4.6 Article

An efficient Pd/C catalyst design based on sequential ligand exchange method for the direct synthesis of H2O2

期刊

MATERIALS LETTERS
卷 234, 期 -, 页码 58-61

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.matlet.2018.09.068

关键词

Sequential ligand exchange; Electrostatic adsorption; Pd/C; Direct synthesis of H2O2

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2016R1D1A3B02006928]
  2. National Research Foundation of Korea [2016R1D1A3B02006928] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

A new catalyst preparation method involving the sequential ligand exchange of anionic palladium complexes to cationic complexes via the formation of palladium hydroxide intermediates is proposed. The novel method enables the electrostatic adsorption of an anionic palladium complex on the negatively charged carbon surface, and therefore makes it possible to obtain small and highly dispersed Pd nanoparticles. The H2O2 productivity and H-2 selectivity of the ligand-exchanged catalyst were 16 and 3.6 times higher than those of the Pd/C catalyst prepared by using the same anionic palladium precursor. The strikingly different activities mainly attributed to the difference in the nanoparticle size and the oxidation state of Pd, which clearly indicates that the activity of Pd/C catalyst for the direct synthesis of H2O2 can be greatly improved by the sequential ligand exchange method. (C) 2018 Elsevier B.V. All rights reserved.

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