Characterization of Lithium Ion-Conducting Blend Biopolymer Electrolyte Based on CH-MC Doped with LiBF4

被引:17
作者
Abdullah, Omed Gh [1 ,2 ]
Hanna, Rawad R. [3 ]
Salman, Yahya A. K. [3 ]
Aziz, Shujahadeen B. [1 ]
机构
[1] Univ Sulaimani, Dept Phys, Coll Sci, Adv Polymer Mat Res Lab, Sulaimani 46001, Kurdistan Regio, Iraq
[2] Komar Univ Sci & Technol, Komar Res Ctr, Sulaimani 46001, Kurdistan Regio, Iraq
[3] Univ Mosul, Dept Phys, Coll Sci, Mosul 41002, Iraq
关键词
Solid polymer electrolyte; Lithium-ion conducting; Conductivity; High refractive index polymer; OPTICAL CHARACTERIZATION; ELECTRICAL-CONDUCTIVITY; POLYMER ELECTROLYTES; CHITOSAN; PVA; FILMS; NANOPARTICLES; BEHAVIOR; ENERGY;
D O I
10.1007/s10904-018-0802-2
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Lithium ion-conducting polymer blend electrolytes based on chitosan and methylcellulose complexed with lithium tetrafluoroborate (LiBF4) were prepared by a solution-casting method. The features of complexation of the solid polymer electrolytes were studied using X-ray diffraction techniques. Electrical conductivity of the prepared films was measured as a function of frequency at a different temperature. The increased trend of the electrical conductivity with increasing temperature and salt concentration can be attributed to increasing the mobility and number of lithium ions, respectively. The polymer electrolyte system exhibited Arrhenius-type, temperature-dependence ion conductivity behavior. Optical properties such as optical band gap, tail due to localized states and complex refractive index were estimated for present polymer electrolyte system from optical absorption measurement in the wavelength region 190-1100 nm. It was found that the optical direct band gap values shifted to lower energies upon addition of LiBF4 salt up to 40 wt% dopant concentration, and showed an increasing tendency for a further increase in dopant concentration. The high refractive index for this composition (2.44-2.63) at visible wavelengths eminently suitable for optical applications.
引用
收藏
页码:1432 / 1438
页数:7
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