Work

Molecular Mechanism and Electrostatic Effect Enabling Symmetric All-Quinone Aqueous Redox Flow Batteries

Year: 2024
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Symmetric all-quinone aqueous redox flow batteries (SQA-RFBs), in which the same quinone derivative is used as the electroactive compound in the negative and positive electrolytes, thereby obviating the need for a species-selective membrane, have been pursued as a potentially cost-effective and sustainable technology for stationary-electrical energy storage. Molecular decomposition during redox activity has frustrated all symmetric organic aqueous RFB development attempts. We used in situ/operando spectroelectrochemistry and density functional theory calculations to demonstrate that during the redox reaction of alizarin red S (ARS), a promising quinone for SQA-RFBs, intramolecular electronic oscillations form positively charged intermediates. Electrodes functionalized with net negative charge stabilize these intermediates via a hybrid adsorptive–diffusive electrochemical reaction mechanism, thereby enabling the cycling of the SQA-RFB. To understand the mechanism, spectroelectrochemical studies were performed on a series of electrodes with and without this functionalization. We report the performance of the first membraneless SQA-RFB prototype, containing ARS in the electrolyte storage reservoirs and instrumented with a reference electrode to evaluate the evolution of the half-cell potentials.
Language: English
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4400899130
FWCI: 0.83
Cites: 41
Cited by: 8
Related to: 10