Nanoscale waterpolymer interactions tune macroscopic diffusivity of water in aqueous poly(ethylene oxide) solutions

The separation and anti-fouling performance of water purification membranes is governed by both macroscopic and molecular-scale water properties near polymer surfaces. However, even for poly(ethylene oxide) (PEO) ubiquitously used in membrane materials there is little understanding of whether or how...

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Published inChemical science (Cambridge) Vol. 15; no. 7; pp. 2495 - 258
Main Authors Moon, Joshua D, Webber, Thomas R, Brown, Dennis Robinson, Richardson, Peter M, Casey, Thomas M, Segalman, Rachel A, Shell, M. Scott, Han, Songi
Format Journal Article
Published 14.02.2024
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Summary:The separation and anti-fouling performance of water purification membranes is governed by both macroscopic and molecular-scale water properties near polymer surfaces. However, even for poly(ethylene oxide) (PEO) ubiquitously used in membrane materials there is little understanding of whether or how the molecular structure of water near PEO surfaces affects macroscopic water diffusion. Here, we probe both time-averaged bulk and local water dynamics in dilute and concentrated PEO solutions using a unique combination of experimental and simulation tools. Pulsed-Field Gradient NMR and Overhauser Dynamic Nuclear Polarization (ODNP) capture water dynamics across micrometer length scales in sub-seconds to sub-nanometers in tens of picoseconds, respectively. We find that classical models, such as the StokesEinstein and MackieMeares relations, cannot capture water diffusion across a wide range of PEO concentrations, but that free volume theory can. Our study shows that PEO concentration affects macroscopic water diffusion by enhancing the water structure and altering free volume. ODNP experiments reveal that water diffusivity near PEO is slower than in the bulk in dilute solutions, previously not recognized by macroscopic transport measurements, but the two populations converge above the polymer overlap concentration. Molecular dynamics simulations reveal that the reduction in water diffusivity occurs with enhanced tetrahedral structuring near PEO. Broadly, we find that PEO does not simply behave like a physical obstruction but directly modifies water's structural and dynamic properties. Thus, even in simple PEO solutions, molecular scale structuring and the impact of polymer interfaces is essential to capturing water diffusion, an observation with important implications for water transport through structurally complex membrane materials. PEO restructures water near the polymer, reducing free volume and slowing local water.
Bibliography:https://doi.org/10.1039/d3sc05377f
Electronic supplementary information (ESI) available. See DOI
ISSN:2041-6520
2041-6539
DOI:10.1039/d3sc05377f