Srinivas Gadipelli, Hanieh Akbari, Juntao Li, Christopher A. Howard, Hong Zhang, Paul R. Shearing, Dan J. L. Brett
{"title":"Structure-guided Capacitance Relationships in Oxidized Graphene Porous Materials Based Supercapacitors","authors":"Srinivas Gadipelli, Hanieh Akbari, Juntao Li, Christopher A. Howard, Hong Zhang, Paul R. Shearing, Dan J. L. Brett","doi":"10.1002/eem2.12637","DOIUrl":null,"url":null,"abstract":"<p>Supercapacitors formed from porous carbon and graphene-oxide (GO) materials are usually dominated by either electric double-layer capacitance, pseudo-capacitance, or both. Due to these combined features, reduced GO materials have been shown to offer superior capacitance over typical nanoporous carbon materials; however, there is a significant variation in reported values, ranging between 25 and 350 F g<sup>−1</sup>. This undermines the structure (e.g., oxygen functionality and/or surface area)-performance relationships for optimization of cost and scalable factors. This work demonstrates important structure-controlled charge storage relationships. For this, a series of exfoliated graphene (EG) derivatives are produced via thermal-shock exfoliation of GO precursors and following controlled graphitization of EG (GEG) generates materials with varied amounts of porosity, redox-active oxygen groups and graphitic components. Experimental results show significantly varied capacitance values between 30 and 250 F g<sup>−1</sup> at 1.0 A g<sup>−1</sup> in GEG structures; this suggests that for a given specific surface area the redox-active and hydrophilic oxygen content can boost the capacitance to 250–300% higher compared to typical mesoporous carbon materials. GEGs with identical oxygen functionality show a surface area governed capacitance. This allows to establish direct structure-performance relationships between 1) redox-active oxygen functional concentration and capacitance and 2) surface area and capacitance.</p>","PeriodicalId":11554,"journal":{"name":"Energy & Environmental Materials","volume":"6 4","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2023-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eem2.12637","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Environmental Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/eem2.12637","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Supercapacitors formed from porous carbon and graphene-oxide (GO) materials are usually dominated by either electric double-layer capacitance, pseudo-capacitance, or both. Due to these combined features, reduced GO materials have been shown to offer superior capacitance over typical nanoporous carbon materials; however, there is a significant variation in reported values, ranging between 25 and 350 F g−1. This undermines the structure (e.g., oxygen functionality and/or surface area)-performance relationships for optimization of cost and scalable factors. This work demonstrates important structure-controlled charge storage relationships. For this, a series of exfoliated graphene (EG) derivatives are produced via thermal-shock exfoliation of GO precursors and following controlled graphitization of EG (GEG) generates materials with varied amounts of porosity, redox-active oxygen groups and graphitic components. Experimental results show significantly varied capacitance values between 30 and 250 F g−1 at 1.0 A g−1 in GEG structures; this suggests that for a given specific surface area the redox-active and hydrophilic oxygen content can boost the capacitance to 250–300% higher compared to typical mesoporous carbon materials. GEGs with identical oxygen functionality show a surface area governed capacitance. This allows to establish direct structure-performance relationships between 1) redox-active oxygen functional concentration and capacitance and 2) surface area and capacitance.
由多孔碳和氧化石墨烯(GO)材料形成的超级电容器通常由双电层电容、伪电容或两者兼而有之。由于这些组合特征,还原GO材料已被证明比典型的纳米多孔碳材料提供了优越的电容;然而,报告的数值有很大的变化,在25到350之间 F g−1.这破坏了优化成本和可扩展因素的结构(如氧功能和/或表面积)-性能关系。这项工作展示了重要的结构控制电荷存储关系。为此,通过GO前体的热冲击剥离产生了一系列剥离石墨烯(EG)衍生物,随后EG(GEG)的受控石墨化产生了具有不同孔隙率、氧化还原活性氧基团和石墨组分的材料。实验结果显示,电容值在30和250之间有显著变化 F 1.0时g−1 A. GEG结构中的g−1;这表明,对于给定的比表面积,与典型的介孔碳材料相比,氧化还原活性和亲水性氧含量可以将电容提高到250-300%。具有相同氧气功能的GEG显示出表面积控制的电容。这允许在1)氧化还原活性氧功能浓度和电容与2)表面积和电容之间建立直接的结构-性能关系。
期刊介绍:
Energy & Environmental Materials (EEM) is an international journal published by Zhengzhou University in collaboration with John Wiley & Sons, Inc. The journal aims to publish high quality research related to materials for energy harvesting, conversion, storage, and transport, as well as for creating a cleaner environment. EEM welcomes research work of significant general interest that has a high impact on society-relevant technological advances. The scope of the journal is intentionally broad, recognizing the complexity of issues and challenges related to energy and environmental materials. Therefore, interdisciplinary work across basic science and engineering disciplines is particularly encouraged. The areas covered by the journal include, but are not limited to, materials and composites for photovoltaics and photoelectrochemistry, bioprocessing, batteries, fuel cells, supercapacitors, clean air, and devices with multifunctionality. The readership of the journal includes chemical, physical, biological, materials, and environmental scientists and engineers from academia, industry, and policy-making.