Cobalt(ii ) containing liquid metal salts for electrodeposition of cobalt and electrochemical nanoparticle formation
Author(s) -
Jeroen Sniekers,
Pieter Geysens,
João C. Malaquías,
Tom Vander Hoogerstraete,
Luc Van Meervelt,
Jan Fransaer,
Koen Binnemans
Publication year - 2017
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/c7dt02604h
Subject(s) - cobalt , electrochemistry , ionic liquid , cyclic voltammetry , inorganic chemistry , chemistry , metal , nanoparticle , imidazole , alkyl , nuclear chemistry , materials science , organic chemistry , electrode , nanotechnology , catalysis
Cobalt(ii)-containing liquid metal salts (LMS) with N-alkylimidazole ligands and bis(trifluoromethanesulfonyl)imide (bistriflimide, Tf 2 N - ) or methanesulfonate (mesylate, OMs - ) anions were synthesized and characterized. The chain length of the alkyl side chain on the imidazole ligand was varied. All compounds were characterized using CHN analysis, DSC and FTIR measurements. Single-crystal X-ray diffraction measurements were performed on six of the compounds for which single crystals of good quality could be obtained. All cobalt(ii) centers are six-coordinate with the N-alkylimidazole ligands in an octahedral configuration and the anions are non-coordinating. The same coordination environment was observed by EXAFS measurements on cobalt(ii) liquid metal salts in the liquid state. The electrochemical properties of the compounds with the lowest melting temperatures were investigated using cyclic voltammetry. It was found that part of the current was consumed in the electrodeposition of cobalt, whereas the other part of the current was consumed in the electrochemical formation of cobalt(0) nanoparticles.
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