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Structure-dependent electrochemical response characteristics of antimony tin oxide nanoparticle-based porous electrodes

机译:锑锡氧化铟锡的多孔电极结构依赖性电化学响应特性

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Antimony tin oxide (ATO) nanoparticle-based porous electrodes have been investigated for use in fast-response electrochromic devices. However, despite their low resistivity, the electrochemical response characteristics of these electrodes are inferior to those of TiO 2 , which was attributed to the effect of small particle and pore size based on structural simulation. Therefore, we investigated the electrochemical response characteristics of ATO porous electrodes with different nanoparticle sizes, to clarify the effect of the porous electrode structure on response characteristics. The time required for charging an electric double layer (EDL) on the surface of a porous electrode increased as the particle size decreased. The ratios of the time constants of the EDL charging current between each porous electrode were larger than the ratios of the effective surface areas although the porous electrodes had almost the same resistivity. When the particle diameter was small (around 20 nm), the electrochromic reaction of dye modification on the porous electrode started 10 s after the application of a potential, because of the extremely low EDL formation rate. It was confirmed that the delay in EDL formation was induced by a lack of electrolyte ions inside the porous electrode. Therefore, to achieve ideal fast-response electrochemical reactions in low-resistivity nanoparticle-based porous electrodes, it is important to optimize the relationship between the electrode structure and the electrolyte ion concentration.
机译:已经研究了锑锡氧化锡(ATO)纳米颗粒基多孔电极用于快速响应电致变色装置。然而,尽管其电阻率低,但是这些电极的电化学响应特性差不多,TiO 2归因于基于结构模拟的小颗粒和孔径的影响。因此,我们研究了具有不同纳米颗粒尺寸的ATO多孔电极的电化学响应特性,以阐明多孔电极结构对响应特性的影响。随着粒度降低,在多孔电极表面上充电的电双层(EDL)所需的时间增加。尽管多孔电极具有几乎相同的电阻率,但是每个多孔电极之间的EDL充电电流的时间常数的比率大于有效表面积的比率。当粒径小(约20nm)时,在施加电位后,在多孔电极上对多孔电极进行染料改性的电致变色反应,因为极低的EDL形成速率。证实,通过多孔电极内的电解质离子缺乏电解质离子诱导ED1形成的延迟。因此,为了在低电阻率纳米粒子基多孔电极中实现理想的快速响应电化学反应,重要的是优化电极结构与电解质离子浓度之间的关系。

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