{"title":"Superior sodium storage anode constructed via chemical bonding between S-doped hard carbon and graphene oxide binder","authors":"Xue Li, Yating Zhang, Youyu Zhu, Yanping Hu, Yicheng Wang, Yizhen Zhang","doi":"10.1007/s11581-024-05776-y","DOIUrl":null,"url":null,"abstract":"<p>Hard carbon stands out as one of the most prospective anode materials for the storage of sodium due to its abundant resources, low cost, high conductivity, and suitable potential. In this study, S-doped hard carbon (SFC/S-3) was synthesized from a mixture of Shenfu bituminous coal (SFC) and S powder via the one-step pyrolysis method. S doping effectively enlarged the carbon layer spacing, formed -C-SO<sub>x</sub>-C- bonds, and increased the specific surface area of the hard carbon, which significantly enhanced the sodium storage capacity of hard carbons. Furthermore, coal-based graphene oxide (CGO) was used as a multi-functional binder to further boost the sodium storage performance of SFC/S-3 by reducing the surface defects and forming a conductive network. Consequently, the SFC/S-3@CGO exhibited an excellent sodium storage performance, delivering a high reversible capacity of 449.4 mAh g<sup>−1</sup>, a high-rate capacity of 224.7 mAh g<sup>−1</sup> at 1 A g<sup>−1</sup>, and approximately 74% capacity retention after 500 cycles at 1 A g<sup>−1</sup>. This study offers a versatile approach for heteroatom doping and promotes the clean utilization of coal.</p>","PeriodicalId":599,"journal":{"name":"Ionics","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2024-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ionics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s11581-024-05776-y","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Hard carbon stands out as one of the most prospective anode materials for the storage of sodium due to its abundant resources, low cost, high conductivity, and suitable potential. In this study, S-doped hard carbon (SFC/S-3) was synthesized from a mixture of Shenfu bituminous coal (SFC) and S powder via the one-step pyrolysis method. S doping effectively enlarged the carbon layer spacing, formed -C-SOx-C- bonds, and increased the specific surface area of the hard carbon, which significantly enhanced the sodium storage capacity of hard carbons. Furthermore, coal-based graphene oxide (CGO) was used as a multi-functional binder to further boost the sodium storage performance of SFC/S-3 by reducing the surface defects and forming a conductive network. Consequently, the SFC/S-3@CGO exhibited an excellent sodium storage performance, delivering a high reversible capacity of 449.4 mAh g−1, a high-rate capacity of 224.7 mAh g−1 at 1 A g−1, and approximately 74% capacity retention after 500 cycles at 1 A g−1. This study offers a versatile approach for heteroatom doping and promotes the clean utilization of coal.
硬碳因其资源丰富、成本低廉、电导率高和具有合适的潜力而成为最有前景的储钠阳极材料之一。本研究以神府烟煤(SFC)和 S 粉的混合物为原料,通过一步热解法合成了 S 掺杂硬碳(SFC/S-3)。S掺杂有效地扩大了碳层间距,形成了-C-SOx-C-键,增加了硬质碳的比表面积,从而显著提高了硬质碳的钠储存能力。此外,煤基氧化石墨烯(CGO)作为一种多功能粘合剂,通过减少表面缺陷并形成导电网络,进一步提高了 SFC/S-3 的储钠性能。因此,SFC/S-3@CGO 表现出了优异的钠存储性能,可提供 449.4 mAh g-1 的高可逆容量,1 A g-1 时的高倍率容量为 224.7 mAh g-1,1 A g-1 时循环 500 次后的容量保持率约为 74%。这项研究为杂质原子掺杂提供了一种多功能方法,促进了煤炭的清洁利用。
期刊介绍:
Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.