Environmentally friendly Mn-alloyed core/shell quantum dots for high-efficiency photoelectrochemical cells
Colloidal quantum dot (QD)-based photoelectrochemical (PEC) cells are cost-effective devices showing remarkable solar-to-fuel conversion efficiency. However, the extensive use of highly toxic elements ( e.g. Pb and Cd) in QDs' synthesis and device fabrication is still a major challenge towards...
Gespeichert in:
Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020, Vol.8 (21), p.1736-1741 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Colloidal quantum dot (QD)-based photoelectrochemical (PEC) cells are cost-effective devices showing remarkable solar-to-fuel conversion efficiency. However, the extensive use of highly toxic elements (
e.g.
Pb and Cd) in QDs' synthesis and device fabrication is still a major challenge towards their practical development. Herein, we fabricate a solar-driven PEC cell based on environmentally friendly Mn-alloyed CuInS
2
(MnCIS)/ZnS core/shell QDs, showing more favorable band alignment, efficient charge transfer, reduced charge recombination and lower charge transfer resistance with respect to the control device fabricated using unalloyed CuInS
2
(CIS)/ZnS core/shell QDs. An unprecedented photocurrent density of ∼5.7 mA cm
−2
with excellent stability was obtained for the as-fabricated MnCIS/ZnS core/shell QD-based PEC device when operated under standard one sun irradiation (AM 1.5G, 100 mW cm
−2
). These results indicate that the transition metal-alloyed environmentally friendly core/shell QDs are promising for next-generation solar technologies.
A high performance photoelectrochemical cell fabricated using eco-friendly Mn-alloyed CuInS
2
/ZnS core/shell quantum dots is demonstrated. |
---|---|
ISSN: | 2050-7488 2050-7496 2050-7496 |
DOI: | 10.1039/d0ta00953a |