TY - JOUR
T1 - Facile synthesis of Fe-modified manganese oxide with high content of oxygen vacancies for efficient airborne ozone destruction
AU - Jia, Jingbo
AU - Yang, Wenjuan
AU - Zhang, Pengyi
AU - Zhang, Junying
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/9/25
Y1 - 2017/9/25
N2 - Oxygen vacancy engineering is an efficient strategy to improve the catalytic performance of nanomaterials. In this work, a highly active Fe-modified manganese oxide (Fe-MnOx) was synthesized and used for airborne ozone decomposition. The addition of Fe3+ during MnO2 synthesis led to higher specific surface area, greatly increased content of oxygen vacancies, evidenced by XPS, H2-TPR analysis and lower oxygen vacancy formation energy (decreased by ∼1.2 eV) based on the density functional theory calculations. The ozone conversion over Fe-MnOx kept 97% after 24 h reaction, while it over MnO2 slowed down to 85% under dry condition. Remarkably, under humid condition (RH = 60%), the ozone conversion over Fe-MnOx kept 73% after 6 h reaction, while ozone conversion over pure MnO2 decreased to 50% within 1 h under the conditions of 100 ppm inlet ozone concentration and weight space velocity of 660 L g−1 h−1. The intermediate peroxide species (O22−) formed on the surface oxygen vacancies of Fe-MnOx and MnO2 during ozone decomposition reaction were observed using in situ Raman spectroscopy. The concentration and depletion rate of O22− on the surface of Fe-MnOx was higher than that on MnO2, illustrating that O22− acted as the key species to boost the catalytic process. The content and dispersity of oxygen vacancies were identified to be mainly responsible for the performance difference. This provides a promising idea for designing novel nanomaterial catalyst for gaseous ozone decomposition.
AB - Oxygen vacancy engineering is an efficient strategy to improve the catalytic performance of nanomaterials. In this work, a highly active Fe-modified manganese oxide (Fe-MnOx) was synthesized and used for airborne ozone decomposition. The addition of Fe3+ during MnO2 synthesis led to higher specific surface area, greatly increased content of oxygen vacancies, evidenced by XPS, H2-TPR analysis and lower oxygen vacancy formation energy (decreased by ∼1.2 eV) based on the density functional theory calculations. The ozone conversion over Fe-MnOx kept 97% after 24 h reaction, while it over MnO2 slowed down to 85% under dry condition. Remarkably, under humid condition (RH = 60%), the ozone conversion over Fe-MnOx kept 73% after 6 h reaction, while ozone conversion over pure MnO2 decreased to 50% within 1 h under the conditions of 100 ppm inlet ozone concentration and weight space velocity of 660 L g−1 h−1. The intermediate peroxide species (O22−) formed on the surface oxygen vacancies of Fe-MnOx and MnO2 during ozone decomposition reaction were observed using in situ Raman spectroscopy. The concentration and depletion rate of O22− on the surface of Fe-MnOx was higher than that on MnO2, illustrating that O22− acted as the key species to boost the catalytic process. The content and dispersity of oxygen vacancies were identified to be mainly responsible for the performance difference. This provides a promising idea for designing novel nanomaterial catalyst for gaseous ozone decomposition.
KW - In situ Raman spectroscopy
KW - Iron modified manganese dioxide
KW - Oxygen vacancy
KW - Ozone decomposition
KW - Peroxide
UR - https://www.scopus.com/pages/publications/85027439944
U2 - 10.1016/j.apcata.2017.08.013
DO - 10.1016/j.apcata.2017.08.013
M3 - 文章
AN - SCOPUS:85027439944
SN - 0926-860X
VL - 546
SP - 79
EP - 86
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
ER -