Charge polarity-dependent ion-insertion asymmetry during electrochemical doping of an ambipolar π-conjugated polymer
Jibin J. Samuel,
Ashutosh Garudapalli,
Chandrasekhar Gangadharappa,
Smruti Rekha Mahapatra,
Satish Patil and
Naga Phani B. Aetukuri ()
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Jibin J. Samuel: Indian Institute of Science
Ashutosh Garudapalli: Indian Institute of Science
Chandrasekhar Gangadharappa: Indian Institute of Science
Smruti Rekha Mahapatra: Indian Institute of Science
Satish Patil: Indian Institute of Science
Naga Phani B. Aetukuri: Indian Institute of Science
Nature Communications, 2022, vol. 13, issue 1, 1-10
Abstract:
Abstract Electrochemical doping is central to a host of important applications such as bio-sensing, neuromorphic computing and charge storage. However, the mechanisms that enable electrochemical dopability and the various parameters that control doping efficiencies are poorly understood. Here, employing complementary electrochemical and spectroelectrochemical measurements, we report a charge-polarity dependent ion insertion asymmetry in a diketopyrrolopyrrole-based ambipolar π-conjugated polymer. We argue that electrostatic interactions are insufficient to fully account for the observed charge-specific ion insertion into the polymer matrix. Using polymer side-chain dependent electrochemical doping studies, we show that electron density donating and accepting tendencies of polymer side-chains sufficiently describe the observed charge-polarity dependent electrochemical doping. Our observations are akin to the solvation of dopant ions by polymer side-chains. We propose that Gutmann donor/acceptor number framework qualifies the ‘solvent-like’ properties of polymer side-chains and provides a rational basis for designing π-conjugated polymers with favorable mixed ionic electronic transport properties.
Date: 2022
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DOI: 10.1038/s41467-022-35408-w
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