Dual redox groups enable organic cathode material with a high capacity for aqueous zinc-organic batteries. (1st February 2022)
- Record Type:
- Journal Article
- Title:
- Dual redox groups enable organic cathode material with a high capacity for aqueous zinc-organic batteries. (1st February 2022)
- Main Title:
- Dual redox groups enable organic cathode material with a high capacity for aqueous zinc-organic batteries
- Authors:
- An, Yongkang
Liu, Yu
Tan, Shuangshuang
Xiong, Fangyu
Liao, Xiaobin
An, Qinyou - Abstract:
- Highlights: An organic cathode with dual redox groups (TBQPH) for aqueous Zn-organic batteries. Utilize dual redox groups to achieve an ultra-high specific capacity of 455 mAh g −1 . Direct evidence of H + insertion was found by liquid 1 H NMR spectrum. Achieved long cycle capabilities of 10, 000 cycles at 5 and 10 a g −1, respectively. Abstract: Organic cathode materials have recently attracted extensive attention in aqueous zinc-organic batteries (ZOBs) due to their safety, abundant resources, and designability. However, the most as-reported organic materials with a single redox site exhibit limited specific capacities. Herein, benzo [i] benzo [6, 7] quinoxalino [2, 3-a] benzo [6, 7] quinoxalino [2, 3-c] phenazine-5, 8, 13, 16, 21, 24-hexaone (TBQPH) with both carbonyls and pyrazines as redox groups is designed and synthesized as ZOBs cathode material. The dual redox sites in TBQPH enable a high specific capacity of 455.8 mAh g −1 at 0.3 A g −1 owing to the 12-electron reaction mechanism. Ex-situ spectroscopic techniques (especially liquid NMR spectrum) and density functional theory calculations provide strong evidence for the insertion/extraction of hydrogen ions. More importantly, the TBQPH electrode exhibits an ultra-long cycle life of 10, 000 cycles at 10 A g −1 with an average decay of only 0.0022% per cycle, which is attributed to the fast reaction kinetics and low charge transfer resistance. This work inspires new inspiration for designing next-generationHighlights: An organic cathode with dual redox groups (TBQPH) for aqueous Zn-organic batteries. Utilize dual redox groups to achieve an ultra-high specific capacity of 455 mAh g −1 . Direct evidence of H + insertion was found by liquid 1 H NMR spectrum. Achieved long cycle capabilities of 10, 000 cycles at 5 and 10 a g −1, respectively. Abstract: Organic cathode materials have recently attracted extensive attention in aqueous zinc-organic batteries (ZOBs) due to their safety, abundant resources, and designability. However, the most as-reported organic materials with a single redox site exhibit limited specific capacities. Herein, benzo [i] benzo [6, 7] quinoxalino [2, 3-a] benzo [6, 7] quinoxalino [2, 3-c] phenazine-5, 8, 13, 16, 21, 24-hexaone (TBQPH) with both carbonyls and pyrazines as redox groups is designed and synthesized as ZOBs cathode material. The dual redox sites in TBQPH enable a high specific capacity of 455.8 mAh g −1 at 0.3 A g −1 owing to the 12-electron reaction mechanism. Ex-situ spectroscopic techniques (especially liquid NMR spectrum) and density functional theory calculations provide strong evidence for the insertion/extraction of hydrogen ions. More importantly, the TBQPH electrode exhibits an ultra-long cycle life of 10, 000 cycles at 10 A g −1 with an average decay of only 0.0022% per cycle, which is attributed to the fast reaction kinetics and low charge transfer resistance. This work inspires new inspiration for designing next-generation high-performance organic electrode materials. Graphical abstract: Image, graphical abstract . … (more)
- Is Part Of:
- Electrochimica acta. Volume 404(2022)
- Journal:
- Electrochimica acta
- Issue:
- Volume 404(2022)
- Issue Display:
- Volume 404, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 404
- Issue:
- 2022
- Issue Sort Value:
- 2022-0404-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-02-01
- Subjects:
- Aqueous Zn-organic batteries -- Organic electrodes -- Carbonyls -- Pyrazines -- High capacity
Electrochemistry -- Periodicals
Electrochemistry, Industrial -- Periodicals
541.37 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00134686 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.electacta.2021.139620 ↗
- Languages:
- English
- ISSNs:
- 0013-4686
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3698.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20356.xml