Please use this identifier to cite or link to this item: https://doi.org/10.1002/anie.202208223
Title: High-Power Near-Neutral Aqueous All Organic Redox Flow Battery Enabled with a Pair of Anionic Redox Species
Authors: Gao, M 
Salla, M 
Song, Y
Qing Wang 
Keywords: All-Organic Redox Flow Battery.
Aqueous Organic Redox Flow Battery
Molecular Engineering
pH-Neutral
Issue Date: 10-Oct-2022
Publisher: Wiley
Citation: Gao, M, Salla, M, Song, Y, Qing Wang (2022-10-10). High-Power Near-Neutral Aqueous All Organic Redox Flow Battery Enabled with a Pair of Anionic Redox Species. Angewandte Chemie - International Edition 61 (41) : e202208223-. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.202208223
Abstract: Aqueous organic redox flow batteries (AORFBs) are regarded as a promising alternative for low-cost and durable grid-scale energy storage. However, the narrow potential gap, chemical lability and membrane fouling in most AORFBs constitute formidable roadblocks for practical applications. Herein, a pair of anionic organic molecules, namely (PPBPy)Br2 and PSS-TEMPO, are proposed. The (PPBPy)Br2 in anolyte reveals remarkable electrochemical stability without degradation after 1000 cycles, while PSS-TEMPO in catholyte presents a capacity decay rate as low as 0.012 %/cycle. At near-neutral conditions, the (PPBPy)Br2/PSS-TEMPO flow cell exhibits a high voltage of 1.61 V, extremely low permeability across cation-exchange membrane and thus excellent cycling stability. Notably, a highest peak power density of 509 mW cm−2 has been achieved among reported all-organic aqueous RFBs. The molecular engineering strategies demonstrated here could provide a credible example of high-performance AORFBs.
Source Title: Angewandte Chemie - International Edition
URI: https://scholarbank.nus.edu.sg/handle/10635/239219
ISSN: 1433-7851
1521-3773
DOI: 10.1002/anie.202208223
Appears in Collections:Staff Publications
Elements

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
Angew manuscript-revised_WQ.pdfAccepted version436.77 kBAdobe PDF

OPEN

Post-printView/Download

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.