Zhou Zhen-Xun, Wang Li Na, Li Zi-Yu, He Sheng-Gui, Ma Tong-Mei
School of Chemistry and Chemical Engineering, South China University of Technology , Wushan Road 381, Tianhe District, Guangzhou, People's Republic of China , 510640.
State Key Laboratory for Structural Chemistry of Unstable and Stable Species, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences , Beijing, People's Republic of China , 100190.
J Phys Chem A. 2016 Jun 9;120(22):3843-8. doi: 10.1021/acs.jpca.6b00108. Epub 2016 May 31.
Cerium oxide cationic clusters (CeO2)1-3(+) were generated through laser ablation and then reacted with sulfur dioxide (SO2) at ambient conditions in an ion trap reactor and those reactions were studied and characterized by combining the art of time-of-flight mass spectrometry (TOF-MS) with density functional theory (DFT) calculations. Molecule association and oxygen atom transfer (OAT) were observed for the CeO2(+) and (CeO2)2,3(+) reaction systems, respectively. The mechanistic analysis indicates that the weak Ce-O bond strength associated with the oxygen release capacity of cerium oxide clusters is considered as the key factor to achieve the oxidation of SO2. To our best knowledge, this research should be the first example to identify the OAT reactivity of metal oxide cluster ions toward sulfur dioxide under thermal collision conditions, and a fundamental understanding of the elementary oxidation of SO2 to SO3 is provided.
通过激光烧蚀产生氧化铈阳离子簇(CeO2)1-3(+),然后在离子阱反应器中于环境条件下与二氧化硫(SO2)反应,并结合飞行时间质谱(TOF-MS)技术和密度泛函理论(DFT)计算对这些反应进行了研究和表征。分别在CeO2(+)和(CeO2)2,3(+)反应体系中观察到了分子缔合和氧原子转移(OAT)。机理分析表明,与氧化铈簇的氧释放能力相关的较弱的Ce-O键强度被认为是实现SO2氧化的关键因素。据我们所知,本研究应是首个在热碰撞条件下确定金属氧化物簇离子对二氧化硫的OAT反应活性的实例,并为SO2向SO3的基本氧化提供了深入理解。