Increasing Redox Potential of Pyromellitic Diimide by Chemical Modifications: Toward High‐Voltage Organic Positive Electrode for Lithium Battery
Source abstract
Abstract
Lithium batteries are considered as the most promising electricity storage solution to support the energy transition but still suffer for cost and sustainable issues related to the use of transition metal‐based electrode materials. Due to their reduced environmental footprint and low cost, organic active materials such as carbonyl family (quinone, anhydride, diimide) are some interesting candidates to replace them but electrochemical performances in particular redox potential have to be increased in order to become a viable alternative. Here benefiting from tunability of organic structure and guided by rational design rules based on Hammett theory, new strategies are proposed to increase the redox potential of molecular diimide by introducing electron‐withdrawing groups such as bromine, cyano, or nitro groups. This work can be considered as a first step to develop some competitive positive electrodes materials based on organic molecules or polymers using diimide derivatives.
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Research context
OpenAlex topics: Synthesis and properties of polymers · Inorganic and Organometallic Chemistry · Thermal and Kinetic Analysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CEA, Liten, DEHT University Grenoble Alpes F‐38054 Grenoble France
CEA, CNRS, IRIG, MEM University Grenoble Alpes F‐38054 Grenoble France
Département de Chimie Moléculaire University Grenoble Alpes F‐38000 Grenoble France
Funding
Agence Nationale de la Recherche · Bundesministerium für Bildung und Forschung
References (30)
Show source-provided references
1. European Commission: E. Directorate‐General for Internal Market Industry, SMEs · 2020
2. 10.1038/nmat237210.1038/nmat2372 ↗
3. 10.1002/aenm.20129003710.1002/aenm.201290037 ↗
4. 10.1021/acs.chemrev.9b0048210.1021/acs.chemrev.9b00482 ↗
5. 10.1039/C0CC04440G10.1039/C0CC04440G ↗
6. 10.1002/anie.20100243910.1002/anie.201002439 ↗
7. 10.1021/jz401735910.1021/jz4017359 ↗
8. 10.1016/j.jpowsour.2018.05.05110.1016/j.jpowsour.2018.05.051 ↗
9. 10.1039/D3MA00805C10.1039/D3MA00805C ↗
10. 10.1039/C5TA02043C10.1039/C5TA02043C ↗
11. 10.1021/acsami.6b0759110.1021/acsami.6b07591 ↗
12. 10.1016/j.jpowsour.2020.22881410.1016/j.jpowsour.2020.228814 ↗
13. 10.1021/acsnano.0c0589610.1021/acsnano.0c05896 ↗
14. 10.1021/cr00002a00410.1021/cr00002a004 ↗
15. 10.1039/B400562G10.1039/B400562G ↗
16. 10.1002/chem.20070007910.1002/chem.200700079 ↗
17. 10.1002/cber.1919052084010.1002/cber.19190520840 ↗
18. 10.1002/jlac.1931488010710.1002/jlac.19314880107 ↗
19. 10.1149/1.210045810.1149/1.2100458 ↗
20. 10.1149/1.208669010.1149/1.2086690 ↗
21. 10.1038/nmat502910.1038/nmat5029 ↗
22. 10.1002/anie.20180783610.1002/anie.201807836 ↗
23. 10.1039/C4SC03671A10.1039/C4SC03671A ↗
24. 10.1002/elan.20206016310.1002/elan.202060163 ↗
25. 10.1002/chem.20190279510.1002/chem.201902795 ↗
26. 10.1021/cg100525h10.1021/cg100525h ↗
27. 10.1002/wcms.8110.1002/wcms.81 ↗
28. 10.1002/wcms.160610.1002/wcms.1606 ↗
29. 10.1063/5.004002110.1063/5.0040021 ↗
30. 10.1002/jcc.2613910.1002/jcc.26139 ↗