4.8 Article

Alkaline soluble 1,3,5,7-tetrahydroxyanthraquinone with high reversibility as anolyte for aqueous redox flow battery

Journal

JOURNAL OF POWER SOURCES
Volume 524, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2022.231001

Keywords

Alkaline aqueous redox flow batteries; Low cost; High solubility; High capacity retention

Funding

  1. National Key Research and Development Program of China [2017YFA0208200]
  2. Fundamental Research Funds for the Central Universities of China [0205-14380266]
  3. National Natural Science Foundation of China [22022505, 21872069]
  4. Natural Science Foundation of Jiangsu Province [BK20180008]
  5. Shenzhen Fundamental Research Program of Science, Technology and Innovation Commission of Shenzhen Municipality [JCYJ20180307155007589]

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In this study, a green and convenient microwave synthesis method was used to successfully synthesize a redox-reversible molecule, 1,3,5,7-tetrahydroxyanthraquinone (1,3,5,7-THAQ), for aqueous redox flow batteries (ARFBs). The ARFBs based on 1,3,5,7-THAQ demonstrated high cell voltage, high power density, and excellent cycling stability. This research provides a reference for the development of low-cost and high-performance ARFBs.
Aqueous redox flow batteries (ARFBs) based on the electrolytes of organic redox-active species with low cost, abundant sources are very attractive for application in large-scale energy storage systems. Herein, we introduce the green and convenient microwave synthesis of a redox-reversible molecule based on an anthraquinone motif, namely 1,3,5,7-tetrahydroxyanthraquinone (1,3,5,7-THAQ), via the dimerization of low-cost 3,5-dihydroxybenzoic acid with high yield and batch production capability. The 1,3,5,7-THAQ presents a high solubility of 1.88 M and a low redox potential of -0.68 V at pH 14, well suited to serving as an anolyte molecule in ARFBs. When paired with a ferrocyanide catholyte, the ARFBs based on 1,3,5,7-THAQ demonstrate a high cell voltage of similar to 1.2 V and a maximum output power density of 0.36 W cm(-2). Detailed battery tests and post-analyses verify the excellent cycling stability of 1,3,5,7-THAQ without electrochemical dimerization in highly alkaline aqueous environment, which contributes to the ultrahigh capacity retention (95.2% after 1100 cycles at 100 mA cm(-2)) and low capacity fade rate (similar to 0.35% per day) of the ARFBs. This work provides an effective paradigm for the design of high performance and low cost ARFBs based on organic redox-active molecules for large-scale and low-cost energy storage applications.

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