Leveraging Long‐Life Alkaline Redox Flow Batteries Using Durable and High‐Hydroxide Exchange N‐Bridged Triazine Framework Membranes

Fluorine-free organic framework polyelectrolyte membranes showing near frictionless ionic conductivities are gaining cognitive insights. However, the co-precipitation of COFs in the membranes often brings trade-offs to commission long-life electrochemical energy storage solutions. Herein, a durable and ionically miscible dual-ion exchange membrane based on triazine organic framework (TOF) is designed for alkaline redox flow batteries (RFB). Bearing dual ion-exchange architectures, the all-hydrocarbon TOF-based PEMs (sTOF's) surpass fluorinated Nafion in terms of energy efficiency (>80%), energy density, and peak power densities. The fabricated sTOF's evidenced the highest net ion-exchange of >2.1 meq g<sup>-1</sup> which encourages electrolyte utilization with ≈100% and offers excellent capacities. Moreover, >97% efficiencies are preserved, and rate capability studies illustrate that, with sTOF-5, the RFB can operate at reduced overpotentials (η ≤200 mV) and can uplift batteries life. The sTOF's supports successful demonstrations of batteries at higher redoxolyte concentrations thereby multiplying the energy densities. The afterlife performance of sTOF-5 revealed efficiencies equivalent to fresh Nafion-117 and surpassed bearing >50% capacity after ≈3000 continuous cycles. With sTOF-5, the cell delivered a peak power (P<sub>max</sub>) of 2.3 W which is ≈60% higher than that of Nafion-117 (P<sub>max</sub> = 1.45 W).

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Publication Details

Journal
Small
Published
2025-01-22
DOI
https://doi.org/10.1002/smll.202406395
Citations
3
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
2.19

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article

Leveraging Long‐Life Alkaline Redox Flow Batteries Using Durable and High‐Hydroxide Exchange N‐Bridged Triazine Framework Membranes

Jeet Sharma, Richa Gupta, Vaibhav Kulshrestha, Kothandaraman Ramanujam
3 citations
Small
Advanced battery technologies research
2.19
article

Leveraging Long‐Life Alkaline Redox Flow Batteries Using Durable and High‐Hydroxide Exchange N‐Bridged Triazine Framework Membranes

Jeet Sharma, Richa Gupta, Vaibhav Kulshrestha, Kothandaraman Ramanujam
article en
3 citations

Abstract

Fluorine-free organic framework polyelectrolyte membranes showing near frictionless ionic conductivities are gaining cognitive insights. However, the co-precipitation of COFs in the membranes often brings trade-offs to commission long-life electrochemical energy storage solutions. Herein, a durable and ionically miscible dual-ion exchange membrane based on triazine organic framework (TOF) is designed for alkaline redox flow batteries (RFB). Bearing dual ion-exchange architectures, the all-hydrocarbon TOF-based PEMs (sTOF's) surpass fluorinated Nafion in terms of energy efficiency (>80%), energy density, and peak power densities. The fabricated sTOF's evidenced the highest net ion-exchange of >2.1 meq g<sup>-1</sup> which encourages electrolyte utilization with ≈100% and offers excellent capacities. Moreover, >97% efficiencies are preserved, and rate capability studies illustrate that, with sTOF-5, the RFB can operate at reduced overpotentials (η ≤200 mV) and can uplift batteries life. The sTOF's supports successful demonstrations of batteries at higher redoxolyte concentrations thereby multiplying the energy densities. The afterlife performance of sTOF-5 revealed efficiencies equivalent to fresh Nafion-117 and surpassed bearing >50% capacity after ≈3000 continuous cycles. With sTOF-5, the cell delivered a peak power (P<sub>max</sub>) of 2.3 W which is ≈60% higher than that of Nafion-117 (P<sub>max</sub> = 1.45 W).

SmallVol. 21(13)
Central Salt and Marine Chemicals Research Institute (IN), Indian Institute of Technology Madras (IN), Council of Scientific and Industrial Research (IN), Academy of Scientific and Innovative Research (IN)
Department of Science and Technology, Government of Rajasthan
Affordable and clean energy
Openalex Percentile: Top 14%
Advanced battery technologies research
2.19
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