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Bimetallic Nickel‐Iridium and Nickel‐Osmium Alloy Nanoparticles and Their Catalytic Performance in Hydrogenation Reactions
Author(s) -
Egeberg Alexander,
Dietrich Christine,
Kind Christian,
Popescu Radian,
Gerthsen Dagmar,
Behrens Silke,
Feldmann Claus
Publication year - 2017
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201700168
Subject(s) - bimetallic strip , catalysis , oleylamine , nanoparticle , materials science , alloy , selectivity , nickel , diphenylacetylene , iridium , chemical engineering , inorganic chemistry , chemistry , nanotechnology , organic chemistry , metallurgy , engineering
Bimetallic NiIr 4 and NiOs 4 alloy nanoparticles are prepared and studied with regard to their performance in catalytic hydrogenation reactions. NiIr 4 and NiOs 4 nanoparticles are obtained by oleylamine‐driven reduction and exhibit mean diameters of (8.9±1.3) and (6.8±1.4) nm at low agglomeration. The phase composition was determined in detail by using different methods, which include high‐resolution TEM, scanning transmission electron microscopy, selected‐area electron diffraction, X‐ray diffraction, and energy‐dispersive X‐ray spectroscopy. This and results in a uniform distribution of both metals Ni‐Ir and Ni‐Os with a ratio of 1:4. The catalytic performance of the NiIr 4 and NiOs 4 nanoparticles for hydrogenation reactions is evaluated using three selected model substrates: 1‐octene, cinnamaldehyde, and diphenylacetylene. Similar sized Ni, Ir, and Os nanoparticles were used as references. Most remarkable are the excellent selectivity of NiOs 4 in the hydrogenation of cinnamaldehyde and the promising formation of ( Z )‐stilbene in terms of conversion activity and selectivity. The alloying of Ir and Os with Ni, moreover, is highly cost efficient. In general, both bimetallic alloy nanoparticles, NiIr 4 and NiOs 4 , are shown here for the first time in terms of synthesis, composition, and catalytic hydrogenation.