The cycling stability and the surface passivation qualities of a heterogeneous polycrystalline NiSi 2 /amorphous Ni x SiO y core-shell nanowires cycled in a Li ion half cell is reported. The nanowire morphology showed stable cycling and excellent charge rate capability having a stable capacity above 1700 mAh/g when cycled in a coin cell at 1/2 C and retaining a capacity of 300 mAhr/g when cycled at a 10 C charge rate. It is shown that the stable cycling is due to the passivation qualities of the oxide components within the amorphous shell which create a stable solid-electrolyte interphase (SEI) during charging which is reduced during discharging through the conductive pathway provided by the Ni doping in the shell and NiSi 2 in the core. The NiSi 2 core interacts with Li through intercalation retaining its rigid core even while Li charged, the overall dimensions of the structure mitigate any pulverization issues, and the conductive core along with the Ni doping disallow any Li trapping leading to high columbic efficiency.Lithium-ion (Li-ion) batteries are the energy storage devices of choice for items ranging from portable electronic devices to electric vehicles (EVs). Most current batteries in this technology family rely on graphite as an anode material, which has relatively low charge storage capacity inhibiting the range of electric vehicles and the lifetime of portable electronics. The use of higher capacity materials for both anode and cathode can alleviate the life-time problems, but are plagued by an array of issues resulting from the materials having an alloying rather than an intercalation reaction with Li. 1-7 For anode materials Si has the highest theoretical capacity (4422 mAh/g 11X higher than graphite at 372 mAh/g) and has been sought after for use in Li-ion batteries. 1-5 Utilizing Si as an anode material creates three different problems in its application namely: pulverization created through strain in volume expansion during alloying, Li trapping due to Si semiconductor to conductor transition when lithiated, and unmitigated creation of a passivation layer on the anode called solid-electrolyte interphase (SEI) growth. 1-8 The SEI is formed due to the bath constituents being unstable at the operating voltage of the Li-ion battery thus decomposing into an insulating layer on the electrode surface. 1-7 Since Si goes through continuous volume expansion during lithiation, Si brings new unpassivated material to the electrode surface to be passivated creating a large SEI layer. [1][2][3][4][5][6][7][8] For Si to achieve such a high capacity Si alloys with Li to create the Li 22 Si 5 silicide causing a 400% volume expansion during the reaction. 1-4 The strain induced pulverization however was shown to be mitigated by going to nano dimensioned materials namely under 150 nm. 6 The second problem in the creation of an unstable SEI passivation layer however has not been solved for Si. 1-5 This passivation layer is created upon the first several cycles of the Si anode material with the electrolyte and is main...