Autor segons l'article: Mozalev, A; Bendova, M; Kalina, L; Prasek, J; Gispert-Guirado, F; Llobet, E
Departament: Enginyeria Electrònica, Elèctrica i Automàtica
Autor/s de la URV: Gispert Guirado, Francesc / Llobet Valero, Eduard
Paraules clau: Alumina-assisted growth; Anodization; Arrays; Films; Layers; Molybdenum; Niobiu; Oxidation; Refinement; Sulfuric-acid
Resum: Nanostructured molybdenum oxide (MoOx) has many exciting properties that are highly dependent on the synthesis procedure. MoOx nanostructures should be aligned on a substrate for nanoelectronic on-chip applications, which has been challenging. Here, for the first time, arrays of MoOx-based nanoprotrusions of various morphologies (nanogoblets and nanorods), dimensions (20-500 nm), and surface densities (up to 1011 cm-2), spatially separated and vertically aligned on a Si wafer, were synthesized via self-organized porous-anodic-alumina (PAA)-assisted anodization of a Mo underlayer covered with a few nm thick Nb interlayer. This creative anodization approach enabled sustainable growth of fully amorphous MoOx within and under the PAA nanopores in several aqueous electrolytes, which other reported methods cannot accomplish. The nanoarrays grow via the outward migration of Mon+ cations enabled by the thin niobium-oxide interlayer, followed by the concurrent migration of Mon+ (n = 4-6) and Nb5+ cations in the PAA barrier layer and along the pore walls, competing with the migration of Mon+ through the anodic molybdenum oxide that grows within the 'empty' pores. The nanorods derived after selective PAA dissolution feature a core/shell heterostructure: The shells are composed of MoO3, several molybdenum suboxides (Mo5+, Mo4+), stoichiometric Nb2O5, and Al2O3, all mixed at the molecular level, whereas the cores are slightly hydrated and reduced MoO3, as revealed by X-ray photoelectron spectroscopy. The annealing in air or vacuum at 550 degrees C increases the oxidation state of Mon+ cations in the shells and causes the formation of monoclinic MoO2 and orthorhombic Nb2O5 nanocrystallites in the bottom oxide. Mott-Schottky analysis disclosed n-type semiconductor properties of the cores, with the charge carrier density reaching 1 x 1022 cm-3, whereas the shells seem more dielectric. The cyclic voltammetry and galvanostatic charge-discharge measurements featured characteristic reversible redox reactions, intensive electron transport, intercalation pseudocapacitive behavior, competitive charge-storage performance, and good rate capability of the rod's cores, which means the potential for nano-energy applications.
Àrees temàtiques: Astronomia / física; Biodiversidade; Biotecnología; Chemistry (all); Chemistry (miscellaneous); Chemistry, physical; Ciências agrárias i; Ciências biológicas i; Ciências biológicas ii; Energy & fuels; Engenharias ii; Engenharias iv; Farmacia; General chemistry; General materials science; Interdisciplinar; Materiais; Materials chemistry; Materials science; Materials science (all); Materials science (miscellaneous); Materials science, multidisciplinary; Medicina i; Odontología; Química; Renewable energy, sustainability and the environment
Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
Adreça de correu electrònic de l'autor: francesc.gispert@urv.cat; francesc.gispert@urv.cat; eduard.llobet@urv.cat
Data d'alta del registre: 2026-02-13
Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
Enllaç font original: https://pubs.rsc.org/en/content/articlelanding/2025/ta/d5ta02921j
Referència a l'article segons font original: Journal Of Materials Chemistry a. 13 (25): 19605-19622
Referència de l'ítem segons les normes APA: Mozalev, A; Bendova, M; Kalina, L; Prasek, J; Gispert-Guirado, F; Llobet, E (2025). MoOx-based high-density nanoarrays on a substrate via smart anodizing as novel 3D electrodes for nano-energy applications. Journal Of Materials Chemistry a, 13(25), 19605-19622. DOI: 10.1039/d5ta02921j
URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
DOI de l'article: 10.1039/d5ta02921j
Entitat: Universitat Rovira i Virgili
Any de publicació de la revista: 2025-06-25
Tipus de publicació: Journal Publications