Nonmetallic doped metal oxides can
be broad in their visible-light-response
range. However, the half-filled or isolated impurity state can also
be the new recombination center for photogenerated electrons/holes,
which seriously influence the photocatalytic activity of the catalyst
in the visible-light region. Therefore, how to prolong the photogenerated
carrier life of nonmetallic doping metal oxides is the difficult and
challenging topic in the field of photocatalysis. In this work, the
hexagonal nanosheets assembled by N-doped C (N–C)-coated N-doped
In2O3 (N–In2O3)
nanoparticles (N–C/N–In2O3 HS)
was obtained by simply pyrolyzing the In(2,5-PDC) hexagonal sheets.
The N–C/N–In2O3 HS catalyst exhibit
good photocatalytic activity and cycle stability in the long-wavelength
region of visible light (λ = 520 and 595 nm). The effective
utilization of long-wavelength visible light for N–C/N–In2O3 HS was mainly attributed to the acceptor–donor–acceptor
compensation mechanism between the oxygen vacancy (VO)
and substitutional N-doping (Ns) sites, which made the
N–C/N–In2O3 HS possess a continuous
band structure, without the half-filled or isolated impurity state
in the band gap, and extended its light absorption edge to 733 nm.
The compensation mechanism of nitrogen doping on In2O3 can promote the photocatalytic activity under longer-wavelength
yellow light (595 nm) irradiation. The N–C layer coated on
the N–In2O3 nanoparticles acted as a
good acceptor of photogenerated electrons, facilitating the effective
spatial separation of photogenerated carriers and extend photogenerated
carrier lifetimes. The comparative photocatalytic experiments (N–In2O3 HS and N–C/N–In2O3 HS) show that the presence of N-doped C layer can enhance
the photocatalytic efficiency by nearly 10-fold. This double-doping
and carbon-coating strategy provided a novel research idea to solve
the problem that nonmetal atoms doped metal oxides led to the secondary
combination of photogenerated electrons/holes.