材料科学
锂(药物)
金属锂
电极
金属
沉积(地质)
电池(电)
中子散射
纳米技术
光电子学
散射
光学
冶金
电解质
物理化学
化学
医学
古生物学
功率(物理)
物理
量子力学
沉积物
生物
内分泌学
作者
Christophe Didier,Elliot P. Gilbert,Jitendra Mata,Vanessa K. Peterson
标识
DOI:10.1002/aenm.202301266
摘要
Abstract Despite being the major cause of safety and performance issues in lithium metal batteries, experimental difficulties in quantifying directly the morphology of lithium deposited at electrode surfaces have meant that the mechanism of metallic lithium growth within batteries remains elusive. This study demonstrates that quantitative detail about the morphology of metallic lithium within batteries can be derived non‐destructively and directly using in situ ultra‐small and small‐angle neutron scattering. This information is obtained over a large electrode area in cells where lithium deposition processes are typical of real‐world applications. Complex variations of surface area and interfacial distances 1–10 µm and 100–300 nm are revealed in size that are influenced by current density and cell cycling history, providing valuable insight into the growth of metallic lithium features detrimental to battery performance. Such quantitative insight into the process of lithium growth is required for the development of safer high‐performance lithium metal batteries.
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