Zn-air batteries (ZABs) present high energy density and high safety but suffer from low oxygen reaction reversibility and dendrite growth at Zn electrode in alkaline electrolytes. Non-alkaline electrolytes have been considered recently for improving the interfacial processes in ZABs. However, the dynamic evolution and reaction mechanisms regulated by electrolytes at both the positive and Zn negative electrodes remain elusive. Herein, using in situ atomic force microscopy, we disclose that thin ZnO nanosheets deposit in non-alkaline electrolyte during discharge, followed by the formation of low-modulus products encircled around them. During recharge, the nanosheets are completely decomposed, revealing the favorable reversibility of the O/ZnO chemistry. The circular outlines with low-modulus, composed of C = C and ZnCO, are left which play a key role in promoting the oxygen reduction reaction (ORR) during the subsequent cycles. In addition, in situ optical microscopy shows that Zn can be uniformly dissolved and deposited in non-alkaline electrolyte, with the formation of homogeneous solid electrolyte interphase. Our work provides straightforward evidence and in-depth understanding of the interfacial reactions at both electrode interfaces in non-alkaline electrolyte, which can inspire strategies of interfacial engineering and material design of advanced ZABs.
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http://dx.doi.org/10.1038/s41467-024-55239-1 | DOI Listing |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11686246 | PMC |
Nat Commun
December 2024
Key Laboratory of Molecular Nanostructure and Nanotechnology, Beijing National Laboratory for Molecular Sciences, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Zn-air batteries (ZABs) present high energy density and high safety but suffer from low oxygen reaction reversibility and dendrite growth at Zn electrode in alkaline electrolytes. Non-alkaline electrolytes have been considered recently for improving the interfacial processes in ZABs. However, the dynamic evolution and reaction mechanisms regulated by electrolytes at both the positive and Zn negative electrodes remain elusive.
View Article and Find Full Text PDFMolecules
November 2024
School of Materials Science and Engineering, Liaocheng University, Liaocheng 252000, China.
Small
November 2023
Department of Materials Science, Fudan University, Shanghai, 200433, China.
Non-alkaline zinc-air batteries (ZABs) that use reversible O /ZnO chemistry exhibit excellent stability and superior reversibility compared to conventional alkaline ZABs. Unlike alkaline ZABs, ZnO discharge products are generated on the surface of the air cathodes in non-alkaline ZABs, requiring more gas-liquid-solid three-phase reaction interfaces. However, the kinetics of reported ZABs based on carbon black (CB) is far from satisfactory due to the insufficient reaction areas.
View Article and Find Full Text PDFChem Commun (Camb)
August 2023
Department of Chemistry and BINA - BIU Center for Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat-Gan 5290002, Israel.
Although non-alkaline rechargeable Zn-air batteries (RZABs) are promising for energy storage, their chemistry is still underdeveloped and unclear. It was suggested that using Zn(OAc) or Zn(OTf) aqueous solutions as electrolytes enables reversible, corrosion-free charge-discharge processes, but the anodic stability of carbon in these cells has remained poorly studied. We report that CO evolution is manifested during the oxygen evolution reaction in non-alkaline RZABs, which is associated with the corrosion of carbon scaffolds.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2022
MEET Battery Research Center, University of Münster, 48149, Münster, Germany.
Electrically rechargeable zinc-air batteries attract extensive research interests due to their potentially high energy density and low cost but suffer from chemical instability and poor electrochemical reversibility caused by the corrosive nature of the conventional alkaline electrolyte. Here we demonstrate a non-alkaline zinc acetate electrolyte for electrically rechargeable zinc-air batteries with long-term operation stability (>600 hours) in ambient air without any special cell engineering. The unique battery chemistry with reversible formation/decomposition of zinc hydroxyacetate dihydrate is systematically revealed using diversified electrochemical and analytical techniques.
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