Electromagnetic and optical characteristics of Nb⁵⁺-doped double-crossover and salmon DNA thin films

We report the fabrication and physical characteristics of niobium ion (Nb⁵⁺)-doped double-crossover DNA (DX-DNA) and salmon DNA (SDNA) thin films. Different concentrations of Nb⁵⁺ ([Nb⁵⁺]) are coordinated into the DNA molecules, and the thin films are fabricated via substrate-assisted growth (DX-DNA) and drop-casting (SDNA) on oxygen plasma treated substrates. We conducted atomic force microscopy to estimate the optimum concentration of Nb⁵⁺ ([Nb⁵⁺]_O = 0.08 mM) in Nb⁵⁺-doped DX-DNA thin films, up to which the DX-DNA lattices maintain their structures without deformation. X-ray photoelectron spectroscopy (XPS) was performed to probe the chemical nature of the intercalated Nb⁵⁺ in the SDNA thin films. The change in peak intensities and the shift in binding energy were witnessed in XPS spectra to explicate the binding and charge transfer mechanisms between Nb⁵⁺ and SDNA molecules. UV-visible, Raman, and photoluminescence (PL) spectra were measured to determine the optical properties and thus investigate the binding modes, Nb⁵⁺ coordination sites in Nb⁵⁺-doped SDNA thin films, and energy transfer mechanisms, respectively. As [Nb⁵⁺] increases, the absorbance peak intensities monotonically increase until ∼[Nb⁵⁺]_O and then decrease. However, from the Raman measurements, the peak intensities gradually decrease with an increase in [Nb⁵⁺] to reveal the binding mechanism and binding sites of metal ions in the SDNA molecules. From the PL, we observe the emission intensities to reduce them at up to ∼[Nb⁵⁺]_O and then increase after that, expecting the energy transfer between the Nb⁵⁺ and SDNA molecules. The current-voltage measurement shows a significant increase in the current observed as [Nb⁵⁺] increases in the SDNA thin films when compared to that of pristine SDNA thin films. Finally, we investigate the temperature dependent magnetization in which the Nb⁵⁺-doped SDNA thin films reveal weak ferromagnetism due to the existence of tiny magnetic dipoles in the Nb⁵⁺-doped SDNA complex.