Abstract
Extensive efforts have been devoted to unraveling the true cause of voltage decay in Li, Mn-rich layered oxides. An initial consensus was reached on structural rearrangement, then leaned toward the newly discovered lattice oxygen activity. It is challenging to differentiate their explicit roles because these events typically coexist during the electrochemical reaction of most Li-rich layered oxides. Here, the voltage decay behavior is probed in Li1.2Ni0.2Ru0.6O2, a structurally and electrochemically relevant compound to Li, Mn-rich layered oxide, but of no oxygen activity. Such intriguing characteristics allow the explicit decoupling of the contribution of transition metal migration and lattice oxygen activity to voltage decay in Li-rich layered oxides. The results demonstrate that the microstructural evolution, mainly originating from transition metal migration, is a direct cause of voltage decay, and lattice oxygen activity likely accelerates the decay.
| Original language | English |
|---|---|
| Article number | 1902258 |
| Journal | Advanced Energy Materials |
| Volume | 9 |
| Issue number | 47 |
| DOIs | |
| Publication status | Published - 1 Dec 2019 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Li-ion battery cathodes
- Li-rich layered oxide
- oxygen activity
- transition metal migration
- voltage decay
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