Phenylene‐Bridged Bispyridinium with High Capacity and Stability for Aqueous Flow Batteries. Issue 7 (14th January 2021)
- Record Type:
- Journal Article
- Title:
- Phenylene‐Bridged Bispyridinium with High Capacity and Stability for Aqueous Flow Batteries. Issue 7 (14th January 2021)
- Main Title:
- Phenylene‐Bridged Bispyridinium with High Capacity and Stability for Aqueous Flow Batteries
- Authors:
- Hu, Shuzhi
Li, Tianyu
Huang, Mingbao
Huang, Jinghua
Li, Wenjin
Wang, Liwen
Chen, Zhenqiang
Fu, Zhiyong
Li, Xianfeng
Liang, Zhenxing - Abstract:
- Abstract: A rotating phenyl ring is introduced between the two pyridinium rings, namely, 1, 1′‐bis[3‐(trimethylamonium)propyl]‐4, 4′‐(1, 4‐phenylene)bispyridinium tetrachloride ((APBPy)Cl4 ), to form a switchable conjugation. In this design, the conjugation is switched "off" in the oxidized state and the two pyridinium rings behave independently during the redox process, yielding a concomitant transfer of two electrons at the same potential and, thus, simplifying the battery management. The conjugation is switched "on" in the reduced state and the charge can be effectively delocalized, lowering the Lewis basicity and improving its chemical stability. By pairing 0.50 m (APBPy)Cl4 with a 2, 2, 6, 6‐tetramethylpiperidin‐1‐yl oxyl derivative as the positive electrolyte, a flow battery delivers a high standard cell voltage of 1.730 V and a high specific capacity of 20.0 Ah L –1 . The battery also shows an exceptionally high energy efficiency of 80.8% and a superior cycling stability at 80 mA cm –2 . This strategy proves itself a great success in engineering viologen as a two‐electron storage mediator with high capacity and stability. Abstract : A self‐regulated conjugation strategy is proposed to engineer viologen for flow batteries. In the oxidized state, the conjugation is "off" and the two pyridinium rings behave independently, yielding concomitant transfer of two electrons and one voltage plateau. In the reduced state, the conjugation is "on" and the charge can be effectivelyAbstract: A rotating phenyl ring is introduced between the two pyridinium rings, namely, 1, 1′‐bis[3‐(trimethylamonium)propyl]‐4, 4′‐(1, 4‐phenylene)bispyridinium tetrachloride ((APBPy)Cl4 ), to form a switchable conjugation. In this design, the conjugation is switched "off" in the oxidized state and the two pyridinium rings behave independently during the redox process, yielding a concomitant transfer of two electrons at the same potential and, thus, simplifying the battery management. The conjugation is switched "on" in the reduced state and the charge can be effectively delocalized, lowering the Lewis basicity and improving its chemical stability. By pairing 0.50 m (APBPy)Cl4 with a 2, 2, 6, 6‐tetramethylpiperidin‐1‐yl oxyl derivative as the positive electrolyte, a flow battery delivers a high standard cell voltage of 1.730 V and a high specific capacity of 20.0 Ah L –1 . The battery also shows an exceptionally high energy efficiency of 80.8% and a superior cycling stability at 80 mA cm –2 . This strategy proves itself a great success in engineering viologen as a two‐electron storage mediator with high capacity and stability. Abstract : A self‐regulated conjugation strategy is proposed to engineer viologen for flow batteries. In the oxidized state, the conjugation is "off" and the two pyridinium rings behave independently, yielding concomitant transfer of two electrons and one voltage plateau. In the reduced state, the conjugation is "on" and the charge can be effectively delocalized, lowering the Lewis basicity and improving the cycling stability of the battery. … (more)
- Is Part Of:
- Advanced materials. Volume 33:Issue 7(2021)
- Journal:
- Advanced materials
- Issue:
- Volume 33:Issue 7(2021)
- Issue Display:
- Volume 33, Issue 7 (2021)
- Year:
- 2021
- Volume:
- 33
- Issue:
- 7
- Issue Sort Value:
- 2021-0033-0007-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-01-14
- Subjects:
- aqueous redox flow batteries -- charge delocalization -- conjugation -- pyridinium
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-4095 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adma.202005839 ↗
- Languages:
- English
- ISSNs:
- 0935-9648
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.897800
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22312.xml