钙钛矿(结构)
磁性
镧
催化作用
无机化学
兴奋剂
氧化物
材料科学
吸附
顺磁性
金属
化学
结晶学
物理化学
冶金
有机化学
物理
量子力学
光电子学
作者
Ran Ao,Tao Pu,Liping Ma,Quxiu Dai,Jie Yang,Wengang Li,Lijuan Xie,Zhiying Guo
标识
DOI:10.1016/j.jenvman.2024.120160
摘要
The partial substitution of A-site in perovskites is a major strategy to enhance the catalytic oxidation activity. This study explores the use of silver (Ag) to partially replace the lanthanum (La) ion at the A-site in LaCoO3 perovskite, investigating the role of Ag in the ABO3 perovskite structure, elucidating the nitric oxide (NO) oxidation mechanism over La1–xAgxCoO3 (x = 0.1–0.5) perovskites. La0.7Ag0.3CoO3 with an Ag-doping amount of 0.3, exhibited the highest NO oxidation activity of 88.5% at 275 °C. Characterization results indicated that Ag substitution enhanced the perovskite, maintaining its original phase structure, existing in the form of a mixture of Ag0 and Ag+ in the La1–xAgxCoO3 (x = 0.1–0.5) perovskites. Notably, Ag substitution improved the specific surface area, reduction performance, Co3+, and surface adsorption oxygen content. Additionally, the study investigated the relationship between magnetism and NO oxidation from a magnetism perspective. Ag-doping strengthened the magnetism of La–Ag perovskite, resulting in stronger adsorption of paramagnetic NO. This study elucidated the NO oxidation mechanism over La–Ag perovskite, considering structural and magnetic properties, providing valuable insights for the subsequent development and industrial application of high oxidation ability perovskite catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI