Direct observation of Sn crystal growth during the lithiation and delithiation processes of SnO2 nanowires

 Micron, doi:10.1016/j.micron.2012.01.016

Tin (Sn) crystal growth on Sn-based anodes in lithium ion batteries is
hazardous for reasons such as possible short-circuit failure by Sn
whiskers and Sn-catalyzed electrolyte decomposition, but the growth mechanism of Sn crystals during battery cycling is not clear. Here we
report different growth mechanisms of Sn crystal during the lithiation
and delithiation processes of SnO2 nanowires revealed by in situ transmission electron microscopy (TEM). Large spherical Sn nanoparticles with sizes of 20–200 nm grew instantaneously upon lithiation of a single-crystalline SnO2 nanowire at large current density (j > 20 A/cm2), which suppressed formation of the LixSn alloy but promoted agglomeration of Sn atoms. Control experiments of Joule-heating (j ≈ 2400 A/cm2) the pristine SnO2 nanowires resulted in melting of the SnO2 nanowires but not Sn particle growth, indicating that the abnormal Sn particle growth was induced by both chemical reduction (i.e., breaking the SnO2
lattice to produce Sn atoms) and agglomeration of the Sn atoms assisted by Joule heating. Intriguingly, Sn crystals grew out of the nanowire
surface via a different “squeeze-out” mechanism during delithiation of the lithiated SnO2 nanowires coated with an ultra-thin solid electrolyte LiAlSiOx
layer. It is attributed to the negative stress gradient generated by
the fast Li extraction in the surface region through the Li+-conducting LiAlSiOx layer. Our previous studies showed that Sn precipitation does not occur in the carbon-coated SnO2
nanowires, highlighting the effect of nanoengineering on tailoring the
electrochemical reaction kinetics to suppress the hazardous Sn whiskers
or nanoparticles formation in a lithium ion battery.