Pd on Nanodiamond/Graphene in Hydrogenation of Propyne with Parahydrogen

被引:5
|
作者
Burueva, Dudari B. [1 ,2 ]
Sviyazov, Sergey, V [1 ,2 ]
Huang, Fei [3 ]
Prosvirin, Igor P. [4 ]
Bukhtiyarov, Andrey, V [4 ]
Bukhtiyarov, Valerii, I [4 ]
Liu, Hongyang [3 ]
Koptyug, Igor, V [1 ]
机构
[1] Int Tomog Ctr SB RAS, Lab Magnet Resonance Microimaging, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
[3] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[4] Boreskov Inst Catalysis SB RAS, Novosibirsk 630090, Russia
关键词
INDUCED POLARIZATION; HETEROGENEOUS HYDROGENATION; SELECTIVE HYDROGENATION; CATALYSTS; PAIRWISE; NMR; PERFORMANCE; HYPERPOLARIZATION; NANOPARTICLES;
D O I
10.1021/acs.jpcc.1c08424
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 catalytic behavior of Pd catalysts supported on a defective nanodiamond/graphene material (ND@G) was studied in propyne hydrogenation with parahydrogen, taking advantage of the possibility to control the character of metal distribution by changing metal loading. Two different catalysts were studied in this work: Pd-1/ND@G with a monoatomic Pd distribution (0.11 wt %) and Pd-n/ND@G comprising supported metal clusters (0.87 wt %). The monoatomic distribution of Pd in Pd-1/ND@G was confirmed by XPS and HAADF-STEM methods. This catalyst demonstrated an outstanding selectivity to propene (up to 100%) in propyne hydrogenation. The activity of the two Pd catalysts in pairwise H-2 addition to propyne was compared under the same experimental conditions by observing H-1 NMR signal enhancements provided by the parahydrogen-induced polarization (PHIP) effect. The enhancements produced by the Pd-1/ND@G catalyst were found to be ca. 6-fold larger than those observed with Pd-n/ND@G, indicating that the character of metal distribution has important consequences for the performance of a catalyst and its efficiency in terms of PHIP effects.
引用
收藏
页码:27221 / 27229
页数:9
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