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  • Wiley  (2)
  • Yan, Zhenhua  (2)
  • Physics  (2)
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  • Wiley  (2)
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  • Physics  (2)
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  • 1
    In: Advanced Materials, Wiley
    Abstract: Layered oxides represent a prominent class of cathode materials extensively employed in lithium‐ion batteries. The structural degradation of layered cathodes causes the capacity decay during battery cycling, which is generally induced by anisotropic lattice strain in the bulk of the cathode particle and undesirable oxygen release at the surface. However, particularly in lithium‐rich layered oxides (LLOs) that undergo intense oxygen redox reactions, the challenge of simultaneously addressing bulk and surface issues through a singular modification technique remains arduous. Here we construct a thin (1‐nm) and coherent spinel‐like phase on the surface of LLOs particle (Li x Mn 0.54 Ni 0.13 Co 0.13 O 2 ) to suppress bulk strain and surface O 2 release by just adjusting the amount of lithium source during synthesis. The spinel‐like phase hinders the surface O 2 release by accommodating O 2 inside the surface layer, while the trapped O 2 in the bulk lattice impedes strain evolution by about 70% at high voltages compared with unmodified LLOs cathodes. Consequently, the enhanced structural stability in bulk and surface leads to a significantly improved capacity retention of 97.6% and a high Coulombic efficiency of about 99.5% after 100 cycles at a rate of 0.1 C. Our findings provide profound mechanistic insights into the functioning of surface structure and offer guidance for synthesizing high‐capacity cathodes with superior cyclability. This article is protected by copyright. All rights reserved
    Type of Medium: Online Resource
    ISSN: 0935-9648 , 1521-4095
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1474949-X
    Location Call Number Limitation Availability
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  • 2
    In: Advanced Materials, Wiley, Vol. 34, No. 15 ( 2022-04)
    Abstract: The metal anode is the pivotal component for advanced sodium‐metal batteries such as Na–O 2 batteries. Designing a 3D confinement scaffold is a promising strategy for constructing dendrite‐free sodium‐metal anodes; however, cycling stability at a large current density ( 〉 10 mA cm −2 ) is still difficult to realize. Herein, the design of new lightweight and fibrous hydroxylated Ti 3 C 2 (h‐Ti 3 C 2 ) MXene based scaffolds with stepped sodiophilic gradient structure (h‐M‐SSG) is reported, and its thickness can be controlled (80−250 µm). The sodiophilic gradient structure (adjusted by h‐Ti 3 C 2 ) can effectively induce sodium ions to preferentially deposit at the bottom of the scaffold, thus inhibiting dendrite growth. h‐M‐SSG/Na‐based symmetrical batteries exhibit a low polarization voltage and long cycling life at a high current density (40 mA cm −2 ) and a high cut‐off capacity (40 mAh cm −2 ). Moreover, a Na–O 2 battery with an h‐M‐SSG/Na anode exhibits a low potential gap of 0.137 V after 45 cycles at 1000 mA g −1 and 1000 mAh g −1 . This deposition‐regulation strategy would inspire the design of 3D scaffolds for high‐performance sodium‐metal‐anode‐based batteries.
    Type of Medium: Online Resource
    ISSN: 0935-9648 , 1521-4095
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1474949-X
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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