Tetrahedrite (CuSbS) is a highly promising environmentally friendly material for energy conversion applications but its synthesis generally requires several days of heating at high temperature conditions. To fabricate tetrahedrite in a more rapid way and under milder conditions, solvothermal synthesis has been recently explored. However, a common problem faced when using this technique is the formation of significant amounts of other ternary Cu-Sb-S phases along with the desired tetrahedrite phase. Here, we present an optimized solvothermal procedure for synthesizing high-purity samples of tetrahedrite at moderate temperatures and reasonable heating times. The as-prepared samples are single-crystalline nanometer-sized structures having multiple voids or pores. By modifying certain experimental parameters such as the reaction temperature and heating time, we have shown that we can alter the nanocrystal architecture. The formation mechanism was investigated and it was found that these porous tetrahedrite nanostructures are a product of the non-classical oriented aggregation growth process. Porosity in nanomaterials is known to improve material properties and is desirable in many important applications so the construction of void-containing tetrahedrite nanostructures will potentially extend the utility of tetrahedrite to a wider range of applications. In this work, we explore its possible use as a photothermal-responsive drug delivery vehicle.
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http://dx.doi.org/10.1039/c7nr07652e | DOI Listing |
Molecules
December 2022
Institute of Geotechnics, Slovak Academy of Sciences, 04001 Košice, Slovakia.
Copper, antimony and sulfur in elemental form were applied for one-pot solid-state mechanochemical synthesis of skinnerite (CuSbS) in a laboratory mill and an industrial mill. This synthesis was completed after 30 min of milling in the laboratory mill and 120 min in the industrial mill, as corroborated by X-ray diffraction. XRD analysis confirmed the presence of pure monoclinic skinnerite prepared in the laboratory mill and around 76% monoclinic skinnerite, with the secondary phases famatinite (CuSbS; 15%), and tetrahedrite (CuSbS; 8%), synthesized in the industrial mill.
View Article and Find Full Text PDFDalton Trans
August 2022
Department of Chemistry, Kamla Nehru Institute of Physical and Social Sciences, Sultanpur-228118, India.
Stibnite SbS and tetrahedrite CuSbS nanostructures being economical, environmentally benign and having a high absorption coefficient are highly promising materials for energy conversion applications. However, producing these materials especially tetrahedrite in the phase pure form is a challenging task. In this report we present a structurally characterized single source molecular precursor [Sb(4,6-MepymS)] for the facile synthesis of binary SbS as well as ternary CuSbS in oleylamine (OAm) at a relatively lower temperature.
View Article and Find Full Text PDFNanomaterials (Basel)
May 2021
Institute of Earth Resources, Technical University Košice, 04001 Košice, Slovakia.
In this study, we demonstrate the feasibility of Bi-doped tetrahedrite CuSbBiS (x = 0.02-0.20) synthesis in an industrial eccentric vibratory mill using Cu, Sb, Bi and S elemental precursors.
View Article and Find Full Text PDFSci Rep
January 2021
Department of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
We report a simple, economical and low temperature route for phase-pure synthesis of two distinct phases of Cu-Sb-S, chalcostibite (CuSbS) and tetrahedrite (CuSbS) nanostructures. Both compounds were prepared by the decomposition of a mixture of bis(O-ethylxanthato)copper(II) and tris(O-ethylxanthato)antimony(III), without the use of solvent or capping ligands. By tuning the molar ratio of copper and antimony xanthates, single-phases of either chalcostibite or tetrahedrite were obtained.
View Article and Find Full Text PDFACS Appl Mater Interfaces
April 2020
State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, P. R. China.
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