TY - JOUR
T1 - Doping Pd2+ into NinCeOx nanofibers promotes low-temperature CO2 methanation
AU - Zhang, Mengyuan
AU - Ye, Jian
AU - Lu, Nana
AU - Lu, Xiaoyan
AU - Luo, Kongliang
AU - Dong, Jiali
AU - Niu, Qiang
AU - Zhang, Pengfei
AU - Dai, Sheng
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2024/6
Y1 - 2024/6
N2 - CO2 methanation at low temperatures is still a challenge. Herein, NinCeOx (n = 1–3) and Ni2.5Pd0.1CeOx nanofibers by electrospinning is reported. The main advantage of this method is to obtain the highly dispersed precursor of palladium, nickel, and cerium, overcoming the difficulty of uniform mixing in conventional preparation methods. The Ni2.5Pd0.1CeOx nanofiber catalyst exhibited outstanding catalytic performance at low temperatures (CO2 conversion rate = 90.4 %, CH4 selectivity = 99.6 % at 230 °C) along with exceptional stability over 300 h. EPR, Raman, and O 1s XPS confirmed that Pd2+ doping increased oxygen vacancy concentration. In-situ infrared spectroscopy indicated that CO2 methanation on Ni2.5CeOx and Ni2.5Pd0.1CeOx catalysts followed the formate pathways. Pd2+ doping increased the number of surface oxygen vacancies and hydroxyl groups, thus increasing the amount of bicarbonates and formates. DFT calculations suggested that Pd2+ doping increased CO2 adsorption energy, and confirmed surface hydroxyl groups and bicarbonate being beneficial for CO2 methanation, consequently enhancing the activity of Ni2.5Pd0.1CeOx catalyst especially at low temperatures.
AB - CO2 methanation at low temperatures is still a challenge. Herein, NinCeOx (n = 1–3) and Ni2.5Pd0.1CeOx nanofibers by electrospinning is reported. The main advantage of this method is to obtain the highly dispersed precursor of palladium, nickel, and cerium, overcoming the difficulty of uniform mixing in conventional preparation methods. The Ni2.5Pd0.1CeOx nanofiber catalyst exhibited outstanding catalytic performance at low temperatures (CO2 conversion rate = 90.4 %, CH4 selectivity = 99.6 % at 230 °C) along with exceptional stability over 300 h. EPR, Raman, and O 1s XPS confirmed that Pd2+ doping increased oxygen vacancy concentration. In-situ infrared spectroscopy indicated that CO2 methanation on Ni2.5CeOx and Ni2.5Pd0.1CeOx catalysts followed the formate pathways. Pd2+ doping increased the number of surface oxygen vacancies and hydroxyl groups, thus increasing the amount of bicarbonates and formates. DFT calculations suggested that Pd2+ doping increased CO2 adsorption energy, and confirmed surface hydroxyl groups and bicarbonate being beneficial for CO2 methanation, consequently enhancing the activity of Ni2.5Pd0.1CeOx catalyst especially at low temperatures.
KW - CO methanation
KW - DFT calculations
KW - In situ DRIFTS
KW - Low-temperature
KW - Nanofiber
UR - http://www.scopus.com/inward/record.url?scp=85192455585&partnerID=8YFLogxK
U2 - 10.1016/j.jcat.2024.115535
DO - 10.1016/j.jcat.2024.115535
M3 - Article
AN - SCOPUS:85192455585
SN - 0021-9517
VL - 434
JO - Journal of Catalysis
JF - Journal of Catalysis
M1 - 115535
ER -