Loading…
Fabrication of Flower-Shaped Sb 2 S 3 /Fe 2 O 3 Heterostructures for Enhanced Photoelectrochemical Performance
Antimony sulfide (Sb S ) has been recognized as a catalytic material for splitting water by solar energy because of its suitable narrow band gap, high absorption coefficient, and abundance of elements. However, many deep-level defects in Sb S result in a significant recombination of photoexcited ele...
Saved in:
Published in: | Langmuir 2024-06, Vol.40 (23), p.12097-12106 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Antimony sulfide (Sb
S
) has been recognized as a catalytic material for splitting water by solar energy because of its suitable narrow band gap, high absorption coefficient, and abundance of elements. However, many deep-level defects in Sb
S
result in a significant recombination of photoexcited electron-hole pairs, weakening its photoelectrochemical performance. Here, by using a simple hydrothermal and spin-coating method, we fabricated a step-scheme heterojunction of Sb
S
/α-Fe
O
to improve the photoelectrochemical performance of pure Sb
S
. Our Sb
S
/α-Fe
O
photoanode has a photocurrent density of 1.18 mA/cm
at 1.23 V vs reversible hydrogen electrode, 1.39 times higher than that of Sb
S
(0.84 mA/cm
). In addition, our heterojunction has a lower onset potential, a higher absorbance intensity, a higher incident photon-to-current conversion efficiency, a higher applied bias photon-to-current efficiency, and a lower charge transfer resistance compared to pure Sb
S
. Based on ultraviolet photoelectron spectroscopy, we constructed a step-scheme band structure of Sb
S
/α-Fe
O
to explain its photoelectrochemical enhancement. This work offers a promising strategy to optimize the performance of Sb
S
photoelectrodes for solar-driven photoelectrochemical water splitting. |
---|---|
ISSN: | 0743-7463 1520-5827 |
DOI: | 10.1021/acs.langmuir.4c00938 |