journal article·2021-09-15

Vertical Channels Design for Polymer Electrolyte to Enhance Mechanical Strength and Ion Conductivity

Yaohui Liang, Nan Chen, Wenjie Qu, Cheng Yang, Li Li, Feng Wu, Renjie Chen

ACS Applied Materials & Interfaces· Volume 13· Issue 36
Publisher page

Abstract

Polymer electrolytes are the key candidates for solid-state batteries benefiting from their intrinsic advantages over inorganic electrolytes in terms of flexibility and easy processability. However, they suffer from low ionic conductivity and poor mechanical strength, which restrict their wide utilization. Conventional ceramic fillers are used to improve the mechanical properties of polymer electrolytes but lack sufficient Li+ conductivity. In this work, a framework with vertical channels that possess fast Li+ movement is designed. It is found that the poly(ethylene oxide) (PEO) compound in the vertical channel framework benefits to improve the ionic conductivity and mechanical strength synchronously. The framework in which ionic liquids are loaded on a zirconium dioxide surface (ZrO2@ILs) helps to improve ionic conductivity by 2 orders of magnitude compared with PEO, which is due to the enhanced orientation of ion transport. By optimizing the content of ZrO2@ILs, the elastic modulus is also tripled. Therefore, the symmetric lithium battery can cycle stably for more than 800 h at a current density of 0.25 mA cm–1, whereas the lithium metal battery has a specific capacity of 135 mAh g–1 at a current density of 2C and can cycle stably for more than 200 cycles at 60 °C.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Supercapacitor Materials and Fabrication

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

Affiliations

Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China

Institute of Advanced Technology, Beijing Institute of Technology, Jinan 250300, China

Shanghai Institute of Space Power-Sources, Shanghai 200245, China

School of Materials Science and Engineering, Harbin Institute of Technology, Harbin 150001, Heilongjiang, China

State Key Laboratory of Space Power-Sources Technology, Shanghai 200245, China

Funding

Beihang University · Natural Science Foundation of Beijing Municipality · Beijing Institute of Technology · National Natural Science Foundation of China

References (58)

Show source-provided references
1. 10.1002/anie.20200447710.1002/anie.202004477 ↗
2. 10.1021/acsnano.9b0378410.1021/acsnano.9b03784 ↗
3. 10.1021/acsenergylett.0c0046810.1021/acsenergylett.0c00468 ↗
4. 10.1002/aenm.20170265710.1002/aenm.201702657 ↗
5. 10.1016/j.ssi.2010.10.01310.1016/j.ssi.2010.10.013 ↗
6. 10.1002/anie.20200762110.1002/anie.202007621 ↗
7. 10.1149/2.0351906jes10.1149/2.0351906jes ↗
8. 10.1038/s41563-021-01019-x10.1038/s41563-021-01019-x ↗
9. 10.1038/s41560-019-0384-410.1038/s41560-019-0384-4 ↗
10. 10.1016/j.nanoen.2020.10462510.1016/j.nanoen.2020.104625 ↗
11. 10.1149/1.185085410.1149/1.1850854 ↗
12. 10.1021/acs.chemmater.5b0385410.1021/acs.chemmater.5b03854 ↗
13. 10.1021/acsami.8b1653610.1021/acsami.8b16536 ↗
14. 10.1016/j.matt.2020.09.01810.1016/j.matt.2020.09.018 ↗
15. 10.1002/smll.20200576210.1002/smll.202005762 ↗
16. 10.1002/adma.20190202910.1002/adma.201902029 ↗
17. 10.1002/aenm.20200004910.1002/aenm.202000049 ↗
18. 10.1016/j.ssi.2020.11541210.1016/j.ssi.2020.115412 ↗
19. 10.1021/jacs.9b1223310.1021/jacs.9b12233 ↗
20. 10.1016/j.memsci.2020.11894010.1016/j.memsci.2020.118940 ↗
21. 10.1016/j.jechem.2021.01.01310.1016/j.jechem.2021.01.013 ↗
22. 10.1002/adma.20180266110.1002/adma.201802661 ↗
23. 10.1021/acs.nanolett.7b0071510.1021/acs.nanolett.7b00715 ↗
24. 10.1038/s41565-019-0465-310.1038/s41565-019-0465-3 ↗
25. 10.1016/j.ensm.2021.06.03010.1016/j.ensm.2021.06.030 ↗
26. 10.1038/nenergy.2017.3510.1038/nenergy.2017.35 ↗
27. 10.1021/acs.nanolett.8b0111110.1021/acs.nanolett.8b01111 ↗
28. 10.1016/j.nanoen.2019.03.05110.1016/j.nanoen.2019.03.051 ↗
29. 10.1016/j.ensm.2020.12.02810.1016/j.ensm.2020.12.028 ↗
30. 10.1016/j.nanoen.2019.04.05810.1016/j.nanoen.2019.04.058 ↗
31. 10.1039/c7ta07653c10.1039/c7ta07653c ↗
32. 10.1016/j.cej.2019.12192510.1016/j.cej.2019.121925 ↗
33. 10.1016/j.polymer.2016.08.10010.1016/j.polymer.2016.08.100 ↗
34. 10.1021/acsami.9b0141710.1021/acsami.9b01417 ↗
35. 10.1021/acsami.9b0783010.1021/acsami.9b07830 ↗
36. 10.1016/j.ssi.2011.06.00110.1016/j.ssi.2011.06.001 ↗
37. 10.1039/d0ta02098b10.1039/d0ta02098b ↗
38. 10.1073/pnas.160042211310.1073/pnas.1600422113 ↗
39. 10.1016/j.nanoen.2019.10439810.1016/j.nanoen.2019.104398 ↗
40. 10.1021/acsami.9b1693610.1021/acsami.9b16936 ↗
41. 10.1002/adfm.20210116810.1002/adfm.202101168 ↗
42. 10.1002/adfm.20190104710.1002/adfm.201901047 ↗
43. 10.1002/anie.20171084110.1002/anie.201710841 ↗
44. 10.1016/s0167-2738(01)00884-010.1016/s0167-2738(01)00884-0 ↗
45. 10.1002/adma.20190562910.1002/adma.201905629 ↗
46. 10.1039/c8ta08391f10.1039/c8ta08391f ↗
47. 10.1021/acs.chemmater.8b0222710.1021/acs.chemmater.8b02227 ↗
48. 10.1016/j.jpowsour.2015.03.05810.1016/j.jpowsour.2015.03.058 ↗
49. 10.1002/adma.20170443610.1002/adma.201704436 ↗
50. 10.1149/1.208590010.1149/1.2085900 ↗
51. 10.1016/j.nanoen.2016.09.00210.1016/j.nanoen.2016.09.002 ↗
52. 10.1002/adfm.20200781510.1002/adfm.202007815 ↗
53. 10.1016/0032-3861(87)90394-610.1016/0032-3861(87)90394-6 ↗
54. 10.1002/anie.20191447810.1002/anie.201914478 ↗
55. 10.1021/acsami.0c0062110.1021/acsami.0c00621 ↗
56. 10.1016/j.ensm.2019.11.01810.1016/j.ensm.2019.11.018 ↗
57. 10.1002/aenm.20200070210.1002/aenm.202000702 ↗
58. 10.1002/adfm.20190095010.1002/adfm.201900950 ↗