α-Fe2O3-supported Co3O4 nanoparticles to construct highly active interfacial oxygen vacancies for ozone decomposition.
Environ Pollut
; 330: 121704, 2023 Aug 01.
Article
de En
| MEDLINE
| ID: mdl-37116569
ABSTRACT
Ozone pollution has become one of the most concerned environmental issue. Developing low-cost and efficient catalysts is a promising alternative for ozone decomposition. This work presents a creative strategy that using α-Fe2O3-supported Co3O4 nanoparticles for constructing interfacial oxygen vacancies (Vo) to remove ozone. The efficiency of Co3O4/α-Fe2O3 was superior to that of pure α-Fe2O3 by nearly two times for 200-ppm ozone removal after 6-h reaction at 25 °C, which is ascribed to the highly active interfacial Vo. X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy suggest that the Fe3+-Vo-Co2+ was formed when Co3O4 was loaded in α-Fe2O3. Furthermore, the density functional theory (DFT) calculations reveal the desorption and electron transfer ability of intermediate peroxide (O22-) on Fe3+-Vo-Co2+ are higher than the Vo from other regions. In situ diffuse reflectance Fourier transform (DRIFT) spectroscopy also demonstrate the higher conversion rate of O22- on Co3O4/α-Fe2O3. Base on the intermediates detected, we propose a recycle mechanism of interfacial Vo for ozone removal O22- is quickly converted to O2- and transformed into O2 on interfacial Vo. Moreover, O2-temperature-programmed desorption (TPD), H2-temperature-programmed reduction (TPR), and electrochemical impedance spectroscopy (EIS) reveal that the oxygen mobility, reducibility, and conductivity of Co3O4/α-Fe2O3 are greatly superior to those of α-Fe2O3, which is contributed to the conversion of O22-. Consequently, our proposed strategy effectively enhances the activity and stability of the bimetallic transition oxides for ozone decomposition.
Mots clés
Texte intégral:
1
Collection:
01-internacional
Base de données:
MEDLINE
Sujet principal:
Ozone
/
Nanoparticules
Langue:
En
Journal:
Environ Pollut
Sujet du journal:
SAUDE AMBIENTAL
Année:
2023
Type de document:
Article
Pays d'affiliation:
Chine