Formaldehyde
is ubiquitously found in the environment, meaning
that real-time monitoring of formaldehyde, particularly indoors, can
have a significant impact on human health. However, the performance
of commercially available interdigital electrode-based sensors is
a compromise between active material loading and steric hindrance.
In this work, a spaced TiO2 nanotube array (NTA) was exploited
as a scaffold and electron collector in a formaldehyde sensor for
the first time. A Sn-based metal–organic framework was successfully
decorated on the inside and outside of TiO2 nanotube walls
by a facile solvothermal decoration strategy. This was followed by
regulated calcination, which successfully integrated the preconcentration
effect of a porous Sn-based metal–organic framework (SnMOF)
structure and highly active SnO2 nanocrystals into the
spaced TiO2 NTA to form a Schottky heterojunction-type
gas sensor. This SnMOF/SnO2@TiO2 NTA sensor
achieved a high room-temperature formaldehyde response (1.7 at 6 ppm)
with a fast response (4.0 s) and recovery (2.5 s) times. This work
provides a new platform for preparing alternatives to interdigital
electrode-based sensors and offers an effective strategy for achieving
target preconcentrations for gas sensing processes. The as-prepared
SnMOF/SnO2@TiO2 NTA sensor demonstrated excellent
sensitivity, stability, reproducibility, flexibility, and convenience,
showing excellent potential as a miniaturized device for medical diagnosis,
environmental monitoring, and other intelligent sensing systems.