Eu-based anolytes for high-voltage and long-lifetime aqueous flow batteries

被引:6
作者
Sun, Pan [1 ]
Liu, Yahua [1 ]
Zuo, Peipei [1 ]
Li, Yuanyuan [1 ]
Chen, Qianru [1 ]
Yang, Zhengjin [1 ,2 ]
Xu, Tongwen [1 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Soft Matter Chem, iCHEM Collaborat Innovat Ctr Chem Energy Mat, Dept Chem,Sch Chem & Mat, Hefei 230026, Anhui, Peoples R China
[2] Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2021年 / 60卷
基金
中国国家自然科学基金;
关键词
Energy storage; Aqueous flow batteries; Anolytes; Europium; HIGH-CAPACITY; VANADIUM; POLYMER; SAFE;
D O I
10.1016/j.jechem.2021.01.041
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Aqueous flow batteries (AFBs) are among the most promising electrochemical energy storage solutions for the massive-scale adoption of renewable electricity because of decoupled energy and power, design flexibility, improved safety and low cost. The development of high-voltage AFB is, however, limited by the lack of stable anolytes that have low redox potential. Here we report Eu-based anolytes for high-voltage pH-neutral AFB applications. Eu3+ has a reduction potential of -0.39 V vs. SHE, which can be dramatically lowered when forming stable complex with inexpensive organic chelates. A typical complex, EuDTPA, features a low redox potential of -1.09 V vs. SHE, fast redox kinetics, and a high water solubility of 1.5 M. When paired with ferrocyanide, the battery had an open-circuit voltage of 1.56 V and demonstrated stable cell cycling performance, including a capacity retention rate of 99.997% per cycle over 500 cycles at 40 mA cm(-2), a current efficiency of >99.9%, and an energy efficiency of >83.3%. A high concentration anolyte at 1.5 M exhibited a volumetric capacity of 40.2 Ah L-1, which is one of the highest known for pH-neutral AFBs, promising a potent solution for the grid-scale storage of renewable electricity. (C) 2021 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
引用
收藏
页码:368 / 375
页数:8
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