Novel cobalt redox materials admitted in natrosol polymer with a thiophene based additive as a gel polymer electrolyte to tune up the efficiency of dye sensitized solar cells

色素敏化染料 电解质 氧化还原 噻吩 聚合物 介电谱 电化学 傅里叶变换红外光谱 无机化学 材料科学 光电流 化学 化学工程 有机化学 物理化学 电极 工程类 光电子学
作者
S. Balamurugan,S. Ganesan
出处
期刊:Electrochimica Acta [Elsevier]
卷期号:329: 135169-135169 被引量:41
标识
DOI:10.1016/j.electacta.2019.135169
摘要

Synthesis of novel cobalt redox pairs such as Co2+/3+[bnbip]2, Co2+/3+[npbi]3, Co2+/3+[b(ttb)bip]2 and unknown organic additive integrated into a new natrosol polymer host act as an polymer gel electrolytes in DSSC. The newly synthesized ligands and organic additive (BNBIT) was characterized by 1H, 13C NMR and HRMS spectroscopy and complexes were confirmed by UV–Visible, FTIR and ESI-MS spectrum. Electrochemical analysis was determined for all new redox pairs in that Co2+/3+[bnbip]2 shows positive E1/2value 0.51 V V NHE and higher formal potential 0.55 V which leads a way to increase in open circuit voltage of DSSC. The new natrosol polymer gel electrolytes was characterized by using UV–Visible, FTIR, DSC, XRD, impedance spectrum and I–V curve. The conductivity increases up to 7.14x10−4Scm−1 for natrosol polymer gel electrolyte with a novel organic additive and stable Co2+/3+[bnbip]2 redox pair. The new organic additive plays a vital role in DSSC device which shields the Co3+ ions of the redox pair in gel electrolytes and interaction with TiO2 surface that made shift in quasi Fermi level of TiO2 which suppresses the recombination processes. The new natrosol polymer gel electrolytes with novel cobalt redox pairs and thiophene based organic additive that enhances the efficiency up to 4.5% under light illumination of 100 mW/cm2 with a better stability. A increase in photocurrent due to BNBIT organic additive and the best E1/2 value of Co2+/3+[bnbip]2 mediator which made shift in (EF,n) quasi Fermi level of TiO2 that mitigate the recombination process in DSSCs. The interfacial studies in DSSCs were focused via EIS to elucidate the charge transport mechanisms at the interfaces of photoelectrodes and electrolyte medium of the devices.
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