Zinc-ion batteries, in which zinc ions and protons do intercalation and de-intercalation during battery cycling with various proposed mechanisms under debate, have been studied. Recently, electrolytic zinc-manganese batteries, exhibiting the pure dissolution-deposition behavior with a large charge capacity, have been accomplished through using electrolytes with Lewis acid. However, the complicated chemical environment and mixed products hinder the investigation though it is crucial to understand the detailed mechanism. Here, cyclic voltammetry coupled electrochemical quartz crystal microbalance (EQCM) and ultraviolet-visible spectrophotometry (UV-Vis) are respectively, for the very first time, used to study the transition from zinc-ion batteries to zinc electrolytic batteries by the continuous addition of acetate ions. These complementary techniques operando trace the mass and the composition evolution. The observed formation and dissolution of zinc hydroxide sulfate (ZHS) and manganese oxides evince the effect of acetate ions on zinc-manganese batteries from an alternative perspective. Both the amount of acetate and the pH value have large impacts on the capacity and Coulombic efficiency of the MnO electrode, and thus they should be optimized when constructing a full zinc-manganese battery with high rate capability and reversibility.
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http://dx.doi.org/10.1002/cssc.202300259 | DOI Listing |
Angew Chem Int Ed Engl
November 2024
School of Materials Science and Engineering, Key Laboratory of Electronic Packaging and Advanced Functional Materials of Hunan Province, Central South University, Changsha, 410083, P.R. China.
Elusive ion behaviors in aqueous electrolyte remain a challenge to break through the practicality of aqueous zinc-manganese batteries (AZMBs), a promising candidate for safe grid-scale energy storage systems. The proposed electrolyte strategies for this issue most ignore the prominent role of proton conduction, which greatly affects the operation stability of AZMBs. Here we report a water-poor quasi-solid electrolyte with efficient proton transfer pathways based on the large-space interlayer of montmorillonite and strong-hydration Pr additive in AZMBs.
View Article and Find Full Text PDFPhys Chem Chem Phys
October 2024
Department of Materials Science and Engineering, The University of Texas at Dallas, Richardson, Texas 75080, USA.
The appeal of safe, energy-dense, and environmentally-friendly MnO as a cathode for rechargeable aqueous zinc-metal oxide batteries (AZMOBs) has attracted significant research attention, but unexpected complexities have resulted in a decade of confusion and conflicting claims. The literature base is near saturation with a mix of efforts to achieve practical, rechargeable Zn-ion batteries and to untangle the presented electrochemical mechanisms. We have summarized the respective mechanisms and contextualized the respective justifications.
View Article and Find Full Text PDFNano Lett
August 2024
Hunan Provincial Key Laboratory of Chemical Power Sources, College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, People's Republic of China.
ACS Appl Mater Interfaces
May 2024
Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing 211816, China.
The continuous advancement in the field of flexible and wearable electronics has led to increased research interest in safe, low-cost, and flexible zinc-ion batteries, particularly with a focus on flexible electrolytes. In this study, we present a leather gel electrolyte (LGE) that offers robust mechanical properties and an excellent electrochemical performance. LGE exhibits an ionic conductivity of 1.
View Article and Find Full Text PDFSmall
August 2024
Division of Energy Storage, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
Mn/MnO aqueous battery is a promising candidate for large-scale energy storage owing to its feature of low-cost and abundant crustal reserves. However, the inherent MnO shedding issue results in a limited areal capacity and poor cycling life, which prohibits its further commercialization. In this manuscript, it is revealed that the cause of shedding is the cracking of MnO layer due to stress.
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