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Advances and Challenges in Multivalent Chemistries for Energy Storage

机译:储能多价化学的进步与挑战

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摘要

TE Modeling assumptions: 1.Cycle life = 1000 cycles 2. Excess MV metal limited to 50% 3. Electrolyte volume: lean condition 4. Energy accessible at C/5 & 25℃ 5. Electrode loading to 20 mg/cm2 a. Can Mg-ion have appreciable transport in solid-state oxides? 1) To date: limited known working cathodes (low voltage -1.1 V vs Mg/Mg~(2+)), e.g., Mo_6S_8· b. Can electrolytes have wide electrochemical operating window? 1)< 4 V vs Mg/Mg~(2+) and retain efficient plating/stripping 1. Yes, Mobility energy barrier can be low for Mg 2. Electrochemical Mg removal at high voltage is possible 3. Some evidence of reversibility is possible seen 4. E_a is not be the complete story: more to it than energy barrier 5. Interfacial transport, kinetics, and stability remain a challenge.
机译:TE建模假设:1.循环寿命= 1000个循环2.过量的中压金属限制为50%3.电解质的体积:稀薄条件4.在C / 5和25℃时可获得的能量5.电极负载为20 mg / cm2 a。镁离子能否在固态氧化物中有明显的迁移? 1)迄今为止:有限的已知工作阴极(低电压-1.1 V vs Mg / Mg〜(2+)),例如Mo_6S_8·b。电解质能否具有宽阔的电化学工作范围? 1)<4 V vs Mg / Mg〜(2+),并保持有效的电镀/剥离1.是的,Mg的移动能垒可能较低2.可以在高压下去除电化学Mg 3.某些可逆性证据见4. E_a并不是完整的故事:它不仅仅是能量屏障。5.界面传输,动力学和稳定性仍然是一个挑战。

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  • 来源
  • 会议地点 Mainz(DE)
  • 作者

    BRIAN J. INGRAM;

  • 作者单位

    Multivalent Intercalation Lead Joint Center for Energy Storage Research Argonne National Laboratory;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
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