Vanadium niobium carbide (VNbCTx) bimetallic MXene derived V5S8-Nb2O5@MXene heterostructures for efficiently boosting the adsorption and catalytic performance of lithium polysulfide.

IF 12.2 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Materials Horizons Pub Date : 2024-10-09 DOI:10.1039/d4mh00674g
Yuqing Chen, Yongjie Huang, Qing Xu, Liying Yang, Ningyi Jiang, Shougen Yin
{"title":"Vanadium niobium carbide (VNbCT<sub><i>x</i></sub>) bimetallic MXene derived V<sub>5</sub>S<sub>8</sub>-Nb<sub>2</sub>O<sub>5</sub>@MXene heterostructures for efficiently boosting the adsorption and catalytic performance of lithium polysulfide.","authors":"Yuqing Chen, Yongjie Huang, Qing Xu, Liying Yang, Ningyi Jiang, Shougen Yin","doi":"10.1039/d4mh00674g","DOIUrl":null,"url":null,"abstract":"<p><p>To alleviate the shuttle effect in lithium-sulfur (Li-S) batteries, the electrocatalytic conversion of polysulfides serves as a vital strategy. However, achieving a synergy that combines robust adsorption with high catalytic activity continues to pose significant challenges. Herein, a simple solid-state sintering method is employed to transform vanadium-niobium carbide MXene (VNbCT<sub><i>x</i></sub>) into a heterogeneous structure of V<sub>5</sub>S<sub>8</sub>-Nb<sub>2</sub>O<sub>5</sub>@VNbCT<sub><i>x</i></sub> MXene (denoted as V<sub>5</sub>S<sub>8</sub>-Nb<sub>2</sub>O<sub>5</sub>@MX). The Nb<sub>2</sub>O<sub>5</sub> component immobilizes lithium polysulfides (LiPSs) at the electrode through its strong chemical affinity, while the V<sub>5</sub>S<sub>8</sub> fraction serves as an outstanding electrochemical catalyst, enhancing the reaction kinetics of sulfur precipitation. Furthermore, the VNbCT<sub><i>x</i></sub> MXene precursor scaffold is preserved through the conversion and uniformly distributed throughout the composite, exhibiting excellent electrical conductivity. Thanks to the synergistic \"capture-adsorption-catalysis\" action on LiPSs, the V<sub>5</sub>S<sub>8</sub>-Nb<sub>2</sub>O<sub>5</sub>@MX composite effectively restrains the shuttle effect. The as-prepared Li-S battery demonstrates a significant increase in specific capacity, reaching 1508 mA h g<sup>-1</sup> at 0.1C and maintaining a capacity decay of approximately 0.027% per cycle after 500 cycles at 1C and 766.1 mA h g<sup>-1</sup> at 5C. Even under a high sulfur loading of 5.75 mg cm<sup>-2</sup>, the battery can maintain a specific capacity of 596.6 mA h g<sup>-1</sup> and exhibit significant cycling stability after 100 cycles. DFT calculations indicate that the V<sub>5</sub>S<sub>8</sub>-Nb<sub>2</sub>O<sub>5</sub>@MX heterostructure exhibits a higher binding energy of 5.34 eV and a lower decomposition barrier energy of 0.68 eV, presenting potential advantages in accelerating the conversion reactions of LiPSs. Our research offers a straightforward approach for designing metal oxide-sulfide heterostructured catalysts that deliver superior performance and enhance the electrocatalytic conversion of LiPSs, clearing the path for high performance Li-S batteries.</p>","PeriodicalId":87,"journal":{"name":"Materials Horizons","volume":null,"pages":null},"PeriodicalIF":12.2000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Horizons","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d4mh00674g","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

To alleviate the shuttle effect in lithium-sulfur (Li-S) batteries, the electrocatalytic conversion of polysulfides serves as a vital strategy. However, achieving a synergy that combines robust adsorption with high catalytic activity continues to pose significant challenges. Herein, a simple solid-state sintering method is employed to transform vanadium-niobium carbide MXene (VNbCTx) into a heterogeneous structure of V5S8-Nb2O5@VNbCTx MXene (denoted as V5S8-Nb2O5@MX). The Nb2O5 component immobilizes lithium polysulfides (LiPSs) at the electrode through its strong chemical affinity, while the V5S8 fraction serves as an outstanding electrochemical catalyst, enhancing the reaction kinetics of sulfur precipitation. Furthermore, the VNbCTx MXene precursor scaffold is preserved through the conversion and uniformly distributed throughout the composite, exhibiting excellent electrical conductivity. Thanks to the synergistic "capture-adsorption-catalysis" action on LiPSs, the V5S8-Nb2O5@MX composite effectively restrains the shuttle effect. The as-prepared Li-S battery demonstrates a significant increase in specific capacity, reaching 1508 mA h g-1 at 0.1C and maintaining a capacity decay of approximately 0.027% per cycle after 500 cycles at 1C and 766.1 mA h g-1 at 5C. Even under a high sulfur loading of 5.75 mg cm-2, the battery can maintain a specific capacity of 596.6 mA h g-1 and exhibit significant cycling stability after 100 cycles. DFT calculations indicate that the V5S8-Nb2O5@MX heterostructure exhibits a higher binding energy of 5.34 eV and a lower decomposition barrier energy of 0.68 eV, presenting potential advantages in accelerating the conversion reactions of LiPSs. Our research offers a straightforward approach for designing metal oxide-sulfide heterostructured catalysts that deliver superior performance and enhance the electrocatalytic conversion of LiPSs, clearing the path for high performance Li-S batteries.

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
碳化钒铌 (VNbCTx) 双金属 MXene 衍生 V5S8-Nb2O5@MXene 异质结构可有效提高多硫化锂的吸附和催化性能。
为缓解锂硫(Li-S)电池中的穿梭效应,多硫化物的电催化转化是一项重要策略。然而,实现强吸附性与高催化活性的协同作用仍是一项重大挑战。本文采用一种简单的固态烧结方法,将碳化钒铌 MXene(VNbCTx)转化为 V5S8-Nb2O5@VNbCTx MXene(简称 V5S8-Nb2O5@MX)的异质结构。Nb2O5 部分通过其强大的化学亲和力将多硫化锂(LiPS)固定在电极上,而 V5S8 部分则可作为出色的电化学催化剂,增强硫沉淀的反应动力学。此外,VNbCTx MXene 前体支架在转化过程中得以保留,并均匀地分布在整个复合材料中,表现出卓越的导电性。得益于对锂离子的 "捕获-吸附-催化 "协同作用,V5S8-Nb2O5@MX 复合材料有效抑制了穿梭效应。制备的锂-S 电池的比容量显著增加,在 0.1C 时达到 1508 mA h g-1,在 1C 时循环 500 次后每次循环的容量衰减约为 0.027%,在 5C 时达到 766.1 mA h g-1。即使在 5.75 mg cm-2 的高硫负荷下,电池也能保持 596.6 mA h g-1 的比容量,并在 100 次循环后表现出显著的循环稳定性。DFT 计算表明,V5S8-Nb2O5@MX 异质结构具有更高的结合能(5.34 eV)和更低的分解势垒能(0.68 eV),在加速锂离子电池的转换反应方面具有潜在优势。我们的研究为设计金属氧化物-硫化物异质结构催化剂提供了一种简单直接的方法,这种催化剂性能优越,能增强锂离子电池的电催化转化,为高性能锂离子电池的发展开辟了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Materials Horizons
Materials Horizons CHEMISTRY, MULTIDISCIPLINARY-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
18.90
自引率
2.30%
发文量
306
审稿时长
1.3 months
期刊介绍: Materials Horizons is a leading journal in materials science that focuses on publishing exceptionally high-quality and innovative research. The journal prioritizes original research that introduces new concepts or ways of thinking, rather than solely reporting technological advancements. However, groundbreaking articles featuring record-breaking material performance may also be published. To be considered for publication, the work must be of significant interest to our community-spanning readership. Starting from 2021, all articles published in Materials Horizons will be indexed in MEDLINE©. The journal publishes various types of articles, including Communications, Reviews, Opinion pieces, Focus articles, and Comments. It serves as a core journal for researchers from academia, government, and industry across all areas of materials research. Materials Horizons is a Transformative Journal and compliant with Plan S. It has an impact factor of 13.3 and is indexed in MEDLINE.
期刊最新文献
Inside back cover Back cover Efficient photodegradation of carbamazepine by organocatalysts incorporating a third component with a more complementary absorption spectrum. Upconversion circularly polarized luminescence of cholesteric liquid crystal polymer networks with NaYF4:Yb,Tm UCNPs. Dopamine-integrated all-hydrogel multi-electrode arrays for neural activity recording.
×
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