Electrochemical studies on tin selenide and fullerene decorated MWCNTs for sensor and dye degradation applications
摘要
In this work, we report the first synthesis of a SnSe/MWCNT/Fullerene ternary nanocomposite via a facile combination of hydrothermal crystallization and mechanical mixing, yielding a well-dispersed network of few-layer SnSe nanosheets intertwined with multi-walled carbon nanotubes and C60 nanoparticles. Structural characterization (XRD, FT-IR, FE-SEM) confirms the retention of SnSe’s orthorhombic phase alongside clear signatures of graphite and face-centered-cubic C60, while cyclic voltammetry and electrochemical impedance spectroscopy demonstrate that the optimal composition (SnSe0.92/MWCNT0.05/Fullerene0.03) achieves a charge transfer resistance as low as ≈ 40 Ω and peak current densities nearly twice those of binary or undoped SnSe analogues. In differential pulse voltammetry, this S4 electrode exhibits a linear Pb2⁺ sensing range up to 10 mM (R2 = 0.969), a limit of detection of 42.94 µM, and a limit of quantification of 14.17 µM, with excellent reproducibility (RSD = 1.36%) and stability over four weeks. Under UV–visible irradiation, S4 displays outstanding photocatalytic performance for Rhodamine B degradation: an optimal catalyst loading of 30 mg in 5 mL of 10 ppm dye yields 92.88% removal in 210 min, and tuning the solution pH to 11 boosts decolorization to 99.60%. The synergistic interplay between SnSe’s narrow, tunable bandgap (1.2–2.8 eV) and Fullerene’s high electron affinity sharply suppresses electron–hole recombination, while MWCNTs furnish robust electron-transport pathways-together delivering a multifunctional material that simultaneously excels as an electrochemical sensor and a visible-light-driven photocatalyst.