Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis

This study presents a prototype non-aqueous redox flow battery that advances the capabilities of conventional systems by achieving a wide operational voltage range, high efficiency, and prolonged cycle life. Leveraging the redox pair 10-[2-(2-methoxy ethoxy)ethyl]-10H-phenothiazine and 2-ethyltereph...

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Main Authors: Mirko D’Adamo, Nicolas Daub, Lluis Trilla, Jose A. Saez-Zamora, Juan Manuel Paz-Garcia
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Batteries
Subjects:
Online Access:https://www.mdpi.com/2313-0105/11/1/8
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author Mirko D’Adamo
Nicolas Daub
Lluis Trilla
Jose A. Saez-Zamora
Juan Manuel Paz-Garcia
author_facet Mirko D’Adamo
Nicolas Daub
Lluis Trilla
Jose A. Saez-Zamora
Juan Manuel Paz-Garcia
author_sort Mirko D’Adamo
collection DOAJ
description This study presents a prototype non-aqueous redox flow battery that advances the capabilities of conventional systems by achieving a wide operational voltage range, high efficiency, and prolonged cycle life. Leveraging the redox pair 10-[2-(2-methoxy ethoxy)ethyl]-10H-phenothiazine and 2-ethylterephthalonitrile, the system delivers a discharge cell voltage ranging from approximately 2.25 V to 1.9 V. To address the economic challenges associated with non-aqueous redox flow batteries, this work explores a cost-efficient design using a symmetric cell architecture and a low-cost, porous separator. To evaluate the feasibility and scalability of this approach, a 2D time-transient reactive transport model is developed, integrating Nernst–Planck electroneutrality principles and porous electrode kinetics. The model is optimized and validated against experimental charge/discharge cycles, accurately predicting voltage behavior. Additionally, the study provides crucial insights into the crossover phenomenon, elucidating the transport dynamics and spatial distribution of active species within the cell. This comprehensive framework establishes a robust foundation for future efforts to scale and optimize non-aqueous redox flow batteries for large-scale energy storage applications, bringing them closer to commercial viability.
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series Batteries
spelling doaj-art-c3b34a10beb34acfa8d6c6a23e4dfde22025-01-24T13:22:23ZengMDPI AGBatteries2313-01052024-12-01111810.3390/batteries11010008Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade AnalysisMirko D’Adamo0Nicolas Daub1Lluis Trilla2Jose A. Saez-Zamora3Juan Manuel Paz-Garcia4NVISION, Gran Via Carles III, 124, ent. 1a, 08034 Barcelona, SpainDepartment of Chemical Engineering and Chemistry, Research Group of Molecular Materials and Nanosystems, Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600 MB Eindhoven, The NetherlandsInstitut de Recerca en Energia de Catalunya—IREC, Jardins de les Dones de Negre 1, 2ª pl., 08930 Sant Adrià del Besòs, SpainNVISION, Gran Via Carles III, 124, ent. 1a, 08034 Barcelona, SpainDepartment of Chemical Engineering, University of Malaga, 29071 Malaga, SpainThis study presents a prototype non-aqueous redox flow battery that advances the capabilities of conventional systems by achieving a wide operational voltage range, high efficiency, and prolonged cycle life. Leveraging the redox pair 10-[2-(2-methoxy ethoxy)ethyl]-10H-phenothiazine and 2-ethylterephthalonitrile, the system delivers a discharge cell voltage ranging from approximately 2.25 V to 1.9 V. To address the economic challenges associated with non-aqueous redox flow batteries, this work explores a cost-efficient design using a symmetric cell architecture and a low-cost, porous separator. To evaluate the feasibility and scalability of this approach, a 2D time-transient reactive transport model is developed, integrating Nernst–Planck electroneutrality principles and porous electrode kinetics. The model is optimized and validated against experimental charge/discharge cycles, accurately predicting voltage behavior. Additionally, the study provides crucial insights into the crossover phenomenon, elucidating the transport dynamics and spatial distribution of active species within the cell. This comprehensive framework establishes a robust foundation for future efforts to scale and optimize non-aqueous redox flow batteries for large-scale energy storage applications, bringing them closer to commercial viability.https://www.mdpi.com/2313-0105/11/1/8redox flow batteriesmultiphysics modelingcrossover diffusionnon-aqueous redox flow batterycapacity fadeoperational voltage window
spellingShingle Mirko D’Adamo
Nicolas Daub
Lluis Trilla
Jose A. Saez-Zamora
Juan Manuel Paz-Garcia
Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis
Batteries
redox flow batteries
multiphysics modeling
crossover diffusion
non-aqueous redox flow battery
capacity fade
operational voltage window
title Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis
title_full Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis
title_fullStr Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis
title_full_unstemmed Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis
title_short Modeling of a Non-Aqueous Redox Flow Battery for Performance and Capacity Fade Analysis
title_sort modeling of a non aqueous redox flow battery for performance and capacity fade analysis
topic redox flow batteries
multiphysics modeling
crossover diffusion
non-aqueous redox flow battery
capacity fade
operational voltage window
url https://www.mdpi.com/2313-0105/11/1/8
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AT joseasaezzamora modelingofanonaqueousredoxflowbatteryforperformanceandcapacityfadeanalysis
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