A composite anode including silicon oxide, amorphous carbon and few -layer graphene (FLG) is investigated for Li -ion battery. The material reflects both the amorphous structure of the silicon oxide and the crystalline one of the FLG, with a morphology consisting of micrometric FLG flakes and carbon surrounded by nanometric particles of silicon oxide. The electrode shows reversible Li -alloying and Li -insertion processes between 0.01 and 0.30 V vs. Li+/Li, as well as an interphase progressively improving and activating upon cell operation, with a decrease of the resistance. Galvanostatic cycling shows maximum capacity of about 400 mAh g-1, rate capability extended to 240 mA g-1, and cell life of 200 cycles with capacity retention of 94%. The anode is chemically pre-lithiated to remove the initial irreversible capacity using direct contact with lithium metal, and combined with a LiNi0.33Mn0.33Co0.33O2 (NCM) layered oxide cathode in a Li -ion battery. The full -cell shows an electrochemical process centered at 3.5 V with a capacity of 158 mAh g-1 retained for 90% over 120 cycles, a coulombic efficiency exceeding 98%, and rate capability extended up to 3C. Ex -situ studies of the electrodes evidence the full retention of the morphology and structure over cycling.
A lithium-ion battery with cycling stability promoted by the progressive activation of a silicon oxide anode in graphene-amorphous carbon matrix
Barcaro, EdoardoPrimo
;Marangon, VittorioSecondo
;Mutarelli, MarcoPenultimo
;Hassoun, Jusef
Ultimo
2024
Abstract
A composite anode including silicon oxide, amorphous carbon and few -layer graphene (FLG) is investigated for Li -ion battery. The material reflects both the amorphous structure of the silicon oxide and the crystalline one of the FLG, with a morphology consisting of micrometric FLG flakes and carbon surrounded by nanometric particles of silicon oxide. The electrode shows reversible Li -alloying and Li -insertion processes between 0.01 and 0.30 V vs. Li+/Li, as well as an interphase progressively improving and activating upon cell operation, with a decrease of the resistance. Galvanostatic cycling shows maximum capacity of about 400 mAh g-1, rate capability extended to 240 mA g-1, and cell life of 200 cycles with capacity retention of 94%. The anode is chemically pre-lithiated to remove the initial irreversible capacity using direct contact with lithium metal, and combined with a LiNi0.33Mn0.33Co0.33O2 (NCM) layered oxide cathode in a Li -ion battery. The full -cell shows an electrochemical process centered at 3.5 V with a capacity of 158 mAh g-1 retained for 90% over 120 cycles, a coulombic efficiency exceeding 98%, and rate capability extended up to 3C. Ex -situ studies of the electrodes evidence the full retention of the morphology and structure over cycling.File | Dimensione | Formato | |
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