4.8 Article

A single-ion conducting covalent organic framework for aqueous rechargeable Zn-ion batteries

期刊

CHEMICAL SCIENCE
卷 11, 期 43, 页码 11692-11698

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc02785e

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资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [2018R1A2A1A05019733, 2018M3D1A1058624]
  2. Samsung Research Funding Centre of Samsung Electronics [SRFC-MA1702-04]
  3. Basic Science Research Program through the NRF - Ministry of Education [2017R1D1A1B03033699, 2020R1I1A1A01064798]
  4. ERC [NRF-2014R1A5A1009799]
  5. National Research Foundation of Korea [2020R1I1A1A01064798, 2017R1D1A1B03033699] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Despite their potential as promising alternatives to current state-of-the-art lithium-ion batteries, aqueous rechargeable Zn-ion batteries are still far away from practical applications. Here, we present a new class of single-ion conducting electrolytes based on a zinc sulfonated covalent organic framework (TpPa-SO3Zn0.5) to address this challenging issue. TpPa-SO3Zn0.5 is synthesised to exhibit single Zn2+ conduction behaviour via its delocalised sulfonates that are covalently tethered to directional pores and achieve structural robustness by its beta-ketoenamine linkages. Driven by these structural and physicochemical features, TpPa-SO3Zn0.5 improves the redox reliability of the Zn metal anode and acts as an ionomeric buffer layer for stabilising the MnO2 cathode. Such improvements in the TpPa-SO3Zn0.5-electrode interfaces, along with the ion transport phenomena, enable aqueous Zn-MnO2 batteries to exhibit long-term cyclability, demonstrating the viability of COF-mediated electrolytes for Zn-ion batteries.

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