Abstract:Cu2S nanoribbons with width of 60–80 nm, length of 200–500 nm, and average thickness of about 8 nm were prepared by means of a simple solid-state reaction at room temperature without surfactants. The product was characterized by various techniques of XRD, XPS, TEM, HRTEM, and UV–vis spectra.
“…Therefore, Δ E g × L y 2 should be a constant. The value of Δ E g × L y 2 calculated from Cu 2 S nanoribbons26 is 40.96 eV nm 2 . As shown in Figure 10, the absorption maximum at λ =274 nm and the absorption edge at λ =293 nm (curves c and d), give Δ E g =0.29 eV, and the average thickness is then calculated to be ≈12 nm, which is in good agreement with the thickness obtained from TEM observations.…”
Section: Resultsmentioning
confidence: 95%
“…22 The quantum size effect of nano Cu 2 S materials23 results in the tunable band gaps of these materials, which is desirable in photoelectric applications. Recently, Cu 2 S nanocrystals with different morphologies, such as wires,17, 24, 25 ribbons,26, 27 tubes,25 rods,14 disks, and plates,10, 13, 14 have been prepared by using different approaches, for example, solid, solution, hydrothermal, and solventless methods. The solventless method has shown advantages in producing uniform nanoproducts,14, 17 however, high yields from this method are impossible because of the extreme difficulty of separating Cu 2 S nanoproducts from the raw products (a mixture of several insoluble byproducts and unreacted reactants).…”
Uniform Cu(2)S nanodisks have been synthesized from a well-characterized layered copper thiolate precursor by structure-controlling solventless thermolysis at 200-220 degrees C under a N(2) atmosphere. The development from small Cu(2)S nanoparticles (diameter approximately 3 nm) to nanodisks (diameter 8.3 nm) and then to faceted nanodisks (diameter 27.5 nm, thickness 12.7 nm) is accompanied by a continuous phase transition from metastable orthorhombic to monoclinic Cu(2)S, the ripening of small particles by aggregation, and finally the crystallization process. The growth of the nanoproduct is constrained by the crystal structure of the precursor and the in situ-generated thiol molecules. Such controlled anisotropic growth leads to a nearly constant thickness of faceted nanodisks with different diameters, which has been confirmed by TEM observations and optical absorption measurements.
“…Therefore, Δ E g × L y 2 should be a constant. The value of Δ E g × L y 2 calculated from Cu 2 S nanoribbons26 is 40.96 eV nm 2 . As shown in Figure 10, the absorption maximum at λ =274 nm and the absorption edge at λ =293 nm (curves c and d), give Δ E g =0.29 eV, and the average thickness is then calculated to be ≈12 nm, which is in good agreement with the thickness obtained from TEM observations.…”
Section: Resultsmentioning
confidence: 95%
“…22 The quantum size effect of nano Cu 2 S materials23 results in the tunable band gaps of these materials, which is desirable in photoelectric applications. Recently, Cu 2 S nanocrystals with different morphologies, such as wires,17, 24, 25 ribbons,26, 27 tubes,25 rods,14 disks, and plates,10, 13, 14 have been prepared by using different approaches, for example, solid, solution, hydrothermal, and solventless methods. The solventless method has shown advantages in producing uniform nanoproducts,14, 17 however, high yields from this method are impossible because of the extreme difficulty of separating Cu 2 S nanoproducts from the raw products (a mixture of several insoluble byproducts and unreacted reactants).…”
Uniform Cu(2)S nanodisks have been synthesized from a well-characterized layered copper thiolate precursor by structure-controlling solventless thermolysis at 200-220 degrees C under a N(2) atmosphere. The development from small Cu(2)S nanoparticles (diameter approximately 3 nm) to nanodisks (diameter 8.3 nm) and then to faceted nanodisks (diameter 27.5 nm, thickness 12.7 nm) is accompanied by a continuous phase transition from metastable orthorhombic to monoclinic Cu(2)S, the ripening of small particles by aggregation, and finally the crystallization process. The growth of the nanoproduct is constrained by the crystal structure of the precursor and the in situ-generated thiol molecules. Such controlled anisotropic growth leads to a nearly constant thickness of faceted nanodisks with different diameters, which has been confirmed by TEM observations and optical absorption measurements.
“…It is well-known that in an alkaline medium S 2– ions are generated by hydrolysis of thiocarbamide The capping groups or surfactants play an important role in nanocrystals growth.…”
Section: Resultsmentioning
confidence: 99%
“…It is well-known that in an alkaline medium S 2À ions are generated by hydrolysis of thiocarbamide. 51 The capping groups or surfactants play an important role in nanocrystals growth. At high temperatures, the surfactant molecules are dynamically adsorbed to the surface of growing crystals, thereby stabilizing the particles in solution and mediating their growth.…”
“…Transition metal complexes are a class of important compounds owing to their good catalytic properties in organic synthesis and some potential uses as sensitizers for photolysis of water . At the same time, they can be used as precursors for preparation of some semiconductors including ZnS, , ZnSe, ZnO, , CuS, and Cu 2 S via thermal decomposition, solvothermal or hydrothermal process, solid-state reaction, and so on. For example, X. Chen et al synthesized copper sulfide hollow spheres via a hydrothermal route utilizing a copper(II)−thiourea complex as the precursor.…”
In the present paper, we report the successful synthesis of a ZnS(en)0.5 complex (en = ethylenediamine) with a
cuboid morphology by a solvothermal method employing zinc powder and sulfur powder as the reactants in ethylenediamine and
further conversion to ZnS and ZnO. Research showed that the morphology hardly changed after the ZnS(en)0.5 complex had been
converted into ZnS in a vacuum at 450 °C for 40 min and that nearly spherical ZnO grains with a mean diameter of 300 nm were
obtained after the ZnS(en)0.5 complex was oxidized in air at 650 °C for 40 min. Also, the experiments indicated that ZnS(en)0.5,
ZnS, and ZnO could degrade safranine T, an organic dye, under irradiation of 254 nm UV light and that ZnS had better photocatalytic
degradation properties than ZnS(en)0.5 and ZnO after irradiation for 30 min. The electrochemical studies showed that ZnS and ZnO
had a stronger ability to promote electron transfers between hemoglobin (Hb) and the Au electrode than ZnS(en)0.5 but had a weaker
ability to accelerate electron transfers between catechol and the Au electrode than ZnS(en)0.5. The possible mechanisms are discussed.
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