Hierarchical Nano-Electrocatalytic Reactor for High Performance Polysulfides Redox Flow Batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 37787504.
- Also identified by DOI 10.1021/acsnano.3c07085.
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Abstract
The aqueous polysulfides is an important Earth-abundant and multielectron redox couple to construct high capacity density and low-cost aqueous redox flow batteries (RFB) ; nevertheless, the sluggish conversion and kinetic behavior of S<sup>2-</sup>/S<sub><i>x</i></sub><sup>2-</sup> result in a low power density output and poor active material utilizations. Herein, we present nanoconfined self-assembled ordered hierarchical porous Co and N codoped carbon (OHP-Co/NC) as an electrocatalytic reactor to enhance the mass transfer and redox activity of aqueous polysulfides. Finite element method simulation proves that the OHP-Co/NC with interconnected macropores and mesopores exhibits an enhanced mass transfer and delivers a larger redox electrolyte utilization of 50.1% compared to 23.3% of conventional Co/NC. Notably, the OHP-Co/NC obtained at 850 °C delivers the smallest redox peak potential difference (Δ<i>E</i> = 99 mV). Comparison studies of <i>in operando</i> Raman for aqueous polysulfides in the redox electrolyte and <i>in situ</i> electrochemical Raman on the single OHP-Co/NC particle for the adsorbed polysulfides were carried out. And it confirms that the OHP-Co/NC-850 catalyst has a strong adsorption of S<sub>4</sub><sup>2-</sup> and can retard the strong disproportionation and hydrolysis behavior of polysulfides on the electrocatalyst interface. Therefore, the polysulfide/ferrocyanide RFB with an OHP-Co/NC-850 based membrane-electrode assembly (MEA) exhibited a high power density of 110 mW cm<sup>-2</sup>, as well as a steady capacity retention over 99.7% in 300 cycles.