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Active Sites on Nickel‐Promoted Transition‐Metal Sulfides That Catalyze Hydrogenation of Aromatic Compounds
Author(s) -
Luo Wanqiu,
Shi Hui,
Schachtl Eva,
Gutiérrez Oliver Y.,
Lercher Johannes A.
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201808428
Subject(s) - vicinal , chemistry , sulfide , nickel sulfide , transition metal , nickel , hydrogen sulfide , metal , selectivity , inorganic chemistry , hydrogen , catalysis , photochemistry , sulfur , organic chemistry
Hydrogenation on Mo and W sulfides occurs at the edges of the sulfide slabs. The rate of hydrogen addition is directly proportional to the concentration of sulfhydryl (SH) groups at the slab edge and the metal atom attached to it. Sulfhydryl groups vicinal to edge‐incorporated Ni hydrogenate with much higher rates than SH close to Mo and W. Each subset of SH groups, however, exhibits nearly identical intrinsic activity and selectivity, independent of the sulfide composition. The higher activity of Ni‐WS 2 compared to Ni‐MoS 2 stems from a higher concentration of SH groups on the former sulfide associated with a higher tendency of its surface vacancies to react with H 2 .