Thermal stability and electrochemical behavior of commercial polycrystalline and single-crystalline cathodes integrated with cubic LiLaZrTaO for all-solid-state lithium batteries

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Vol. 13; no. 32; pp. 26647 - 26659
• Main Authors: Ma, Ziting, LaBriola, Grant, Salazar, Karlo Adrian, Mi, Chunting Chris, Kong, Lingping
• Format: Journal Article
• Published: 12.08.2025
• ISSN: 2050-7488; 2050-7496
• DOI: 10.1039/d5ta03114a

All-solid-state lithium batteries (ASSLBs) have emerged as promising next-generation energy storage systems, offering enhanced safety and higher energy density compared to conventional Li-ion batteries. However, their practical performance remains limited by interfacial instabilities. In this work, we systematically investigate the interfacial reactions and secondary phase formation between garnet-type cubic Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) and a variety of commercial cathode materials, including polycrystalline LiNi 0.5 Mn 1.5 O 4 (pc-LNMO), LiCoO 2 (pc-LCO), LiNi 1− x − y Mn x Co y O 2 (pc-NMC811, 631, 532, 111), and single-crystalline NMC631 (sc-NMC631). Structural analyses reveal that interfacial phase evolution is highly dependent on cathode composition, crystal structure, and sintering temperature. Among all compositions studied, sc-NMC631 exhibits superior thermal compatibility with LLZTO, maintaining phase integrity up to 1000 °C. In contrast, polycrystalline cathodes undergo distinct interfacial degradation: La 2 Zr 2 O 7 and LaCoO 3 form at 700 °C in pc-LCO + LLZTO, while Li 2 MnO 3 and La 2 Zr 2 O 7 emerge as early as 400 °C in pc-LNMO + LLZTO. In pc-NMC + LLZTO composites, LaMO 3 -type (M: Ni, Mn, Co) phases are consistently observed. Additionally, La 2 (Ni 0.5 Li 0.5 )O 4 phase is present in these Ni-rich compositions and Li 2 MnO 3 is in the Ni-lean NMC111. Electrochemical studies reveal a 63% capacity loss in pc-NMC631 + LLZTO-900, primarily due to resistive interfacial phases and poor solid–solid contact that impede Li-ion transport. In comparison, sc-NMC631 + LLZTO-900 demonstrates a lower capacity loss of 48%, attributed to enhanced interfacial stability over its polycrystalline counterpart. However, the remaining capacity loss is likely due to misaligned Li-ion transport pathways across the rigid solid–solid interface. These results highlight the critical role of cathode selection and interface engineering in garnet-based ASSLBs and establish sc-NMC631 as a promising candidate for high-performance composite cathodes. All-solid-state lithium batteries (ASSLBs) have emerged as promising next-generation energy storage systems, offering enhanced safety and higher energy density compared to conventional Li-ion batteries.