In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries

The Zn‐MnO2 primary alkaline battery (PAB) is widely utilized in low‐power and portable applications due to its low cost and favorable energy density. The accumulation of inactive materials during discharge and its effect on the capacity and internal impedance in PAB cells are investigated in this w...

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Main Authors: Giancarlo Dominador D. Sanglay, Michael T. Castro, Lawrence A. Limjuco, Joey D. Ocon
Format: Article
Language:English
Published: Wiley-VCH 2025-07-01
Series:ChemElectroChem
Subjects:
Online Access:https://doi.org/10.1002/celc.202400714
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author Giancarlo Dominador D. Sanglay
Michael T. Castro
Lawrence A. Limjuco
Joey D. Ocon
author_facet Giancarlo Dominador D. Sanglay
Michael T. Castro
Lawrence A. Limjuco
Joey D. Ocon
author_sort Giancarlo Dominador D. Sanglay
collection DOAJ
description The Zn‐MnO2 primary alkaline battery (PAB) is widely utilized in low‐power and portable applications due to its low cost and favorable energy density. The accumulation of inactive materials during discharge and its effect on the capacity and internal impedance in PAB cells are investigated in this work. AA‐sized PABs are partially discharged using 25, 50, and 100 mA constant currents at 25% depth of discharge (DoD) intervals until 100% DoD. The cells are imaged via in situ X‐ray micro‐computed tomography (micro‐CT) while the impedances are measured through electrochemical impedance spectroscopy. At low discharge rates, a higher capacity at 100% DoD is obtained while more inactive materials are formed, particularly ZnO throughout the Zn anode, resulting in a higher internal resistance. At higher discharge rate, oxide formation is concentrated on the anode surface, limiting access to the bulk anode—preventing further reaction, leading to a lower capacity and internal resistance. These observations are supported by multiphysics modeling simulations on the distribution of porosity, ZnO, and Zn(OH)42− and OH− ions. The observations from this work provide insights that can be useful in optimizing electrode design and maximizing cell capacity.
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spelling doaj-art-3f90bd7f079d4620bfdf4458bab27cfb2025-08-20T03:14:01ZengWiley-VCHChemElectroChem2196-02162025-07-011215n/an/a10.1002/celc.202400714In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline BatteriesGiancarlo Dominador D. Sanglay0Michael T. Castro1Lawrence A. Limjuco2Joey D. Ocon3Laboratory of Electrochemical Engineering (LEE) Department of Chemical Engineering University of the Philippines Diliman Quezon City 1101 PhilippinesLaboratory of Electrochemical Engineering (LEE) Department of Chemical Engineering University of the Philippines Diliman Quezon City 1101 PhilippinesLaboratory of Electrochemical Engineering (LEE) Department of Chemical Engineering University of the Philippines Diliman Quezon City 1101 PhilippinesLaboratory of Electrochemical Engineering (LEE) Department of Chemical Engineering University of the Philippines Diliman Quezon City 1101 PhilippinesThe Zn‐MnO2 primary alkaline battery (PAB) is widely utilized in low‐power and portable applications due to its low cost and favorable energy density. The accumulation of inactive materials during discharge and its effect on the capacity and internal impedance in PAB cells are investigated in this work. AA‐sized PABs are partially discharged using 25, 50, and 100 mA constant currents at 25% depth of discharge (DoD) intervals until 100% DoD. The cells are imaged via in situ X‐ray micro‐computed tomography (micro‐CT) while the impedances are measured through electrochemical impedance spectroscopy. At low discharge rates, a higher capacity at 100% DoD is obtained while more inactive materials are formed, particularly ZnO throughout the Zn anode, resulting in a higher internal resistance. At higher discharge rate, oxide formation is concentrated on the anode surface, limiting access to the bulk anode—preventing further reaction, leading to a lower capacity and internal resistance. These observations are supported by multiphysics modeling simulations on the distribution of porosity, ZnO, and Zn(OH)42− and OH− ions. The observations from this work provide insights that can be useful in optimizing electrode design and maximizing cell capacity.https://doi.org/10.1002/celc.202400714in situ X‐ray micro‐CTinterfacesmanganesemultiphysics modelzinc
spellingShingle Giancarlo Dominador D. Sanglay
Michael T. Castro
Lawrence A. Limjuco
Joey D. Ocon
In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries
ChemElectroChem
in situ X‐ray micro‐CT
interfaces
manganese
multiphysics model
zinc
title In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries
title_full In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries
title_fullStr In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries
title_full_unstemmed In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries
title_short In Situ X‐Ray Microtomographic and Multiphysics Modeling Investigation of the Discharge Process and Impedance Evolution of Zn‐MnO2 Primary Alkaline Batteries
title_sort in situ x ray microtomographic and multiphysics modeling investigation of the discharge process and impedance evolution of zn mno2 primary alkaline batteries
topic in situ X‐ray micro‐CT
interfaces
manganese
multiphysics model
zinc
url https://doi.org/10.1002/celc.202400714
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