Enhancing formic acid dehydrogenation for hydrogen production with the metal/organic interface

被引:43
|
作者
Wang, Hongli [1 ]
Chi, Yue [1 ]
Gao, Dawei [1 ]
Wang, Zhili [2 ]
Wang, Cong [1 ]
Wang, Liying [1 ]
Wang, Minggang [1 ]
Cheng, Daowen [1 ]
Zhang, Jingjing [1 ]
Wu, Chen [1 ]
Zhao, Zhankui [1 ]
机构
[1] Changchun Univ Technol, Coll Mat Sci & Engn, Minist Educ, Key Lab Adv Struct Mat, Changchun 130012, Jilin, Peoples R China
[2] Jilin Univ, Dept Mat Sci & Engn, Minist Educ, Key Lab Automobile Mat, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Formic acid; Metal/organic interface; Hydrogen production; Heterogeneous catalyst; REDUCED GRAPHENE OXIDE; METAL-ORGANIC FRAMEWORK; ROOM-TEMPERATURE DEHYDROGENATION; ALLOY NANOPARTICLES; PALLADIUM NANOPARTICLES; EFFICIENT NANOCATALYST; SYNERGISTIC CATALYSIS; IN-SITU; GENERATION; DECOMPOSITION;
D O I
10.1016/j.apcatb.2019.117776
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
Ultrafine and well-dispersed CrPd nanoparticles are successfully immobilized on 3-aminopropyl triethoxysilane functionalized monochlortriaziny beta-cyclodeztrin (M-beta-CD-A) by a facile wet-chemical method. Benefiting from the strong metal/organic interfacial interactions between the CrPd nanoparticles and M-beta-CD-A support, the Cr-0.4 Pd-0.6/M-beta-CD-A catalyst exhibits excellent catalytic activity towards formic acid dehydrogenation for hydrogen production, affording a high initial turn over frequency of 5771 mol H-2 mol Pd( )(-1)h(-1) without any additive at 323 K, which is much higher than those obtained for most of the reported noble metal catalysts under similar conditions. This work provides a promising lead for the design of efficient heterogeneous catalysts toward formic acid dehydrogenation for hydrogen production.
引用
收藏
页数:8
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