journal article·2026-05-26

Continuous Long-ch a in PEG Design in Polyimide Binders Enables Durable High-Voltage Cycling of NCM811 Cathodes

Xia Yan, Junhao Xin, Qinghai Chen, Zixin Lv, Zhaozan Xu, Quanyuan Zhang, Nanwen Li

Chemistry of Materials· Volume 38· Issue 10
Publisher page

Abstract

High-nickel LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811) cathodes suffer from severe structural degradation, interfacial side reactions, and mechanical failure under high-voltage operation. To address these challenges, a novel polyimide-polyethylene glycol binder, denoted PI-PEG3(2000), was designed by integrating flexible long-chain PEG segments into a rigid polyimide backbone via a one-step synthesis. The rigid framework enables high-voltage tolerance, while the continuous PEG segments simultaneously establish efficient Li + transport channels and provide outstanding elasticity to accommodate cycling-induced stress. When applied to NCM811 cathodes, PI-PEG3(2000) forms a uniform and dense coating that effectively suppresses interfacial side reactions, transition metal dissolution and phase transformation. As a result, cells with this binder exhibit significantly improved high-voltage cycling stability, retaining 86.2% and 76.7% capacity after 100 cycles at 4.5 and 4.7 V versus Li/Li +, respectively, outperforming conventional PVDF-based cells (66.1% and 54.2%). The binder also enables excellent rate capability, delivering 146 mAh g –1 at 5C in the 2.5–4.7 V versus Li/Li + window compared with 113 mAh g –1 for PVDF. In long-term cycling tests, the PI-PEG3(2000) binder retains 71.4% capacity after 250 cycles (2.5–4.5 V vs Li/Li + ) and 65.2% after 200 cycles (2.5–4.7 V vs Li/Li + ). Additionally, the thermal stability of fully charged cathodes is significantly improved by reducing heat release, enhancing overall battery safety. This study presents a chain-length-based design strategy for advanced binders that simultaneously achieve high-voltage stability, high ionic conductivity, and mechanical resilience, providing a promising approach for developing high-energy-density lithium-ion batteries.
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Research context

OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Conducting polymers and applications

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Affiliations

Shanxi Collaborative Innovation Center of High Value-added Utilization of Coal-related Wastes, Institute of Resources and Environmental Engineering

Shanxi University

State Key Laboratory of Coal Conversion

Institute of Coal Chemistry, Chinese Academy of Sciences

Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science and Engineering

Hubei University

Faculty of Materials Science and Energy Engineering

Shenzhen University of Advanced Technology

Funding

National Natural Science Foundation of China

References (50)

Show source-provided references
1. 10.1021/acsami.0c2065710.1021/acsami.0c20657 ↗
2. 10.1016/j.electacta.2021.13844010.1016/j.electacta.2021.138440 ↗
3. 10.1016/j.mattod.2014.10.04010.1016/j.mattod.2014.10.040 ↗
4. 10.1021/acsami.1c0182410.1021/acsami.1c01824 ↗
5. 10.1021/acsami.9b0288910.1021/acsami.9b02889 ↗
6. 10.1039/D0TA08038A10.1039/D0TA08038A ↗
7. 10.1021/acs.jpcc.7b0636310.1021/acs.jpcc.7b06363 ↗
8. 10.1002/aenm.20200106910.1002/aenm.202001069 ↗
9. 10.1016/j.cej.2020.12644210.1016/j.cej.2020.126442 ↗
10. 10.1016/j.nanoen.2018.09.06610.1016/j.nanoen.2018.09.066 ↗
11. 10.1038/nmat241810.1038/nmat2418 ↗
12. 10.1016/j.jallcom.2014.06.04910.1016/j.jallcom.2014.06.049 ↗
13. 10.1002/aenm.20190159710.1002/aenm.201901597 ↗
14. 10.1016/j.matchemphys.2020.12308510.1016/j.matchemphys.2020.123085 ↗
15. 10.1007/s10008-019-04308-310.1007/s10008-019-04308-3 ↗
16. 10.1002/adfm.20210534310.1002/adfm.202105343 ↗
17. 10.1016/j.ensm.2020.11.02110.1016/j.ensm.2020.11.021 ↗
18. 10.1002/adfm.20210485810.1002/adfm.202104858 ↗
19. 10.1016/j.eml.2015.11.00510.1016/j.eml.2015.11.005 ↗
20. 10.1002/adma.20241687210.1002/adma.202416872 ↗
21. 10.1002/aenm.20230284510.1002/aenm.202302845 ↗
22. 10.1039/c2ee03389e10.1039/c2ee03389e ↗
23. 10.1002/eem2.1287110.1002/eem2.12871 ↗
24. 10.1016/j.cej.2022.13795910.1016/j.cej.2022.137959 ↗
25. 10.1016/j.apenergy.2022.11928210.1016/j.apenergy.2022.119282 ↗
26. 10.1016/j.cej.2024.15867010.1016/j.cej.2024.158670 ↗
27. 10.1002/adfm.20251607410.1002/adfm.202516074 ↗
28. 10.1016/j.mtener.2017.11.00110.1016/j.mtener.2017.11.001 ↗
29. 10.1021/acsami.3c1700810.1021/acsami.3c17008 ↗
30. 10.1002/aenm.20170313810.1002/aenm.201703138 ↗
31. 10.1016/j.jpowsour.2025.23662910.1016/j.jpowsour.2025.236629 ↗
32. 10.1021/ja405446510.1021/ja4054465 ↗
33. 10.1002/adma.20250626610.1002/adma.202506266 ↗
34. 10.1016/j.nanoen.2021.10624010.1016/j.nanoen.2021.106240 ↗
35. 10.1038/srep2577110.1038/srep25771 ↗
36. 10.1002/aenm.20130078710.1002/aenm.201300787 ↗
37. 10.1016/j.jpowsour.2017.05.06310.1016/j.jpowsour.2017.05.063 ↗
38. 10.1002/adfm.20242541710.1002/adfm.202425417 ↗
39. 10.1016/j.ensm.2016.10.00710.1016/j.ensm.2016.10.007 ↗
40. 10.1039/C6TA01061J10.1039/C6TA01061J ↗
41. 10.1021/acs.accounts.9b0003310.1021/acs.accounts.9b00033 ↗
42. 10.1007/s11664-019-07489-910.1007/s11664-019-07489-9 ↗
43. 10.1016/j.nanoen.2021.10585410.1016/j.nanoen.2021.105854 ↗
44. 10.1016/j.jechem.2022.09.00810.1016/j.jechem.2022.09.008 ↗
45. 10.1021/acsami.9b1672710.1021/acsami.9b16727 ↗
46. 10.1016/j.jechem.2020.12.02810.1016/j.jechem.2020.12.028 ↗
47. 10.1002/aenm.20190273110.1002/aenm.201902731 ↗
48. 10.1002/adfm.20170469010.1002/adfm.201704690 ↗
49. 10.1149/1.355663810.1149/1.3556638 ↗
50. 10.1002/aenm.20140182610.1002/aenm.201401826 ↗