Effect of Manganese-Doping on the chemical and optical properties of cobalt ferrite nanoparticles

Abstract

We report on the effect of manganese (Mn) doping on the structural, chemical and optical properties of cobalt ferrite (CFO) nanoparticles (NPs). The Mn(II)-substituted CFO NPs with variable chemical composition (Co1-xMnxFe2O4; x = 0.0–0.5; CMFO) were synthesized by an eco-friendly hydrothermal route. The CMFO NPs produced were with a crystallite size varying in the range of 8–14 nm, where the chemical valence state, chemical bonding, electronic structure and optical properties are strongly influenced by the Mn-substitution. The X-ray diffraction (XRD) studies revealed the Mn-substitution induced changes in CFO crystal structure. The Mn-substitution in CFO causes the lattice parameter enhancement (a), crystallite size increase, and micro-strain (ε) as evident in the XRD studies. The chemical composition driven direct, functional relationship reflected in a-D-ε correlation, which suggests the Mn-substitution allows the ability to control the size and strain in CFMO NPs. Chemical bonding analyses using Fourier transform infrared spectroscopy (FTIR) corroborates with structural assessment made with XRD studies. The MTd–O (MTd = metal ions in tetrahedral locations) absorption bands shifting to higher wavenumbers in FTIR studies indicate that, Mn-substitution induce changes in the metal cation distribution between the tetrahedral and octahedral locations of the ferrite lattice. The X-ray photoelectron spectroscopic (XPS) analyses indicate the presence of iron as Fe+3, cobalt as Co+2, and manganese in Mn+2 chemical state. With increasing Mn-content, the XPS revealed that the binding energy (BE) separation of Fe, as well as Mn, does not change compared to Co, indicating the chemical stability and valence state of Fe+3 and Mn+2 cations maintained well in the CMFO samples. While the overall chemistry of CFO is maintained, and is not influenced by the increasing Mn-concentration, the remarkable effect of Mn-substitution is seen on the optical properties of CFO NPs. The optical studies indicate that the band gap of CFO NPs exhibits a direct, functional dependence on Mn-concentration; the band gap varies in a wide range of 2.38–3.12 eV. The analyses indicate the exponential dependence of CFO optical band gap with Mn-content which provide a roadmap to engineer the materials with tunable band gap for desired technological applications.