A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V

Abstract As a promising stationary energy storage device, aqueous redox flow battery (ARFB) still faces the challenge of low open-circuit voltage, due to the limitation of the potential of water splitting (1.23 V theoretically). Herein, we present a low potential anolyte design by using Na substitut...

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Main Authors: Weipeng Li, Weizhuo Xu, Zhaopeng Sun, Linning Tang, Guohao Xu, Xinyue He, Yulin Deng, Wei Sun, Bingjie Zhou, Jianfei Song, Wei Liu
Format: Article
Language:English
Published: Nature Portfolio 2025-05-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-60018-7
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author Weipeng Li
Weizhuo Xu
Zhaopeng Sun
Linning Tang
Guohao Xu
Xinyue He
Yulin Deng
Wei Sun
Bingjie Zhou
Jianfei Song
Wei Liu
author_facet Weipeng Li
Weizhuo Xu
Zhaopeng Sun
Linning Tang
Guohao Xu
Xinyue He
Yulin Deng
Wei Sun
Bingjie Zhou
Jianfei Song
Wei Liu
author_sort Weipeng Li
collection DOAJ
description Abstract As a promising stationary energy storage device, aqueous redox flow battery (ARFB) still faces the challenge of low open-circuit voltage, due to the limitation of the potential of water splitting (1.23 V theoretically). Herein, we present a low potential anolyte design by using Na substituted phosphotungstic acid (3Na-PW12) for an aqueous redox flow battery with the high open-circuit voltage up to 2.0 V. The 3Na-PW12 can store 5 electrons in the charging process and simultaneously capture Na+ or protons from the dissociation of water, resulting in the increase of electrolyte pH to 11. Because of the high pH value, the hydrogen evolution reaction (HER) is highly suppressed, and the 3Na-PW12 is partially degraded into a lacunary structured PW11 with extremely low potential down to −1.1 V (vs. SHE). After discharging, the captured protons are re-released into the solution, therefore, pH and the structure of 3Na-PW12 are recovered. Based on the cyclic pH change and self-regulation process of 3Na-PW12 in the charge and discharge process, the aqueous flow battery offered a high-power density of 200 mW cm−2 and 160 mW cm−2 coupled with Br2/Br− and I2/I− catholyte respectively.
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spelling doaj-art-904d23b597da47ff9914f7959f3fee852025-08-20T03:48:18ZengNature PortfolioNature Communications2041-17232025-05-0116111010.1038/s41467-025-60018-7A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 VWeipeng Li0Weizhuo Xu1Zhaopeng Sun2Linning Tang3Guohao Xu4Xinyue He5Yulin Deng6Wei Sun7Bingjie Zhou8Jianfei Song9Wei Liu10School of Chemistry and Chemical Engineering, Central South UniversitySchool of Chemistry and Chemical Engineering, Central South UniversitySchool of Chemistry and Chemical Engineering, Central South UniversitySchool of Chemistry and Chemical Engineering, Central South UniversitySchool of Chemistry and Chemical Engineering, Central South UniversitySchool of Chemistry and Chemical Engineering, Central South UniversitySchool of Chemical & Biomolecular Engineering and RBI at Georgia Tech, Georgia Institute of TechnologySchool of Chemistry and Chemical Engineering, Shihezi UniversityNational Engineering Laboratory for Mobile Source Emission Control Technology, China Automotive Technology & Research Center Co. Ltd.Changsha New Energy Innovation InstituteSchool of Chemistry and Chemical Engineering, Central South UniversityAbstract As a promising stationary energy storage device, aqueous redox flow battery (ARFB) still faces the challenge of low open-circuit voltage, due to the limitation of the potential of water splitting (1.23 V theoretically). Herein, we present a low potential anolyte design by using Na substituted phosphotungstic acid (3Na-PW12) for an aqueous redox flow battery with the high open-circuit voltage up to 2.0 V. The 3Na-PW12 can store 5 electrons in the charging process and simultaneously capture Na+ or protons from the dissociation of water, resulting in the increase of electrolyte pH to 11. Because of the high pH value, the hydrogen evolution reaction (HER) is highly suppressed, and the 3Na-PW12 is partially degraded into a lacunary structured PW11 with extremely low potential down to −1.1 V (vs. SHE). After discharging, the captured protons are re-released into the solution, therefore, pH and the structure of 3Na-PW12 are recovered. Based on the cyclic pH change and self-regulation process of 3Na-PW12 in the charge and discharge process, the aqueous flow battery offered a high-power density of 200 mW cm−2 and 160 mW cm−2 coupled with Br2/Br− and I2/I− catholyte respectively.https://doi.org/10.1038/s41467-025-60018-7
spellingShingle Weipeng Li
Weizhuo Xu
Zhaopeng Sun
Linning Tang
Guohao Xu
Xinyue He
Yulin Deng
Wei Sun
Bingjie Zhou
Jianfei Song
Wei Liu
A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V
Nature Communications
title A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V
title_full A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V
title_fullStr A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V
title_full_unstemmed A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V
title_short A tungsten polyoxometalate mediated aqueous redox flow battery with high open-circuit voltage up to 2 V
title_sort tungsten polyoxometalate mediated aqueous redox flow battery with high open circuit voltage up to 2 v
url https://doi.org/10.1038/s41467-025-60018-7
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