Binder Effect on Electrochemical and Mechanical Properties of Flexible Electrodes
Source abstract
Abstract
Binders are essential electrode materials used to bond active and conductive materials together and fix them to the current collector. Therefore, binders are essential in ensuring mechanical stability and maintaining the microstructure to ensure a smooth flow of ions and electrons. In flexible electrodes, binders have the additional role of enhancing flexibility. Ultraflexible electrodes can be fabricated by exploiting the thermoplastic properties of the poly(vinylidene fluoride) (PVDF) binder using thermally induced phase separation (TIPS). Because binders are insulating materials, excess amounts can affect the specific capacity; therefore, their amount should be determined by considering the interplay between flexibility and capacity. In this study, four TIPS-based electrodes having 10, 20, 30, and 40 wt % PVDF were investigated to understand the effect of binder amount on the electrode properties. The electrodes with 10 and 20 wt % PVDF attained a high capacity (180 mAh g −1 ), significantly outperforming those containing 30 and 40 wt %. Notably, the electrodes containing less PVDF (≤20 wt %) had considerably higher porosity than those containing larger amounts, suggesting that the outstanding capacity is attributed to high porosity, which enhances ionic conductivity. The poor capacity of the higher PVDF electrodes (≥30 wt %) is associated with high ionic and electronic resistances resulting from low porosity and polymer adsorption that blocks the electron conductive network. Conversely, the electrodes containing larger amounts of PVDF achieved a higher tensile strain and greater flexibility. Considering the trade-off between electrochemical and mechanical properties, the preparation of electrodes with smaller quantities of PVDF is suggested. This study provides a systematic approach to understanding the effect of binder on flexible electrodes and can be extended to other devices where binder is applied, including energy storage and biomedical devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Dielectric materials and actuators · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Nano-devices and Displays, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea
Department of Nanomechatronics, University of Science and Technology (UST), Daejeon 34113, Republic of Korea
Funding
Korea Institute of Machinery and Materials · National Research Foundation of Korea
References (40)
Show source-provided references
1. 10.1002/advs.20220487510.1002/advs.202204875 ↗
2. 10.1021/acsami.6b1471910.1021/acsami.6b14719 ↗
3. 10.1002/adma.20200441910.1002/adma.202004419 ↗
4. 10.1016/j.ensm.2019.04.01910.1016/j.ensm.2019.04.019 ↗
5. 10.1073/pnas.200725011710.1073/pnas.2007250117 ↗
6. 10.1016/S0376-7388(00)85130-310.1016/S0376-7388(00)85130-3 ↗
7. 10.1016/j.memsci.2005.11.03610.1016/j.memsci.2005.11.036 ↗
8. 10.1002/smll.20230541610.1002/smll.202305416 ↗
9. Hatsey, N. H.; Kim, A.; Ha, H.; Lee, J. Y.; Oh, M.; Kim, K. S.; So, H. M.; Hyun, S.High-Performance Stainless-Steel-Fiber-Reinforced Thick Ultra-Flexible Electrode Applicable to 3D Free-Form Batteries Adv. Fiber Mater. 202410.1007/s42765-024-00468-8.10.1007/s42765-024-00468-8 ↗
10. 10.1021/acs.chemrev.8b0024110.1021/acs.chemrev.8b00241 ↗
11. 10.1007/s41918-023-00198-210.1007/s41918-023-00198-2 ↗
12. 10.1007/s42114-021-00217-010.1007/s42114-021-00217-0 ↗
13. 10.1007/s12598-021-01816-y10.1007/s12598-021-01816-y ↗
14. 10.1149/1.216804910.1149/1.2168049 ↗
15. 10.1021/acsnano.1c0649110.1021/acsnano.1c06491 ↗
16. 10.1039/C8TA05049J10.1039/C8TA05049J ↗
17. 10.1016/j.jpowsour.2023.23332710.1016/j.jpowsour.2023.233327 ↗
18. 10.1007/s10800-017-1047-410.1007/s10800-017-1047-4 ↗
19. 10.1021/acsami.1c0701910.1021/acsami.1c07019 ↗
20. 10.1016/j.apsusc.2021.14956410.1016/j.apsusc.2021.149564 ↗
21. 10.1016/j.mtcomm.2021.10254910.1016/j.mtcomm.2021.102549 ↗
22. 10.1002/aenm.20170303110.1002/aenm.201703031 ↗
23. 10.1002/adma.20170674510.1002/adma.201706745 ↗
24. 10.1002/adma.20210127510.1002/adma.202101275 ↗
25. 10.1149/1.349599210.1149/1.3495992 ↗
26. 10.1016/j.jpowsour.2020.22940210.1016/j.jpowsour.2020.229402 ↗
27. 10.1016/j.apsusc.2018.01.20210.1016/j.apsusc.2018.01.202 ↗
28. 10.1002/er.767010.1002/er.7670 ↗
29. 10.1039/B512304F10.1039/B512304F ↗
30. 10.1002/aenm.20120032010.1002/aenm.201200320 ↗
31. 10.1002/aenm.20190145710.1002/aenm.201901457 ↗
32. 10.1149/1945-7111/ab8b9910.1149/1945-7111/ab8b99 ↗
33. 10.1021/acs.nanolett.0c0205310.1021/acs.nanolett.0c02053 ↗
34. 10.1038/s41598-017-16711-910.1038/s41598-017-16711-9 ↗
35. 10.1016/j.mser.2023.10073710.1016/j.mser.2023.100737 ↗
36. 10.1038/nmat481010.1038/nmat4810 ↗
37. 10.3389/fmats.2019.0017610.3389/fmats.2019.00176 ↗
38. 10.1002/asia.20200033410.1002/asia.202000334 ↗
39. 10.1039/D2CC02517E10.1039/D2CC02517E ↗
40. 10.1039/D2TA05960F10.1039/D2TA05960F ↗