双金属片
材料科学
微球
锂(药物)
硫化物
金属
钠
化学工程
硫化铁
过渡金属
硫化钠
无机化学
化学
冶金
催化作用
有机化学
硫黄
医学
工程类
内分泌学
作者
Baole Guan,Sheng Li,Nan Zhang,Ting Sun,Yan‐Rong Zhu,Junhong Zhang,Ting‐Feng Yi
标识
DOI:10.1016/j.cej.2022.137154
摘要
• A novel ZCS@NC@MS hierarchical composite was synthesized for the first time. • N-doped carbon and MoS 2 synergistically improve the electrochemical properties. • The heterointerface effectively facilitate the ions/electrons diffusion kinetics. • ZCS@NC@MS exhibits excellent electrochemical performance for LIBs and SIBs. MoS 2 as a promising electrode has aroused widely attention because of the high theoretical capacity. However, the poor electrical conductivity and large volume expansion seriously impede the practical application. Herein, we propose a novel hydrangea-like hierarchical Zn 0.76 Co 0.24 S@NC@MoS 2 (denoted as ZCS@NC@MS) composite by cultivating ultrathick MoS 2 nanoplates on N-doped carbon matrix derived from the bimetallic metal–organic framework. On the one hand, the N-doped carbon matrix can not only improve the electrical conductivity, but also mitigate the volume expansion. In addition, the heterointerfaces can induce the built-in electric field, thus facilitating the ion diffusion kinetics. Integrating the above advantages, ZCS@NC@MS as anode for lithium-ion batteries delivers an outstanding specific capacity of 1040.5 mAh g −1 at 0.1 A g −1 and a high reversible capacity of 680 mAh g −1 over 1000 cycles at 1.0 A g −1 . ZCS@NC@MS as anode for sodium-ion batteries also manifests an excellent specific capacity of 723.6 mAh g −1 at 0.1 A g −1 . The density functional theory calculation further confirms that heterointerfaces can effectively improve the reaction kinetic. Consequently, this novel strategy provides a new pathway to improve the energy storage performance of two-dimension transition metal sulfides.
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