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用于高性能锂/钠存储的由氮掺杂碳包裹的分级C/MoS纳米带的构建。

Construction of hierarchical C/MoS nanobelts wrapped by N-doped carbon toward high-performance lithium/sodium storage.

作者信息

Ye Bingqing, Cai Xingke, Zhao Ruo

机构信息

College of Civil and Transportation Engineering, Shenzhen University, Shenzhen 518060, Guangdong, China; Institute for Advanced Study, Shenzhen University, Shenzhen 518060, Guangdong, China.

Institute for Advanced Study, Shenzhen University, Shenzhen 518060, Guangdong, China.

出版信息

J Colloid Interface Sci. 2025 Dec 15;700(Pt 2):138458. doi: 10.1016/j.jcis.2025.138458. Epub 2025 Jul 16.

Abstract

As an ideal choice for anode materials in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs), molybdenum disulfide (MoS) still encounters the obstacles of undesirable conductivity, volume expansion and self-agglomeration during cycling that need to be conquered. Herein, a novel hierarchical nanobelt structure of N-doped carbon-coated C/MoS (denoted as C/MoS@NC) was synthesized by self-sacrificing template method and facile double carbon coating process. In this hierarchical structure, MoS nanosheets grown vertically along the nanobelt axis offer a plethora of active sites for electrode reaction and expedite the transport of Li/Na, thus promoting the electrochemical process. Furthermore, the double carbon coating effectively enhances the conductivity of MoS and alleviates its volume expansion, wherein the inner carbon playing a pivotal role in preserving the nanobelt structure, while the outermost N-doped carbon effectively prevents polysulfide dissolution and further reinforce structural stability. Consequently, the C/MoS@NC-2 electrode presents exceptional electrochemical behavior for both LIBs (1254 mAh g at 0.2 A g after 100 cycles, 884 mAh g at 1 A g after 500 cycles, and rate capacity of 629 mAh g at 10 A g) and SIBs (441 mAh g at 0.2 A g after 100 cycles and capacity retention rate of 80.4 % after 1000 cycles at 1 A g). Moreover, the Li/Na-ion full cells show good cycling stability, confirming the C/MoS@NC-2 electrode's viability for practical applications in these energy storage systems.

摘要

作为锂离子电池(LIBs)和钠离子电池(SIBs)阳极材料的理想选择,二硫化钼(MoS)在循环过程中仍面临着导电性差、体积膨胀和自团聚等需要克服的障碍。在此,通过自牺牲模板法和简便的双碳包覆工艺合成了一种新型的N掺杂碳包覆C/MoS分级纳米带结构(表示为C/MoS@NC)。在这种分级结构中,沿纳米带轴垂直生长的MoS纳米片为电极反应提供了大量活性位点,并加快了Li/Na的传输,从而促进了电化学过程。此外,双碳包覆有效地提高了MoS的导电性并减轻了其体积膨胀,其中内层碳在保持纳米带结构方面起关键作用,而最外层的N掺杂碳有效地防止了多硫化物的溶解并进一步增强了结构稳定性。因此,C/MoS@NC-2电极在LIBs(100次循环后在0.2 A g下为1254 mAh g,500次循环后在1 A g下为884 mAh g,10 A g下的倍率容量为629 mAh g)和SIBs(100次循环后在0.2 A g下为441 mAh g,1 A g下1000次循环后的容量保持率为80.4%)中均表现出优异的电化学性能。此外,Li/Na离子全电池显示出良好的循环稳定性,证实了C/MoS@NC-2电极在这些储能系统中实际应用的可行性。

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