Abstract

It was recently reported that inclusion of Cu in Bi-modified MnO2 cathodes allowed over 1000 cycles at nearly the full capacity of 617 mAh/g-MnO2, at a high areal capacity of 28 mAh/cm2. To better understand the molecular mechanism by which Bi and Cu impart rechargeability, cathodes prepared by physical mixing of MnO2 and Bi2O3 were studied during initial discharge at an areal capacity of 57.4 mAh/cm2, both with Cu (MDBC) and without (MDB). These were compared to the base case with MnO2 only (MD). It is demonstrated that there are two distinct regimes of MnII production during the second electron regime of discharge. In standard MD cathodes, the first regime results in an amorphous product formed simultaneously with Mn3O4, while the second results in crystalline Mn(OH)2. When MnO2 is Bi-modified, crystalline Mn(OH)2 is formed in both regimes and Mn3O4 is absent. Bi and Cu are observed to have a structural effect on the α-MnOOH discharge intermediate. CuII is shown to be electrochemically active at the surfaces of MnO2 particles, reducing to CuI and Cu0. Reversible potentials suggest MnII would act as a redox mediator, reducing CuII. Fluorescence mapping provides evidence for occurrence of this phenomenon.

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