Li2O:Li–Mn–O Disordered Rock‐Salt Nanocomposites as Cathode Prelithiation Additives for High‐Energy Density Li‐Ion Batteries
Source abstract
Abstract
Abstract The irreversible loss of lithium from the cathode material during the first cycles of rechargeable Li‐ion batteries notably reduces the overall cell capacity. Here, a new family of sacrificial cathode additives based on Li2O:Li2/3Mn1/3O5/6 composites synthesized by mechanochemical alloying is reported. These nanocomposites display record (but irreversible) capacities within the Li–Mn–O systems studied, of up to 1157 mAh g−1, which represents an increase of over 300% of the originally reported capacity in Li2/3Mn1/3O5/6 disordered rock salts. Such a high irreversible capacity is achieved by the reaction between Li2O and Li2/3Mn1/3O5/6 during the first charge, where electrochemically active Li2O acts as a Li+ donor. A 13% increase of the LiFePO4 and LiCoO2 first charge gravimetric capacities is demonstrated by the addition of only 2 wt% of the nanosized composite in the cathode mixture. This result shows the great potential of these newly discovered sacrificial additives to counteract initial losses of Li+ ions and improve battery performance.
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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
ISIS Facility STFC Rutherford Appleton Laboratory Didcot OX11 0QX UK
Diamond Light Source Ltd. Diamond House Harwell Science and Innovation Campus Didcot OX11 0DE UK
Institut Néel CNRS Grenoble Alpes Université 38000 Grenoble France
SAFT 111‐113 Bd Alfred Daney 33074 Bordeaux France
Crismat CNRS Unicaen Ensicaen Normandie Université 14000 Caen France
Funding
Agence Nationale de la Recherche
References (31)
Show source-provided references
1. 10.1149/1.204866510.1149/1.2048665 ↗
2. 10.1016/j.jpowsour.2009.01.00710.1016/j.jpowsour.2009.01.007 ↗
3. 10.1021/nn201716710.1021/nn2017167 ↗
4. 10.1016/j.jpowsour.2011.11.06010.1016/j.jpowsour.2011.11.060 ↗
5. 10.1016/j.jpowsour.2005.07.05110.1016/j.jpowsour.2005.07.051 ↗
6. 10.1016/j.jpowsour.2014.02.11210.1016/j.jpowsour.2014.02.112 ↗
7. 10.1016/j.jpowsour.2005.03.02310.1016/j.jpowsour.2005.03.023 ↗
8. 10.1038/ncomms608810.1038/ncomms6088 ↗
9. 10.1016/j.elecom.2010.07.01610.1016/j.elecom.2010.07.016 ↗
10. 10.1002/chem.20180180910.1002/chem.201801809 ↗
11. 10.1016/S0013-4686(00)00395-910.1016/S0013-4686(00)00395-9 ↗
12. Gyu M. · J. Mater. Chem. · 2008 · 3 · 5880
13. 10.1149/2.085208jes10.1149/2.085208jes ↗
14. 10.1016/S0378-7753(03)00236-210.1016/S0378-7753(03)00236-2 ↗
15. 10.1002/adma.20100071710.1002/adma.201000717 ↗
16. 10.1039/C7QM00175D10.1039/C7QM00175D ↗
17. 10.1038/nenergy.2015.810.1038/nenergy.2015.8 ↗
18. 10.1002/aenm.20160015410.1002/aenm.201600154 ↗
19. 10.1021/acs.nanolett.5b0522810.1021/acs.nanolett.5b05228 ↗
20. 10.1002/aenm.20150253410.1002/aenm.201502534 ↗
21. 10.1038/nmat447910.1038/nmat4479 ↗
22. 10.1039/C5CC08034G10.1039/C5CC08034G ↗
23. 10.1016/j.jpowsour.2017.09.06010.1016/j.jpowsour.2017.09.060 ↗
24. 10.1039/C7EE03195E10.1039/C7EE03195E ↗
25. 10.1016/j.elecom.2015.08.00310.1016/j.elecom.2015.08.003 ↗
26. 10.1038/s41586-018-0015-410.1038/s41586-018-0015-4 ↗
27. 10.1002/smll.20190246210.1002/smll.201902462 ↗
28. 10.1039/C8TA00234G10.1039/C8TA00234G ↗
29. 10.1021/acs.jpcc.8b0939710.1021/acs.jpcc.8b09397 ↗
30. 10.1038/3503504510.1038/35035045 ↗
31. 10.1021/ja202174710.1021/ja2021747 ↗