化学
动力学
电子顺磁共振
阿累尼乌斯方程
催化作用
光谱学
钙长石
氧化还原
分析化学(期刊)
化学动力学
离子
物理化学
无机化学
光化学
活化能
核磁共振
有机化学
沸石
物理
量子力学
作者
Yiqing Wu,Yue Ma,Yilin Wang,Kenneth G. Rappé,Nancy Washton,Yong Wang,Éric Walter,Feng Gao
摘要
A series of seven Cu/SSZ-13 catalysts with Si/Al = 6.7 are used to elucidate key rate-controlling factors during low-temperature standard ammonia-selective catalytic reduction (NH3-SCR), via a combination of SCR kinetics and operando electron paramagnetic resonance (EPR) spectroscopy. Strong Cu-loading-dependent kinetics, with Cu atomic efficiency increasing nearly by an order of magnitude, is found when per chabazite cage occupancy for Cu ion increases from ∼0.04 to ∼0.3. This is due mainly to the release of intercage Cu transfer constraints that facilitates the redox chemistry, as evidenced from detailed Arrhenius analysis. Operando EPR spectroscopy studies reveal strong connectivity between Cu-ion dynamics and SCR kinetics, based on which it is concluded that under low-temperature steady-state SCR, kinetically most relevant Cu species are those with the highest intercage mobility. Transient binuclear Cu species are mechanistically relevant species, but their splitting and cohabitation are indispensable for low-temperature kinetics.
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