用于无铂染料敏化太阳能电池的分层结构Cu2MnSnS4-PVP对电极提高了光伏效率

IF 6.3 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
P. Baskaran, K.D. Nisha
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Cyclic voltammetry analysis revealed that the catalytic properties enhanced due to increase the PVP concentration. For the 1<!-- --> <!-- -->g of PVP with CMTS exhibited high cathodic current density 0.0022<!-- --> <!-- -->mA/cm<sup>2</sup> compared to the Pt CE. With increase in PVP concentration the resistivity decreased, and the mobility increased. Highest carrier concentration was observed for highest PVP concentration in CMTS. Nyquist plot displayed a decrease in series resistance and charge transfer resistance. DSSCs were fabricated using the CMTS samples as CE. I-V characterization were learned out to determine the efficiency of the devices. Open circuit voltage V<sub>oc</sub> of 1<!-- --> <!-- -->g of PVP with CMTS 0.74<!-- --> <!-- -->V and short circuit current J<sub>sc</sub> of 7.06<!-- --> <!-- -->mA. cm<sup>-2</sup> which is comparable to Pt CE V<sub>oc</sub> of 0.74<!-- --> <!-- -->V and J<sub>sc</sub> of 7.65<!-- --> <!-- -->mA. cm<sup>-2</sup>. 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引用次数: 0

摘要

采用水热法制备了季硫系化合物Cu2MnSnS4 (CMTS)作为染料敏化太阳能电池(DSSCs)的非贵重对电极。不同浓度的PVP与CMTS共同作用,生成了不同的纳米结构。本文主要研究PVP对不同CMTS纳米结构电催化性能的影响。研究了其结构、形态和电催化性能。XRD测定证实了CMTS的锡酸盐结构。FESEM分析显示,带有PVP的CMTS具有花状形态。PVP浓度改变了CMTS纳米结构的形貌。除了形貌外,电学和电化学性能也发生了变化。循环伏安分析表明,PVP浓度的增加使催化剂的催化性能增强。与Pt CE相比,1 g PVP与CMTS表现出较高的阴极电流密度0.0022 mA/cm2。随着PVP浓度的增加,电阻率降低,迁移率增加。在CMTS中,PVP浓度最高,载体浓度最高。奈奎斯特图显示串联电阻和电荷转移电阻减小。以CMTS样品为CE制备DSSCs。了解了I-V表征,以确定器件的效率。开路电压Voc为1g PVP, CMTS 0.74 V,短路电流Jsc为7.06 mA。cm-2与Pt CE的Voc为0.74 V, Jsc为7.65 mA相当。cm-2。1 g PVP与CMTS的功率转换效率PCE比其他CMTS的CE高3.33%。说明1 g PVP加CMTS对I-/I3-氧化还原反应的电催化活性较好。因此,它是一种与Pt CE相当的DSSC对电极材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced photovoltaic efficiency of hierarchically structured Cu2MnSnS4-PVP counter electrodes for platinum-free dye-sensitized solar cells
Quaternary chalcogenide, Cu2MnSnS4 (CMTS) was synthesized by hydrothermal method as a non-precious counter electrode (CE) for dye sensitized solar cells (DSSCs). PVP in different concentration was used along with CMTS, to generate various nanostructures. This work focusses on investigating the role of PVP on electrocatalytic properties of the different CMTS nanostructures. The structural, morphological, and electrocatalytic properties was done. XRD measurement confirmed stannite structure of CMTS. FESEM analysis showed flower like morphology of CMTS with PVP. The PVP concentration tunned the morphology of the CMTS nanostructure. In addition to morphology, electrical and electrochemical properties were changed. Cyclic voltammetry analysis revealed that the catalytic properties enhanced due to increase the PVP concentration. For the 1 g of PVP with CMTS exhibited high cathodic current density 0.0022 mA/cm2 compared to the Pt CE. With increase in PVP concentration the resistivity decreased, and the mobility increased. Highest carrier concentration was observed for highest PVP concentration in CMTS. Nyquist plot displayed a decrease in series resistance and charge transfer resistance. DSSCs were fabricated using the CMTS samples as CE. I-V characterization were learned out to determine the efficiency of the devices. Open circuit voltage Voc of 1 g of PVP with CMTS 0.74 V and short circuit current Jsc of 7.06 mA. cm-2 which is comparable to Pt CE Voc of 0.74 V and Jsc of 7.65 mA. cm-2. Power conversion efficiency PCE of 1 g of PVP with CMTS 3.33% higher than other CMTS CE. This indicates electrocatalytic activity of flower like 1 g of PVP with CMTS was better for I-/I3- redox reaction. Hence it is a good counter electrode material comparable to Pt CE for DSSC.
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来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
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