Improved chemical deposition of cobalt-doped CdS nanostructured thin films via nucleation-doping strategy: Surface and optical properties
[Display omitted] •The colloidal nucleation-doping strategy was extended to the thin film deposition.•It improves the chemical bath deposition technique for doping deposited nanostructures.•Developed CBD technique results in high-quality smoothed Co:CdS thin films.•Strategy is simple, low-cost, and...
Gespeichert in:
Veröffentlicht in: | Materials science & engineering. B, Solid-state materials for advanced technology Solid-state materials for advanced technology, 2021-10, Vol.272, p.115328, Article 115328 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | [Display omitted]
•The colloidal nucleation-doping strategy was extended to the thin film deposition.•It improves the chemical bath deposition technique for doping deposited nanostructures.•Developed CBD technique results in high-quality smoothed Co:CdS thin films.•Strategy is simple, low-cost, and effective with scaling-up ability at acidic medium.•PL emission results were optimized to reach impurity-related PL emission.
In the majority of the chemical deposition techniques used for doping thin films, dopant cations are usually added to the reaction simultaneously with the host cations, or even after the formation of the host matrix. This approach reduces the dopant efficiency and reproducibility of dopant-related properties. In the present work, the nucleation-doping strategy usually used for colloidal nanocrystals is extended into the chemical bath deposition technique to prepare cobalt-doped CdS nanostructured thin films. The Co:CdS thin films showed %2.5 doping yield with a root-mean-square roughness below 22 nm and absorption edge below 510 nm. The PL emission spectra of the films revealed two distinct peaks at 490 and 530 nm, attributed to the recombination processes through excitonic states and impurity levels, respectively. Almost all the experimental variables were optimized to reach a partially single-emission peak at 530 nm, which can prove the successful incorporation of Co ions into CdS nanostructures. |
---|---|
ISSN: | 0921-5107 1873-4944 |
DOI: | 10.1016/j.mseb.2021.115328 |