Atomic rearrangement on YMn2O5 modified Pt-based diesel oxidation catalyst for promoted performance

被引:9
|
作者
Liang, Yanli [1 ]
Hu, Chao [2 ]
Zou, Wei [1 ]
Ma, Xiaoyan [1 ]
He, Darong [3 ]
Wang, Jianli [3 ]
Zhao, Ming [3 ]
Chen, Yaoqiang [3 ]
机构
[1] Sichuan Univ Sci & Engn, Sch Chem Engn, Zigong 643000, Peoples R China
[2] Sichuan Univ Sci & Engn, Sch Civil Engn, Zigong 643000, Peoples R China
[3] Sichuan Univ, Coll Chem, Sichuan Prov Environm Protect Environm Catalyt Mat, Chengdu 610064, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Diesel oxidation catalyst; Redox cycles; Atomic rearrangement; Oxidation performance; NO OXIDATION; CO; NANOPARTICLES; OXIDES; MODEL;
D O I
10.1016/j.apcata.2022.118742
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
To improve the stability of Pt nanoparticles, the redox cycles with oxidation at 800 degrees C and reduction at 250 degrees C for three times were adopted on the Mn-mullite doped Pt-based catalysts (Pt-YMO/SA-Red) to rearrange the Pt atoms. The light-off temperature toward CO/C3H6/NO oxidation on Pt-YMO/SA-Red decreases by 20-60 degrees C, and the NO maximum conversion is improved by 27 % than the catalyst with only oxidation treatment at 800 degrees C (Pt-YMO/SA-Oxi). Characterization results verify that the interaction of Pt with YMn2O5 on Pt-YMO/SA-Red is reinforced via redox cyclic treatment to inhibit the aggregation of platinum particles and promote the formation of active oxygen species, in comparison to Pt-YMO/SA-Oxi. The easier active oxygen regeneration and more active platinum sites contribute to the excellent catalytic performances and stability. In addition, the mechanism for the high CO/C3H6/NO oxidation performance are analyzed via the detected reaction intermediate species.
引用
收藏
页数:11
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