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Influence of cathodic overpotential and zincate concentration on zinc deposition in alkaline solution

机译:阴极过电位和锌酸盐浓度对碱性溶液中锌沉积的影响

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摘要

Understanding zinc deposition during charging is important for the development of electrically rechargeable zinc-air batteries. For this purpose, the influences of cathodic overpotential and zincate concentration on zinc deposition in 6 M KOH solution were investigated by electrochemical and morphology characterization. When the zincate concentration is lower than 0.1 M, or the cathodic overpotential is more positive than -30 mV, the first charge-transfer reaction (Zn(OH)(2) + e(-) -> Zn(OH) + OH-) tends to be the rate-determining step. The second charge-transfer reaction (Zn(OH) + e(-) -> Zn + OH-) becomes the rate-determining step at zincate concentration higher than 0.2 M and cathodic overpotentials larger than -50 mV. A low zincate concentration and small cathodic overpotential help suppress dendritic zinc deposition. These results will promote the performance of zinc anodes during the charging of zinc-air batteries.
机译:了解充电过程中的锌沉积对于可充电锌空气电池的开发很重要。为此,通过电化学和形态表征研究了阴极超电势和锌酸盐浓度对6 M KOH溶液中锌沉积的影响。当锌酸盐浓度低于0.1 M或阴极超电势高于-30 mV时,第一次电荷转移反应(Zn(OH)(2)+ e(-)-> Zn(OH)+ OH- )往往是决定速率的步骤。在锌酸盐浓度高于0.2 M且阴极超电势大于-50 mV时,第二个电荷转移反应(Zn(OH)+ e(-)-> Zn + OH-)成为速率确定步骤。低锌酸盐浓度和小的阴极过电位有助于抑制树突状锌的沉积。这些结果将在锌空气电池充电期间提高锌阳极的性能。

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