Reversible redox chemistry in azobenzene-based organic molecules for high-capacity and long-life nonaqueous redox flow batteries

被引:106
作者
Zhang, Leyuan [1 ,2 ]
Qian, Yumin [1 ,2 ]
Feng, Ruozhu [3 ]
Ding, Yu [1 ,2 ]
Zu, Xihong [1 ,2 ]
Zhang, Changkun [1 ,2 ]
Guo, Xuelin [1 ,2 ]
Wang, Wei [3 ]
Yu, Guihua [1 ,2 ]
机构
[1] Univ Texas Austin, Mat Sci & Engn Program, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Mech Engn, Austin, TX 78712 USA
[3] Pacific Northwest Natl Lab, Energy & Environm Directorate, Richland, WA 99352 USA
关键词
ENERGY-STORAGE; AZO-COMPOUNDS; FAST-CHARGE; ELECTROLYTES; DENSITY; REDUCTION; CATHOLYTE; PROSPECTS; PROGRESS; ANOLYTE;
D O I
10.1038/s41467-020-17662-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Redox-active organic molecules have drawn extensive interests in redox flow batteries (RFBs) as promising active materials, but employing them in nonaqueous systems is far limited in terms of useable capacity and cycling stability. Here we introduce azobenzene-based organic compounds as new active materials to realize high-performance nonaqueous RFBs with long cycling life and high capacity. It is capable to achieve a stable long cycling with a low capacity decay of 0.014% per cycle and 0.16% per day over 1000 cycles. The stable cycling under a high concentration of 1M is also realized, delivering a high reversible capacity of similar to 46 Ah L-1. The unique lithium-coupled redox chemistry accompanied with a voltage increase is observed and revealed by experimental characterization and theoretical simulation. With the reversible redox activity of azo group in -conjugated structures, azobenzene-based molecules represent a class of promising redox-active organics for potential grid-scale energy storage systems.
引用
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页数:11
相关论文
共 43 条
[1]  
Armand M, 2009, NAT MATER, V8, P120, DOI [10.1038/NMAT2372, 10.1038/nmat2372]
[2]   Photoisomerization in different classes of azobenzene [J].
Bandara, H. M. Dhammika ;
Burdette, Shawn C. .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (05) :1809-1825
[3]   Azobenzene photoswitches for biomolecules [J].
Beharry, Andrew A. ;
Woolley, G. Andrew .
CHEMICAL SOCIETY REVIEWS, 2011, 40 (08) :4422-4437
[4]   ELECTROGENERATED BASES - THE ROLE OF WEAK ELECTROINACTIVE PROTON DONORS AND THE EFFECT OF ELECTROCATALYSIS ON THE REDOX BEHAVIOR OF AZOBENZENE [J].
CHENG, S ;
HAWLEY, MD .
JOURNAL OF ORGANIC CHEMISTRY, 1985, 50 (18) :3388-3392
[5]   A Highly Concentrated Catholyte Enabled by a Low-Melting-Point Ferrocene Derivative [J].
Cong, Guangtao ;
Zhou, Yucun ;
Li, Zhejun ;
Lu, Yi-Chun .
ACS ENERGY LETTERS, 2017, 2 (04) :869-875
[6]   Pathways to Widespread Applications: Development of Redox Flow Batteries Based on New Chemistries [J].
Ding, Yu ;
Zhang, Changkun ;
Zhang, Leyuan ;
Zhou, Yangen ;
Yu, Guihua .
CHEM, 2019, 5 (08) :1964-1987
[7]   Molecular engineering of organic electroactive materials for redox flow batteries [J].
Ding, Yu ;
Zhang, Changkun ;
Zhang, Leyuan ;
Zhou, Yangen ;
Yu, Guihua .
CHEMICAL SOCIETY REVIEWS, 2018, 47 (01) :69-103
[8]   A Bio-Inspired, Heavy-Metal-Free, Dual-Electrolyte Liquid Battery towards Sustainable Energy Storage [J].
Ding, Yu ;
Yu, Guihua .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (15) :4772-4776
[9]   "Wine-Dark Sea" in an Organic Flow Battery: Storing Negative Charge in 2,1,3-Benzothiadiazole Radicals Leads to Improved Cyclability [J].
Duan, Wentao ;
Huang, Jinhua ;
Kowalski, Jeffrey A. ;
Shkrob, Ilya A. ;
Vijayakumar, M. ;
Walter, Eric ;
Pan, Baofei ;
Yang, Zheng ;
Milshtein, Jarrod D. ;
Li, Bin ;
Liao, Chen ;
Zhang, Zhengcheng ;
Wang, Wei ;
Liu, Jun ;
Moore, Jeffery S. ;
Brushett, Fikile R. ;
Zhang, Lu ;
Wei, Xiaoliang .
ACS ENERGY LETTERS, 2017, 2 (05) :1156-1161
[10]   Electrical Energy Storage for the Grid: A Battery of Choices [J].
Dunn, Bruce ;
Kamath, Haresh ;
Tarascon, Jean-Marie .
SCIENCE, 2011, 334 (6058) :928-935