丙炔
催化作用
纳米金刚石
氢的自旋异构体
金属
材料科学
丙烯
石墨烯
化学
光化学
无机化学
氢
纳米技术
有机化学
钻石
作者
Dudari B. Burueva,Sergey V. Sviyazov,Fei Huang,Igor P. Prosvirin,Andrey V. Bukhtiyarov,Valerii I. Bukhtiyarov,Hongyang Li,Igor V. Koptyug
标识
DOI:10.1021/acs.jpcc.1c08424
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: Pd1/ND@G with a monoatomic Pd distribution (0.11 wt %) and Pdn/ND@G comprising supported metal clusters (0.87 wt %). The monoatomic distribution of Pd in Pd1/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 H2 addition to propyne was compared under the same experimental conditions by observing 1H NMR signal enhancements provided by the parahydrogen-induced polarization (PHIP) effect. The enhancements produced by the Pd1/ND@G catalyst were found to be ca. 6-fold larger than those observed with Pdn/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.
科研通智能强力驱动
Strongly Powered by AbleSci AI