材料科学
阳极
钾
钠
钾离子电池
锂(药物)
离子
电池(电)
钠离子电池
锂离子电池
化学工程
无机化学
光电子学
磷酸钒锂电池
电极
化学
冶金
物理化学
法拉第效率
有机化学
功率(物理)
内分泌学
工程类
物理
医学
量子力学
作者
Zhenwei Li,Meisheng Han,Yuanbo Zhang,Yuan Fu,Ying Fu,Jie Yu
出处
期刊:Advanced Science
[Wiley]
日期:2023-03-22
卷期号:10 (15): e2207234-e2207234
被引量:76
标识
DOI:10.1002/advs.202207234
摘要
Abstract Single‐layered MoS 2 is a promising anode material for lithium‐ion batteries (LIBs), sodium‐ion batteries (SIBs), and potassium‐ion batteries (PIBs) due to its high capacity and isotropic ion transport paths. However, the low intrinsic conductivity and easy‐agglomerated feature hamper its applications. Here, a charge‐driven interlayer expansion strategy that Co 2+ replaces Mo 4+ in the doping form to endow MoS 2 layers with negative charges, thus inducing electrostatic repulsion, together with the insertion of gaseous groups, to drive interlayer expansion which once breaks the confinement of interlayer van der Waals force, single‐layered MoS 2 is obtained and uniformly dispersed into carbon matrix arising from the transformation of carbonaceous gaseous groups under high vapor pressure, is proposed. Co atom doping helps enhance the intrinsic conductivity of single‐layered MoS 2 . Carbon matrix effectively prevents agglomeration of single‐layered MoS 2 . The doped Co atoms can be fully transformed into ultrasmall Co nanoparticles during conversion reaction, which enables strong spin‐polarized surface capacitance and thus significantly boosts ion transport and storage. Consequently, the prepared material delivers superb Li/Na/K‐ion storage performances, which are best in the reported MoS 2 ‐based anodes. The proposed charge‐driven interlayer expansion strategy provides a novel perspective for preparing single‐layered MoS 2, which shows huge potential for energy storage.
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