Acetaldehyde polymerization on Co(0001): the role of CO

被引:1
作者
Chen, Jun [1 ,2 ]
Guo, Qing [2 ,3 ]
Wu, Jiawei [2 ]
Dai, Dongxu [2 ]
Chen, Maodu [1 ]
Yang, Xueming [2 ]
机构
[1] Dalian Univ Technol, Sch Phys, Minist Educ, Key Lab Mat Modificat Laser Electron & Ion Beams, Dalian 116023, Liaoning, Peoples R China
[2] Dalian Inst Chem Phys, State Key Lab Mol React Dynam, 457 Zhongshan Rd, Dalian 116023, Liaoning, Peoples R China
[3] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
SURFACE REACTIVITY; ADSORPTION; DECOMPOSITION; OXIDATION; DECARBONYLATION; ACTIVATION; CATALYSTS; MECHANISM; ACETATE;
D O I
10.1039/c9cp00441f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption and polymerization of acetaldehyde (CH3CHO) have been investigated on clean and CO pre-covered Co(0001) surfaces using the temperature programmed desorption (TPD) method. On the clean Co(0001) surface, CH3CHO molecules can polymerize to produce paraldehyde with very low efficiency. With pre-dosed CO molecules on Co(0001), the decomposition of CH3CHO is greatly inhibited. When the coverage of pre-dosed CO is <0.33 ML, no enhancement of CH3CHO polymerization is observed. However, when the pre-dosed CO coverage is >0.33 ML, the polymerization of CH3CHO is significantly enhanced during the TPD process. Further results suggest that CO molecules adsorbed at the bridge/hollow sites may initialize the polymerization by nucleophilic attack of CH3CHO molecules with their O atoms. Moreover, the polymerization product induced by CO molecules is not paraldehyde, but linear polymer chains of CH3CHO at low CH3CHO coverages and probably three dimensional polymer structures at high CH3CHO coverages.
引用
收藏
页码:8275 / 8281
页数:7
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