Conductive Binder for Si Anode with Boosted Charge Transfer Capability via n-Type Doping
Source abstract
Abstract
Employing conductive binders in silicon (Si) anode has been considered as a fundamental solution to the pulverization of Si particles. Therefore, it is still a great challenge to improve the charge transfer capability of the conductive binder. Herein, a copolymer (PFPQ-COONa) is synthesized, characterized, and electrochemically tested as conductive binder for Si anode. It is found that PFPQ-COONa exhibits not only excellent cycling stability, but also satisfactory rate performance with relatively high areal loading, which outperforms currently reported single-component conductive binders. The superior electrochemical performance can be attributed to the molecular-level contact between binder and Si particles and to the enhanced intrinsic conductivity of PFPQ-COONa at reductive potential. This method provides a fresh perspective to design and develop conductive binder for high-capacity battery anode.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, P. R. China
Department of Nano Engineering, University of California San Diego, 9500 Gilman Drive 0448, La Jolla, California 92093-0448, United States
School of Materials Science and Engineering, Zhengzhou University, Zhengzhou 450001, P. R. China
Funding
Ministry of Science and Technology of the People's Republic of China · Shenzhen Science and Technology Innovation Committee · Guangdong Innovation Team
References (33)
Show source-provided references
1. 10.1021/cm901452z10.1021/cm901452z ↗
2. 10.1038/nnano.2016.20710.1038/nnano.2016.207 ↗
3. 10.1149/1.240986210.1149/1.2409862 ↗
4. 10.1149/1.179224210.1149/1.1792242 ↗
5. 10.1038/nnano.2007.41110.1038/nnano.2007.411 ↗
6. 10.1038/nnano.2014.610.1038/nnano.2014.6 ↗
7. 10.1039/B417492E10.1039/B417492E ↗
8. 10.1021/nn901632g10.1021/nn901632g ↗
9. 10.1002/aenm.20160090410.1002/aenm.201600904 ↗
10. 10.1002/anie.20131041210.1002/anie.201310412 ↗
11. 10.1002/aenm.20170118510.1002/aenm.201701185 ↗
12. 10.1021/am100871y10.1021/am100871y ↗
13. 10.1016/j.jpowsour.2013.08.07310.1016/j.jpowsour.2013.08.073 ↗
14. 10.1021/jp204817h10.1021/jp204817h ↗
15. 10.1126/science.120915010.1126/science.1209150 ↗
16. 10.1002/adma.20120398110.1002/adma.201203981 ↗
17. 10.1149/1.205642710.1149/1.2056427 ↗
18. 10.1038/ncomms294110.1038/ncomms2941 ↗
19. 10.1002/celc.20140221010.1002/celc.201402210 ↗
20. 10.1002/adfm.20187001610.1002/adfm.201870016 ↗
21. 10.1021/acsnano.6b0021810.1021/acsnano.6b00218 ↗
22. 10.1002/adfm.20150058910.1002/adfm.201500589 ↗
23. 10.1002/adma.20110242110.1002/adma.201102421 ↗
24. 10.1021/nl503490h10.1021/nl503490h ↗
25. 10.1021/ja405446510.1021/ja4054465 ↗
26. 10.1016/j.nanoen.2017.04.04310.1016/j.nanoen.2017.04.043 ↗
27. 10.1039/C5EE00472A10.1039/C5EE00472A ↗
28. 10.1149/1.321289410.1149/1.3212894 ↗
29. 10.1002/anie.20120156810.1002/anie.201201568 ↗
30. 10.1016/j.jpowsour.2014.03.02710.1016/j.jpowsour.2014.03.027 ↗
31. 10.1021/acs.chemmater.5b0099010.1021/acs.chemmater.5b00990 ↗
32. 10.1063/1.167752710.1063/1.1677527 ↗
33. 10.1063/1.44426710.1063/1.444267 ↗