催化作用
氧化态
氧化还原
催化循环
化学
选择性催化还原
氮氧化物
红外光谱学
吸收(声学)
相(物质)
光化学
吸收光谱法
无机化学
产量(工程)
分析化学(期刊)
材料科学
物理化学
有机化学
物理
量子力学
冶金
复合材料
燃烧
作者
Hiroe Kubota,Yuan Jing,Wan Li,Jiahuan Tong,Ningqiang Zhang,Shinya Mine,Takashi Toyao,Ryo Toyoshima,Hiroshi Kondoh,Davide Ferri,Ken‐ichi Shimizu
标识
DOI:10.1021/acscatal.3c01665
摘要
Operando spectroscopies (in situ Ce and W L3-edge X-ray absorption near-edge structure, ultraviolet–visible (UV–vis), and infrared (IR) spectroscopies, combined with online analysis of gas-phase products) were exploited to elucidate reduction/oxidation half-cycles in the selective catalytic reduction of NO with NH3 (NH3–SCR) over WO3-loaded CeO2. The Ce4+ species was reduced by NO + NH3 to yield N2 and Ce3+ species (reduction half-cycle), which was then reoxidized by O2 (oxidation half-cycle). The oxidation state of the W6+ species remained unchanged under redox conditions. IR and theoretical results indicated that the reduction half-cycle started with the reaction of W6+–OH and adjacent Ce4+–O with NO to afford Ce3+ species and gaseous HONO, which was converted to NO+ species on the catalyst. The NO+ species then reacted with NH3 to generate N2.
科研通智能强力驱动
Strongly Powered by AbleSci AI