Advances in WO(3)-Based Supercapacitors: State-of-the-Art Research and Future Perspectives

基于WO(3)的超级电容器的研究进展:最新研究成果与未来展望

阅读:1

Abstract

Electrochemical energy storage devices are one of the main protagonists in the ongoing technological advances in the energy field, whereby the development of efficient, sustainable, and durable storage systems aroused a great interest in the scientific community. Batteries, electrical double layer capacitors (EDLC), and pseudocapacitors are characterized in depth in the literature as the most powerful energy storage devices for practical applications. Pseudocapacitors bridge the gap between batteries and EDLCs, thus supplying both high energy and power densities, and transition metal oxide (TMO)-based nanostructures are used for their realization. Among them, WO(3) nanostructures inspired the scientific community, thanks to WO(3)'s excellent electrochemical stability, low cost, and abundance in nature. This review analyzes the morphological and electrochemical properties of WO(3) nanostructures and their most used synthesis techniques. Moreover, a brief description of the electrochemical characterization methods of electrodes for energy storage, such as Cyclic Voltammetry (CV), Galvanostatic Charge-Discharge (GCD), and Electrochemical Impedance Spectroscopy (EIS) are reported, to better understand the recent advances in WO(3)-based nanostructures, such as pore WO(3) nanostructures, WO(3)/carbon nanocomposites, and metal-doped WO(3) nanostructure-based electrodes for pseudocapacitor applications. This analysis is reported in terms of specific capacitance calculated as a function of current density and scan rate. Then we move to the recent progress made for the design and fabrication of WO(3)-based symmetric and asymmetric supercapacitors (SSCs and ASCs), thus studying a comparative Ragone plot of the state-of-the-art research.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。