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Improved Selectivity by Stabilizing and Exposing Active Phases on Supported Pd Nanoparticles in Acetylene-Selective Hydrogenation

MPS-Authors
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Shao,  Lidong
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Zhang,  Bing Sen
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Shenyang National Laboratory for Materials Science Institute of Metal Research, Chinese Academy of Science;

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Zhang,  Wei
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Teschner,  Detre
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Girgsdies,  Frank
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Su,  Dang Sheng
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Shenyang National Laboratory for Materials Science Institute of Metal Research, Chinese Academy of Science;

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201202608.pdf
(Preprint), 132KB

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Citation

Shao, L., Zhang, B. S., Zhang, W., Teschner, D., Girgsdies, F., Schlögl, R., et al. (2012). Improved Selectivity by Stabilizing and Exposing Active Phases on Supported Pd Nanoparticles in Acetylene-Selective Hydrogenation. Chemistry-a European Journal, 18(47), 14962-14966. doi:10.1002/chem.201202608.


Cite as: https://hdl.handle.net/11858/00-001M-0000-000E-6FB9-C
Abstract
Palladium dynamics: Under hydrogenation conditions, saturating over-active palladium by carbon diffusion leads to a stable and selective particle surface. By choosing supports with suitable geometric structures and establishing a strong interaction between supports and metal particles, accumulated species can be regularly rearranged and reaction-selective phases can be exposed.