journal article·2025-05Open access

Green Electrode Processing Enabled by Fluoro‐Free Multifunctional Binders for Lithium‐Ion Batteries

Xiuyu Jin, Ziting Zhu, Qiusu Miao, Chen Fang, Di Huang, Raynald Giovine, Linfeng Chen, Chaochao Dun, Jeffrey J. Urban, Yanbao Fu, Defu Li, Katie Liu, Yunfei Wang, Tianyu Zhu, Chenhui Zhu, Wei Tong, Gao Liu

Advanced Science· Volume 12· Issue 17

Abstract

Abstract The eco‐friendly processing of conjugated polymer binder for lithium‐ion batteries demands improved polymer solubility by introducing functional moieties, while this strategy will concurrently sacrifice polymer conductivity. Employing the polyfluorene‐based binder poly(2,7‐9,9 (di(oxy‐2,5,8‐trioxadecane))fluorene) (PFO), soluble in water‐ethanol mixtures, a novel approach is presented to solve this trade‐off, which features integration of aqueous solution processing with subsequent controlled thermal‐induced cleavage of solubilizing side chains, to produce hierarchically ordered structures (HOS). The thermal processing can enhance the intermolecular π–π stacking of polyfluorene backbone for better electrochemical performance. Notably, HOS‐PFO demonstrated a substantial 6–7 orders of magnitude enhancement in electronic conductivity, showcasing its potential as a functional binder for lithium‐ion batteries. As an illustration, HOS‐PFO protected SiOx anodes, utilizing in situ side chain decomposition of PFO surrounding SiOx particles after aqueous processing are fabricated. HOS‐PFO contributed to the stable cycling and high‐capacity retention of practical SiOx anodes (3.0 mAh cm −2 ), without the use of any conducting carbon additives or fluorinated electrolyte additives. It is proposed that this technique represents a universal approach for fabricating electrodes with conjugated polymer binders from aqueous solutions without compromising conductivity.
Source: crossref · Quality: baseline

Research context

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

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

The Energy Storage and Distributed Resources Division (ESDR) Lawrence Berkeley National Laboratory Berkeley CA 94720 USA

Pines Magnetic Resonance Center (PMRC)‐Core Facility College of Chemistry University of California Berkeley CA 94720 USA

The Molecular Foundry Lawrence Berkeley National Laboratory Berkeley CA 94720 USA

Advanced Light Source Lawrence Berkeley National Laboratory Berkeley CA 94720 USA

School of Polymer Science and Engineering The University of Southern Mississippi Hattiesburg MS 39406 USA

Department of Materials Science and Engineering Clemson University Clemson SC 29634 USA

Funding

National Science Foundation

References (38)

Show source-provided references
1. 10.1039/C7CS00863E10.1039/C7CS00863E ↗
2. 10.1016/j.jpowsour.2020.22870810.1016/j.jpowsour.2020.228708 ↗
3. 10.1021/acsenergylett.0c0258410.1021/acsenergylett.0c02584 ↗
4. 10.1039/C7CS00858A10.1039/C7CS00858A ↗
5. 10.1002/adma.20180056110.1002/adma.201800561 ↗
6. 10.1016/j.nanoen.2017.04.04310.1016/j.nanoen.2017.04.043 ↗
7. 10.1021/acs.accounts.7b0040210.1021/acs.accounts.7b00402 ↗
8. 10.1039/C8EE00640G10.1039/C8EE00640G ↗
9. 10.1016/j.jpowsour.2014.04.09010.1016/j.jpowsour.2014.04.090 ↗
10. 10.1021/ma00238a04010.1021/ma00238a040 ↗
11. 10.1002/pol.1974.17012010210.1002/pol.1974.170120102 ↗
12. 10.1016/0379-6779(94)02412-R10.1016/0379-6779(94)02412-R ↗
13. 10.1016/j.progpolymsci.2013.05.01510.1016/j.progpolymsci.2013.05.015 ↗
14. 10.1016/0379-6779(89)90798-410.1016/0379-6779(89)90798-4 ↗
15. 10.1016/S0379-6779(99)00267-210.1016/S0379-6779(99)00267-2 ↗
16. 10.1039/D0TC03610B10.1039/D0TC03610B ↗
17. 10.1002/pola.2848210.1002/pola.28482 ↗
18. 10.1002/aenm.20140020710.1002/aenm.201400207 ↗
19. 10.1149/1945-7111/ab856b10.1149/1945-7111/ab856b ↗
20. 10.1002/celc.20140221010.1002/celc.201402210 ↗
21. 10.1002/app.4977410.1002/app.49774 ↗
22. 10.1021/acsami.7b0893710.1021/acsami.7b08937 ↗
23. 10.1002/aenm.20170231410.1002/aenm.201702314 ↗
24. 10.1016/j.ensm.2023.10307410.1016/j.ensm.2023.103074 ↗
25. 10.1021/cr200263w10.1021/cr200263w ↗
26. 10.1021/cm402080510.1021/cm4020805 ↗
27. 10.1002/adma.20190310410.1002/adma.201903104 ↗
28. 10.1016/j.trechm.2022.05.00210.1016/j.trechm.2022.05.002 ↗
29. 10.1021/jacs.1c1155810.1021/jacs.1c11558 ↗
30. 10.1021/jp021114v10.1021/jp021114v ↗
31. 10.1002/smll.20210225610.1002/smll.202102256 ↗
32. 10.1557/jmr.2015.32810.1557/jmr.2015.328 ↗
33. 10.1038/pj.2010.5810.1038/pj.2010.58 ↗
34. 10.1039/C9PY01469A10.1039/C9PY01469A ↗
35. 10.1038/s41560-022-01176-610.1038/s41560-022-01176-6 ↗
36. 10.1002/adfm.20217014910.1002/adfm.202170149 ↗
37. 10.1002/adfm.20160598910.1002/adfm.201605989 ↗
38. 10.1002/aenm.20230289910.1002/aenm.202302899 ↗