Loading…
Efficient harvesting and storage of solar energy of an all-vanadium solar redox flow battery with a MoS2@TiO2 photoelectrode
Solar redox flow batteries constitute an emerging technology that provides a smart alternative for the capture and storage of discontinuous solar energy through the photo-generation of the discharged redox species employed in traditional redox flow batteries. Here, we show that a MoS2-decorated TiO2...
Saved in:
Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022, Vol.10 (19), p.10484-10492 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Solar redox flow batteries constitute an emerging technology that provides a smart alternative for the capture and storage of discontinuous solar energy through the photo-generation of the discharged redox species employed in traditional redox flow batteries. Here, we show that a MoS2-decorated TiO2 (MoS2@TiO2) photoelectrode can successfully harvest light to be stored in a solar redox flow battery using vanadium ions as redox active species in both the catholyte and anolyte, and without the use of any bias. The MoS2@TiO2 photoelectrode achieved an average photocurrent density of ∼0.4 mA cm−2versus 0.08 mA cm−2 for bare TiO2, when tested for the oxidation of V4+ to V5+, attributed to a more efficient light harvesting and charge separation for the MoS2@TiO2 relative to TiO2. The designed solar redox flow cell exhibited an optimal overall solar-to-output energy conversion efficiency (SOEE) of ∼4.78%, which outperforms previously reported solar redox flow batteries. This work demonstrates the potential of the MoS2@TiO2 photoelectrode to efficiently convert solar energy into chemical energy in a solar redox flow battery, and it also validates the great potential of this technology to increase reliability in renewable energies. |
---|---|
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d2ta00739h |