Direct Visualization of Metastable Charged States in Positive Electrode Materials by Cryo-STEM
Source abstract
Abstract
LiNiO 2 is regarded as an ideal positive electrode material for Li-ion battery applications, offering a large reversible capacity, >200 mA h g –1, with a lower cutoff voltage, 4.3 V. The fully charged state, Li 1– x NiO 2 ( x ≈ 0.9), is a metastable phase obtained by electrochemical oxidation in Li cells. Due to its instability, atomic-scale imaging of this phase by using scanning transmission electron microscopy (STEM) is particularly challenging, as it readily decomposes under electron beam exposure. In this study, the effect of cryogenic conditions during STEM observation is examined. While as-prepared LiNiO 2 shows strong resistance to beam damage, Li 1– x NiO 2 ( x ≈ 0.9) undergoes structural changes under room-temperature beam exposure. In contrast, beam-induced damage is substantially suppressed under cryogenic conditions (−150 °C), enabling successful acquisition of atomic-resolution STEM images. These findings underscore the importance of cryo-STEM techniques for imaging metastable battery materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Transition Metal Oxide Nanomaterials · Advancements in Battery Materials · Gas Sensing Nanomaterials and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Life Science, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa 240-8501, Japan
Advanced Chemical Energy Research Center, Institute of Advanced Sciences
Yokohama National University
Tsukuba Satellite Laboratory
Sumika Chemical Analysis Service, Ltd.
Funding
Ministry of Education, Culture, Sports, Science and Technology · Japan Society for the Promotion of Science · Japan Science and Technology Agency
References (23)
Show source-provided references
1. 10.1021/acsenergylett.7b0030410.1021/acsenergylett.7b00304 ↗
2. 10.1149/2.0381813jes10.1149/2.0381813jes ↗
3. 10.1021/acsami.2c1342110.1021/acsami.2c13421 ↗
4. 10.1002/adfm.20221146110.1002/adfm.202211461 ↗
5. 10.1039/D4EE02398F10.1039/D4EE02398F ↗
6. 10.1021/acsami.4c1226210.1021/acsami.4c12262 ↗
7. 10.5796/electrochemistry.25-0010310.5796/electrochemistry.25-00103 ↗
8. 10.1039/D1TA03066C10.1039/D1TA03066C ↗
9. 10.1016/j.ensm.2024.10320010.1016/j.ensm.2024.103200 ↗
10. 10.1016/j.trechm.2023.07.00310.1016/j.trechm.2023.07.003 ↗
11. 10.1039/D3EE04354A10.1039/D3EE04354A ↗
12. 10.1039/D1EE01678D10.1039/D1EE01678D ↗
13. 10.1016/j.isci.2021.10340210.1016/j.isci.2021.103402 ↗
14. 10.1002/aenm.20200175310.1002/aenm.202001753 ↗
15. 10.1016/0167-2738(94)90415-410.1016/0167-2738(94)90415-4 ↗
16. 10.1021/acsami.5b1208110.1021/acsami.5b12081 ↗
17. 10.1038/s41563-022-01421-z10.1038/s41563-022-01421-z ↗
18. 10.1021/acsami.9b1560810.1021/acsami.9b15608 ↗
19. 10.1021/jp050486b10.1021/jp050486b ↗
20. 10.1016/j.oceram.2023.10049410.1016/j.oceram.2023.100494 ↗
21. 10.1038/s41563-025-02144-710.1038/s41563-025-02144-7 ↗
22. 10.1039/D4TA07033J10.1039/D4TA07033J ↗
23. 10.1016/j.mtener.2025.10196210.1016/j.mtener.2025.101962 ↗