4.8 Article

High-Energy-Density Supercapacitors Based on High-Areal-Specific-Capacity Ti3C2Tx and a Redox-Active Organic-Molecule Hybrid Electrode

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 32, 期 48, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202208403

关键词

hybrid electrodes; photorechargeable; solar cells; specific capacity; supercapacitors

资金

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA17040506]
  2. National Nature Science Foundation of China [U20A20252, U21A20102, 62174103]
  3. Innovation Fund Project of Dalian Institute of Chemical Physics [DICP I202025, DICP I202032]
  4. Cooperation Foundation of Dalian National Laboratory For Clean Energy of the Chinese Academy of Sciences [DNL202015]
  5. Natural Science Foundation of Liaoning Province [2021-MS-016]
  6. Youth Science and Technology Star Project of Dalian [2021RQ121]
  7. 111 Project [B1404]
  8. Transformational Technologies for Clean Energy and Demonstration, Strategic Priority Research Program of the Chinese Academy of Sciences [XDA21061001, XDA21061002]
  9. Fundamental Research Funds for the Central Universities [GK202103106]
  10. Shanxi Science and Technology Department [20201101012]
  11. Project of Knowledge Innovation Engineering [Y261261606]

向作者/读者索取更多资源

Photorechargeable supercapacitors with enhanced energy density were achieved by utilizing organic-inorganic hybrid electrodes. The covalent cross-linking of organic molecules on Ti3C2Tx was shown to improve ion absorption and storage, increasing the energy density of supercapacitors.
Photorechargeable supercapacitors are perfect energy storage devices, particularly for solar cells that output electricity only during sunshine hours. The lower energy density of supercapacitors is due to fewer redox-active sites, poor electrolyte accessibility at the electrodes, and charge loss during charge transfer from solar cells to the supercapacitor. Here, an electrolyte-accessible organic-inorganic hybrid electrode with synergistic pseudocapacitance of Ti3C2Tx and high theoretical specific capacity C(sic)O active centers to enhance the energy density of the supercapacitor is proposed. Density functional theory (DFT) calculations show that the covalent cross-linking of organic molecules changes the charge density redistribution of Ti3C2Tx, enhances ion absorption and storage, and increases the energy density of the supercapacitors. Based on these DFT calculation results, hybrid electrodes are successfully prepared using p-phenylene diisocyanate to covalently cross-link pseudocapacitors Ti3C2Tx with anthraquinone such as 1-hydroxyanthraquinone (HA) or 1-amino-4-bromoanthraquinone-2-sodium sulfonate (ABS). The Ti3C2Tx-HA hybrid electrodes exhibit high areal specific capacity (2532.5 mF cm(-2)), excellent ion absorption storage capability, and long-term stability. The asymmetric supercapacitor yields a decent area specific capacity (1686.72 mF cm(-2) at 0.25 mA cm(-2)) and energy density (599.72 mWh cm(-2) at a power density of 200 mW cm(-2)). These high-energy-density supercapacitors are coupled with perovskite solar cells to prepare photorechargeable supercapacitors with fast energy storage.

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