相容性(地球化学)
分离器(采油)
复合数
材料科学
陶瓷
烧结
电解质
阳极
阴极
化学工程
复合材料
化学
物理化学
工程类
电极
物理
热力学
作者
Christoph Roitzheim,Yoo Jung Sohn,Liang‐Yin Kuo,Grit Häuschen,Markus Mann,Doris Sebold,Martin Finsterbusch,Payam Kaghazchi,Olivier Guillon,Dina Fattakhova‐Rohlfing
标识
DOI:10.1021/acsaem.2c00533
摘要
Garnet-based all-solid-state batteries (ASBs) with high energy density require composite cathodes with high areal loading and high-capacity cathode active materials. While all ceramic cathodes can typically be manufactured via cosintering, the elevated temperatures necessary for this process pose challenges with respect to material compatibility. High-capacity cathode active materials like Ni-rich LiNixCoyMn1–x–yO2 (NCM) show insufficient material compatibility toward the solid electrolyte Li6.45Al0.05La3Zr1.6Ta0.4O12 (LLZO:Ta) during cosintering, leading to the formation of highly resistive interphases. We investigated this secondary phase formation both experimentally and via density functional theory calculation to get a mechanistic understanding of the cosintering behavior of LLZO:Ta with NCM111 and Ni-rich NCM811. Furthermore, we employed B doping of both NCM materials in order to assess its impact on the cation interchange and subsequent secondary phase formation. While secondary phases were formed for all four NCM materials, their onset temperature, nature, and amount strongly depend on the NCM composition and doping. Surprisingly, Ni-rich NCM811 turned out to be the most promising cathode active material for the combination with garnet-type LLZO:Ta. As proof of concept, fully inorganic, ceramic all-solid-state lithium batteries featuring only a Li-metal anode, an LLZO:Ta separator, and a composite cathode, consisting of LLZO:Ta, Li3BO3, and NCM811, were prepared by conventional sintering. The purely inorganic full cells delivered a high specific areal discharge capacity of 0.7 mA h cm–2 in the initial cycle.
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