The development of
highly efficient catalysts for ambient formaldehyde
(HCHO) destruction is of great interest for indoor air purification.
Here, we show that a sodium (Na)-doped iridium (Ir) catalyst (Ir/TiO2) is a highly active catalyst for the catalytic oxidation
of HCHO at room temperature. We observed that Na addition dramatically
enhanced the activity of the Ir/TiO2-R catalyst, and 100%
HCHO conversion was achieved over Na-Ir/TiO2-R catalyst
at a gas hourly space velocity of 100,000 h–1 and
HCHO inlet concentration of 120 ppm at 25 °C. The Ir/TiO2 and Na-Ir/TiO2 catalysts were characterized using
X-ray powder diffraction, Brunauer–Emmett–Teller surface
area testing, high-angle annular dark-field scanning transmission
electron microscopy, H2 temperature-programmed reduction
(TPR), X-ray absorption fine structure, X-ray photoelectron spectroscopy,
and CO-TPR. The characterization results show that the addition of
Na species had no influence on Ir dispersion on the TiO2 surface but greatly promoted the activation of both chemisorbed
oxygen and H2O. The reaction mechanism of HCHO oxidation
was investigated by using in situ diffuse reflectance infrared transform
spectroscopy. The results show that the reaction mechanisms on Ir/TiO2-R and Na-Ir/TiO2-R both followed the direct formate
oxidation pathway (HCHO → HCOO + OH → CO2 + H2O), and the activated oxygen species mainly participated
in the formate formation step while the activated OH groups were primarily
responsible for the subsequent formate oxidation. Because of the improved
capacities for the activation of oxygen and H2O induced
by Na addition, the Na-Ir/TiO2 catalyst demonstrated much
better performance than Ir/TiO2 for ambient HCHO oxidation.