催化作用
锰
臭氧
掺杂剂
X射线光电子能谱
分解
氧气
无机化学
铜
空间速度
材料科学
共沉淀
反应性(心理学)
化学
兴奋剂
化学工程
冶金
选择性
有机化学
替代医学
病理
工程类
医学
光电子学
作者
Yi Wei,Xiubo Min,Yunhe Li,Haonan Wang,Fengshi Qi,Peiyuan Liang,Hao Li,Jiangliang Hu,Tianjun Sun
标识
DOI:10.1016/j.apcata.2022.118659
摘要
Mn-based catalysts modified by copper, alumina and/or rGOs were synthesized by a simple coprecipitation method to decompose ozone under high humidity conditions, and their intrinsic mechanisms of ozone decomposition were investigated deeply. Hereinto, Mn-based catalysts doped by Cu-Al and Cu-Al-rGOs exhibited excellent activity and durability, maintaining above 94% and 98% ozone conversion for nearly 40 h under 85% RH and GHSV of 300 L·g −1 ·h −1 at 25 °C. The characterization results showed that the Cu dopants enhance the reducibility and regeneration speed owing to the formation of CuMn 2 O 4 solid solutions, and the additions of Al and rGO significantly increase the amount of surface and sub-surface lattice oxygen, promoting effectually catalytic performances. XPS results revealed that the abundant surface oxygen species with high reactivity and stability were generated from the sites associated with Cu–O, Al–O bonds, and large amounts of Mn 2+ /Mn 3+ in Mn-based catalysts modified by Cu, Al and GOs. • Cu/Mn-Al-rGO catalyst maintained 98% ozone conversion under 85% RH at 298 K. • CuMn 2 O 4 phase in catalysts enhances the activity of ozone decomposition. • Al and GOs dopants increase surface and sub-surface lattice oxygen significantly. • Superior stability and activity attributed to extensive surface oxygen and Mn 2+ /Mn 3+ .
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