One of the weaknesses
of silicon-based batteries is the rapid deterioration
of the charge-storage capacity with increasing cycle numbers. Pure
silicon anodes tend to suffer from poor cycling ability due to the
pulverization of the crystal structure after repeated charge and discharge
cycles. In this work, we present the synthesis of a hollow nanostructured
SiO2 material for lithium-ion anode applications to counter
this drawback. To improve the understanding of the synthesis route,
the crucial synthesis step of removing the ZnO template core is shown
using an in situ closed gas-cell sample holder for transmission electron
microscopy. A direct visual observation of the removal of the ZnO
template from the SiO2 shell is yet to be reported in the
literature and is a critical step in understanding the mechanism by
which these hollow nanostructures form from their core–shell
precursors for future electrode material design. Using this unique
technique, observation of dynamic phenomena at the individual particle
scale is possible with simultaneous heating in a reactive gas environment.
The electrochemical benefits of the hollow morphology are demonstrated
with exceptional cycling performance, with capacity increasing with
subsequent charge–discharge cycles. This demonstrates the criticality
of nanostructured battery materials for the development of next-generation
Li+-ion batteries