Defects are widely
present in nanomaterials, and they are recognized
as the active sites that tune surface properties in the local region
for catalysis. Recently, the theory linking defect structures and
catalytic properties of nanocatalysts has been most commonly described.
In this study, we prepared boron-doped carbon nano-onions (B-CNOs)
by applying an annealing treatment of ultradispersed nanodiamond particles
and amorphous boron. These experimental conditions guarantee doping
of CNOs with boron atoms in the entire carbon nanostructure, thereby
ensuring structural homogeneity. In our research, we discuss the correlations
between defective structures of B-CNOs with their catalytic properties
toward SO
2
and
tert
-butanol dehydration.
We show that there is a close relationship between the catalytic properties
of the B-CNOs and the experimental conditions for their formation.
It is not only the mass of the substrates used for the formation of
B-CNOs that is crucial, that is, the mass ratio of NDs to amorphous
B, but also the process, including temperature and gas atmosphere.
As it was expected, all B-CNOs demonstrated significant catalytic
activity in HSO
3
–
oxidation. However,
the subsequent annealing in an air atmosphere diminished their catalytic
activity. Unfortunately, no direct relationship between the catalytic
activity and the presence of heteroatoms on the B-CNO surface was
observed. There was a linear dependence between catalytic activity
and Raman reactivity factors for each of the B-CNO materials. In contrast
to SO
2
oxidation, the B-CNO-a samples showed higher catalytic
activity in
tert
-butanol dehydration due to the presence
of Brønsted and Lewis acid sites. The occurence of three types
of boron-Lewis sites differing in electron donor properties was confirmed
using quantitative infrared spectroscopic measurements of pyridine
adsorption.