In Situ Confinement of Ultrasmall Pd Clusters within Nanosized Silicalite-1 Zeolite for Highly Efficient Catalysis of Hydrogen Generation

被引:600
作者
Wang, Ning [1 ]
Sun, Qiming [1 ]
Bai, Risheng [1 ]
Li, Xu [1 ]
Guo, Guanqi [1 ]
Yu, Jihong [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
FORMIC-ACID DECOMPOSITION; METAL-CLUSTERS; SYNERGISTIC CATALYSIS; ROOM-TEMPERATURE; DEHYDROGENATION; NANOPARTICLES; STORAGE; CONSEQUENCES;
D O I
10.1021/jacs.6b03518
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Well-dispersed and ultrasmall Pd clusters in nanosized silicalite-1 (MFI) zeolite have been prepared under direct hydrothermal conditions using [Pd(NH2CH2-CH2NH2)(2)] Cl-2 as precursor. High-resolution scanning transmission electron microscopy studies indicate that the Pd clusters are encapsulated within the intersectional channels of MFI, and the Pd clusters in adjacent channels visually aggregate, forming nanoparticles (NPs) of similar to 1.8 nm. The resultant catalysts show an excellent activity and highly efficient H-2 generation toward the complete decomposition of formic acid (FA) under mild conditions. Notably, thanks to the further reduced Pd NP size (similar to 1.5 nm) and the additionally introduced basic sites, the Pd/S-1-in-K catalyst affords turnover frequency values up to 856 h(-1) at 25 degrees C and 3027 h(-1) at 50 degrees C. The easy in situ confinement synthesis of metal clusters in zeolites endows the catalysts with superior catalytic activities, excellent recyclability, and high thermal stability, thus opening new perspectives for the practical application of FA as a viable and effective H-2 storage material for use in fuel cells.
引用
收藏
页码:7484 / 7487
页数:4
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