Investigation of Thermal Stability of P2–NaxCoO2 Cathode Materials for Sodium Ion Batteries Using Real-Time Electron Microscopy
Source abstract
Abstract
Here, we take advantage of in situ transmission electron microscopy (TEM) to investigate the thermal stability of P2-type Na x CoO 2 cathode materials for sodium ion batteries, which are promising candidates for next-generation lithium ion batteries. A double-tilt TEM heating holder was used to directly characterize the changes in the morphology and the crystallographic and electronic structures of the materials with increase in temperature. The electron diffraction patterns and the electron energy loss spectra demonstrated the presence of cobalt oxides (Co 3 O 4, CoO) and even metallic cobalt (Co) at higher temperatures as a result of reduction of Co ions and loss of oxygen. The bright-field TEM images revealed that the surface of Na x CoO 2 becomes porous at high temperatures. Higher cutoff voltages result in degrading thermal stability of Na x CoO 2 . The observations herein provide a valuable insight that thermal stability is one of the important factors to be considered in addition to the electrochemical properties when developing new electrode materials for novel battery systems.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Extraction and Separation Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Energy Convergence, Korea Institute of Science and Technology (KIST), Seoul 02792, Republic of Korea
Carbon Composite Materials Research Centre, Institute of Advanced Composite Materials, KIST, Wanju-gun 55324, Republic of Korea
Funding
Korea Institute of Science and Technology · Brookhaven National Laboratory
References (22)
Show source-provided references
1. 10.1002/aenm.20120002610.1002/aenm.201200026 ↗
2. 10.1021/cr500192f10.1021/cr500192f ↗
3. 10.1038/nmat292010.1038/nmat2920 ↗
4. 10.1038/nmat330910.1038/nmat3309 ↗
5. 10.1149/2.002201esl10.1149/2.002201esl ↗
6. 10.1016/j.electacta.2012.09.05810.1016/j.electacta.2012.09.058 ↗
7. 10.1016/0378-4363(80)90214-410.1016/0378-4363(80)90214-4 ↗
8. 10.1039/c1ee01782a10.1039/c1ee01782a ↗
9. 10.1149/1.209540710.1149/1.2095407 ↗
10. 10.1021/ja053056810.1021/ja0530568 ↗
11. 10.1021/cm303096e10.1021/cm303096e ↗
12. 10.1021/am503278f10.1021/am503278f ↗
13. 10.1021/acs.chemmater.5b0070910.1021/acs.chemmater.5b00709 ↗
14. 10.1149/2.102205jes10.1149/2.102205jes ↗
15. 10.1149/2.007305jes10.1149/2.007305jes ↗
16. 10.1039/C5EE00695C10.1039/C5EE00695C ↗
17. 10.1038/nmat477710.1038/nmat4777 ↗
18. 10.1021/cm403332s10.1021/cm403332s ↗
19. 10.1016/j.ssc.2005.02.00610.1016/j.ssc.2005.02.006 ↗
20. 10.1046/j.1365-2818.2001.00898.x10.1046/j.1365-2818.2001.00898.x ↗
21. 10.1103/PhysRevB.69.23510310.1103/PhysRevB.69.235103 ↗
22. 10.1063/1.348201310.1063/1.3482013 ↗