Hollow Carbon and MXene Dual‐Reinforced MoS2 with Enlarged Interlayers for High‐Rate and High‐Capacity Sodium Storage Systems

Author:

Pan Hanqing1,Huang Yan1,Cen Xinnuo1,Zhang Ming1,Hou Jianhua2,Wu Chao3,Dou Yuhai3,Sun Bing4,Wang Ying1,Zhang Binwei56,Zhang Lei7ORCID

Affiliation:

1. Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials School of Chemistry & Materials Science Jiangsu Normal University Xuzhou Jiangsu 221116 P. R. China

2. College of Environmental Science and Engineering Yangzhou University Yangzhou Jiangsu 225009 P. R. China

3. Institute of Energy Materials Science University of Shanghai for Science and Technology Shanghai 200093 P. R. China

4. Centre for Clean Energy Technology School of Mathematical and Physical Sciences Faculty of Science University of Technology Sydney Ultimo NSW 2007 Australia

5. School of Chemistry and Chemical Engineering Chongqing University Chongqing 401331 P. R. China

6. Center of Advanced Electrochemical Energy Institute of Advanced Interdisciplinary Studies Chongqing University Chongqing 401331 P. R. China

7. Centre for Catalysis and Clean Energy Gold Coast Campus Griffith University Gold Coast QLD 4222 Australia

Abstract

AbstractSodium‐ion batteries (SIBs) and sodium‐ion capacitors (SICs) are promising candidates for cost‐effective and large‐scale energy storage devices. However, sluggish kinetics and low capacity of traditional anode materials inhibit their practical applications. Herein, a novel design featuring a layer‐expanded MoS2 is presented that dual‐reinforced by hollow N, P‐codoped carbon as the inner supporter and surface groups abundant MXene as the outer supporter, resulting in a cross‐linked robust composite (NPC@MoS2/MXene). The hollow N, P‐codoped carbon effectively prevents agglomeration of MoS2 layers and facilitates shorter distances between the electrolyte and electrode. The conductive MXene outer surface envelops the NPC@MoS2 units inside, creating interconnected channels that enable efficient charge transfer and diffusion, ensuring rapid kinetics and enhanced electrode utilization. It exhibits a high reversible capacity of 453 mAh g−1, remarkable cycling stability, and exceptional rate capability with 54% capacity retention when the current density increases from 100 to 5000 mA g−1 toward SIBs. The kinetic mechanism studies reveal that the NPC@MoS2/MXene demonstrates a pseudocapacitance dominated hybrid sodiation/desodiation process. Coupled with active carbon (AC), the NPC@MoS2/MXene//AC SICs achieve both high energy density of 136 Wh kg−1 at 254 W kg−1 and high‐power density of 5940 W kg−1 at 27 Wh g−1, maintaining excellent stability.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Griffith University

Australian Research Council

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3