يعرض 1 - 10 نتائج من 1,558 نتيجة بحث عن '"Ryoji Kanno"', وقت الاستعلام: 0.75s تنقيح النتائج
  1. 1
    دورية أكاديمية

    المصدر: Communications Materials, Vol 5, Iss 1, Pp 1-14 (2024)

    الوصف: Abstract All-solid-state lithium–sulfur batteries exhibit high energy densities, operate safely, and suppress polysulfide shuttling. However, their electrochemical performance is restricted by the insulating nature of sulfur and Li2S, and by severe cathode-related volumetric changes during cycling. Here, we prepare a Li2S-based cathode composite with high mixed-conductivity and stability, by infiltrating a Li2S–LiI active material solution into a mesoporous carbon replica with ~10-nm-sized pores, followed by mixing with a liquid-phase-synthesized Li6PS5Br solid electrolyte and vapour-grown carbon fibres. Benefiting from a mechanically reinforced, three-dimensional ion/electron-conducting structure, the cathode exhibits high discharge capacity (1009 mAh g−1, 20 cycles, 298 K, 0.05 C) and high reversible capacity (650 mAh g−1, 100 cycles, 298 K, 0.1 C). These findings underscore the feasibility of developing high-performance all-solid-state lithium-sulfur batteries by designing three-dimensional mixed-conducting mechanically robust cathodes.

    وصف الملف: electronic resource

  2. 2
    دورية أكاديمية

    المصدر: Advanced Materials Interfaces, Vol 11, Iss 5, Pp n/a-n/a (2024)

    الوصف: Abstract Information on the cathode/organic–electrolyte interface structure provides clues regarding the rate and reversibility of lithium intercalation reactions in lithium‐ion batteries. Herein, structural changes within the LiCoO2 electrode, throughout the interphase region, and in the LiPF6/propylene carbonate electrolyte are observed concurrently by in situ neutron reflectometry. The formation of an electrical double layer (EDL) during the early stages of charging and discharging is investigated and compared with that at an intercalation‐inactive Nb:SrTiO3 electrode. At the intercalation‐inactive interface between Nb:SrTiO3 and the electrolyte, a voltage‐dependent ionic distribution corresponding to the EDL forms on the electrolyte side without the formation of a cathode/electrolyte interphase (CEI) layer. In contrast, at the intercalation‐active LiCoO2/electrolyte interface, a CEI layer forms immediately after cell construction, and the ionic distribution in the electrolyte formed outside the CEI layer scarcely changes upon voltage application. The CEI/electrolyte interface is shielded from potential changes by the electronically insulating CEI; therefore, structural changes in the EDL are restricted. This supports the prevailing understanding that the CEI layer defines the rates of solvation/de‐solvation and adsorption/desorption reactions of lithium ions.

    وصف الملف: electronic resource

  3. 3
    دورية أكاديمية
  4. 4
    دورية أكاديمية
  5. 5
    دورية أكاديمية
  6. 6
    دورية أكاديمية
  7. 7
    دورية أكاديمية

    المصدر: Electrochemistry, Vol 92, Iss 3, Pp 037008-037008 (2024)

    الوصف: A thin-film battery composed of a LiFePO4 cathode/Li3PO4 electrolyte/Li anode was fabricated on a Pt/Ti/Si (PTS) substrate via RF magnetron sputtering. The amorphous Li3PO4 film was densely stacked on a 60 nm-thick LiFePO4 film, which provided a suitable reaction field for understanding the electrochemical properties of LiFePO4 at the interface with the solid electrolyte. The LiFePO4 cathode film exhibited highly reversible lithium desertion/insertion at the interface at room temperature and 60 °C, without any side reactions. An irreversible oxidation reaction occurred during the initial charging process at 100 °C, leading to an increase in the charge-transfer resistance of the LiFePO4/Li3PO4 interface with no significant decrease in the lithium desertion/insertion capacity of LiFePO4. This result suggests the formation of a resistive interphase via the decomposition of Li3PO4 at 100 °C. A severe decrease in capacity is observed at 125 °C, which indicates the LiFePO4-side interface contributed to the side reactions. The film battery exhibits a severe decrease in capacity at 125 °C.

    وصف الملف: electronic resource

  8. 8
    دورية أكاديمية

    المصدر: Communications Chemistry, Vol 5, Iss 1, Pp 1-9 (2022)

    مصطلحات موضوعية: Chemistry, QD1-999

    الوصف: The electronic structure evolution within a battery during cycling can provide crucial cues for its optimization, but insights on operando band structures are extremely challenging to obtain. Here, the authors determine the overall band structure of a model thin-film solid-state lithium battery via operando hard X-ray photoelectron spectroscopy, considering the cathode and anode sides.

    وصف الملف: electronic resource

  9. 9
    دورية أكاديمية
  10. 10
    دورية أكاديمية

    المصدر: Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)

    مصطلحات موضوعية: Science

    الوصف: Fundamental investigations at the electrode/electrolyte interface are essential for developing high-energy batteries. Here, the authors investigate the degradation mechanisms at the LGPS/NCM622 interface providing a quantitative model to interpret the interfacial resistance growth.

    وصف الملف: electronic resource