4.6 Article

Electrochemical Stability of ZnMn2O4: Understanding Zn-Ion Rechargeable Battery Capacity and Degradation

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 126, Issue 27, Pages 10957-10967

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.2c01900

Keywords

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Funding

  1. Salient Energy
  2. NSERC Alliance program
  3. Mitacs Globalink program
  4. International Manganese Institute (IMnI)
  5. Mitacs Accelerate program [FR49801]

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We present a refined Mn-Zn-H2O Pourbaix diagram relevant for Zn/MnO2 rechargeable cells, which helps to rationalize experimental observations and guide the selection of operating conditions for existing aqueous Zn/MnO2 rechargeable cells. The proposed Pourbaix diagram is validated through pH-dependent transformations of electrolytic manganese dioxide. The relation between electrochemical stability boundaries and operating conditions can also be used as a design criterion for future cathode materials in aqueous rechargeable batteries.
We present a refined Mn-Zn-H2O Pourbaix diagram with the emphasis on parameters relevant for the Zn/MnO2 rechargeable cells. It maps out boundaries of electrochemical stability for MnO2, ZnMn2O4, ZnMn3O7, and MnOOH. The diagram helps to rationalize experimental observation on processes and phases occurring during charge/discharge, including the position of charge/discharge redox peaks and capacity fade observed in rechargeable aqueous Zn-ion batteries for stationary storage. The proposed Pourbaix diagram is validated by observing the pH-dependent transformation of electrolytic manganese dioxide to hetaerolite and chalcophanite during discharge and charge, respectively. Our results can guide the selection of operating conditions (the potential range and pH) for existing aqueous Zn/MnO2 rechargeable cells to maximise their longevity. In addition, the relation between electrochemical stability boundaries and operating conditions can be used as an additional design criterion in exploration of future cathode materials for aqueous rechargeable batteries.

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