掺杂电子富铁杂原子的卵黄壳 MoS2 纳米球用于超长寿命锰离子电池

IF 7.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY ACS Sustainable Chemistry & Engineering Pub Date : 2024-08-04 DOI:10.1021/acssuschemeng.4c04400
Mingjing Chu, Xin Xu, Wenqing Zhao, Yue Dai, Xu Zhou, Guanwei Xue, Yiwei Xue, Liang Cao, Shuoran Chen
{"title":"掺杂电子富铁杂原子的卵黄壳 MoS2 纳米球用于超长寿命锰离子电池","authors":"Mingjing Chu, Xin Xu, Wenqing Zhao, Yue Dai, Xu Zhou, Guanwei Xue, Yiwei Xue, Liang Cao, Shuoran Chen","doi":"10.1021/acssuschemeng.4c04400","DOIUrl":null,"url":null,"abstract":"Molybdenum disulfide (MoS<sub>2</sub>) has been extensively studied as an anode for sodium-ion batteries owing to its large theoretical specific capacity and steady crystal texture. Nevertheless, the unsatisfactory rate capability and short cycling lifespan of MoS<sub>2</sub> derived from its inferior electrical conductivity and extensive volume variation among Na<sup>+</sup> insertion and extraction have greatly impeded its practical exploitation. Hence, we proposed an electron coupling strategy with the rational incorporation of iron heteroatoms in a novel yolk–shell MoS<sub>2</sub> nanostructure (FMS@C) through an advanced micelle-confined microemulsion technology. In this configuration, the doping of electron-rich Fe heteroatoms breaks the long-range ordered texture of pristine MoS<sub>2</sub> with extensively activated electronic structures, thus enabling accelerated mass transfer and charge diffusion. Meanwhile, the novel yolk–shell nanoarchitecture with enough inner room can efficiently accommodate the volume variation during repeated charge/discharge cycles, thus favoring the high stability of the structure. Consequently, the prepared FMS@C anode delivers superior rate capability and impressive reversible capacity retention, and it can achieve 201.5 mA h<sup>–1</sup> after 5500 cycles at 5 A g<sup>–1</sup> with a low capacity decay of 0.0057% per cycle. Accordingly, this work opens up a brilliant way to improve the performance of metal sulfur compounds as advanced energy storage electrodes.","PeriodicalId":25,"journal":{"name":"ACS Sustainable Chemistry & Engineering","volume":null,"pages":null},"PeriodicalIF":7.1000,"publicationDate":"2024-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Yolk–Shell MoS2 Nanosphere-Doped Electron-Rich Iron Heteroatoms for Ultralong Lifespan Na-Ion Batteries\",\"authors\":\"Mingjing Chu, Xin Xu, Wenqing Zhao, Yue Dai, Xu Zhou, Guanwei Xue, Yiwei Xue, Liang Cao, Shuoran Chen\",\"doi\":\"10.1021/acssuschemeng.4c04400\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Molybdenum disulfide (MoS<sub>2</sub>) has been extensively studied as an anode for sodium-ion batteries owing to its large theoretical specific capacity and steady crystal texture. Nevertheless, the unsatisfactory rate capability and short cycling lifespan of MoS<sub>2</sub> derived from its inferior electrical conductivity and extensive volume variation among Na<sup>+</sup> insertion and extraction have greatly impeded its practical exploitation. Hence, we proposed an electron coupling strategy with the rational incorporation of iron heteroatoms in a novel yolk–shell MoS<sub>2</sub> nanostructure (FMS@C) through an advanced micelle-confined microemulsion technology. In this configuration, the doping of electron-rich Fe heteroatoms breaks the long-range ordered texture of pristine MoS<sub>2</sub> with extensively activated electronic structures, thus enabling accelerated mass transfer and charge diffusion. Meanwhile, the novel yolk–shell nanoarchitecture with enough inner room can efficiently accommodate the volume variation during repeated charge/discharge cycles, thus favoring the high stability of the structure. Consequently, the prepared FMS@C anode delivers superior rate capability and impressive reversible capacity retention, and it can achieve 201.5 mA h<sup>–1</sup> after 5500 cycles at 5 A g<sup>–1</sup> with a low capacity decay of 0.0057% per cycle. Accordingly, this work opens up a brilliant way to improve the performance of metal sulfur compounds as advanced energy storage electrodes.\",\"PeriodicalId\":25,\"journal\":{\"name\":\"ACS Sustainable Chemistry & Engineering\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":7.1000,\"publicationDate\":\"2024-08-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Sustainable Chemistry & Engineering\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acssuschemeng.4c04400\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Sustainable Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acssuschemeng.4c04400","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

由于二硫化钼(MoS2)具有较大的理论比容量和稳定的晶体结构,作为钠离子电池的阳极已被广泛研究。然而,由于 MoS2 的导电性较差,且在 Na+ 插入和萃取过程中体积变化较大,因此其速率能力并不理想,循环寿命也较短,这极大地阻碍了其实际应用。因此,我们提出了一种电子耦合策略,通过先进的胶束封闭微乳液技术,在新型卵黄壳 MoS2 纳米结构(FMS@C)中合理掺入铁杂质原子。在这种结构中,富电子铁杂原子的掺杂打破了原始 MoS2 的长程有序结构,使其具有广泛活化的电子结构,从而加速了传质和电荷扩散。同时,新颖的蛋黄壳纳米结构具有足够的内部空间,可以有效地适应反复充放电循环过程中的体积变化,从而有利于结构的高稳定性。因此,所制备的 FMS@C 阳极具有优异的速率能力和令人印象深刻的可逆容量保持能力,在 5 A g-1 的条件下循环 5500 次后可达到 201.5 mA h-1,且容量衰减较低,每循环为 0.0057%。因此,这项工作为提高金属硫化合物作为先进储能电极的性能开辟了一条光明大道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Yolk–Shell MoS2 Nanosphere-Doped Electron-Rich Iron Heteroatoms for Ultralong Lifespan Na-Ion Batteries
Molybdenum disulfide (MoS2) has been extensively studied as an anode for sodium-ion batteries owing to its large theoretical specific capacity and steady crystal texture. Nevertheless, the unsatisfactory rate capability and short cycling lifespan of MoS2 derived from its inferior electrical conductivity and extensive volume variation among Na+ insertion and extraction have greatly impeded its practical exploitation. Hence, we proposed an electron coupling strategy with the rational incorporation of iron heteroatoms in a novel yolk–shell MoS2 nanostructure (FMS@C) through an advanced micelle-confined microemulsion technology. In this configuration, the doping of electron-rich Fe heteroatoms breaks the long-range ordered texture of pristine MoS2 with extensively activated electronic structures, thus enabling accelerated mass transfer and charge diffusion. Meanwhile, the novel yolk–shell nanoarchitecture with enough inner room can efficiently accommodate the volume variation during repeated charge/discharge cycles, thus favoring the high stability of the structure. Consequently, the prepared FMS@C anode delivers superior rate capability and impressive reversible capacity retention, and it can achieve 201.5 mA h–1 after 5500 cycles at 5 A g–1 with a low capacity decay of 0.0057% per cycle. Accordingly, this work opens up a brilliant way to improve the performance of metal sulfur compounds as advanced energy storage electrodes.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering CHEMISTRY, MULTIDISCIPLINARY-ENGINEERING, CHEMICAL
CiteScore
13.80
自引率
4.80%
发文量
1470
审稿时长
1.7 months
期刊介绍: ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment. The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.
期刊最新文献
Toward Sustainable Adhesives with Biodegradability, Scalability, and Removability: Poly(butylene succinate)-Based Hot-Melt Adhesives Renewables-Based Routes to Paracetamol: A Green Chemistry Analysis Visible Light Induced Synthesis of 2-Benzoxazolecarboxamides Promoted by a Conjugated Microporous Polymer Modulating Molecular Interactions in Bulk and Electrochemical Interfaces of Deep Eutectic Solvent-Based Tailored Electrolytes for Facilitating Reactive CO2 Capture Crafting an Exceptionally Redox-Active Organic Molecule Boasting Superior Electron Mobility for High-Performance Electrochemical Desalination
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1