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Updated: Sep 16, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Mn-Co Dual-Metal Single-Atom Catalytic Sites for Boosted Redox Kinetics in Aqueous Polysulfide/Ferricyanide Flow
Hong Zhang1, Ziyu Feng2,3, Tianhang Ding2,3
1Key Laboratory of Automobile Materials (Jilin University), Ministry of Education, and School of Material Science and Engineering, Jilin University, Changchun 130022, China.
None:
The sluggish redox kinetics of Na2Sx/Na2S and the uncontrollable crossover of polysulfides often result in limited reutilization of active materials, hindering the practical scalable application of polysulfide/ferricyanide flow batteries. By leveraging the bidirectional manipulation of redox kinetics of active species, diatomic Mn and Co sites anchored on nitrogen-doped carbon encapsulated graphite carbon felt was prepared. And a progressive "optimized d-band model" was revealed, in which the tunable d-band centers of Mn and Co were, respectively, regulated to enable facile electron extraction and injection during the Na2S2-Na2S redox; then the synergistic catalytic effect renders the matrix with bidirectional acceleration. The electrocatalytic capability was also witnessed within the catholyte chamber. The assembled polysulfide-ferricyanide flow cell exhibits high energy efficiency of 76.4% at 20 mA cm-2, and an impressively power density of 119.3 mW cm-2, along with a very low capacity decay rate of 0.0146% per cycle over 1000 cycles.
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