4.5 Article

Role of Silver Salts Lattice Energy on Conductivity Drops in Chitosan Based Solid Electrolyte: Structural, Morphological and Electrical Characteristics

Journal

JOURNAL OF ELECTRONIC MATERIALS
Volume 47, Issue 7, Pages 3800-3808

Publisher

SPRINGER
DOI: 10.1007/s11664-018-6250-5

Keywords

Chitosan biopolymer; XRD analysis; UV-Vis study; optical micrograph; lattice energy of salts; electrical properties

Funding

  1. Ministry of Higher Education and Scientific Research-Kurdistan Regional Government
  2. Department of Physics, College of Science, University of Sulaimani, Sulaimani
  3. Komar Research Center (KRC)-KomarUniversity for Science and Technology

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The influence of anion type on silver ion reduction and drop in direct current (DC) conductivity was investigated experimentally. The structural, optical, morphological and electrical properties of the samples were investigated using x-ray diffraction (XRD), ultraviolet-visible (UV-Vis), optical micrographs (OM) and impedance spectroscopy. The XRD results reveal significant disruption in the crystalline structure of chitosan (CS) for different concentrations of silver nitrate (AgNt) salt. The localized surface resonance plasmonic (LSRP) peaks that were observed for CS:AgNt samples, along with the white silver specs detected by OM technique confirm the formation of Ag nanoparticles. The appearance of obvious dark regions in the CS:AgNt system reveals the existence of a large percentage of amorphous domains. The nonexistence of spherulitic texture confirms the amorphous nature of the samples. The second semicircle in an impedance plot can be attributed to an Ag nanoparticle grain boundary. The established relationships between dielectric constant and carrier concentration and the behavior of dielectric constant versus salt concentration were used to explain the phenomenon of ion-ion association. The continuous increase of DC conductivity was noticed at high temperatures, which was then explained on the basis of lattice energy of silver salts. The influences of anion size on the rate of silver ion reductions are also interpreted.

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