Investigating the Structure–Function Relationships of Fluorinated Interfaces for PFAS Capture and Electrochemically‐Mediated Release

Abstract Fluorinated materials are promising sorbents for the selective removal of per‐ and polyfluoroalkyl substances (PFAS) due to their unique fluorophilic interactions. However, there are gaps in the understanding of design principles toward fluorinated materials for optimized PFAS remediation. In this work, we vary the length of fluorinated side‐chains in copolymer‐functionalized electrodes to study their effect on electrochemically‐mediated PFAS capture and release. Molecular dynamics simulations and adsorption experiments reveal that binding is governed by the total amount of fluorophilic interactions rather than the length of the fluorinated side‐chain. Moreover, the length of the fluorinated side‐chain alters the polymer packing and porosity, which in turn affects PFAS capture and release. Simulations reveal that short‐chain PFAS percolate into the pores of the polymer matrix, while long‐chain PFAS aggregate on the surface, facilitating a faster desorption. Experiments show that desorption is enhanced upon applying potential, regenerating over 80% of the electrode and providing a reversible mechanism for the adsorption and release of PFAS. Additionally, the copolymer sorbents demosntrate selectivity between PFAS, achieving separation factors >190 for perfluorooctanoic acid (PFOA, 7 C–F) over perfluorobutanoic acid (PFBA, 3 C–F). This study provides insights into the design of functional fluorinated materials for electrochemical PFAS separations.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-04-29
DOI
https://doi.org/10.1002/adfm.202502317
Citations
10
Primary Topic
Per- and polyfluoroalkyl substances research
Type
article
Field-Weighted Citation Impact
8.60

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article

Investigating the Structure–Function Relationships of Fluorinated Interfaces for PFAS Capture and Electrochemically‐Mediated Release

Anaira Román Santiago, Amartya Dutta, Xiao Su, Diwakar Shukla et al.
10 citations
Advanced Functional Materials
Per- and polyfluoroalkyl substances research
8.60
article

Investigating the Structure–Function Relationships of Fluorinated Interfaces for PFAS Capture and Electrochemically‐Mediated Release

Anaira Román Santiago, Amartya Dutta, Xiao Su, Diwakar Shukla, Ye Won Lee, Jhen‐Cih Wu, Yin Song, Chia‐Hung Hou
article en
10 citations

Abstract

Abstract Fluorinated materials are promising sorbents for the selective removal of per‐ and polyfluoroalkyl substances (PFAS) due to their unique fluorophilic interactions. However, there are gaps in the understanding of design principles toward fluorinated materials for optimized PFAS remediation. In this work, we vary the length of fluorinated side‐chains in copolymer‐functionalized electrodes to study their effect on electrochemically‐mediated PFAS capture and release. Molecular dynamics simulations and adsorption experiments reveal that binding is governed by the total amount of fluorophilic interactions rather than the length of the fluorinated side‐chain. Moreover, the length of the fluorinated side‐chain alters the polymer packing and porosity, which in turn affects PFAS capture and release. Simulations reveal that short‐chain PFAS percolate into the pores of the polymer matrix, while long‐chain PFAS aggregate on the surface, facilitating a faster desorption. Experiments show that desorption is enhanced upon applying potential, regenerating over 80% of the electrode and providing a reversible mechanism for the adsorption and release of PFAS. Additionally, the copolymer sorbents demosntrate selectivity between PFAS, achieving separation factors >190 for perfluorooctanoic acid (PFOA, 7 C–F) over perfluorobutanoic acid (PFBA, 3 C–F). This study provides insights into the design of functional fluorinated materials for electrochemical PFAS separations.

Advanced Functional MaterialsVol. 35(36)
University of Illinois Urbana-Champaign (US), National Taiwan University (TW)
National Science Foundation, National Natural Science Foundation of China
Openalex Percentile: Top 2%
Per- and polyfluoroalkyl substances research
8.60
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