Synergistic Defect Modification in FexII/Zn1-xFeIII2O4 Nanostructures via Controlled FeII Doping (x = 0.0–0.4) for Enhanced Photocatalytic Crystal Violet Degradation

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FeII-doped zinc ferrite nanocrystals (FeIIxZn1-xFeIII2O4) were prepared via a sol–gel approach in the presence of polyvinyl alcohol as a stabilizer and assessed for their capability to eliminate crystal violet (CV) dye from water-based solutions. The structural and surface characteristics of the prepared materials were examined by XRD, HRTEM, FESEM, ATR–FTIR, XPS, UV–visible spectrophotometer and BET analyses. XRD patterns confirmed the formation of a cubic spinel ferrite structure (Fd-3m), indicating successful incorporation of FeII into the ZnFe2O4 lattice. ATR–FTIR spectra showed characteristic metal–oxygen vibrations at the tetrahedral and octahedral sites. XPS analysis confirmed the coexistence of FeII and FeIII species, which may promote interfacial charge transfer and redox reactions. HRTEM and FESEM images showed particle agglomeration and grain growth after calcination at 700 °C. FeII0.2Zn0.8FeIII2O4 exhibited the highest photocatalytic performance, achieving 97.2% degradation of CV under optimized conditions. The effects of contact time, catalyst dosage, initial dye concentration, and pH were systematically studied. The maximum removal efficiency was obtained at pH 10 using 0.075 g catalyst for 20 mg L−1 CV solution within 40 min. Freundlich isotherm models exhibited the strongest correlation (R2 = 0.918), pointing to multilayer adsorption occurring across a non-uniform nanoparticle surface. The Dubinin–Radushkevich analysis returned an adsorption energy of 3.01 kJ mol−1, implying that physical forces predominantly control the adsorption mechanism. Kinetic investigations revealed a two-stage CV uptake pathway: fast initial binding at exterior surface sites, succeeded by a slower migration of dye molecules into the internal pores of the adsorbent.

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