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Surface Chemistry Mechanism of Ultra-Low Interfacial Resistance in the Solid-State Electrolyte Li7La3Zr2O12

机译:固态电解质Li7La3zR2O12中超低界面抗性的表面化学机制

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摘要

The impact of surface chemistry on the interfacial resistance between the Li7La3Zr2O12 (LLZO) solid-state electrolyte and a metallic Li electrode is revealed. Control of surface chemistry allows the interfacial resistance to be reduced to 2 Omega cm(2), lower than that of liquid electrolytes, without the need for interlayer coatings. A mechanistic understanding of the origins of ultra-low resistance is provided by quantitatively evaluating the linkages between interfacial chemistry, Li wettability, and electrochemical phenomena. A combination of Li contact angle measurements, X-ray photoelectron spectroscopy (XPS), first-principles calculations, and impedance spectroscopy demonstrates that the presence of common LLZO surface contaminants, Li2CO3 and LiOH, result in poor wettability by Li and high interfacial resistance. On procedure for removing these surface layers is demonstrated, which results in a dramatic increase in Li wetting and the elimination of nearly all interfacial resistance. The low interfacial resistance is maintained over one-hundred cycles and suggests a straightforward pathway to achieving high energy and power density solid-state batteries.
机译:揭示了表面化学对Li7La3zR2O12(LLZO)固态电解质和金属Li电极之间的界面抗性的影响。表面化学的控制允许界面抗性降至2ωcm(2),低于液体电解质的2℃,而不需要夹层涂层。通过定量评估界面化学,锂润湿性和电化学现象之间的联系来提供对超低电阻的起源的机械理解。 Li接触角测量,X射线光电子能谱(XPS),第一原理计算和阻抗光谱的组合表明,常见的LLZO表面污染物,Li2CO3和LiOH的存在导致Li和高界面抗性差。在去除这些表面层的过程中,证明了Li润湿和消除几乎所有界面抗性的显着增加。低界面抗性保持超过一百个循环,并表明了实现高能量和功率密度固态电池的直接路径。

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