4.2 Article

The next big thing for silicon nanostructures - CO2photocatalysis

期刊

FARADAY DISCUSSIONS
卷 222, 期 -, 页码 424-432

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9fd00104b

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资金

  1. Ontario Ministry of Research and Innovation (MRI)
  2. Ministry of Economic Development, Employment and Infrastructure (MEDI)
  3. Ministry of the Environment and Climate Change's (MOECC) Best in Science (BIS) Award
  4. Ontario Center of Excellence Solutions 2030 Challenge Fund
  5. Ministry of Research Innovation and Science (MRIS) Low Carbon Innovation Fund (LCIF)
  6. Imperial Oil
  7. University of Toronto's Connaught Innovation Fund (CIF)
  8. Connaught Global Challenge (CGC) Fund
  9. Natural Sciences and Engineering Research Council of Canada (NSERC)
  10. Young Professor Program from Zhejiang University [ZJU100]
  11. National Natural Science Foundation of China [51902287, 21878203]
  12. Shanxi International Cooperation Project [201703D421037]
  13. Natural Science Foundation of Shanxi Province [201801D121061]

向作者/读者索取更多资源

Silicene is a relatively new member of the growing family of two-dimensional single-element materials. Both top-down and bottom-up approaches provide access to silicene, the formerviavapor deposition on a substrate and the latterviaexfoliation of the layered CaSi(2)precursor. Most top-down research has been concerned with understanding the various electronic, optical, magnetic, mechanical, electrical, thermal transport and gas-adsorption properties of silicene. By contrast, the focus on bottom-up silicene has primarily been on its synthesis, structure and chemical properties as they relate to its function and utility. Herein, emphasis is placed on the bottom-up strategy because of its scalability and the ease of subsequent silicene modification, with both qualities being important prerequisites for heterogeneous catalysis applications. In this context, synthetic freestanding silicene exists as single sheets or multilayer assemblies, depending on the CaSi(2)exfoliation synthesis conditions. The structure of a sheet comprises three connected chair-configuration silicon 6-rings. This connectivity creates buckled sheets in which the hybridization around the unsaturated silicon atoms is sp(2)-sp(3). By adjusting the CaSi(2)exfoliation synthesis conditions, either layered silane (Si6H6) or siloxene (Si6H3(OH)(3)) nanosheets can be obtained. In our studies, we have explored the nucleation and growth of different transition metal nanoparticles on and within the layer spaces of these nanosheets, and explored their thermochemical and photochemical reactivity in CO(2)hydrogenation reactions. An overview of these findings, related works and a new-and-optimized catalyst are provided in this article.

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