4.8 Article

Mn-incorporated Co3O4 bifunctional electrocatalysts for zinc-air battery application: An experimental and DFT study

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 319, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2022.121909

关键词

Zinc-air battery; Bifunctional electrocatalyst; Manganese incorporation; Oxygen vacancy; DFT calculation

资金

  1. National Natural Science Foundation of China [22076088, 21607163]
  2. Natural Sci- ence Foundation of Anhui Province [2008085ME134]
  3. Qingdao Science and Technology Plan Key Research and Development Special Project [21-1-2-17-xx]

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Manganese-incorporated Co3O4 catalysts, prepared through thermal pyrolysis of ZIF-67, showed enhanced electrocatalytic activity for oxygen reduction and evolution reactions. The catalyst annealed at 450 degrees C exhibited the best performance in terms of catalytic activity, delivering high power density and good cycling stability in zinc-air battery applications. The improved catalytic activity can be attributed to the introduction of manganese and the induced structural changes.
Manganese-incorporated Co3O4 catalysts were prepared via thermal pyrolysis of ZIF-67, and the effect of manganese incorporation and annealing temperature on their catalytic performances for oxygen reduction and evolution reactions (ORR, OER) were investigated. Notable crystalline distortion was induced by manganese insertion into Co(3)O(4 )lattice, resulting in smaller crystallite size, more abundant Co2+ and considerable oxygen vacancies. All these properties were regarded as the crucial origins for electrocatalytic activity elevation. The catalyst annealed at 450 degrees C (denoted as Mn/Co-450) exhibited the optimal catalytic activity with an ultra-low potential gap (0.83 V). Using Mn/Co-450 as an air cathode, the zinc-air battery delivered high power density (115.5 mW cm(-2)), competitive specific capacity (783.4 mAh g(-1)) and good cycling stability. The theoretical overpotentials of ORR and OER were respectively decreased by 0.18 V and 0.05 V by DFT calculation due to the weakened interaction between Co and OH group and the strengthened Co-OOH interaction.

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