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      • KCI등재

        Inclusion of polyaniline in electrodeposited bismuth sulphide thin films: Synthesis and characterization

        S. Subramanian,P. Chithra lekha,D. Pathinettam Padiyan 한국물리학회 2009 Current Applied Physics Vol.9 No.5

        Structural, electrical and optical properties of polyaniline (PAni) doped Bi2S3 composite thin films prepared by electrodeposition method are reported. X-ray diffraction pattern indicates its polycrystalline nature and crystallite size increases with increase in the concentration of PAni. FTIR studies reveal that the dopant PAni has affected the absorption phenomenon in the IR region of the Bi2S3 thin films. The optical band gap energy is found to be 1.91 eV for as-deposited Bi2S3 thin film and it decreases with increase in the concentration of PAni. The morphology of the doped films changes due to the addition of PAni. in the concentration of PAni. The morphology of the doped films changes due to the addition of PAni. The conduction results from a hopping due to localized states in the temperature range 300–358 K. Above 358 K, the conduction process is explained by the traps at grain boundaries of partially depleted grains.

      • KCI등재

        Sensing properties of polyoxomolybdate doped polyaniline nanomaterials for oxidising and reducing volatile organic compounds

        P. Chithra lekha,M. Balaji,S. Subramanian,D. Pathinettam Padiyan 한국물리학회 2010 Current Applied Physics Vol.10 No.2

        The polyoxomolybdates encapsulated PAni hybrid materials are prepared by interfacial polymerisation. In P12MPA, the crystal structure of 12MPA is not modified on doping with PAni. However, P11MPA have the polycrystallinity due to the presence of vanadium in the dopant molecule. Though, the hybrids prepared by interfacial polymerisation are in emaraldine salt form, there is a blue shift in the absorption spectra due to dopant induced decrease in conjugation length and over-oxidation. Interfacially polymerised PAniPOM hybrid materials are exposed with various concentrations of vapours of different volatile organic compounds (VOC) such as acetone, methanol, chloroform and carbon tetrachloride. The oxidising VOCs like acetone and methanol on exposure to PAni decrease the resistivity by hydrogen bonding with the redox cites of the polymer. Among these two, the sensitivity towards acetone is more in PAni and its hybrids which can be linked with the vapour pressure of the analyte. Due to the weak acidic characteristics of chlorinated hydrocarbons which are reducing vapours, the resistivity of PAni and its hybrids increases on exposure to chloroform and CCl4. Here, the chlorinated hydrocarbons interact with the redox sites of PAni and reduce it to base form. Bridging of polymer chains is also proposed for the reduction of conductivity on exposure to the analyte. The sensitivity is higher for the reducing analytes than that of the oxidising one.

      • KCI등재

        High-energy ion induced physical and surface modifications in antimony sulphide thin films

        S. Subramanian,M. Balaji,P. Chithra Lekha,K. Asokan,D. Kanjilal,Indra Sulania,Jai Prakash,D. Pathinettam Padiyan 한국물리학회 2010 Current Applied Physics Vol.10 No.4

        Sb2S3 thin films prepared by electrodeposition on indium tin oxide coated glass substrate were irradiated with 150 MeV Ni11+ ions for various fluence in the range of 1011–1013 ions/㎠. The modifications in the structure, surface morphology and optical properties have been studied as a function of ion fluence. X-ray diffraction (XRD) analysis indicates a shift in the (2 4 0) peak position towards lower diffraction angle and a decrease in grain size with increase in ion fluence. Presence of microcracks due to irradiation induced grain splitting effect has been observed from the SEM micrograph at higher ion fluence. The optical absorbance spectrum revealed a shift in the fundamental absorption edge and the band gap energy increased from a value of 1.63 eV for as-deposited films to 1.80 eV for the films irradiated with 1013 ions/㎠.

      • Electronic structure studies of nanoferrite Cu(x)Co(1-x)Fe2O4 by X-ray absorption spectroscopy.

        Gautam, S,Muthurani, S,Balaji, M,Thakur, P,Padiyan, D Pathinettam,Chae, K H,Kim, S S,Asokan, K American Scientific Publishers 2011 Journal of Nanoscience and Nanotechnology Vol.11 No.1

        <P>Pure and mixed cobalt copper ferrites are of great interest due to their widespread application in electronics and medicine. We report on the electronic structure of a nanoferrite Cu(x)Co(1-x)Fe2O4 (0.0 < or = x < or = 1.0) system studied by X-ray absorption spectroscopy. These magnetic nanoferrites (average crystallite size approximately 31-43 nm) were synthesized by an auto combustion method and are characterized by high resolution X-ray diffraction and near edge X-ray absorption fine structure measurements at the O K and Co, Cu, and Fe L-edges. The O K-edge spectra suggest that there is a strong hybridization between O 2p and 3d electrons of Co, Cu and Fe cations and Fe L3,2-edge spectra indicate that Fe ions coexist in mixed valence states (Fe3+ and Fe2+) at tetrahedral and octahedral sites of the spinel structure. Copper and cobalt ions are distributed in the divalent state in octahedral sites of the spinel structure. The origin of high saturation magnetization and coercivity in cobalt-copper ferrites are explained in light of these results.</P>

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