3D interconnected N-doped graphene architecture encapsulated with oxygen-deficient TiO2 nanotube array: synergism of oxygen vacancy and carbon materials on enhanced sulfur conversion and catalytic activity of TiO2 nanotube array in Li–S batteries†
{"title":"3D interconnected N-doped graphene architecture encapsulated with oxygen-deficient TiO2 nanotube array: synergism of oxygen vacancy and carbon materials on enhanced sulfur conversion and catalytic activity of TiO2 nanotube array in Li–S batteries†","authors":"Shaymaa Jabbar Abdulrazzaq","doi":"10.1039/D3ME00163F","DOIUrl":null,"url":null,"abstract":"<p >The main challenges to Li–S battery use include poor conductivity, the shuttling effect, and slow LiPS transition. In this work, a 3D framework of N-doped graphene interconnected with defect-rich TiO<small><sub>2</sub></small> nanotubes acts as a sulfur host. A narrow TiO<small><sub>2</sub></small> nanotube reduces lithium-ion diffusion length and facilitates fast charge transport. The unique 3D porous nanostructure holds a wide range of sulfur species and provides optimal pathways for electrolyte penetration. It also counters volume expansion during cycling and serves as a platform for the successful absorption of LiPSs. The TiO<small><sub>2</sub></small> nanowire with oxygen vacancy/N-doped graphene aerogel/sulfur (S-OVTNW/NGA) electrode has a small aspect ratio and is attached to graphene layers, which anchors LiPSs through a strong chemical interaction. Oxygen deficiency boosts electrical conductivity, reduces LiPS flow into the electrolyte, improves catalytic performance, and speeds up LiPS transformation. This design provides excellent electrochemical performance. The cathode has a notable primary specific capacity of 1370.2 mAh g<small><sup>−1</sup></small> at <em>J</em> = 0.2 C, with a sulfur ratio of 80%. Following 100 cycles, the observed capacity of the specimen remains at 879.2 mAh g<small><sup>−1</sup></small>, signifying a retention rate of 66.5%. Its capacity of 635.5 mAh g<small><sup>−1</sup></small> under 4 C shows its excellent rate performance. The findings may accelerate the development of electrode materials for lithium–sulfur (Li–S) batteries that are more efficient and cost-effective.</p>","PeriodicalId":91,"journal":{"name":"Molecular Systems Design & Engineering","volume":" 2","pages":" 158-170"},"PeriodicalIF":3.2000,"publicationDate":"2023-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Systems Design & Engineering","FirstCategoryId":"5","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/me/d3me00163f","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The main challenges to Li–S battery use include poor conductivity, the shuttling effect, and slow LiPS transition. In this work, a 3D framework of N-doped graphene interconnected with defect-rich TiO2 nanotubes acts as a sulfur host. A narrow TiO2 nanotube reduces lithium-ion diffusion length and facilitates fast charge transport. The unique 3D porous nanostructure holds a wide range of sulfur species and provides optimal pathways for electrolyte penetration. It also counters volume expansion during cycling and serves as a platform for the successful absorption of LiPSs. The TiO2 nanowire with oxygen vacancy/N-doped graphene aerogel/sulfur (S-OVTNW/NGA) electrode has a small aspect ratio and is attached to graphene layers, which anchors LiPSs through a strong chemical interaction. Oxygen deficiency boosts electrical conductivity, reduces LiPS flow into the electrolyte, improves catalytic performance, and speeds up LiPS transformation. This design provides excellent electrochemical performance. The cathode has a notable primary specific capacity of 1370.2 mAh g−1 at J = 0.2 C, with a sulfur ratio of 80%. Following 100 cycles, the observed capacity of the specimen remains at 879.2 mAh g−1, signifying a retention rate of 66.5%. Its capacity of 635.5 mAh g−1 under 4 C shows its excellent rate performance. The findings may accelerate the development of electrode materials for lithium–sulfur (Li–S) batteries that are more efficient and cost-effective.
Li-S电池使用的主要挑战包括导电性差、穿梭效应和缓慢的lip过渡。在这项工作中,n掺杂石墨烯的3D框架与富含缺陷的TiO2纳米管相互连接,作为硫宿主。窄的TiO2纳米管减少了锂离子的扩散长度,促进了电荷的快速传输。独特的3D多孔纳米结构容纳了广泛的硫种,并为电解质渗透提供了最佳途径。它还可以在循环过程中对抗体积膨胀,并作为成功吸收LiPSs的平台。带有氧空位/ n掺杂石墨烯气凝胶/硫(S-OVTNW/NGA)电极的TiO2纳米线具有小宽高比,附着在石墨烯层上,通过强化学相互作用锚定LiPSs。缺氧可提高导电率,减少LiPS进入电解液,提高催化性能,加速LiPS的转化。这种设计提供了优异的电化学性能。在J = 0.2 C,硫比为80%时,阴极的初级比容量为1370.2 mAh g−1。循环100次后,观察到样品的容量保持在879.2 mAh g−1,保留率为66.5%。其在4℃下的容量为635.5 mAh g−1,具有优异的倍率性能。这一发现可能会加速锂硫(Li-S)电池电极材料的开发,从而提高效率和成本效益。
期刊介绍:
Molecular Systems Design & Engineering provides a hub for cutting-edge research into how understanding of molecular properties, behaviour and interactions can be used to design and assemble better materials, systems, and processes to achieve specific functions. These may have applications of technological significance and help address global challenges.