Boron nitride nanotubes (BNNTs) are emerging nanomaterials
with
impressive mechanical properties and unique multifunctional properties
including high thermal stability, electrical insulation, optical transparency,
neutron absorption capability, and piezoelectricity. To harness the
true potential of BNNTs for applications from drug delivery to advanced
coatings and composites, functionalization is necessary to enhance
their solubility and processability. Current functionalization approaches
require aggressive reaction conditions such as long reaction times,
high temperatures, high pressures, aggressive reagents, and an inert
atmosphere. Herein, we present the development of a low temperature
covalent functionalization method for enhanced solution processing
of BNNTs utilizing a nitrene based (2 + 1) cycloaddition reaction
that results in enhanced BNNT processability and solubility in N-methyl-2-pyrrolidone and N,N-dimethylformamide. Confirmation and degree of covalent functionalization
are established using infrared (IR) spectroscopy, X-ray photoelectron
spectroscopy (XPS), and thermal gravimetric analysis (TGA). Poly(3-hexylthiophene)
(P3HT) is used to assess the quality of the BNNTs postfunctionalization
to again confirm covalent functionalization. Finally, secondary functionalization
of the functionalized BNNTs with propargyl chloride is achieved to
demonstrate that this functionalization not only enhances the processability
of the BNNTs but also results in a BNNT surface platform in which
a plethora of molecules and nanomaterials can be grafted based on
the application case. This nondestructive method preserves the extraordinary
properties of BNNTs while opening their widespread use in many new
and exciting opportunities in materials development.