电解质
锌
溶解
储能
锰
水溶液
插层(化学)
化学工程
电化学
化学
氧化还原
材料科学
无机化学
电极
冶金
物理
工程类
有机化学
量子力学
功率(物理)
物理化学
作者
Lijuan Wu,Yingying Mei,Yuanhao Liu,Wen Xu,Minghui Zhang,Yanfeng Dong,Zhong‐Shuai Wu
标识
DOI:10.1016/j.cej.2023.141662
摘要
Low-cost and nontoxic manganese dioxide (MnO2) cathodes have shown promising application in high-capacity and high-voltage rechargeable zinc ion batteries (ZIBs), but suffer from limited cycling life and energy density mainly due to poor electrical conductivity and structural failure induced by manganese dissolution and H+/Zn2+ co-intercalation in traditional aqueous electrolytes. Herein, two-dimensional strongly-coupled δ-MnO2/MXene heteronanosheets are efficiently developed for high-performance ZIBs, which mainly includes an in-situ polymerization of dopamine on Ti3C2 MXene surface and subsequent redox reaction between KMnO4 and polydopamine. Benefited from the conductive MXene nanosheets for fast electron transfer, and the thin thickness of δ-MnO2 nanosheets for improved Zn2+ insertion kinetics and structural stability, the δ-MnO2/MXene heteronanosheets exhibit unique Zn2+-exclusive storage mechanism without proton storage induced disadvantages (e.g., Mn dissolution in traditional aqueous electrolytes) and superior zinc storage performance in 0.5 M zinc triflate in triethyl phosphate organic electrolyte (Zn(OTf)2/TEP), offering a capacity of ∼163 mAh g−1 at 100 mA g−1, a high capacity retention of 84.5 % after 1000 cycles, and an areal capacity of 1.9 mAh cm−2 when the mass loading is up to 10.5 mg cm−2. This work provides unique Zn2+-exclusive storage mechanism of δ-MnO2 in organic electrolyte and opens up a new approach for building high-performance ZIBs.
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