Studies on Electrochemical Properties of Polycarbazole Prepared Via Self-Support Polymerization and Self-Doping

S. Shakshooki, F. A. El-Akari, L. A. Abouderbala, A. A. Alahemmer
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Abstract

Mixed glassy zirconium-tin phosphate, g-Zr0.64.Sn.0.36(HPO4)2.3H2O(g-ZrSnP), nano fibrous cerium phosphate, Ce(HPO4)2 2,9H2O(nCePf), and mixed glassy zirconium-tin phosphate / fibrous cerium phosphate nanocomposite membrane, [g-Zr0.64 Sn0.36 (HPO4)2]0.25 [Ce(HPO4)2]0.75 ..4.43H2O, were prepared and characterized. By chemical , x-ray diffraction (XRD), thermogravimetric analysis (TGA), and Fourier transform spectroscopy (FTIR), Zirconium tin mole ratio were estimated using (EDAX). Novel [g-Zr0.64 Sn0.36 (HPO4)2]0.25 [Ce(HPO4)2]0.75 / polycarbazole nanocomposite membrane was prepared via self-support polymerization of carbazole, which was promoted by the reduction of Ce(iv) phosphate present in the inorganic matrix. Possible explanation is nCePf present on the surface of the nanocomposite is attacked by carbazole, converted to cerium (III) orthophosphate(CePO4). The resultant polycarbazole was characterized by C,H,N analysis, SEM ,FT-IR. UV-Vis and electrical conductance measurements. From elemental (C,H,N) analysis, the amount of polycarbazole present in the composite found to be (2.15 % in wt.). Polycarbazole is considered as one of modern material used in solar cells, furthermore it has become an important material for optoelectronic applications in recent years. The dc conductivity of polycarbazole nanocomposite membrane at 280C (using RC-Circuit) found to be equal to 3x10-5 Scm-1, range of semi-conductors. We suggest self-doping occurred on polymerization, which is due to H+ present in (O3POH)2 groups of [g-Zr0.64 Sn0.36 (HPO4)2]0.25. The electrochemistry of resultant polycarbazole in acetonitrile solution for a range of concentrations from 1.06 x10-4 to 2.19 x 10–3 mol dm-3 was carried out using CV techniques. Investigation of its electrochemical properties affords insight into the mechanisms for their oxidation and reduction, therefore provides the basis for evaluating the stabilities of the material and for designing novel polycarbazole-derived materials with desired properties as well as new devices. That will be discussed.
自支撑聚合和自掺杂法制备聚咔唑的电化学性能研究
制备了混合玻璃状磷酸锆锡g-Zr0.64. sn .0.36(HPO4)2.3H2O(g-ZrSnP)、纳米纤维状磷酸铈Ce(HPO4) 2,9h2o (nCePf)和混合玻璃状磷酸锆锡/纤维状磷酸铈纳米复合膜[g-Zr0.64 Sn0.36 (HPO4)2]0.25 [Ce(HPO4)2]0.75 .4.43H2O。通过化学、x射线衍射(XRD)、热重分析(TGA)、傅立叶变换光谱(FTIR)等方法,用EDAX法估算了锆锡摩尔比。通过还原无机基质中存在的Ce(iv)磷酸,以咔唑为载体进行自支撑聚合,制备了新型的[g-Zr0.64 Sn0.36 (HPO4)2]0.25 [Ce(HPO4)2]0.75 /聚咔唑纳米复合膜。可能的解释是纳米复合材料表面的nCePf被咔唑攻击,转化为正磷酸铈(CePO4)。用C、H、N分析、SEM、FT-IR对产物进行了表征。UV-Vis和电导测量。通过元素(C,H,N)分析,发现复合材料中聚咔唑的含量为(2.15%)。聚咔唑是一种现代太阳能电池材料,近年来已成为光电子领域的重要材料。聚咔唑纳米复合膜在280C时的直流电导率(使用rc电路)等于3 × 10-5 cm-1,半导体范围。我们认为自掺杂发生在聚合过程中,这是由于H+存在于[g-Zr0.64 Sn0.36 (HPO4)2]0.25的(O3POH)2基团中。在1.06 × 10-4 ~ 2.19 × 10-3 mol dm-3的乙腈溶液中,用CV技术对合成的聚咔唑进行了电化学反应。对其电化学性质的研究有助于深入了解其氧化和还原的机制,从而为评估材料的稳定性以及设计具有理想性能的新型聚咔唑衍生材料和新器件提供基础。我们会讨论这个问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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