论文标题

通过同时进行电化学和颜色阻抗测量研究的电致氧化氧化物的电荷颜色动力学

Charge coloration dynamics of electrochromic amorphous tungsten oxide studied by simultaneous electrochemical and color impedance measurements

论文作者

Rojas-González, Edgar A., Niklasson, Gunnar A.

论文摘要

可以通过比较电气和光学响应的​​动力学来探测电致(EC)系统中的着色机制。在本文中,通过两种技术的组合$ \ text {----} $的组合,即电化学障碍光谱(EIS)和所谓的有色化的色谱光谱(CIS)。这是在不同的偏差电位上完成的,这可能与不同的插入水平有关。与EIS光谱的等效电路拟合用于提取参与总阻抗响应的法拉达分量。后者被分配到插入之前的中间吸附步骤,并在膜中电子离子对的扩散。将表示复杂的光学电容的数量与复杂的电容$ \ text {---} $进行比较,它们的表达式与法拉达的过程有关。低插入水平的着色遵循吸附和扩散现象。相反,扩散贡献在高插入水平上是主要的,在这种情况下,吸附的贡献似乎可以忽略不计。对于完美同步的电响应和光学响应,其复杂光谱只有多元因素有所不同。除了高频率下的小偏差外,在低插入水平下就是这种情况。随着插入水平的增加,观察到了与此行为的明显不同。在本工作中提出的频率依赖性技术的组合可以帮助理解各种条件下EC材料中色彩机理的动力学,例如,在不同的互相级别和光学波长下,$ \ text {----} $。

The coloration mechanisms in electrochromic (EC) systems can be probed by comparing the dynamics of the electrical and optical responses. In this paper, the linear frequency-dependent electrical and optical responses of an amorphous tungsten oxide thin film were measured simultaneously by a combination of two techniques$\text{---}$that is, electrochemical impedance spectroscopy (EIS) and the so-called color impedance spectroscopy (CIS). This was done at different bias potentials, which can be associated with different intercalation levels. Equivalent circuit fitting to the EIS spectra was used to extract the Faradaic components participating in the total impedance response. The latter were assigned to an intermediate adsorption step before the intercalation and to the diffusion of the electron-ion couple in the film. A quantity denoted complex optical capacitance is compared to the complex electrical capacitance$\text{---}$in particular, their expressions are related to the Faradaic processes. The coloration at low intercalation levels followed both the adsorption and diffusion phenomena. Conversely, the diffusion contribution was dominant at high intercalation levels and the adsorption one seemed to be negligible in this case. For perfectly synchronized electrical and optical responses, their complex spectra are expected to differ only by a multiplying factor. This was the case at low intercalation levels, apart from small deviations at high frequencies. A clear departure from this behavior was observed as the intercalation level increased. A combination of frequency-dependent techniques, as presented in this work, can help in the understanding of the dynamics of the coloration mechanisms in EC materials at various conditions$\text{---}$for example, at different intercalation levels and optical wavelengths.

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