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DOI 10.1038/s41598-025-13516-z

Медицинская библиотека · Scientific reports · 2025

Nickel doping induced morphological and structural transformation of electrochemically deposited ZnO nanostructures via ethylene glycol based electrolyte.

Rana Parvaj, Islam Md Earul, Tabassum Samia, Ismail Abu Bakar Md

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Аннотация

The synthesis of undoped and Ni-doped-ZnO (NZO) has been successfully demonstrated through an in-situ electrochemical deposition process using ethylene glycol (EG) electrolyte on FTO glass substrates. The doping concentration varied as 0, 1, 3, 4, and 5 mol%. Chronoamperometry studies show a significant increase in current density with higher doping levels, confirming typical electrochemical deposition behavior. SEM and EDX studies show a sponge-like porous ZnO with a lack of Zn-ions at 0 mol%, and the morphology turned into a spherical nanostructure when the doping concentration increased. Interestingly, at 5 mol%, multiple homogeneous and independent nuclei of NZO formed, resulting in a thin-film NZO nanostructure with three-dimensional grain growth mode. Further, the XRD analysis indicates that both undoped and NZO possess a pure-phase hexagonal wurtzite structure with dominant preferential orientation along the [101] plane. The undoped and NZO show nearly 100% atomic packing fraction (APF), implying a good atomic arrangement, and the density of NZO is nearly 50% higher than that of the undoped-ZnO. The sponge-like, undoped, and highly dense spherical nanostructure NZO can be tailored for energy storage applications and mechanical properties enhancement. Experimental results indicate that highly dense with nearly 100% APF, having a tunable morphology of ZnO structure, can be synthesized by electrochemical deposition using an EG-based electrolyte.

Для цитирования: Rana Parvaj, Islam Md Earul, Tabassum Samia, Ismail Abu Bakar Md. Nickel doping induced morphological and structural transformation of electrochemically deposited ZnO nanostructures via ethylene glycol based electrolyte.. Scientific reports. 2025. DOI: 10.1038/s41598-025-13516-z.
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