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In Situ Synthesis and Integration of Polymer Electrolytes in Nanostructured Electrodes for Photovoltaic Applications

机译:用于光伏应用纳米结构电极中聚合物电解质的原位合成和整合

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The conventional dye sensitized solar cell (DSSC) is limited by the use of a liquid electrolyte that is prone to leakage and evaporation. Efforts to replace the liquid with a solid equivalent have been met with difficulties in penetrating the mesoporous TiO_2 nanostructured photoanode with liquid processing, particularly for photoanode layer thickness greater than 2 μm. Here, initiated chemical vapor deposition (iCVD) is successfully applied to directly synthesize and fill the pores of the mesoporous TiO_2 network of up to 12 μm thickness with poly(2-hydroxyethyl methacrylate) (PHEMA) polymer electrolyte. Comparing with equivalent liquid electrolyte cells, DSSCs integrated with PHEMA polymer electrolyte showed consistently higher open circuit voltage, which is attributed to a decrease in electron recombination with the redox couple at the electrode-electrolyte interface.
机译:传统的染料敏化太阳能电池(DSSC)受到易于泄漏和蒸发的液体电解质的限制。已经努力用固体等同物替换液体,难以穿透介于液体处理的介孔TiO_2纳米结构光磁极,特别是对于大于2μm的光电层厚度。此处,已成功地应用引发的化学气相沉积(ICVD)以直接合成并填充具有多达12μm厚度的介孔TiO_2网络的孔与聚(2-羟乙基甲基丙烯酸酯)(PHEMA)聚合物电解质。与等效液体电解质细胞相比,与PHEMA聚合物电解质集成的DSSCs呈始终较高的开路电压,其归因于电极 - 电解质界面处的氧化还原耦合的电子复合的降低。

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