Abstract

Aqueous processing of positive electrode active materials (AMs) could enable a more economical and environmentally friendly production of lithium‐ion batteries. Intrinsically, aqueous processing of positive AMs is hampered by lithium‐proton exchange in the AM surface, leading to a poor electrochemical performance and a resulting strong increase in the pH value in the electrode paste, thereby corroding the aluminum current collector. Herein, the influence of different lithium salts as processing additive to tailor the pH value of the electrode paste, the manganese dissolution during processing, and the electrochemical performance is described for aqueous processing of LiNi0.5Mn1.5O4‐based positive electrodes. Positive electrodes, based on an aqueous LiNi0.5Mn1.5O4‐based electrode paste which is mixed with LiN(SO2CF3)2 (LiTFSI), achieve a comparable electrochemical performance to state‐of‐the‐art nonaqueous‐processed electrodes. Manganese dissolution into the electrode paste is examined by inductively coupled plasma‐mass spectrometry (ICP‐MS), showing that the addition of lithium salts to the electrode paste substantially decreases manganese leaching during processing. Furthermore, postmortem analysis shows that the addition of LiTFSI to the electrode paste has a positive effect not only during processing but also on charge/discharge cycling performance.

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