4.8 Article

Operando NMR electrochemical gating studies of ion dynamics in PEDOT:PSS

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NATURE MATERIALS
卷 22, 期 6, 页码 746-+

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NATURE PORTFOLIO
DOI: 10.1038/s41563-023-01524-1

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Operando NMR spectroscopy is used to quantify cation and water movement in organic mixed conductors, providing insights into charge-compensating interactions and ionic dynamics. The study sheds light on the working principles of organic mixed conductors and demonstrates the utility of operando NMR spectroscopy in revealing structure-property relationships in electroactive polymers.
Understanding charge-compensating interactions and ionic dynamics in organic mixed conductors can be challenging. Operando NMR spectroscopy is now used to quantify cation and water movement during doping/dedoping in mixed conductor films. Although organic mixed ionic-electronic conductors are widely proposed for use in bioelectronics, energy generation/storage and neuromorphic computing, our fundamental understanding of the charge-compensating interactions between the ionic and electronic carriers and the dynamics of ions remains poor, particularly for hydrated devices and on electrochemical cycling. Here we show that operando Na-23 and H-1 nuclear magnetic resonance (NMR) spectroscopy can quantify cation and water movement during the doping/dedoping of films comprising the widely used mixed conductor poly(3,4-ethylene dioxythiophene) poly(styrene sulfonate) (PEDOT:PSS). A distinct Na-23 quadrupolar splitting is observed due to the partial ordering of the PSS chains within the PEDOT:PSS-rich domains, with respect to the substrate. Operando Na-23 NMR studies reveal a close-to-linear correlation between the quadrupolar splitting and the charge stored, which is quantitatively explained by a model in which the holes on the PEDOT backbone are bound to the PSS SO3- groups; an increase in hole concentration during doping inversely correlates with the number of Na+ ions bound to the PSS chains within the PEDOT-rich ordered domains, leading to a decrease in ions within the ordered regions and a decrease in quadrupolar splitting. The Na+-to-electron coupling efficiency, measured via Na-23 NMR intensity changes, is close to 100% when using a 1 M NaCl electrolyte. Operando H-1 NMR spectroscopy confirms that the Na+ ions injected into/extracted from the wet films are hydrated. These findings shed light on the working principles of organic mixed conductors and demonstrate the utility of operando NMR spectroscopy in revealing structure-property relationships in electroactive polymers.

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