Publications by authors named "Yonas Tesfamhret"

Transition metal (TM) dissolution is a direct consequence of cathode-electrolyte interaction, having implications not only for the loss of redox-active material from the cathode but also for the alteration of solid electrolyte interphase (SEI) composition and stability at the counter electrode. It has widely been reported that the limited anodic stability of typical carbonate-based electrolytes, specifically ethylene carbonate (EC)-based electrolytes, makes high-voltage cathode performance problematic. Hence, the more anodically stable tetramethylene sulfone (SL) has herein been utilized as a co-solvent and a substitute for EC in combination with diethyl carbonate (DEC) to investigate the TM dissolution behavior of LiNCAl (NCA) and LiMnO (LMO).

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Two water-soluble binders of carboxymethyl cellulose (CMC) and sodium alginate (SA) have been studied in comparison with N-methylpyrrolidone-soluble poly(vinylidene difluoride-co-hexafluoropropylene) (PVdF-HFP) to understand their effect on the electrochemical performance of a high-voltage lithium nickel manganese oxide (LNMO) cathode. The electrochemical performance has been investigated in full cells using a Li Ti O (LTO) anode. At room temperature, LNMO cathodes prepared with aqueous binders provided a similar electrochemical performance as those prepared with PVdF-HFP.

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TiO -coating of LiNi Mn O (LNMO) by atomic layer deposition (ALD) has been studied as a strategy to stabilize the cathode/electrolyte interface and mitigate transition metal (TM) ion dissolution. The TiO coatings were found to be uniform, with thicknesses estimated to 0.2, 0.

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This study demonstrates the application of AlO coatings for the high-voltage cathode material LiNi Mn O (LNMO) by atomic layer deposition. The ultrathin and uniform coatings (0.6-1.

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