TY - JOUR
T1 - Investigation into the Phase–Activity Relationship of MnO2 Nanomaterials toward Ozone-Assisted Catalytic Oxidation of Toluene
AU - Yang, Ruijie
AU - Guo, Zhongjie
AU - Cai, Lixin
AU - Zhu, Rongshu
AU - Fan, Yingying
AU - Zhang, Yuefeng
AU - Han, Pingping
AU - Zhang, Wanjian
AU - Zhu, Xiangang
AU - Zhao, Qitong
AU - Zhu, Zhenye
AU - Chan, Chak Keung
AU - Zeng, Zhiyuan
N1 - Generated from Scopus record by KAUST IRTS on 2023-07-06
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Manganese dioxide (MnO2), with naturally abundant crystal phases, is one of the most active candidates for toluene degradation. However, it remains ambiguous and controversial of the phase–activity relationship and the origin of the catalytic activity of these multiphase MnO2. In this study, six types of MnO2 with crystal phases corresponding to α-, β-, γ-, ε-, λ-, and δ-MnO2 are prepared, and their catalytic activity toward ozone-assisted catalytic oxidation of toluene at room temperature are studied, which follow the order of δ-MnO2 > α-MnO2 > ε-MnO2 > γ-MnO2 > λ-MnO2 > β-MnO2. Further investigation of the specific oxygen species with the toluene oxidation activity indicates that high catalytic activity of MnO2 is originated from the rich oxygen vacancy and the strong mobility of oxygen species. This work illustrates the important role of crystal phase in determining the oxygen vacancies’ density and the mobility of oxygen species, thus influencing the catalytic activity of MnO2 catalysts, which sheds light on strategies of rational design and synthesis of multiphase MnO2 catalysts for volatile organic pollutants’ (VOCs) degradation.
AB - Manganese dioxide (MnO2), with naturally abundant crystal phases, is one of the most active candidates for toluene degradation. However, it remains ambiguous and controversial of the phase–activity relationship and the origin of the catalytic activity of these multiphase MnO2. In this study, six types of MnO2 with crystal phases corresponding to α-, β-, γ-, ε-, λ-, and δ-MnO2 are prepared, and their catalytic activity toward ozone-assisted catalytic oxidation of toluene at room temperature are studied, which follow the order of δ-MnO2 > α-MnO2 > ε-MnO2 > γ-MnO2 > λ-MnO2 > β-MnO2. Further investigation of the specific oxygen species with the toluene oxidation activity indicates that high catalytic activity of MnO2 is originated from the rich oxygen vacancy and the strong mobility of oxygen species. This work illustrates the important role of crystal phase in determining the oxygen vacancies’ density and the mobility of oxygen species, thus influencing the catalytic activity of MnO2 catalysts, which sheds light on strategies of rational design and synthesis of multiphase MnO2 catalysts for volatile organic pollutants’ (VOCs) degradation.
UR - https://onlinelibrary.wiley.com/doi/10.1002/smll.202103052
UR - http://www.scopus.com/inward/record.url?scp=85118306048&partnerID=8YFLogxK
U2 - 10.1002/smll.202103052
DO - 10.1002/smll.202103052
M3 - Article
SN - 1613-6829
VL - 17
JO - Small
JF - Small
IS - 50
ER -