Mesoscopic framework in hierarchical Pt/Silicate-1 zeolite catalyst enables stable low-temperature CO conversion

被引:0
|
作者
Cui, Ronghua [1 ]
Liu, Yatian [1 ]
Dong, Zejian [1 ]
Zhang, Lifeng [1 ]
Xian, Quangang [2 ]
Luo, Langli [1 ,3 ]
机构
[1] Tianjin Univ, Inst Mol Plus, 92 Weijin Rd, Tianjin 300072, Peoples R China
[2] Chinese Acad Sci, Inst Met Res, Shenyang 110016, Peoples R China
[3] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
中国国家自然科学基金;
关键词
Hierarchical zeolite; Silicate-1; CO oxidation; Pt; Mesoscopic channels; METAL-CLUSTERS; 1ST STEPS; PLATINUM; ATOMS; PORES;
D O I
10.1016/j.mtener.2023.101406
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
Hierarchical porous zeolites often exhibit improved diffusion and enhanced catalytic performance compared to conventional microporous zeolites. Meanwhile, metal encapsulation in a zeolite framework becomes an efficient way to achieve a highly dispersed and stable metal loading for heterogeneous catalysts. Herein, we synthesize a hierarchical Silicate-1 (S-1) zeolite catalyst with three-dimensional mesoscopic channels, which achieves both improved diffusion and uniform encapsulation of Pt species. We find that the optimized zeolite possesses atom-precise mesoscopic channels (2 and 4 nm) formed during the controlled crystallization process, which enables a better catalytic performance (100% CO conversion at a low temperature of similar to 60 degrees C for over 250 h) compared with other mesoscopic S-1 catalysts with varied pore sizes and also superior to micropore-only S-1 with an even smaller Pt size. This unique channel structure enables a balance between maximizing the effective encapsulation of Pt and prohibiting aggregation of Pt species, further broadening the scope of hierarchical porous zeolite catalysts.(c) 2023 Elsevier Ltd. All rights reserved.
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页数:8
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