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Anodic electrochemical mechanism and performance dominant factors of the VB2-air battery
Schematic diagrams for the anodic discharge and self-discharge of the VB2-air battery. [Display omitted] •The new charge transfer reaction for the anode: VB2+12OH-→VO2++2BOH4-+2H2O+11e-.•No passivation layer formed on the surface of the VB2 during storage and discharge.•The main factors determining...
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Published in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2020-05, Vol.388, p.124257, Article 124257 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Schematic diagrams for the anodic discharge and self-discharge of the VB2-air battery.
[Display omitted]
•The new charge transfer reaction for the anode: VB2+12OH-→VO2++2BOH4-+2H2O+11e-.•No passivation layer formed on the surface of the VB2 during storage and discharge.•The main factors determining the anodic electrochemical performance.
The vanadium diboride air battery (VB2-air battery) is a primary battery with the highest intrinsic anode capacity of 4060 mAh g−1 and a theoretical open circuit potential of 1.55 V. So far, the studies of the battery are particularly limited by the elusive anodic electrochemical mechanism. In this work, the following new mechanism for the charge transfer reaction of the anode is proposed: VB2+12OH-→VO2++2BOH4-+2H2O+11e-. From the possible reactions of the anode, we conclude that the surface of the VB2 is not passivated during the battery's standing and discharging processes, which is further verified by specially designed experiments. The surface density of the active substance, the direct contact area of the active substance with the electrolyte, and the hydroxide ion concentration are considered as the dominant factors of the battery's discharge voltage and discharge capacity. A series of measurements on pouch cells have been conducted to ensure the direct proportion between the evolution tendency of charge transfer reaction and the concentration of the hydroxide ions. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2020.124257 |