It
remains
challenging
for
the
fabrication
of
metal-organic
framework
(MOF)/semiconductor
heterojunction
photocatalysts
with
close
contact
interfaces.
In
this
work,
a
novel
MOF/semiconductor
photocatalyst
consisting
H2O2-modified
TiO2
nanotubes
(H2O2-TNTs)
and
MIL-88B(Fe)-NH2
(labeled
as
H-T/M)
was
firstly
constructed
based
on
hydrogen-bonded
combination
between
O
atoms
from
–OOH
groups
resulting
H2O2
absorbed
surface
H
–NH2
group
in
MOF.
The
significantly
enhanced
photocatalytic
property
H-T/M
reducing
Cr(VI)
under
visible
light
irradiation
could
be
ascribed
to
accelerated
interfacial
electron
transfer
dynamics
by
channel
hydrogen
bonds
(N···H–O–O–Ti),
which
extracted
femtosecond
transient
absorption
spectroscopy
(fs-TAS).
Moreover,
built-in
electric
field
differences
charge
density
functional
theory
(DFT)
calculations
provide
driving
force
transfer.
It
remains
challenging
for
the
fabrication
of
metal-organic
framework
(MOF)/semiconductor
heterojunction
photocatalysts
with
close
contact
interfaces.
In
this
work,
a
novel
MOF/semiconductor
photocatalyst
consisting
H2O2-modified
TiO2
nanotubes
(H2O2-TNTs)
and
MIL-88B(Fe)-NH2
(labeled
as
H-T/M)
was
firstly
constructed
based
on
hydrogen-bonded
combination
between
O
atoms
from
–OOH
groups
resulting
H2O2
absorbed
surface
H
–NH2
group
in
MOF.
The
significantly
enhanced
photocatalytic
property
H-T/M
reducing
Cr(VI)
under
visible
light
irradiation
could
be
ascribed
to
accelerated
interfacial
electron
transfer
dynamics
by
channel
hydrogen
bonds
(N···H–O–O–Ti),
which
extracted
femtosecond
transient
absorption
spectroscopy
(fs-TAS).
Moreover,
built-in
electric
field
differences
charge
density
functional
theory
(DFT)
calculations
provide
driving
force
transfer.