MXene/Organics Heterostructures Enable Ultrastable and High-Rate Lithium/Sodium Batteries
Source abstract
Abstract
Organic electrode materials have shown potential for rechargeable batteries because they are environmentally friendly, earth-abundant sources, recyclable, high sustainable, designable, flexible, and lightweight. However, low electrical conductivity and dissolution in organic liquid electrolytes hinder their further development. Herein, MXene/organics heterostructures are designed to address the problems of organic electrodes via a scalable and simple electrostatic self-assembly strategy. Under the effect of the electrostatic interaction, organic cathode material, 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA), is tightly attached to MXene nanosheets. Owing to the high electronic conductivity and special two-dimensional (2D) structure of MXene nanosheets, the issues of PTCDA cathode are effectively relieved. When applied in lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs), the MXene@PTCDA heterostructure exhibits significantly enhanced rate capability and cycling performance than bare PTCDA. The heterostructures proposed here can be applied to other (K, Zn, Al, Mg, Ca, etc.) battery systems. In addition to energy storage and conversion, the heterostructures can be also extended to many fields such as catalysis, sensors, electronics, optics, membranes, semiconductors, biomedicines, etc.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Advancements in Battery Materials · Advanced Battery Materials and Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory for Liquid−Solid Structural Evolution & Processing of Materials (Ministry of Education), Research Center for Carbon Nanomaterials, School of Materials Science and Engineering, Shandong University, Jinan 250061, P. R. China
School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, P. R. China
Funding
National Natural Science Foundation of China
References (63)
Show source-provided references
1. 10.1126/science.121274110.1126/science.1212741 ↗
2. 10.1038/451652a10.1038/451652a ↗
3. 10.1002/adma.20180056110.1002/adma.201800561 ↗
4. 10.1039/C6CS00776G10.1039/C6CS00776G ↗
5. 10.1016/j.ensm.2020.09.00610.1016/j.ensm.2020.09.006 ↗
6. 10.1002/adfm.20200943310.1002/adfm.202009433 ↗
7. 10.1002/adfm.20201083210.1002/adfm.202010832 ↗
8. 10.1039/C7TA10500B10.1039/C7TA10500B ↗
9. 10.1016/j.ensm.2021.03.00610.1016/j.ensm.2021.03.006 ↗
10. 10.1016/j.chphma.2021.09.00310.1016/j.chphma.2021.09.003 ↗
11. 10.1039/c2cs35307e10.1039/c2cs35307e ↗
12. 10.1016/j.mattod.2015.10.00910.1016/j.mattod.2015.10.009 ↗
13. 10.1021/acs.accounts.0c0046510.1021/acs.accounts.0c00465 ↗
14. 10.1021/acs.chemrev.9b0048210.1021/acs.chemrev.9b00482 ↗
15. 10.1021/acsami.9b2038410.1021/acsami.9b20384 ↗
16. 10.1038/s41570-020-0160-910.1038/s41570-020-0160-9 ↗
17. 10.1039/c3ee40709h10.1039/c3ee40709h ↗
18. 10.1002/smll.20190646210.1002/smll.201906462 ↗
19. 10.1002/adfm.20170543210.1002/adfm.201705432 ↗
20. 10.1002/adfm.20180713710.1002/adfm.201807137 ↗
21. 10.1002/smll.20180506110.1002/smll.201805061 ↗
22. 10.1039/C9EE03637G10.1039/C9EE03637G ↗
23. 10.1016/j.joule.2018.07.00810.1016/j.joule.2018.07.008 ↗
24. 10.1002/adma.20170468210.1002/adma.201704682 ↗
25. 10.1016/j.jechem.2020.05.02110.1016/j.jechem.2020.05.021 ↗
26. 10.1002/anie.20200896010.1002/anie.202008960 ↗
27. 10.1002/cey2.210.1002/cey2.2 ↗
28. 10.1002/adma.20110230610.1002/adma.201102306 ↗
29. 10.1038/natrevmats.2016.9810.1038/natrevmats.2016.98 ↗
30. 10.1002/adma.20180477910.1002/adma.201804779 ↗
31. 10.1021/acs.chemmater.7b0284710.1021/acs.chemmater.7b02847 ↗
32. 10.1002/adfm.20200461310.1002/adfm.202004613 ↗
33. 10.1002/smll.20190321410.1002/smll.201903214 ↗
34. 10.1002/adfm.20180810710.1002/adfm.201808107 ↗
35. 10.1002/inf2.1211810.1002/inf2.12118 ↗
36. 10.1002/adfm.20180594610.1002/adfm.201805946 ↗
37. 10.1021/acs.nanolett.0c0321510.1021/acs.nanolett.0c03215 ↗
38. 10.1039/C8TA02068J10.1039/C8TA02068J ↗
39. 10.1002/adfm.20200070610.1002/adfm.202000706 ↗
40. 10.1016/j.ensm.2020.01.00510.1016/j.ensm.2020.01.005 ↗
41. 10.1039/C8CS00324F10.1039/C8CS00324F ↗
42. 10.1016/j.cclet.2019.12.03310.1016/j.cclet.2019.12.033 ↗
43. 10.1002/smll.20190208510.1002/smll.201902085 ↗
44. 10.1021/acs.chemrev.9b0034810.1021/acs.chemrev.9b00348 ↗
45. 10.1002/adma.20210314810.1002/adma.202103148 ↗
46. 10.1021/acsnano.1c0549710.1021/acsnano.1c05497 ↗
47. 10.1007/s12274-021-3433-910.1007/s12274-021-3433-9 ↗
48. 10.1002/adfm.20210119410.1002/adfm.202101194 ↗
49. 10.1016/j.nantod.2020.10099110.1016/j.nantod.2020.100991 ↗
50. 10.1016/j.electacta.2019.04.09410.1016/j.electacta.2019.04.094 ↗
51. 10.1007/s40820-019-0296-710.1007/s40820-019-0296-7 ↗
52. 10.1016/j.nanoen.2016.06.00510.1016/j.nanoen.2016.06.005 ↗
53. 10.1016/j.electacta.2018.04.15510.1016/j.electacta.2018.04.155 ↗
54. 10.1002/aenm.20200139410.1002/aenm.202001394 ↗
55. 10.1002/aenm.20140055410.1002/aenm.201400554 ↗
56. 10.1039/C8CC00649K10.1039/C8CC00649K ↗
57. 10.1007/s40820-019-0312-y10.1007/s40820-019-0312-y ↗
58. 10.1002/adfm.20170126410.1002/adfm.201701264 ↗
59. 10.1016/j.cej.2019.12262210.1016/j.cej.2019.122622 ↗
60. 10.1016/j.apsusc.2015.11.08910.1016/j.apsusc.2015.11.089 ↗
61. 10.1002/adfm.20180462910.1002/adfm.201804629 ↗
62. 10.1039/C9TA06663B10.1039/C9TA06663B ↗
63. 10.1039/C5RA07356A10.1039/C5RA07356A ↗