Related Experiment Video
Updated: May 25, 2025

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
Published on: August 12, 2013
Chemical Compatibility of Li1.3Al0.3Ti1.7(PO4)3 Solid-State Electrolyte Co-Sintered with Li4Ti5O12 Anode for
Jiangtao Li1,2, Mingsheng Ma1,2, Ya Mao3
1State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201899, China.
Abstract:
Multilayer ceramic lithium batteries (MLCBs) are regarded as a new type of oxide-based all-solid-state microbattery for integrated circuits and various wearable devices. The chemical compatibility between the solid electrolyte and electrode active materials during the high-temperature co-sintering process is crucial for determining the structural stability and cycling performance of MLCBs. This study focuses on the typical MLCB composite electrodes composed of the NASICON-type Li1.3Al0.3Ti1.7(PO4)3 (LATP) solid electrolyte and the spinel-type Li4Ti5O12 (LTO) anode material. The thermal behavior, phase structure, morphological evolution, and elemental chemical states of these composite electrodes were systematically investigated over a co-sintering temperature range of 400-900 °C. The results indicate that the reactivity between LATP and LTO during co-sintering is primarily driven by the diffusion of Li from the LTO anode, leading to the formation of TiO2, Li3PO4, and LiTiOPO4. Furthermore, the co-sintered LATP-LTO multilayer composites reveal that the generation of Li3PO4 at the LATP/LTO interface facilitates their co-sintering integration at 800-900 °C, which is essential for the successful fabrication of MLCBs. These findings provide direct evidence and valuable references for the structural and performance optimization of MLCBs in the future.
Related Concept Videos
Comparing Intermolecular Forces: Melting Point, Boiling Point, and Miscibility
Temporary attractive forces like dispersion are present in all molecules, whether they are polar or nonpolar. They...
Extraction: Advanced Methods
Ionic Bonding and Electron Transfer
Alkali Metals
Table 1: Properties of the alkali metals
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Solubility of Ionic Compounds

