journal article·2023-03Open access

Isomeric Triptycene Triquinones as Universal Cathode Materials for High Energy Alkali Metal Batteries

Hyunji Park, Yoshiaki Shuku, Jihyun Lee, Kyunam Lee, Dong Joo Min, Byeong‐Kwan An, Kuino Awaga, Soo Young Park, Ji Eon Kwon

Batteries & Supercaps· Volume 6· Issue 3

Abstract

Abstract Organic electrode materials have been extensively researched for alkali metal batteries such as Li, Na, and K batteries due to their unique redox mechanism independent of types of charge‐carrying ions and flexible intermolecular structures facilitating the insertion of bulky metal‐ions. This study presents an ortho‐isomer of triptycene tribenzoquinone (o‐TT) as a universal organic cathode material for alkali metal batteries. To elevate the redox potentials of previously reported triptycene tribenzoquinone (TT) without sacrificing its large specific capacity (∼386 mAh g−1), the structural isomers of benzoquinone units in the TT molecule were designed by changing their carbonyl group position from para‐ to ortho‐position. Due to multi‐electron redox reactions and the elevated redox potentials, o‐TT shows high energy densities of 945, 767, and 597 Wh kg−1 in Li, Na, and K cells, respectively. Finally, its cycle stability is significantly improved by fabricating composite electrodes with disordered mesoporous carbon (DOMC).
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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

Laboratory for Supramolecular Optoelectronic Materials (LSOM) Department of Materials Science and Engineering Research Institute of Advanced Materials (RIAM) Seoul National University 1 Gwanak-ro, Gwanak-gu Seoul 08826 Republic of Korea

Functional Composite Materials Research Center Institute of Advanced Composite Materials Korea Institute of Science and Technology (KIST) 92 Chudong-ro, Bongdong-eup, Wanju-gun Jeonbuk 55324 Republic of Korea

Department of Chemistry Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8602 Japan

Department of Chemistry Catholic University of Korea 43 Jibong-ro, Bucheon Gyeonggido 14662 Republic of Korea

References (66)

Show source-provided references
1.
2. 10.1039/c1ee01598b10.1039/c1ee01598b ↗
3. 10.1021/acs.chemrev.9b0048210.1021/acs.chemrev.9b00482 ↗
4.
5. 10.1039/C6CS00173D10.1039/C6CS00173D ↗
6. 10.1002/adma.20170000710.1002/adma.201700007 ↗
7. 10.1149/2.0251701jes10.1149/2.0251701jes ↗
8.
9. 10.1002/adfm.20120069110.1002/adfm.201200691 ↗
10. 10.1039/C6CS00776G10.1039/C6CS00776G ↗
11. 10.1016/j.chempr.2018.11.00510.1016/j.chempr.2018.11.005 ↗
12.
13. 10.1002/adfm.20190948610.1002/adfm.201909486 ↗
14. 10.1039/C8EE01023D10.1039/C8EE01023D ↗
15. Kim H. · Adv. Mater. · 2017 · 29
16. 10.1016/j.chempr.2018.09.00510.1016/j.chempr.2018.09.005 ↗
17.
18. 10.1002/aenm.20170027810.1002/aenm.201700278 ↗
19. 10.1002/aenm.20160179210.1002/aenm.201601792 ↗
20. 10.1002/advs.20190043110.1002/advs.201900431 ↗
21.
22. 10.1002/anie.20130258610.1002/anie.201302586 ↗
23. 10.1021/ja507852t10.1021/ja507852t ↗
24.
25. 10.1039/C7QI00453B10.1039/C7QI00453B ↗
26. 10.1021/acs.chemmater.9b0260110.1021/acs.chemmater.9b02601 ↗
27. 10.1016/j.elecom.2016.07.01110.1016/j.elecom.2016.07.011 ↗
28. 10.1039/B814515F10.1039/B814515F ↗
29.
30. 10.1039/C4TA02812K10.1039/C4TA02812K ↗
31. 10.1002/aenm.20170131610.1002/aenm.201701316 ↗
32. 10.1021/acs.chemmater.5b0256910.1021/acs.chemmater.5b02569 ↗
33.
34. 10.1002/aenm.20120094710.1002/aenm.201200947 ↗
35. 10.1021/acs.chemmater.0c0366110.1021/acs.chemmater.0c03661 ↗
36. 10.1016/j.jpowsour.2014.05.05010.1016/j.jpowsour.2014.05.050 ↗
37. 10.1021/am405470p10.1021/am405470p ↗
38. 10.1039/C8CP00597D10.1039/C8CP00597D ↗
39. 10.1039/C7TA09968A10.1039/C7TA09968A ↗
40. 10.1039/C8CC00753E10.1039/C8CC00753E ↗
41. 10.1080/00397911.2022.207711510.1080/00397911.2022.2077115 ↗
42. 10.1021/acs.joc.8b0270610.1021/acs.joc.8b02706 ↗
43. 10.1002/poc.186810.1002/poc.1868 ↗
44. 10.1021/acsaem.7b0015610.1021/acsaem.7b00156 ↗
45. 10.1016/j.electacta.2009.06.04110.1016/j.electacta.2009.06.041 ↗
46. 10.1021/acs.chemmater.7b0195310.1021/acs.chemmater.7b01953 ↗
47.
48. 10.1002/advs.20150001810.1002/advs.201500018 ↗
49. 10.1002/anie.20160111910.1002/anie.201601119 ↗
50. 10.1039/D0TA03562A10.1039/D0TA03562A ↗
51.
52. 10.1039/C8TA09960J10.1039/C8TA09960J ↗
53. 10.1039/C9TA06430C10.1039/C9TA06430C ↗
54.
55. 10.1002/adfm.20190959710.1002/adfm.201909597 ↗
56. 10.1002/advs.20220039710.1002/advs.202200397 ↗
57.
58. 10.1002/aenm.20140055410.1002/aenm.201400554 ↗
59. 10.1016/j.chempr.2018.08.01510.1016/j.chempr.2018.08.015 ↗
60. 10.1039/C9CC01859J10.1039/C9CC01859J ↗
61.
62. 10.1038/s41467-020-20314-w10.1038/s41467-020-20314-w ↗
63. 10.1016/j.bbabio.2020.14817310.1016/j.bbabio.2020.148173 ↗
64. 10.1021/j100012a02910.1021/j100012a029 ↗
65. 10.1016/j.carbon.2013.11.00110.1016/j.carbon.2013.11.001 ↗
66. 10.1021/ma100640m10.1021/ma100640m ↗