催化作用
分解
纳米棒
化学
吸附
一氧化二氮
解吸
多相催化
氧化物
纳米颗粒
氧气
化学工程
氮氧化物
无机化学
光化学
纳米技术
氧化铈
光催化
化学分解
光解
污染物
析氧
材料科学
作者
Yuxin Sun,Yunshuo Wu,Haiqiang Wang,Zhong-biao Wu,Yuxin Sun,Yunshuo Wu,Haiqiang Wang,Zhong-biao Wu
标识
DOI:10.1021/acs.est.5c11651
摘要
Nitrous oxide (N2O) has gained increasing attention as a potent greenhouse gas, and its catalytic decomposition offers a promising mitigation strategy. In this study, single-atom Ru embedded in a rod-shaped CeO2 catalyst was synthesized via a H2O2 chemical etching strategy. The single-atom Ru catalyst demonstrated an exceptional N2O decomposition performance with only 0.48 wt % Ru loading, exhibiting a 34-fold increase in the turnover frequency compared to Ru nanoparticle catalysts. Under simulated exhaust conditions (NO, CO, and N2O), Ru1/CeO2 enabled complete conversion of all three pollutants at 280 °C. Mechanistic studies revealed that N2O decomposition over Ru1/CeO2 and Run/CeO2 followed the Mars-van Krevelen (MvK) and Langmuir-Hinshelwood (L-H) mechanisms, respectively. The exceptional N2O decomposition activity of the single-atom catalyst stems from enhanced O2 desorption through the recombination of oxygen atoms that dissociate from N2O with adjacent lattice oxygen. Notably, Ru1/CeO2 exhibits remarkable O2 tolerance due to the selective adsorption: N2O binds to single Ru atoms, whereas O2 occupies oxygen vacancies. In contrast, the high energy barrier associated with O2 combination and desorption in Run/CeO2 hindered N2O decomposition, and the competitive adsorption of O2 on its surface led to poor O2 resistance. This study demonstrates Ru1/CeO2 as an efficient catalyst for abating N2O and multipollutant removal.
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