材料科学
膜
电解质
多孔性
烧结
电流密度
空隙(复合材料)
储能
制作
化学工程
陶瓷
纳米技术
复合材料
电极
工程类
物理
生物
病理
物理化学
功率(物理)
化学
医学
替代医学
量子力学
遗传学
作者
Huanyu Zhang,Faruk Okur,Bharat Pant,Matthias Klimpel,Sofiia Butenko,Dogan Tarik Karabay,Annapaola Parrilli,A. Neels,Ye Cao,Kostiantyn V. Kravchyk,Maksym V. Kovalenko
标识
DOI:10.1021/acsami.3c14422
摘要
Rechargeable garnet-based solid-state Li batteries hold immense promise as nonflammable, nontoxic, and high energy density energy storage systems, employing Li7La3Zr2O12 (LLZO) with a garnet-type structure as the solid-state electrolyte. Despite substantial progress in this field, the advancement and eventual commercialization of garnet-based solid-state Li batteries are impeded by void formation at the LLZO/Li interface at practical current densities and areal capacities beyond 1 mA cm-2 and 1 mAh cm-2, respectively, resulting in limited cycling stability and the emergence of Li dendrites. Additionally, developing a fabrication approach for thin LLZO electrolytes to achieve high energy density remains paramount. To address these critical challenges, herein, we present a facile methodology for fabricating self-standing, 50 μm thick, porous LLZO membranes with a small pore size of ca. 2.3 μm and an average porosity of 51%, resulting in a specific surface area of 1.3 μm-1, the highest reported to date. The use of such LLZO membranes significantly increases the Li/LLZO contact area, effectively mitigating void formation. This methodology combines two key elements: (i) the use of small pore formers of ca. 1.5 μm and (ii) the use of ultrafast sintering, which circumvents ceramics overdensification using rapid heating/cooling rates of ca. 50 °C per second. The fabricated porous LLZO membranes demonstrate exceptional cycling stability in a symmetrical Li/LLZO/Li cell configuration, exceeding 600 h of continuous operation at a current density of 0.1 mA cm-2.
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