TY - JOUR
T1 - Enhancement of soot oxidation activity of manganese oxide (Mn2O3) through doping by the formation of Mn1.9M0.1O3–δ (M = Co, Cu, and Ni)
AU - Neelapala, Satya Deepika
AU - Patnaik, Harsh
AU - Dasari, Harshini
N1 - Funding Information:
This project was supported by Korea Institute of Science and Technology, the Republic of Korea, under KIST School Partnership project with the project code 2Z05280‐18‐007.
Publisher Copyright:
© 2018 Curtin University and John Wiley & Sons, Ltd.
PY - 2018/9/1
Y1 - 2018/9/1
N2 - The current work describes the catalytic soot oxidation activity of metal-doped manganese oxide (Mn1.9M0.1O3–δ; M = Co, Cu, and Ni) materials, synthesized by coprecipitation method. All the fabricated materials were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Brunauer–Emmett–Teller surface area analysis, and X-ray photoelectron spectroscopy (XPS). XRD analysis confirmed the formation of solid solution Mn1.9M0.1O3–δ (M = Co, Cu, and Ni). M-doped samples exhibited different morphology when compared with pure Mn2O3 as evidenced by FESEM analysis, and Co-doped Mn2O3 possessed the highest specific surface area. XPS analysis revealed the presence of multiple oxidation states of Mn (+4, +3, and +2) and Co (+2 and +3). Soot oxidation activity tests, performed using thermogravimetric analysis, showed that Mn1.9Co0.1O3–δ exhibited better catalytic performance (T50 = 390°C) when compared with pure Mn2O3 (T50 = 490°C). The incorporation of dopants greatly enhanced the oxygen vacancies and redox properties of Mn2O3.
AB - The current work describes the catalytic soot oxidation activity of metal-doped manganese oxide (Mn1.9M0.1O3–δ; M = Co, Cu, and Ni) materials, synthesized by coprecipitation method. All the fabricated materials were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Brunauer–Emmett–Teller surface area analysis, and X-ray photoelectron spectroscopy (XPS). XRD analysis confirmed the formation of solid solution Mn1.9M0.1O3–δ (M = Co, Cu, and Ni). M-doped samples exhibited different morphology when compared with pure Mn2O3 as evidenced by FESEM analysis, and Co-doped Mn2O3 possessed the highest specific surface area. XPS analysis revealed the presence of multiple oxidation states of Mn (+4, +3, and +2) and Co (+2 and +3). Soot oxidation activity tests, performed using thermogravimetric analysis, showed that Mn1.9Co0.1O3–δ exhibited better catalytic performance (T50 = 390°C) when compared with pure Mn2O3 (T50 = 490°C). The incorporation of dopants greatly enhanced the oxygen vacancies and redox properties of Mn2O3.
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U2 - 10.1002/apj.2234
DO - 10.1002/apj.2234
M3 - Article
AN - SCOPUS:85052649364
SN - 1932-2135
VL - 13
JO - Asia-Pacific Journal of Chemical Engineering
JF - Asia-Pacific Journal of Chemical Engineering
IS - 5
M1 - e2234
ER -