In the literature, Zn-Mn aqueous batteries (ZMABs) confront abnormal capacity behavior, such as capacity fluctuation and diverse "unprecedented performances." Because of the electrolyte additive-induced complexes, various charge/discharge behaviors associated with different mechanisms are being reported. However, the current performance assessment remains unregulated, and only the electrode or the electrolyte is considered. The lack of a comprehensive and impartial performance evaluation protocol for ZMABs hinders forward research and commercialization. Here, a pH clue (proton-coupled reaction) to understand different mechanisms is proposed and the capacity contribution is normalized. Then, a series of performance metrics, including rated capacity (C ) and electrolyte contribution ratio from Mn (CfM), are systematically discussed based on diverse energy storage mechanisms. The relationship between Mn (II) ↔ Mn (III) ↔ Mn (IV) conversion chemistry and protons consumption/production is well-established. Finally, the concrete design concepts of a tunable H /Zn /Mn storage system for customized application scenarios, opening the door for the next-generation high-safety and reliable energy storage system, are proposed.
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http://dx.doi.org/10.1002/adma.202300053 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
MOE Key Laboratory for UV Light-Emitting Materials and Technology, Northeast Normal University, Changchun, 130024, P. R. China.
Zn-Mn aqueous batteries (ZMABs) are widely recognized as a promising candidate for large-scale energy storage due to their cost-effectiveness, high safety and environmental friendliness. However, the practical application of ZMABs is hindered by inherent electrical contact loss, hydrogen evolution and dendrite growth on traditional anodes. Here, a three-tiered golf anode with high conductivity is developed to simultaneously enhance the reversibility of Zn and Mn metals.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Department of Chemistry, University College London, London, WC1H 0AJ, UK.
Compared to near-neutral electrolytes (pH=3-6), Zn||Mn batteries in acidic environments can achieve voltages up to ~2 V. However, high proton concentrations raise concerns about Zn anode stability. Current strategies for inhibiting hydrogen evolution corrosion (HEC) on the anode in Zn-based batteries mainly focus on the near-neutral electrolytes.
View Article and Find Full Text PDFSmall Methods
December 2024
Academy of Interdisciplinary Studies on Intelligent Molecules, Tianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin, 300387, China.
MnO is a promising candidate for aqueous zinc ion batteries (ZIBs) due to its high theoretical capacity (468.5 mAh g) and environmental friendliness, while its practical application is hindered by slow kinetics and rapid capacity degradation. Herein, a porous MnO with segregated and interlaced carbon framework (HCF-MnO) is introduced.
View Article and Find Full Text PDFRSC Adv
November 2024
CRRC Qingdao Sifang Rolling Stock Research Insititute Co Ltd People's Republic of China.
Small
January 2025
Department of Chemistry and the Tsinghua Center for Frontier Polymer Research, Tsinghua University, Beijing, 100084, China.
The low plating/stripping efficiency of zinc anodes, dendrite growth, and high freezing points of aqueous solutions hinder the practical application of aqueous zinc-ion batteries. This paper proposes a zwitterionic permeable network solid-state electrolyte based on the "anchor-capture" effect to address these problems by incorporating proline (Pro, a biological antifreeze agent) into the electrolyte. Extensive validation tests, Quantum Chemistry (QC) calculations, Molecular Dynamics (MD) Simulations, and ab initio molecular dynamics simulations consistently indicate that the amino groups in proline adsorb onto the Zn metal surface, stabilizing the zinc anode-electrolyte interface, suppressing side reactions from water decomposition, and homogenizing zinc-ion flux.
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