Surface modification of superparamagnetic Fe3O4 nanoparticles using polymers (polyaniline/polypyrrole) was done by radio frequency (r.f.) plasma polymerization technique and characterized by XRD, TEM, TG/DTA and VSM. Surface-passivated Fe3O4 nanoparticles with polymers were having spherical/rod-shaped structures with superparamagnetic properties. Broad visible photoluminescence emission bands were observed at 445 and 580 nm for polyaniline-coated Fe3O4 and at 488 nm for polypyrrole-coated Fe3O4. These samples exhibit good fluorescence emissions with L929 cellular assay and were non-toxic. Magnetic hyperthermia response of Fe3O4 and polymer (polyaniline/polypyrrole)-coated Fe3O4 was evaluated and all the samples exhibit hyperthermia activity in the range of 42–45 °C. Specific loss power (SLP) values of polyaniline and polypyrrole-coated Fe3O4 nanoparticles (5 and 10 mg/ml) exhibit a controlled heat generation with an increase in the magnetic field.

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Silver nanoparticles were dispersed in the pores of monolithic mesoporous silica prepared by a modified sol-gel method. Structural and microstructural analyses were carried out by Fourier transform infrared spectroscopy and transmission electron microscopy. X-ray photoelectron spectroscopy was employed to determine the chemical states of silver in the silica matrix. Optical absorption studies show the evolution absorption band around 300 nm for silver (Ag) in a silica matrix and it was found to be redshifted to 422 nm on annealing. Photoluminescence studies indicate the presence of various luminescent emitting centers corresponding to silver ions and silver dimers in the SiO2 matrix. The enhancement of absorption and photoluminescence properties is attributed to plasmon resonance energy transfer from Ag nanoparticles to luminescent species in the matrix.

Plasma-assisted synthesis of transparent, environment friendly, lightweight, flexible and stable organic thin films from naturally occurring precursors were emerging as potential candidates for organic semiconductor industry. In the present study, tea tree (Malaleuca alternifolia) oil based polymer thin films were deposited on glass and silicon substrate by using radio frequency plasma polymerization technique. The polymer thin films were characterized with atomic force microscopy (AFM) and Fourier transform infrared (FTIR) spectroscopy techniques. AFM images indicate the formation of homogenous film on the substrate surface. FTIR spectra gives bands related to methyl and methylene groups which confirms the formation of chain branching in the polymer films. Relatively intense infrared (IR) bands obtained from films deposited on glass substrate reveals that glass substrate is more favourable for the growth of polymers than silicon substrate. Optical band gap of the polymerized thin film on glass substrate was estimated using Tauc plot which gives a value of 3.19 eV, indicating the semiconducting nature of the material. Photoluminescence (PL) emission in the yellow region were observed from both the samples and its CIE colour coordinates also matches with yellow emission. Broad visible emission observed in the wavelength range 465-695 nm indicates the presence of multichromophores in the polymer film. Samples also gives IR emission in the wavelength range of 850-1090 nm, upon excitation with a wavelength of 785 nm contributed to polaronic transitions.