Wood‐inspired High Ionic Conductivity Hydrogel Electrolytes for Flexible Supercapacitors
Source abstract
Abstract
Abstract Hydrogel is a promising electrolyte substrate, but its ionic conductivity needs further improvement. In this paper, we propose a strategy to improve the ionic conductivity of hydrogels with flexible wood and fabricate a flexible wood‐based poly(acrylic acid‐acrylamide) composite hydrogel electrolyte (WHE) by delignification and in‐situ polymerization. The flexible wood as a porous backbone for hydrogels can regulate ion transport pathways to improve the ionic conductivity of hydrogels. The straight pores of wood confine the transport of electrolyte ions along the shortest path, resulting in a high ionic conductivity of 3.0×10−2 S cm−1, which is great in composite polymer electrolytes. We have systematically investigated the effect of the degree of delignification and the polymerization process on the overall performance of the electrolyte. The optimized supercapacitor exhibits a specific capacitance of 155.64 F g−1 and an energy density of 7.45 W h kg−1. The WHE is applied to flexible supercapacitor, which exhibits good flexibility under bending conditions and can maintain similar electrochemical performance at a wide range of bending angles. This work provides an effective strategy for the efficient use of wood resources and the development of low‐cost, environmentally friendly, and high‐performance hydrogel electrolyte materials.
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Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Advanced Battery Materials and Technologies · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Chemical Engineering Northwestern Polytechnical University Xi'an 710072 China
Key Laboratory of Bio-based Material Science and Technology of Ministry of Education Northeast Forestry University Harbin 150040 China
School of Science RMIT University Melbourne, VIC 3000 Australia
Funding
Fundamental Research Funds for the Central Universities · China Postdoctoral Science Foundation
References (50)
Show source-provided references
1. 10.1002/adma.20160343610.1002/adma.201603436 ↗
2. 10.1016/j.jechem.2022.02.01210.1016/j.jechem.2022.02.012 ↗
3. 10.1016/j.jechem.2020.07.01410.1016/j.jechem.2020.07.014 ↗
4. 10.1016/j.jpowsour.2021.22946110.1016/j.jpowsour.2021.229461 ↗
5. 10.1016/j.jpowsour.2021.22996210.1016/j.jpowsour.2021.229962 ↗
6. 10.1038/s41467-017-00550-310.1038/s41467-017-00550-3 ↗
7. 10.1002/adma.20170381710.1002/adma.201703817 ↗
8. 10.1002/adma.20190191610.1002/adma.201901916 ↗
9. 10.1016/j.electacta.2018.04.12710.1016/j.electacta.2018.04.127 ↗
10. 10.1002/adma.20230499710.1002/adma.202304997 ↗
11. 10.1016/j.jcis.2018.09.02710.1016/j.jcis.2018.09.027 ↗
12. 10.1002/anie.20171084110.1002/anie.201710841 ↗
13. 10.1021/acsaem.0c0290210.1021/acsaem.0c02902 ↗
14. 10.1016/j.jpowsour.2021.22961810.1016/j.jpowsour.2021.229618 ↗
15. 10.1021/acs.accounts.8b0039110.1021/acs.accounts.8b00391 ↗
16. 10.1021/acsomega.0c0577810.1021/acsomega.0c05778 ↗
17. 10.1038/s41578-020-0195-z10.1038/s41578-020-0195-z ↗
18. 10.1021/acs.chemmater.1c0080610.1021/acs.chemmater.1c00806 ↗
19. 10.1002/adfm.20210047710.1002/adfm.202100477 ↗
20. 10.1073/pnas.232294412110.1073/pnas.2322944121 ↗
21. 10.1021/acsami.0c1396210.1021/acsami.0c13962 ↗
22. 10.1021/acs.biomac.1c0114110.1021/acs.biomac.1c01141 ↗
23. 10.1002/adfm.20201006810.1002/adfm.202010068 ↗
24. 10.1021/acsnano.0c0429810.1021/acsnano.0c04298 ↗
25. 10.1002/anie.20190257810.1002/anie.201902578 ↗
26. J. Li Z. Hu S. Zhang H. Zhang S. Guo G. Zhong Y. Qiao Z. Peng Y. Li S. Chen G. Chen A. Cao Nat. Sustain.2024.
27. 10.1021/acsnano.8b0576310.1021/acsnano.8b05763 ↗
28. 10.1021/acsami.7b0652910.1021/acsami.7b06529 ↗
29. 10.1002/aenm.20180128910.1002/aenm.201801289 ↗
30. 10.1016/j.reactfunctpolym.2005.11.00210.1016/j.reactfunctpolym.2005.11.002 ↗
31. 10.1002/anie.20170521210.1002/anie.201705212 ↗
32. 10.1002/adma.20180193410.1002/adma.201801934 ↗
33. 10.1021/acsnano.0c1011710.1021/acsnano.0c10117 ↗
34. 10.1039/D0TA09730F10.1039/D0TA09730F ↗
35. 10.1002/aenm.20200003510.1002/aenm.202000035 ↗
36. 10.1016/j.jechem.2020.02.02310.1016/j.jechem.2020.02.023 ↗
37. 10.1039/C8RA08403C10.1039/C8RA08403C ↗
38. 10.1039/C9TA03519B10.1039/C9TA03519B ↗
39. 10.1016/j.est.2021.10266310.1016/j.est.2021.102663 ↗
40. 10.1016/j.est.2019.10098810.1016/j.est.2019.100988 ↗
41. 10.1007/s10853-015-9576-x10.1007/s10853-015-9576-x ↗
42. 10.1016/j.renene.2020.08.09210.1016/j.renene.2020.08.092 ↗
43. 10.1039/C7GC01681F10.1039/C7GC01681F ↗
44. 10.1016/j.biombioe.2020.10573010.1016/j.biombioe.2020.105730 ↗
45. 10.1007/s42823-021-00235-410.1007/s42823-021-00235-4 ↗
46. 10.1016/j.cej.2019.12317010.1016/j.cej.2019.123170 ↗
47. 10.1016/j.jpowsour.2019.22715010.1016/j.jpowsour.2019.227150 ↗
48. 10.1016/j.carbon.2019.09.00310.1016/j.carbon.2019.09.003 ↗
49. 10.1002/aenm.20160076310.1002/aenm.201600763 ↗
50. 10.1002/aenm.20190379410.1002/aenm.201903794 ↗