Li-Chyong Chen

Improved broadband and quasi-omnidirectional anti-reflection properties with biomimetic silicon nanostructures

Nature routinely produces nanostructured surfaces with useful properties, such as the self-cleaning lotus leaf, the colour of the butterfly wing, the photoreceptor in brittlestar and the anti-reflection observed in the moth eye. Scientists and engineers have been able to mimic some of these natural structures in the laboratory and in real-world applications. Here, we report a simple aperiodic array of silicon nanotips on a 6-inch wafer with a sub-wavelength structure that can suppress the reflection of light at a range of wavelengths from the ultraviolet, through the visible part of the spectrum, to the terahertz region. Reflection is suppressed for a wide range of angles of incidence and for both s- and p-polarized light. The antireflection properties of the silicon result from changes in the refractive index caused by variations in the height of the silicon nanotips, and can be simulated with models that have been used to explain the low reflection from moth eyes. The improved anti-reflection properties of the surfaces could have applications in renewable energy and electro-optical devices for the military.

Tunable Photoluminescence from Graphene Oxide

Graphene oxide (GO) is a graphene sheet modified with oxygen functional groups in the form of epoxy and hydroxy groups on the basal plane and various other types at the edges. It exhibits interesting steady-state photoluminescence (PL) properties. For example, low-energy fluorescence in red to near infrared (NIR) wavelengths (from 600– 1100 nm) has been detected for suspensions and solid thin films of as-synthesized GO. 3] In addition, broad luminescence from 400 to 800 nm from oxygen plasma-treated, mechanically exfoliated, single-layer graphene sheet has been reported. Blue fluorescence with a relatively narrow bandwidth when excited with UV irradiation has also been detected from chemically reduced GO (rGO) and graphene quantum dots. 6] Recently, chemically modified GO or rGO with n-butylamine or Mn has also demonstrated PL emission at a range of energies. 10] A detailed explanation of the origin of such variable energy PL in GO has yet to be elucidated. This is partly because the sample preparation and reduction methods varied, making it difficult to compare the results. Herein, we have prepared GO suspensions that exhibit virtually all of the PL features observed by different groups, through careful and gradual reduction of the GO. The systematic evolution of the electronic structure and comprehensive analysis of steady-state and transient PL along with photoluminescence excitation (PLE) spectroscopy measurements indicate that two different types of electronically excited states are responsible for the observed emission characteristics. GO was synthesized using the modified Hummers method, the details of which have been reported. GO usually contains a large fraction of sp hybridized carbon atoms bound to oxygen functional groups, which makes it an insulator. Reduction can be achieved chemically (e.g. hydrazine exposure) or by thermal annealing in inert environments. Photothermal reduction of GO can be achieved by exposing GO samples to a Xenon flash in ambient conditions. In this study, we prepared aqueous GO solutions and subjected them to steady-state Xe lamp irradiation (500 W) with different exposure times of up to three hours. In contrast to reduction by an instantaneous flash, this method provides a controllable, gradual transformation from GO to rGO, allowing exploration of the PL evolution and emission mechanisms from as-synthesized GO to rGO. The deoxygenation of GO after reduction was confirmed by X-ray photoelectron spectroscopy (XPS), as shown in Figure 1. The C 1s signals of the original GO can be deconvoluted into signals for the C=C bond in aromatic rings (284.6 eV), C O bond (286.1 eV), C=O bond (287.5 eV), and C(=O) OH bond (289.2 eV), in agreement with previous assignments. Increased sp carbon bonding with increased reduction time can be clearly measured, which

Heterostructures of ZnO-Zn coaxial nanocables and ZnO nanotubes

The heterostructures of Zn–ZnO coaxial nanocables and ZnO nanotubes with an average diameter of 30 nm have been synthesized by simple pyrolysis of zinc acetylacetonate. High-resolution transmission electron microscopy analyses reveal that the Zn core and the ZnO sheath of the nanocables have an epitaxial relationship with their longitudinal axis oriented along the 〈001〉 direction. ZnO nanotubes with a wall thickness of 4 nm possess a single-crystal structure and appear to be the extension of the ZnO sheath of the coaxial nanocables. It is suggested that the ZnO nanotubes are formed by partial evaporation of Zn core of the Zn–ZnO coaxial nanocables.

Polymer Structure and Solvent Effects on the Selective Dispersion of Single-Walled Carbon Nanotubes

Combinations of different aromatic polymers and organic solvents have been studied as dispersing agents for preparing single-walled carbon nanotubes solutions, using optical absorbance, photoluminescence-excitation mapping, computer modeling, and electron microscopic imaging to characterize the solutions. Both the polymer structure and solvent used strongly influence the dispersion of the nanotubes, leading in some cases to very high selectivity in terms of diameter and chiral angle. The highest selectivities are observed using toluene with the rigid polymers PFO-BT and PFO to suspend isolated nanotubes. The specific nanotube species selected are also dependent on the solvent used and can be adjusted by the use of THF or xylene. Where the structure has more flexible conformations, the polymers are shown to be less selective but show an enhanced overall solubilization of nanotube material. When chloroform is used as the solvent, there is a large increase in the overall solubilization, but the nanotubes are suspended as bundles rather than as isolated tubes which leads to a quenching of their photoluminescence.

Elastic, mechanical, and thermal properties of nanocrystalline diamond films

Nanocrystalline columnar-structured diamond films with column diameters less than 100 nm and thicknesses in the range of 1–5 μm were grown on silicon substrates by chemical vapor deposition (CVD) in a microwave plasma reactor with purified methane and hydrogen used as the reactants. Uniform conformal nucleation densities in excess of 1012 cm−2 were accomplished prior to growth by seeding with explosively formed nanodiamonds, which resulted in good optical quality films. The film thickness was measured in situ by the laser reflectometry method. The grain size and optical quality of the films were characterized by scanning electron microscopy and Raman measurements. Broadband surface acoustic wave pulses were used to measure the anomalous dispersion in the layered systems. The experimental dispersion curves were fitted by theory, assuming the diamond film as an isotropic layer on an anisotropic silicon substrate, to determine mean values of the density and Young’s modulus of the diamond films. The density w...

Top laminated graphene electrode in a semitransparent polymer solar cell by simultaneous thermal annealing/releasing method.

In this article, we demonstrate a semitransparent inverted-type polymer solar cell using a top laminated graphene electrode without damaging the underlying organic photoactive layer. The lamination process involves the simultaneous thermal releasing deposition of the graphene top electrode during thermal annealing of the photoactive layer. The resulting semitransparent polymer solar cell exhibits a promising power conversion efficiency of approximately 76% of that of the standard opaque device using an Ag metal electrode. The asymmetric photovoltaic performances of the semitransparent solar cell while illuminated from two respective sides were further analyzed using optical simulation and photocarrier recombination measurement. The devices consisting of the top laminated transparent graphene electrode enable the feasible roll-to-roll manufacturing of low-cost semitransparent polymer solar cells and can be utilized in new applications such as power-generated windows or multijunction or bifacial photovoltaic devices.

Band Gap Engineering of Chemical Vapor Deposited Graphene by in-situ BN Doping

Band gap opening and engineering is one of the high priority goals in the development of graphene electronics. Here, we report on the opening and scaling of band gap in BN doped graphene (BNG) films grown by low-pressure chemical vapor deposition method. High resolution transmission electron microscopy is employed to resolve the graphene and h-BN domain formation in great detail. X-ray photoelectron, micro-Raman, and UV-vis spectroscopy studies revealed a distinct structural and phase evolution in BNG films at low BN concentration. Synchrotron radiation based XAS-XES measurements concluded a gap opening in BNG films, which is also confirmed by field effect transistor measurements. For the first time, a significant band gap as high as 600 meV is observed for low BN concentrations and is attributed to the opening of the π-π* band gap of graphene due to isoelectronic BN doping. As-grown films exhibit structural evolution from homogeneously dispersed small BN clusters to large sized BN domains with embedded diminutive graphene domains. The evolution is described in terms of competitive growth among h-BN and graphene domains with increasing BN concentration. The present results pave way for the development of band gap engineered BN doped graphene-based devices.

Highly Efficient Visible Light Photocatalytic Reduction of CO2 to Hydrocarbon Fuels by Cu-Nanoparticle Decorated Graphene Oxide

The production of renewable solar fuel through CO2 photoreduction, namely artificial photosynthesis, has gained tremendous attention in recent times due to the limited availability of fossil-fuel resources and global climate change caused by rising anthropogenic CO2 in the atmosphere. In this study, graphene oxide (GO) decorated with copper nanoparticles (Cu-NPs), hereafter referred to as Cu/GO, has been used to enhance photocatalytic CO2 reduction under visible-light. A rapid one-pot microwave process was used to prepare the Cu/GO hybrids with various Cu contents. The attributes of metallic copper nanoparticles (∼4-5 nm in size) in the GO hybrid are shown to significantly enhance the photocatalytic activity of GO, primarily through the suppression of electron-hole pair recombination, further reduction of GOs bandgap, and modification of its work function. X-ray photoemission spectroscopy studies indicate a charge transfer from GO to Cu. A strong interaction is observed between the metal content of the Cu/GO hybrids and the rates of formation and selectivity of the products. A factor of greater than 60 times enhancement in CO2 to fuel catalytic efficiency has been demonstrated using Cu/GO-2 (10 wt % Cu) compared with that using pristine GO.

Anomalous blueshift in emission spectra of ZnO nanorods with sizes beyond quantum confinement regime

Cathodoluminescence (CL) spectroscopy has been employed to study the electronic and optical properties of well-aligned ZnO nanorods with diameters ranging from 50to180nm. Single-nanorod CL studies reveal that the emission peak moves toward higher energy as the diameter of the ZnO nanorod decreases, despite that their sizes are far beyond the quantum confinement regime. Blueshift of several tens of meV in the CL peak of these nanorods has been observed. Moreover, this anomalous energy shift shows a linear relation with the inverse of the rod diameter. Possible existence of a surface resonance band is suggested and an empirical formula for this surface effect is proposed to explain the size dependence of the CL data.

Ultrahigh photocurrent gain in m-axial GaN nanowires

An ultrahigh photocurrent gain has been found in the ultraviolet-absorbed GaN nanowires with m-directional long axis grown by chemical vapor deposition. The quantitative results have shown the gain values at 5.0×104–1.9×105 of the GaN nanowires with diameters from 40to135nm are near three orders of magnitude higher than the values of 5.2×101–1.6×102 estimated from the thin film counterparts. The intensity-dependent gain study has shown that the gain value is very sensitive to the excitation intensity following an inverse power law and no gain saturation observed in this investigated intensity range from 0.75to250W∕m2. This behavior has strongly suggested a surface-dominant rather than trap-dominant high gain mechanism in this one-dimensional nanostructure. The strong carrier localization effect induced by the surface electric field in the GaN nanowires is also discussed.