Tailoring hierarchical MnO 2 nanostructures on self-supporting cathodes for high-mass-loading zinc-ion batteries
Aqueous zinc-ion batteries (AZIBs) with MnO cathodes have promising application prospects; however, their performance is hindered by their low efficiency and insufficient life. By leveraging the nanomicellar properties of cetyltrimethylammonium bromide (CTAB), a hierarchical δ-MnO with 2D/3D structu...
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Veröffentlicht in: | Chemical science (Cambridge) 2024-11 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aqueous zinc-ion batteries (AZIBs) with MnO
cathodes have promising application prospects; however, their performance is hindered by their low efficiency and insufficient life. By leveraging the nanomicellar properties of cetyltrimethylammonium bromide (CTAB), a hierarchical δ-MnO
with 2D/3D structure was directionally grown on a modified carbon cloth (CC) collector for realizing high-mass-loading AZIBs. Experimental results reveal the synergistic effects of micro/nano hierarchically structured MnO
-CC heterointerfaces in accelerating the electron migration and transfer rate of Zn
/H
. Functioning as a conductive skeleton and flexible substrate, CC efficiently improves the reaction kinetics and buffers the interfacial stress resulting from the structural evolution of MnO
during the long-term electrode reaction. This phenomenon is investigated using advanced characterisation techniques, including X-ray absorption fine structure spectroscopy, Kelvin probe force microscopy, and theoretical simulations. The fabricated electrode exhibits superior electrochemical properties, such as high capacity (409.6 mA h g
at 0.1 A g
) and reliable cycling performance (with 86.6% capacity retention after 2000 cycles at 1.0 A g
). Even at a high mass loading of 6.0 mg cm
, the battery retains 81.8% of its original capacity after 1300 cycles. The proposed interface engineering strategy provides valuable insights into realising high-loading and long-life AZIBs. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/D4SC06182A |