Stacking of Tailored Chalcogenide Nanosheets around MoO2-C Conductive Stakes Modulated by a Hybrid POM⊂MOF Precursor Template: Composite Conversion–Insertion Cathodes for Rechargeable Mg–Li Dual-Salt Batteries

材料科学 硫系化合物 堆积 阴极 导电体 复合数 化学工程 盐(化学) 光电子学 纳米技术 复合材料 有机化学 电气工程 化学 工程类
作者
Chenglong Wu,Jiulin Hu,Jingjing Tian,Fulu Chu,Zhenguo Yao,Yongjian Zheng,Dongguang Yin,Chilin Li
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (6): 5966-5977 被引量:54
标识
DOI:10.1021/acsami.8b18607
摘要

Mg anode has pronounced advantages in terms of high volumetric capacity, resource abundance, and dendrite-free electrochemical plating, which make rechargeable Mg-based batteries stand out as a representative next-generation energy storage system utilized in the field of large-scale stationary electric grid. However, sluggish Mg2+ diffusion in cathode lattices and facile passivation on the Mg anode hinder the commercialization of Mg batteries. Exploring a highly electroactive cathode prototype with hierarchical nanostructure and compatible electrolyte system with the capability of activating both an anode and a cathode is still a challenge. Here, we propose a POM⊂MOF (NENU-5) core-shell architecture as a hybrid precursor template to achieve the stacking of tailored chalcogenide nanosheets around MoO2-C conductive stakes, which can be employed as conversion-insertion cathodes (Cu1.96S-MoS2-MoO2 and Cu2Se-MoO2) for Mg-Li dual-salt batteries. Li-salt modulation further activates the capacity and rate performance at the cathode side by preferential Li-driven displacement reaction in Cu+ extrusible lattices. The heterogeneous conductive network and conformal dual-doped carbon coating enable a reversible capacity as high as 200 mAh/g with a coulombic efficiency close to 100%. The composite cathode can endure a long-term cycling up to 400 cycles and a high current density up to 2 A/g. The diversity of MOF-based materials infused by functional molecules or clusters would enrich the nanoengineering of electrodes to meet the performance demand for future multivalent batteries.
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