Antonia Kotronia , Habtom Desta Asfaw , Cheuk-Wai Tai , Kristina Edström , Daniel Brandell
{"title":"Catalytically graphitized freestanding carbon foams for 3D Li-ion microbatteries","authors":"Antonia Kotronia , Habtom Desta Asfaw , Cheuk-Wai Tai , Kristina Edström , Daniel Brandell","doi":"10.1016/j.powera.2020.100002","DOIUrl":null,"url":null,"abstract":"<div><p>A long-range graphitic ordering in carbon anodes is desirable since it facilitates Li<sup>+</sup> transport within the structure and minimizes irreversible capacity loss. This is of vital concern in porous carbon electrodes that exhibit high surface areas and porosity, and are used in 3D microbatteries. To date, it remains a challenge to graphitize carbon structures with extensive microporosity, since the two properties are considered to be mutually exclusive. In this article, carbon foams with enhanced graphitic ordering are successfully synthesized, while maintaining their bicontinuous porous microstructures. The carbon foams are synthesized from high internal phase emulsion-templated polymers, carbonized at 1000 °C and subsequently graphitized at 2200 °C. The key to enhancing the graphitization of the bespoke carbon foams is the incorporation of Ca- and Mg-based salts at early stages in the synthesis. The carbon foams graphitized in the presence of these salts exhibit higher gravimetric capacities when cycled at a specific current of 10 mA g<sup>−1</sup> (140 mAh g<sup>−1</sup>) compared to a reference foam (105 mAh g<sup>−1</sup>), which amounts to 33% increase.</p></div>","PeriodicalId":34318,"journal":{"name":"Journal of Power Sources Advances","volume":null,"pages":null},"PeriodicalIF":5.4000,"publicationDate":"2020-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.powera.2020.100002","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Power Sources Advances","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666248520300020","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 5
Abstract
A long-range graphitic ordering in carbon anodes is desirable since it facilitates Li+ transport within the structure and minimizes irreversible capacity loss. This is of vital concern in porous carbon electrodes that exhibit high surface areas and porosity, and are used in 3D microbatteries. To date, it remains a challenge to graphitize carbon structures with extensive microporosity, since the two properties are considered to be mutually exclusive. In this article, carbon foams with enhanced graphitic ordering are successfully synthesized, while maintaining their bicontinuous porous microstructures. The carbon foams are synthesized from high internal phase emulsion-templated polymers, carbonized at 1000 °C and subsequently graphitized at 2200 °C. The key to enhancing the graphitization of the bespoke carbon foams is the incorporation of Ca- and Mg-based salts at early stages in the synthesis. The carbon foams graphitized in the presence of these salts exhibit higher gravimetric capacities when cycled at a specific current of 10 mA g−1 (140 mAh g−1) compared to a reference foam (105 mAh g−1), which amounts to 33% increase.
碳阳极的长期石墨有序是可取的,因为它有利于Li+在结构内的传输,并最大限度地减少不可逆的容量损失。这对于多孔碳电极来说是至关重要的,因为多孔碳电极具有高表面积和孔隙度,并用于3D微电池。迄今为止,石墨化具有广泛微孔隙度的碳结构仍然是一个挑战,因为这两种性质被认为是相互排斥的。本文成功合成了石墨有序度增强的泡沫碳,同时保持了其双连续的多孔微结构。碳泡沫由高内相乳液模板聚合物合成,在1000 °C下碳化,随后在2200 °C下石墨化。提高定制泡沫碳石墨化的关键是在合成的早期阶段加入钙基和镁基盐。在这些盐存在下石墨化的碳泡沫在10 mA g−1 (140 mAh g−1)的特定电流下循环时,与参考泡沫(105 mAh g−1)相比,其重量容量增加了33%。