3D CoNi-MOF nanoflowers anchored on 1D g-C3N4 nanorods: An efficient electrode platform for detection of paracetamol

Ashamary, Francis; Purusothaman, Muruganantham; Elancheziyan, Mari; Atchudan, Raji; Annamalai, Padmanaban; Nellaiappan, Subramanian; Kalambate, Pramod K.; Manoj, Devaraj

Abstract

The rational integration of metal organic frameworks (MOFs) with distinct structural dimensionalities offers a powerful strategy for constructing advanced hybrid architectures with enhanced physiochemical properties. In this work, a new-class of hetero structured electrode platform composed of a three-dimensional (3D) CoNi-based bimetallic MOF were grown in-situ on one-dimensional (1D) graphitic carbon nitride (g-C3N4) nanorod via facile coprecipitation method for detection of pharmaceutically important analgesic and antipyretic drug namely paracetamol. The structural, phase purity and composition of CoNi-MOF@g-C3N4 were confirmed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopic (XPS) analysis. Furthermore, CoNi-MOF@g-C3N4 modified SPE exhibited higher current response with strong redox peak for paracetamol in 0.1 M PBS (pH 7.2) when compared with CoNi-MOF and g-C3N4, with anodic and cathodic peak potentials at +0.25 V and - 0.10 V (vs. Ag/AgCl), respectively. At fixed potential of +0.60 V, CoNi-MOF@g-C3N4 achieved a wide linear range (0.0019 to 1.05 mM), high sensitivity (1.41 mu A mu M- 1 cm- 2), and low detection limit (0.73 mu M). The enhanced analytical performance is attributed to the synergistic interaction between Co2+/Ni2+ bimetallic active sites and the nitrogen-rich g-C3N4 framework, which collectively facilitate rapid electron transfer, increased electrochemically active surface area, and efficient adsorption of paracetamol molecules. Therefore, CoNi-MOF@g-C3N4 demonstrated good selectivity, repeatability, and operational stability, highlighting the broader applicability of this hybrid design of advanced electrode platform for human health and early medical diagnostics.

Más información

Título según WOS: ID WOS:001823890800001 Not found in local WOS DB
Título de la Revista: MICROCHEMICAL JOURNAL
Volumen: 228
Editorial: Elsevier
Fecha de publicación: 2026
DOI:

10.1016/j.microc.2026.119023

Notas: ISI