Water-mediated ion transport in an anion exchange membrane

Abstract Water is a critical component in polyelectrolyte anion exchange membranes (AEMs). It plays a central role in ion transport in electrochemical systems. Gaining a better understanding of molecular transport and conductivity in AEMs has been challenged by the lack of a general methodology capa...

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Main Authors: Zhongyang Wang, Ge Sun, Nicholas H. C. Lewis, Mrinmay Mandal, Abhishek Sharma, Mincheol Kim, Joan M. Montes de Oca, Kai Wang, Aaron Taggart, Alex B. Martinson, Paul A. Kohl, Andrei Tokmakoff, Shrayesh N. Patel, Paul F. Nealey, Juan J. de Pablo
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-55621-z
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author Zhongyang Wang
Ge Sun
Nicholas H. C. Lewis
Mrinmay Mandal
Abhishek Sharma
Mincheol Kim
Joan M. Montes de Oca
Kai Wang
Aaron Taggart
Alex B. Martinson
Paul A. Kohl
Andrei Tokmakoff
Shrayesh N. Patel
Paul F. Nealey
Juan J. de Pablo
author_facet Zhongyang Wang
Ge Sun
Nicholas H. C. Lewis
Mrinmay Mandal
Abhishek Sharma
Mincheol Kim
Joan M. Montes de Oca
Kai Wang
Aaron Taggart
Alex B. Martinson
Paul A. Kohl
Andrei Tokmakoff
Shrayesh N. Patel
Paul F. Nealey
Juan J. de Pablo
author_sort Zhongyang Wang
collection DOAJ
description Abstract Water is a critical component in polyelectrolyte anion exchange membranes (AEMs). It plays a central role in ion transport in electrochemical systems. Gaining a better understanding of molecular transport and conductivity in AEMs has been challenged by the lack of a general methodology capable of capturing and connecting water dynamics, water structure, and ionic transport over time and length scales ranging from those associated with individual bond vibrations and molecular reorientations to those pertaining to macroscopic AEM performance. In this work, we use two-dimensional infrared spectroscopy and semiclassical simulations to examine how water molecules are arranged into successive solvation shells, and we explain how that structure influences the dynamics of bromide ion transport processes in polynorbornene-based materials. We find that the transition to the faster transport mechanism occurs when the reorientation of water molecules in the second solvation shell is fast, allowing a robust hydrogen bond network to form. Our findings provide molecular-level insights into AEMs with inherent transport of halide ions, and help pave the way towards a comprehensive understanding of hydroxide ion transport in AEMs.
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spelling doaj-art-9d8272ea33da4e5090e4ab1e755956b82025-02-02T12:32:00ZengNature PortfolioNature Communications2041-17232025-01-0116111010.1038/s41467-024-55621-zWater-mediated ion transport in an anion exchange membraneZhongyang Wang0Ge Sun1Nicholas H. C. Lewis2Mrinmay Mandal3Abhishek Sharma4Mincheol Kim5Joan M. Montes de Oca6Kai Wang7Aaron Taggart8Alex B. Martinson9Paul A. Kohl10Andrei Tokmakoff11Shrayesh N. Patel12Paul F. Nealey13Juan J. de Pablo14Pritzker School of Molecular Engineering, University of ChicagoPritzker School of Molecular Engineering, University of ChicagoDepartment of Chemistry, James Franck Institute, The University of ChicagoSchool of Chemical and Biomolecular Engineering, Georgia Institute of TechnologyPritzker School of Molecular Engineering, University of ChicagoPritzker School of Molecular Engineering, University of ChicagoPritzker School of Molecular Engineering, University of ChicagoPritzker School of Molecular Engineering, University of ChicagoMaterials Science Division, Argonne National LaboratoryMaterials Science Division, Argonne National LaboratorySchool of Chemical and Biomolecular Engineering, Georgia Institute of TechnologyDepartment of Chemistry, James Franck Institute, The University of ChicagoPritzker School of Molecular Engineering, University of ChicagoPritzker School of Molecular Engineering, University of ChicagoPritzker School of Molecular Engineering, University of ChicagoAbstract Water is a critical component in polyelectrolyte anion exchange membranes (AEMs). It plays a central role in ion transport in electrochemical systems. Gaining a better understanding of molecular transport and conductivity in AEMs has been challenged by the lack of a general methodology capable of capturing and connecting water dynamics, water structure, and ionic transport over time and length scales ranging from those associated with individual bond vibrations and molecular reorientations to those pertaining to macroscopic AEM performance. In this work, we use two-dimensional infrared spectroscopy and semiclassical simulations to examine how water molecules are arranged into successive solvation shells, and we explain how that structure influences the dynamics of bromide ion transport processes in polynorbornene-based materials. We find that the transition to the faster transport mechanism occurs when the reorientation of water molecules in the second solvation shell is fast, allowing a robust hydrogen bond network to form. Our findings provide molecular-level insights into AEMs with inherent transport of halide ions, and help pave the way towards a comprehensive understanding of hydroxide ion transport in AEMs.https://doi.org/10.1038/s41467-024-55621-z
spellingShingle Zhongyang Wang
Ge Sun
Nicholas H. C. Lewis
Mrinmay Mandal
Abhishek Sharma
Mincheol Kim
Joan M. Montes de Oca
Kai Wang
Aaron Taggart
Alex B. Martinson
Paul A. Kohl
Andrei Tokmakoff
Shrayesh N. Patel
Paul F. Nealey
Juan J. de Pablo
Water-mediated ion transport in an anion exchange membrane
Nature Communications
title Water-mediated ion transport in an anion exchange membrane
title_full Water-mediated ion transport in an anion exchange membrane
title_fullStr Water-mediated ion transport in an anion exchange membrane
title_full_unstemmed Water-mediated ion transport in an anion exchange membrane
title_short Water-mediated ion transport in an anion exchange membrane
title_sort water mediated ion transport in an anion exchange membrane
url https://doi.org/10.1038/s41467-024-55621-z
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