A novel strategy to improve the electrochemical performance of a germanium anode is proposed via encapsulating germanium nanoparticles in carbon nanoboxes by carbon coating the precursor, germanium dioxide cubes, and then subjecting them to a reduction treatment. The complete and robust carbon boxes are shown to not only provide extra void space for the expansion of germanium nanoparticles after lithium insertion but also offer a large reactive area and reduced distance for the lithium diffusion. Furthermore, the thus-obtained composite, composed of densely stacked carbon nanoboxes encapsulating germanium nanoparticles (germanium at carbon cubes (Ge at CC)), exhibits a high tap density and improved electronic conductivity. Compared to carbon-coated germanium bulks, the Ge at CC material shows excellent electrochemical properties in terms of both rate capability and cycling stability, due to the unique cubic coreshell structure and the effective carbon coating, so that the Ge at CC electrode delivers ≈497 mA h g-1 at a current rate of 30 C and shows excellent cycling stability of 1065.2 mA h g-1 at 0.5 C for over 500 cycles.
AbstractA novel strategy to improve the electrochemical performance of germanium anode is proposed in this paper via encapsulating germanium nanoparticles in carbon nanoboxes by carbon coating the precursor, germanium dioxide cubes, and then subjecting them to a reduction treatment. The complete and robust carbon boxes are shown to not only provide extra void space for the expansion of germanium nanoparticles after lithium insertion, but also offer a large reactive area and reduced distance for the lithium diffusion. Furthermore, the thus-obtained composite, composed of densely stacked carbon nanoboxes encapsulating germanium nanoparticles (Ge@CC), exhibits a high tap density and improved electronic conductivity. Compared to carbon-coated germanium bulks, the Ge@CC material shows excellent electrochemical properties in terms of both rate capability and cycling stability, due to the unique cubic core-shell structure and the effective carbon coating, so that the Ge@CC electrode delivers about 497 mA h g -1 at a current rate of 30 C and shows excellent cycling stability of 1065.2 mA h g -1 at 0.5 C for over 500 cycles.