posted on 2019-12-31, 17:06authored byGary K. Ong, Camila A. Saez Cabezas, Manuel N. Dominguez, Susanne Linn Skjærvø, Sungyeon Heo, Delia J. Milliron
Niobium oxide (Nb2O5) is an interesting
active
material for technologies ranging from catalysis and sensors to energy
storage and electrochromic devices owing to its unique optical, electronic,
and electrochemical properties. These properties vary between different
phases and morphologies in the Nb2O5 system,
but systematic studies that correlate properties to phase and morphology
are limited by current synthetic methods, which require postsynthetic
high temperature treatments and suffer from a lack of direct and precise
control over morphology, crystal structure, and stoichiometry. Here,
we report a heat-up colloidal synthesis method that produces orthorhombic
Nb2O5 nanorods 1 nm in width by 31 nm in length
that preferentially grow along the [001] direction. The synthesis
is based on aminolysis of niobium oleate in octadecene, and nanorods
are formed through three distinct steps: aminolysis-driven formation
of niobium oxo clusters, condensation into amorphous Nb2O5 seeds below the reaction temperature (240 °C,
under atmospheric pressure), and crystallization and growth of Nb2O5 nanorods. We investigated the electrochromic
behavior of nanorod thin films upon Li+ intercalation and
observed predominantly near-infrared coloration, fast switching
kinetics, and durability for at least 500 charge–discharge
cycles.