AI Article Synopsis

  • The aqueous Zn-vanadium oxide battery faces electrochemical failures due to large volumetric expansion in cathodes, slow transport kinetics, dendrite growth, and hydrogen evolution at the anode.
  • A multifunctional anti-proton electrolyte, particularly with PEG 400, has been developed to address these issues by regulating Zn solvation and reducing lattice expansion in vanadium oxide.
  • This innovative electrolyte helps achieve a high-rate and stable battery performance, with significant capacity retention after extensive cycling, thus presenting a promising strategy for enhancing aqueous Zn-ion batteries.

Article Abstract

Large volumetric expansion of cathode hosts and sluggish transport kinetics in the cathode-electrolyte interface, as well as dendrite growth and hydrogen evolution at Zn anode side are considered as the system problems that cause the electrochemical failure of aqueous Zn-vanadium oxide battery. In this work, a multifunctional anti-proton electrolyte was proposed to synchronously solve all those issues. Theoretical and experimental studies confirm that PEG 400 additive can regulate the Zn solvation structure and inhibit the ionization of free water molecules of the electrolyte. Then, smaller lattice expansion of vanadium oxide hosts and less associated by-product formation can be realized by using such electrolyte. Besides, such electrolyte is also beneficial to guide the uniform Zn deposition and suppress the side reaction of hydrogen evolution. Owing to the integrated synergetic modification, a high-rate and ultrastable aqueous Zn-VO/C battery can be constructed, which can remain a specific capacity of 222.8 mAh g after 6000 cycles at 5 A g, and 121.8 mAh g even after 18,000 cycles at 20 A g, respectively. Such "all-in-one" solution based on the electrolyte design provides a new strategy for developing high-performance aqueous Zn-ion battery.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346040PMC
http://dx.doi.org/10.1007/s40820-022-00907-4DOI Listing

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