Low temperature solution-phase growth of ZnSe and ZnSe/CdSe core/shell nanowires

High quality ZnSe nanowires (NWs) and complementary ZnSe/CdSe core/shell species have been synthesized using a recently developed solution-liquid-solid (SLS) growth technique. In particular, bismuth salts as opposed to pre-synthesized Bi or Au/Bi nanoparticles have been used to grow NWs at low temperatures in solution. Resulting wires are characterized using transmission electron microscopy and possess mean ensemble diameters between 15 and 28 nm with accompanying lengths ranging from 4-10 μm. Subsequent solution-based overcoating chemistry results in ZnSe wires covered with CdSe nanocrystals. By varying the shell's growth time, different thicknesses can be obtained and range from 8 to 21 nm. More interestingly, the mean constituent CdSe nanocrystal diameter can be varied and results in size-dependent shell emission spectra.Fil: Petchsang, Nattasamon. University of Notre Dame; Estados Unidos. Thailand Ministry of Education; Tailandia. Mahidol University; TailandiaFil: Shapoval, Liubov. Herzen State Pedagogical University Of Russia; RusiaFil: Vietmeyer, Felix. University of Notre Dame; Estados UnidosFil: Yu, Yanghai. University Of Wisconsin Madison;Fil: Hodak, Jose Hector. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Tang, I-Ming. Mahidol University; Tailandia. Thailand Ministry Of Education; TailandiaFil: Kosel, Thomas H.. University of Notre Dame; Estados UnidosFil: Kuno, Masaru. University of Notre Dame; Estados Unido

Direct Observation of Single Layer Graphene Oxide Reduction through Spatially Resolved, Single Sheet Absorption/Emission Microscopy

Laser reduction of graphene oxide (GO) offers unique opportunities for the rapid, nonchemical production of graphene. By tuning relevant reduction parameters, the band gap and conductivity of reduced GO can be precisely controlled. In situ monitoring of single layer GO reduction is therefore essential. In this report, we show the direct observation of laser-induced, single layer GO reduction through correlated changes to its absorption and emission. Absorption/emission movies illustrate the initial stages of single layer GO reduction, its transition to reduced-GO (rGO) as well as its subsequent decomposition upon prolonged laser illumination. These studies reveal GO’s photoreduction life cycle and through it native GO/rGO absorption coefficients, their intrasheet distributions as well as their spatial heterogeneities. Extracted absorption coefficients for unreduced GO are α_405 nm ≈ 6.5 ± 1.1 × 10⁴ cm^–1, α_520 nm ≈ 2.1 ± 0.4 × 10⁴ cm^–1, and α_640 nm ≈ 1.1 ± 0.3 × 10⁴ cm^–1 while corresponding rGO α-values are α_405 nm ≈ 21.6 ± 0.6 × 10⁴ cm^–1, α_520 nm ≈ 16.9 ± 0.4 × 10⁴ cm^–1, and α_640 nm ≈ 14.5 ± 0.4 × 10⁴ cm^–1. More importantly, the correlated absorption/emission imaging provides us with unprecedented insight into GO’s underlying photoreduction mechanism, given our ability to spatially resolve its kinetics and to connect local rate constants to activation energies. On a broader level, the developed absorption imaging is general and can be applied toward investigating the optical properties of other two-dimensional materials, especially those that are nonemissive and are invisible to current single molecule optical techniques

Direct Observation of Spatially Heterogeneous Single-Layer Graphene Oxide Reduction Kinetics

Graphene oxide (GO) is an important precursor in the production of chemically derived graphene. During reduction, GO’s electrical conductivity and band gap change gradually. Doping and chemical functionalization are also possible, illustrating GO’s immense potential in creating functional devices through control of its local hybridization. Here we show that laser-induced photolysis controllably reduces individual single-layer GO sheets. The reaction can be followed in real time through sizable decreases in GO’s photoluminescence efficiency along with spectral blueshifts. As-produced reduced graphene oxide (rGO) sheets undergo additional photolysis, characterized by dramatic emission enhancements and spectral redshifts. Both GO’s reduction and subsequent conversion to photobrightened rGO are captured through movies of their photoluminescence kinetics. Rate maps illustrate sizable spatial and temporal heterogeneities in sp² domain growth and reveal how reduction “flows” across GO and rGO sheets. The observed heterogeneous reduction kinetics provides mechanistic insight into GO’s conversion to chemically derived graphene and highlights opportunities for overcoming its dynamic, chemical disorder

Direct Observation of Spatially Heterogeneous Single-Layer Graphene Oxide Reduction Kinetics

Graphene oxide (GO) is an important precursor in the production of chemically derived graphene. During reduction, GO’s electrical conductivity and band gap change gradually. Doping and chemical functionalization are also possible, illustrating GO’s immense potential in creating functional devices through control of its local hybridization. Here we show that laser-induced photolysis controllably reduces individual single-layer GO sheets. The reaction can be followed in real time through sizable decreases in GO’s photoluminescence efficiency along with spectral blueshifts. As-produced reduced graphene oxide (rGO) sheets undergo additional photolysis, characterized by dramatic emission enhancements and spectral redshifts. Both GO’s reduction and subsequent conversion to photobrightened rGO are captured through movies of their photoluminescence kinetics. Rate maps illustrate sizable spatial and temporal heterogeneities in sp² domain growth and reveal how reduction “flows” across GO and rGO sheets. The observed heterogeneous reduction kinetics provides mechanistic insight into GO’s conversion to chemically derived graphene and highlights opportunities for overcoming its dynamic, chemical disorder

Direct Observation of Spatially Heterogeneous Single-Layer Graphene Oxide Reduction Kinetics

Graphene oxide (GO) is an important precursor in the production of chemically derived graphene. During reduction, GO’s electrical conductivity and band gap change gradually. Doping and chemical functionalization are also possible, illustrating GO’s immense potential in creating functional devices through control of its local hybridization. Here we show that laser-induced photolysis controllably reduces individual single-layer GO sheets. The reaction can be followed in real time through sizable decreases in GO’s photoluminescence efficiency along with spectral blueshifts. As-produced reduced graphene oxide (rGO) sheets undergo additional photolysis, characterized by dramatic emission enhancements and spectral redshifts. Both GO’s reduction and subsequent conversion to photobrightened rGO are captured through movies of their photoluminescence kinetics. Rate maps illustrate sizable spatial and temporal heterogeneities in sp² domain growth and reveal how reduction “flows” across GO and rGO sheets. The observed heterogeneous reduction kinetics provides mechanistic insight into GO’s conversion to chemically derived graphene and highlights opportunities for overcoming its dynamic, chemical disorder

Direct Observation of Spatially Heterogeneous Single-Layer Graphene Oxide Reduction Kinetics

Graphene oxide (GO) is an important precursor in the production of chemically derived graphene. During reduction, GO’s electrical conductivity and band gap change gradually. Doping and chemical functionalization are also possible, illustrating GO’s immense potential in creating functional devices through control of its local hybridization. Here we show that laser-induced photolysis controllably reduces individual single-layer GO sheets. The reaction can be followed in real time through sizable decreases in GO’s photoluminescence efficiency along with spectral blueshifts. As-produced reduced graphene oxide (rGO) sheets undergo additional photolysis, characterized by dramatic emission enhancements and spectral redshifts. Both GO’s reduction and subsequent conversion to photobrightened rGO are captured through movies of their photoluminescence kinetics. Rate maps illustrate sizable spatial and temporal heterogeneities in sp² domain growth and reveal how reduction “flows” across GO and rGO sheets. The observed heterogeneous reduction kinetics provides mechanistic insight into GO’s conversion to chemically derived graphene and highlights opportunities for overcoming its dynamic, chemical disorder

Direct Observation of Spatially Heterogeneous Single-Layer Graphene Oxide Reduction Kinetics

Graphene oxide (GO) is an important precursor in the production of chemically derived graphene. During reduction, GO’s electrical conductivity and band gap change gradually. Doping and chemical functionalization are also possible, illustrating GO’s immense potential in creating functional devices through control of its local hybridization. Here we show that laser-induced photolysis controllably reduces individual single-layer GO sheets. The reaction can be followed in real time through sizable decreases in GO’s photoluminescence efficiency along with spectral blueshifts. As-produced reduced graphene oxide (rGO) sheets undergo additional photolysis, characterized by dramatic emission enhancements and spectral redshifts. Both GO’s reduction and subsequent conversion to photobrightened rGO are captured through movies of their photoluminescence kinetics. Rate maps illustrate sizable spatial and temporal heterogeneities in sp² domain growth and reveal how reduction “flows” across GO and rGO sheets. The observed heterogeneous reduction kinetics provides mechanistic insight into GO’s conversion to chemically derived graphene and highlights opportunities for overcoming its dynamic, chemical disorder