Open AccessHeavy Chalcogenide‐Based Ionic Liquids in Syntheses of Metal Chalcogenide Materials near Room Temperature
Author(s) -
Guschlbauer Jannick,
Sundermeyer Jörg
Publication year - 2021
Publication title -
chemistryopen
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.644
H-Index - 29
ISSN - 2191-1363
DOI - 10.1002/open.202000346
Subject(s) - chalcogenide , chalcogen , homoleptic , ternary operation , ionic liquid , tellurium , chemistry , metastability , ionic bonding , metal , main group element , selenium , inorganic chemistry , crystallography , transition metal , nanotechnology , materials science , ion , organic chemistry , catalysis , programming language , computer science
This minireview describes two strategically different and unexplored approaches to use ionic liquids (IL) containing weakly solvated and highly reactive chalcogenide anions [E‐SiMe 3 ] − and [E−H] − of the heavy chalcogens (E=S, Se, Te) in materials synthesis near room temperature. The first strategy involves the synthesis of unprecedented trimethylsilyl chalcogenido metalates Cat + [M(E‐SiMe 3 ) n ] − (Cat=organic IL cation) of main group and transition metals (M=Ga, In, Sn, Zn, Cu, Ag, Au). These fully characterized homoleptic metalates serve as thermally metastable precursors in low‐temperature syntheses of binary, ternary and even quaternary chalcogenide materials such as CIGS and CZTS relevant for semiconductor and photovoltaics (PV) applications. Furthermore, thermally and protolytically metastable coinage metalates Cat + [M(ESiMe 3 ) 2 ] − (M=Cu, Ag, Au; E=S, Se) are accessible. Finally, the use of precursors BMPyr[E‐SiMe 3 ] (E=Se,Te; BMPyr=1‐butyl‐1‐methylpyrrolidinium) as sources of activated selenium and tellurium in the synthesis of high‐grade thermoelectric nanoparticles Bi 2 Se 3 and Bi 2 Te 3 is shortly highlighted. The second synthesis strategy involves the metalation of ionic liquids Cat[S−H] and Cat[Se−H] by protolytically highly active metal alkyls or amides R n M. This rather general approach towards unknown chalcogenido metalates Cat m [R n‐1 M(E)] m (E=S, Se) will be demonstrated in a research paper following this short review head‐to‐tail.