Single-crystal tin selenide (SnSe), a record holder of high-performance thermoelectric materials, enables high-efficient interconversion between heat and electricity for power generation or refrigeration. However, the rigid bulky SnSe cannot satisfy the applications for flexible and wearable devices. Here, a method is demonstrated to achieve ultralong single-crystal SnSe wire with rock-salt structure and high thermoelectric performance with diameters from micro- to nanoscale. This method starts from thermally drawing SnSe into a flexible fiber-like substrate, which is polycrystalline, highly flexible, ultralong, and mechanically stable. Then a CO laser is employed to recrystallize the SnSe core to single-crystal over the entire fiber. Both theoretical and experimental studies demonstrate that the single-crystal rock-salt SnSe fibers possess high thermoelectric properties, significantly enhancing the ZT value to 2 at 862 K. This simple and low-cost approach offers a promising path to engage the fiber-shaped single-crystal materials in applications from 1D fiber devices to multidimensional wearable fabrics.
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http://dx.doi.org/10.1002/adma.202002702 | DOI Listing |
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December 2024
Department of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE, 68588, USA.
Tin diselenide (SnSe), a layered transition metal dichalcogenide (TMDC), stands out among other TMDCs for its extraordinary photoactive ability and low thermal conductivity. Consequently, it has stimulated many influential researches on photodetectors, ultrafast pulse shaping, thermoelectric devices, etc. However, the carrier mobility in SnSe, as determined experimentally, remains limited to tens of cmVs.
View Article and Find Full Text PDFInorg Chem
June 2024
Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada.
The ternary rare-earth sulfides SnS ( = La-Nd) and the partial solid solutions Sn(SSe) ( = La, Ce; = 0-0.8) were prepared in the form of polycrystalline samples by reaction of the elements at 900 °C and as single crystals in the presence of KBr flux. They adopt the LaSnS-type structure (orthorhombic, space group , = 2) consisting of chains of edge-sharing Sn octahedra separated by atoms.
View Article and Find Full Text PDFAdv Sci (Weinh)
February 2024
Molecular Inorganic Chemistry and Catalysis, Inorganic and Structural Chemistry, Center for Molecular Materials, Faculty of Chemistry, Universität Bielefeld, Universitätsstrasse 25, 33615, Bielefeld, Germany.
Decarbonylation of a cyclic bis-phosphaethynolatostannylene [(ADC)Sn(PCO)] based on an anionic dicarbene framework (ADC = PhC{N(Dipp)C} ; Dipp = 2,6-iPr C H ) under UV light results in the formation of a Sn P cluster compound [(ADC)SnP] as a green crystalline solid. The electronic structure of [(ADC)SnP] is analyzed by quantum-chemical calculations. At room temperature, [(ADC)SnP] reversibly binds with CO and forms [(ADC) {SnOC(O)P}SnP].
View Article and Find Full Text PDFInorg Chem
April 2023
Institute of Inorganic Chemistry, University of Cologne, Greinstraße 6, D-50939 Cologne, Germany.
Two-dimensional tin monoselenide (SnSe) and tin diselenide (SnSe) materials were efficiently produced by the thermolysis of molecular compounds based on a new class of seleno-ligands. Main group metal chalcogenides are of fundamental interest due to their layered structures, thickness-dependent modulation in electronic structure, and small effective mass, which make them attractive candidates for optoelectronic applications. We demonstrate here the synthesis of stable tin selenide precursors by reductive bond cleavage in the dimeric diselenide ligand (SeCHN(Me)CHSe) in the presence of SnCl.
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