Sun Shuo, Han Zhen, Liu Wei, Xia Qiuying, Xue Liang, Lei Xincheng, Zhai Teng, Su Dong, Xia Hui
School of Materials Science and Engineering, Nanjing University of Science and Technology, 210094, Nanjing, PR China.
Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, China.
Nat Commun. 2023 Oct 20;14(1):6662. doi: 10.1038/s41467-023-42335-x.
Large lattice expansion/contraction with Li intercalation/deintercalation of electrode active materials results in severe structural degradation to electrodes and can negatively impact the cycle life of solid-state lithium-based batteries. In case of the layered orthorhombic MoO (α-MoO), its large lattice variation along the b axis during Li insertion/extraction induces irreversible phase transition and structural degradation, leading to undesirable cycle life. Herein, we propose a lattice pinning strategy to construct a coherent interface between α-MoO and η-MoO with epitaxial intergrowth structure. Owing to the minimal lattice change of η-MoO during Li insertion/extraction, η-MoO domains serve as pin centers that can effectively suppress the lattice expansion of α-MoO, evidenced by the noticeably decreased lattice expansion from about 16% to 2% along the b direction. The designed α-MoO/η-MoO intergrown heterostructure enables robust structural stability during cycling (about 81% capacity retention after 3000 cycles at a specific current of 2 A g and 298 ± 2 K) by harnessing the merits of epitaxial stabilization and the pinning effect. Finally, benefiting from the stable positive electrode-solid electrolyte interface, a highly durable and flexible all-solid-state thin-film lithium microbattery is further demonstrated. This work advances the fundamental understanding of the unstable structure evolution for α-MoO, and may offer a rational strategy to develop highly stable electrode materials for advanced batteries.
电极活性材料在锂嵌入/脱嵌过程中发生的大晶格膨胀/收缩会导致电极严重的结构退化,并可能对固态锂基电池的循环寿命产生负面影响。以层状正交晶系的MoO(α-MoO)为例,其在锂嵌入/脱出过程中沿b轴的大晶格变化会引发不可逆的相变和结构退化,从而导致不理想的循环寿命。在此,我们提出一种晶格钉扎策略,以构建具有外延共生结构的α-MoO与η-MoO之间的相干界面。由于η-MoO在锂嵌入/脱出过程中的晶格变化最小,η-MoO域充当钉扎中心,可有效抑制α-MoO的晶格膨胀,这一点可从沿b方向晶格膨胀明显从约16%降至2%得到证明。通过利用外延稳定化和钉扎效应的优点,设计的α-MoO/η-MoO共生异质结构在循环过程中实现了强大的结构稳定性(在2 A g的特定电流和298±2 K下3000次循环后容量保持率约为81%)。最后,受益于稳定的正极-固体电解质界面,进一步展示了一种高度耐用且灵活的全固态薄膜锂微型电池。这项工作推进了对α-MoO不稳定结构演变的基本理解,并可能为开发用于先进电池的高度稳定电极材料提供一种合理策略。