Abstract

The lithiation/delithiation properties of α-Si3 N4 and β-Si3 N4 are compared and the carbon coating effects are examined. Then, β-Si3 N4 at various fractions is used as the secondary phase in a Si anode to modify the electrode properties. The incorporated β-Si3 N4 decreases the crystal size of Si and introduces a new NSiO species at the β-Si3 N4 /Si interface. The nitrogen from the milled β-Si3 N4 diffuses into the surface carbon coating during the carbonization heat treatment, forming pyrrolic nitrogen and CNO species. The synergistic effects of combining β-Si3 N4 and Si phases on the specific capacity are confirmed. The operando X-ray diffraction and X-ray photoelectron spectroscopy data indicate that β-Si3 N4 is partially consumed during lithiation to form a favorable Li3 N species at the electrode. However, the crystalline structure of the hexagonal β-Si3 N4 is preserved after prolonged cycling, which prevents electrode agglomeration and performance deterioration. The carbon-coated β-Si3 N4 /Si composite anode shows specific capacities of 1068 and 480 mAh g-1 at 0.2 and 5 A g-1 , respectively. A full cell consisting of the carbon-coated β-Si3 N4 /Si anode and a LiNi0.8 Co0.1 Mn0.1 O2 cathode is constructed and its properties are evaluated. The potential of the proposed composite anodes for Li-ion battery applications is demonstrated.

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