Attention
to semiconductor nanostructures with a narrow band gap
energy and low production cost has increased in recent years, due
to practical demands for use in various optoelectronics and communication
devices. Colloidal nanostructures from the IV–VI semiconductors,
such as lead and tin chalcogenides, seem to be the most suitable materials
platform; however, their poor chemical and spectral stability has
impeded practical applications. The present work explored the mechanism
for formation of new nanostructures, SnTe/PbTe/SnO2, with
a core/shell/shell heterostructure architecture. The preparation involved
a single-step post-treatment for the preprepared SnTe cores, which
simultaneously generated two different consecutive shells. The process
followed a remarkable Kirkendall effect, where Sn ions diffused to
the exterior surface from a region below the surface and left a ringlike
vacancy area. Then Pb ions diffused inward and created a PbTe shell,
filling the Sn-deficient region. Finally, the ejected Sn ions at the
exterior surface underwent oxidation and formed a disordered SnO2 layer. These intriguing processes were corroborated by a
theoretical estimation of the relative diffusion length of the individual
elements at the reaction temperature. The nanostructures which were
comprised of low-toxicity elements were endowed with optical tunability
and chemical stability, which lasted more than one month at ambient
conditions.