2005
DOI: 10.1002/adma.200400894
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Spontaneous Transformation of Stabilizer‐Depleted Binary Semiconductor Nanoparticles into Selenium and Tellurium Nanowires

Abstract: Se and Te nanowires (NWs) are spontaneously formed in solution through chemical decomposition of stabilizer‐depleted nanoparticles (NPs) in the presence of a strong complexing agent. Highly crystalline Se and Te NWs with monodisperse lateral sizes, in the range 10–100 nm, are produced (see Figure and cover). This work provides a new approach to nanoscale synthesis, which takes advantage of the transformation of NPs to NWs induced by stabilizer shell depletion and ensuing chemical reactions.

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Cited by 142 publications
(182 citation statements)
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“…The distance between two neighboring lattice fringes in Figure 2B is about 0.58 nm, corresponding to the Te (006) crystal planes and suggesting the growth direction for Te nanowires is along c-axis, which is mainly due to the anisotropic crystal structure in hexagonal Te phase. 22,23 19,24 Notably, the concentration and the amount of hydrazine have been found to significantly impact the composition of the final product as well as the size and the density of the Te nanowires and Bi 2 Te 3 plates. Using anhydrous hydrazine in the reaction will only lead to the formation of pure Bi 2 Te 3 nanowires with a much thinner diameter, which is consistent with our previous report.…”
mentioning
confidence: 99%
“…The distance between two neighboring lattice fringes in Figure 2B is about 0.58 nm, corresponding to the Te (006) crystal planes and suggesting the growth direction for Te nanowires is along c-axis, which is mainly due to the anisotropic crystal structure in hexagonal Te phase. 22,23 19,24 Notably, the concentration and the amount of hydrazine have been found to significantly impact the composition of the final product as well as the size and the density of the Te nanowires and Bi 2 Te 3 plates. Using anhydrous hydrazine in the reaction will only lead to the formation of pure Bi 2 Te 3 nanowires with a much thinner diameter, which is consistent with our previous report.…”
mentioning
confidence: 99%
“…26 Other methods for wet chemical synthesis of 1D tellurium nanostructures are also reported. [27][28][29] However, the vapor phase synthesis of Te nanotubes is not common. In a particular case, it results in the formation of tubular structures of Te with micrometer diameters.…”
Section: Introductionmentioning
confidence: 99%
“…This anisotropic structure induces Te toward 1D growth. 3,[21][22][23][24][25][26][27][28][29][30][31][32] Mayer and Xia reported the synthesis of Te nanotubes with hexagonal cross sections by reducing orthotelluric acid in ethylene glycol. 3 Wei et al synthesized Te nanotubes by a solvothermal process using N,N-dimethylformamide as a solvent and porous silica (MCM-41) as a growth assisting agent.…”
Section: Introductionmentioning
confidence: 99%
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“…Previous reports on the synthesis of Te and Se nanomaterials [29][30][31] did not relate to the chirality or chiroptical activity of the nanostructures, and there were no attempts to direct their handedness. Here, in addition to lattice chirality of nanocrystals, the overall shape of Te nanocrystals is made chiral, to achieve a new level of control over chirality.…”
mentioning
confidence: 99%