor photocatalyst enables the photocatalytic production of H
2
O
2
from H
2
O and O
2
under visible light without any external cocatalysts or sacrificial agents |
---|---|
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-024-53896-w |