Source abstract
Abstract
While α-MnO2 has been intensively studied for zinc batteries, δ-MnO2 is usually believed to be more suitable for ion storage with its layered structure. Unfortunately, the extraordinary Zn ion storage performance that δ-MnO2 should exhibit has not yet been achieved due to the frustrating structural degradation during charge–discharge cycles. Here, we found the Na ion and water molecules pre-intercalation can effectively activate stable Zn ion storage of δ-MnO2. Our results reveal that the resulted Zn//pre-intercalated δ-MnO2 battery delivers an extraordinarily high-rate performance, with a high capacity of 278 mAh g–1 at 1 C and up to 20 C, and a high capacity of 106 mAh g–1 can still be measured. The capacity retention is as high as 98% after charged–discharged up to 10,000 cycles benefiting from smooth Zn ion diffusion in the pre-intercalated structure. Further in situ/ex situ characterization confirms the superfast Zn ion diffusion in the pre-intercalated structure at room temperature. In addition, utilizing the well-chosen electrode material and modified polyurethane shell, we fabricated a quasi-solid-state healable Zn-δ-MnO2, which can be self-healed after multiple catastrophic damages, emphasizing the advanced features of aqueous Zn ion battery for wearable applications.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China
Department of Chemistry, Capital Normal University, 105 West Third Ring Road North, Haidian District, Beijing 100048, P.R. China
Shenzhen Research Institute, City University of Hong Kong, Shenzhen 518057, P.R. China
Funding
Research Grants Council, University Grants Committee · National Natural Science Foundation of China · Science Technology and Innovation Committee of Shenzhen Municipality