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膜厚对通过氧化分子层沉积(oMLD)生长的纳米级聚乙撑二氧噻吩(PEDOT)薄膜电化学性能的影响。

Effects of film thickness on electrochemical properties of nanoscale polyethylenedioxythiophene (PEDOT) thin films grown by oxidative molecular layer deposition (oMLD).

作者信息

Brathwaite Katrina G, Wyatt Quinton K, Atassi Amalie, Gregory Shawn A, Throm Eric, Stalla David, Yee Shannon K, Losego Mark D, Young Matthias J

机构信息

Chemical and Biomedical Engineering, University of Missouri, Columbia, Missouri, 65211, USA.

Department of Chemistry, University of Missouri, Columbia, Missouri, 65211, USA.

出版信息

Nanoscale. 2023 Mar 30;15(13):6187-6200. doi: 10.1039/d3nr00708a.

Abstract

Poly(3,4-ethylene dioxythiophene) (PEDOT) has a high theoretical charge storage capacity, making it of interest for electrochemical applications including energy storage and water desalination. Nanoscale thin films of PEDOT are particularly attractive for these applications to enable faster charging. Recent work has demonstrated that nanoscale thin films of PEDOT can be formed using sequential gas-phase exposures oxidative molecular layer deposition, or oMLD, which provides advantages in conformality and uniformity on high aspect ratio substrates over other deposition techniques. But to date, the electrochemical properties of these oMLD PEDOT thin films have not been well-characterized. In this work, we examine the electrochemical properties of 5-100 nm thick PEDOT films formed using 20-175 oMLD deposition cycles. We find that film thickness of oMLD PEDOT films affects the orientation of ordered domains leading to a substantial change in charge storage capacity. Interestingly, we observe a minimum in charge storage capacity for an oMLD PEDOT film thickness of ∼30 nm (60 oMLD cycles at 150 °C), coinciding with the highest degree of face-on oriented PEDOT domains as measured using grazing incidence wide angle X-ray scattering (GIWAXS). Thinner and thicker oMLD PEDOT films exhibit higher fractions of oblique (off-angle) orientations and corresponding increases in charge capacity of up to 120 mA h g. Electrochemical measurements suggest that higher charge capacity in films with mixed domain orientation arise from the facile transport of ions from the liquid electrolyte into the PEDOT layer. Greater exposure of the electrolyte to PEDOT domain edges is posited to facilitate faster ion transport in these mixed domain films. These insights will inform future design of PEDOT coated high-aspect ratio structures for electrochemical energy storage and water treatment.

摘要

聚(3,4 - 亚乙基二氧噻吩)(PEDOT)具有较高的理论电荷存储容量,这使其在包括能量存储和海水淡化在内的电化学应用中备受关注。PEDOT的纳米级薄膜对于这些应用尤其具有吸引力,因为它能够实现更快的充电速度。最近的研究表明,可以通过连续气相曝光——氧化分子层沉积(oMLD)来形成PEDOT纳米级薄膜,与其他沉积技术相比,oMLD在高纵横比衬底上的保形性和均匀性方面具有优势。但迄今为止,这些oMLD PEDOT薄膜的电化学性能尚未得到充分表征。在这项工作中,我们研究了使用20 - 175个oMLD沉积循环形成的5 - 100纳米厚的PEDOT薄膜的电化学性能。我们发现,oMLD PEDOT薄膜的厚度会影响有序域的取向,从而导致电荷存储容量发生显著变化。有趣的是,我们观察到,当oMLD PEDOT薄膜厚度约为30纳米(在150°C下进行60个oMLD循环)时,电荷存储容量出现最小值,这与使用掠入射广角X射线散射(GIWAXS)测量的最高程度的面取向PEDOT域相吻合。更薄和更厚的oMLD PEDOT薄膜表现出更高比例的倾斜(非角度)取向,并且电荷容量相应增加,最高可达120 mA h/g。电化学测量表明,具有混合域取向的薄膜中较高的电荷容量源于离子从液体电解质向PEDOT层的便捷传输。电解质与PEDOT域边缘的更大接触被认为有助于这些混合域薄膜中更快的离子传输。这些见解将为未来用于电化学能量存储和水处理的PEDOT涂层高纵横比结构的设计提供参考。

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