English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Facile synthesis of tellurium nano- And microstructures by trace HCl in ionic liquids

MPS-Authors
/persons/resource/persons126823

Ruck,  Michael
Michael Ruck, Max Planck Fellow, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Zhang, T., Doert, T., Schwedtmann, K., Weigand, J. J., & Ruck, M. (2020). Facile synthesis of tellurium nano- And microstructures by trace HCl in ionic liquids. Dalton Transactions, 49, 1891-1896. doi:10.1039/c9dt04604f.


Cite as: https://hdl.handle.net/21.11116/0000-0005-BB3E-4
Abstract
Ionic liquids (ILs) are widely used as versatile solvents for the synthesis of nanomaterials. However, the effect of IL impurities on the formation of nanomaterials is often neglected. Herein, we report on the formation of tellurium (Te) nanoparticles from the reaction of trialkylphosphane tellurides, formed by reactive dissolution of Te in dried commercial trihexyltetradecylphosphonium chloride ([P66614]Cl) at high temperatures, with common polar protic solvents (e.g. water, alcohols, or amides). Highly homogeneous Te nano- and microstructures with various sizes and morphologies including three-dimensional (3D) Te fusiform assemblies and 3D aloe-like Te microarchitectures are obtained. Our investigation shows that trace amounts of HCl impurities in [P66614]Cl tend to remain as [P66614][HCl2] due to the strong interaction with Cl-. The addition of a polar, protic solvent liberates active HCl from the HCl2- anion which we found to play an essential role in the formation of Te particles due to the accelerating effect of P-Te bond cleavage. This approach presents a general and convenient synthetic strategy for the preparation of Te nano- and microstructures. This journal is © The Royal Society of Chemistry.