Field electron emission of carbon-based nanocone films

Diamond nanocone, graphitic nanocone, and mixed diamond and graphitic nanocone films have been synthesized through plasma enhanced hot filament chemical vapor deposition (HFCVD). The field emission properties of these films have been experimentally investigated. The studies have revealed that all three kinds of nanocone films have excellent field electron emission (FEE) properties including low turn-on electric field and large emission current at low electric field. Compared with the diamond nanocone films (emission current of 86 μA at 26 V/μm with the turn-on field of 10 V/μm), the graphitic nanocone films exhibit higher FEE current of 1.8×10² μA at 13 V/μm and a lower turn-on filed of 4 V/μm. The mixed diamond and graphitic nanocone films have been found to posses FEE properties similar to graphitic nanocone films (emission current of 1.7×10² μA at 20 V/μm with the turn-on field of 5 V/μm), but have much better FEE stability than the graphitic nanocone films. PACS 81.07.Bc; 81.05.Uw; 79.70.+q     

Waveguides and quasi-waveguides based on pyrromethene 597-doped poly(methyl methacrylate)

The characteristics of amplified spontaneous emission (ASE) from asymmetric planar waveguides and quasi-waveguides consisting of thin films of poly(methyl methacrylate) incorporating lasing dye pyrromethene 597 deposited onto quartz and glass substrates, respectively, are investigated. The variable stripe length and moving constant stripe methods, together with appropriate theoretical expressions which take into account gain saturation and a simple model based on a four-level laser, allow for obtaining the net gain coefficients as a function of pump intensity, losses, pump thresholds for the onset of ASE, effective stimulated emission cross sections, pump saturation intensities, and saturation lengths. Net gain coefficients of up to 84±3 cm⁻¹ at a pump intensity of 404 kW/cm² (28 μJ/pulse) for quasi-waveguides and up to 59±6 cm⁻¹ at a pump intensity of 360 kW/cm² (25 μJ/pulse) for waveguides were obtained, with pump thresholds of 15.7 kW/cm² (1.1 μJ/pulse) and 6.3 kW/cm² (0.43 μJ/pulse), respectively. When waveguides 8 μm thick were irradiated with pulses of 200 kW/cm² at 10 Hz repetition rate, the ASE remained at 79% of its initial value after 1000 pump pulses in the same position of the sample. In quasi-waveguides 10 μm thick, the emission remained at 82% of the initial value under the same conditions.     

Luminescence of Eu<Superscript>2+</Superscript> ions in alkaline earth dilithiosilicates

Spectral-luminescent properties of Eu²⁺ ions in alkaline earth dilithiosilicates of composition MLi₂SiO₄ (M = Ca, Sr, Ba) have been studied at 77 K. The reasons for the different positions of the Eu²⁺ 4f ⁶5 d → 4f ⁷ emission band maximum in spectra of MLi₂SiO₄ were found based on the obtained results. It was shown that the increase in the decay time of the Eu²⁺ emission on going from CaLi₂SiO₄ (0.41μs) through BaLi₂SiO₄ (0.64 μs) to Sr-silicate (1.11μs) correlates with the shift of the emission maximum to longer wavelengths.     

Mechanism of field emission from carbon materials

Field emission in diamond and graphite-like polycrystalline films is investigated experimentally. It is shown that the emission efficiency increases as the nondiamond carbon phase increases; for graphite-like films the threshold electric field is less than 1.5 V/μm, and at 4 V/μm the emission current reaches 1 mA/cm², while the density of emission centers exceeds 10⁶ cm⁻². A general mechanism explaining the phenomenon of electron field emission from materials containing graphite-like carbon is proposed. Pis’ma Zh. éksp. Teor. Fiz. 68, No. 1, 56–60 (10 July 1998)     

Optimization of field emission properties from multi-walled carbon nanotubes using ceramic fillers

The field emission properties of multi-walled carbon nanotubes were examined using a screen-printed thick film with a diode-type configuration in a vacuum. The effects of various concentrations of two different ceramic fillers, indium tin oxide (ITO) powder and a glass frit, on the emission current density and turn-on field were evaluated. The emission properties of both pastes were dependent on the amount of filler. Considerably enhanced emission properties were obtained with the paste containing 5–10 wt.% of either ITO or the glass frit compared with those without a filler. The paste containing the ceramic filler showed enhanced emission properties compared with that containing the 5 wt.% Ag conventionally used, which confirmed the importance of the filler. The paste containing 10 wt.% ITO represented an emission current density of 176.4 μA/cm² at 5 V/μA, a turn-on field of 1.87 V/μA for an emission current density of 1 μA/cm² and a field enhancement factor of 7580. The paste formulation was also found to be suitable for fine patterning using UV-lithography techniques. A long-term stability test for 110 h of a paste containing 10 wt.% ITO revealed a half-life of approximately 30000 h, which is appropriate for commercial applications.     

Low threshold field electron emission from solvothermally synthesized WO2.72 nanowires

Field emission studies of WO_2.72 nanowires synthesized by a solvothermal method have been performed in the planar diode configuration under ultra high vacuum conditions. Fowler–Nordheim plots obtained from the current-voltage characteristics follow the quantum mechanical tunneling process and a current density of ∼8.3×10⁶ μA/cm² can be drawn at an applied electric field of 2 V/μm. The field enhancement factor is 33025, while the turn-on field is only 1.4 V/μm. The emission current-time plot recorded at the pre-set value of emission current of 1 μA over a period of more than 3 h exhibits an initial increase and a subsequent stabilization of the emission current. The results reveal that the WO_2.72 nanowire emitters synthesized by the solvothermal method are promising cathode materials for practical applications.     

Field emission from lotiform-like ZnO nanostructures synthesized via thermal evaporation method

Novel lotiform ZnO nanostructures were synthesized on silicon substrate via simple thermal evaporation. The average diameter of the ZnO nanostructures is ∼1.5 μm. The lotiform-like ZnO structures were formed by nanorods arrays with the average diameter of 70 nm. The as-grown lotiform ZnO nanostructures have excellent field-emission properties such as the low turn-on field of 3.4 V/μm, and very high emission current density of 12.4 mA/cm² at the field of 9.6 V/μm. These features make the lotiform-like ZnO nanostructures competitive candidates for field-emission-based displays. PACS 61.46.-w; 61.82.Rx; 78.67.-n; 73.63.Bd; 74.78.Na     

Spectroscopic and lasing properties of Er3+:Yb3+-doped fluoride phosphate glasses

Er³⁺ emission and lasing properties at 1.5 μm were studied in fluoride phosphate glasses (FP20) with different doping concentrations as well as in a commercial phosphate glass (Kigre QX). Emission decay behaviour at 1 μm and 1.5 μm was examined with respect to energy transfer between ytterbium and erbium. Emission cross-sections were determined using the reciprocity and Füchtbauer–Ladenburg methods. Gain spectra were calculated for the glasses and related to differences in the tuning curves and lasing properties. The temperature rise due to the quantum defect was determined via the ratios of green upconversion luminescence for different pump powers. The results from the laser and tuning experiments indicate that the FP20 glass offers good possibilities in broadband amplification and the generation of ultrashort pulses. Received: 24 August 2000 / Revised version: 27 October 2000 / Published online: 7 February 2001     

Synthesis and field emission of two kinds of ZnO nanotubes: taper-like and flat-roofed tubes

Two kinds of ZnO nanotubes, including taper-like and flat-roofed tubes, have been successfully fabricated using a simple aqueous solution route by changing the experimental conditions. All the obtained nanotubes have a uniform size of 500 nm in diameter, 10–50 nm in wall thickness, and 2–5 μm in length. The growth mechanism of two kinds of ZnO nanotubes was investigated. Field emission measurements showed that tapering nanotubes have the good field emission performance with a low turn-on field of ∼ 2.1 V μm^-1 and a low threshold field of ∼ 3.8 V μm^-1, which suggests the possible applications of the ZnO tubular structures in field emission microelectronic devices. PACS 73.61.Ga; 73.63. Fg; 85.45.Db     

Spectroscopic properties of 1.8 μm emission of thulium ions in germanate glass

A new type host of germanate glass (GeO₂− BaO−BaF₂−Ga₂O₃−La₂O₃) codoped with Tm₂O₃ has been investigated for application as laser material. It possesses a large emission cross section with the value of 9.3×10⁻²¹ cm² at 1.8 μm. Judd-Ofelt intensity parameters and radiative transition probability are calculated and analyzed by Judd-Ofelt theory and absorption spectra. The infrared emission spectra at 1.8 μm have been obtained by using a 794 nm laser diode as excitation resource. The emission intensity ratio of 1.8 (³F₄→³H₆) to 1.47 μm (³H₄→³F₄) increases, while the experimental lifetime of the Tm³⁺:³H₄ level decreases by increasing Tm₂O₃ concentration, which is attributed to the presence of a cross relaxation process. The most intensive emission at 1.8 μm is achieved from the germanate glass with the concentration of Tm₂O₃ reaches 1.0 wt%. The extended overlap integral method is used to calculate the microparameter of the energy transfer and the critical distance, which are derived to better understand the energy transfer process of thulium ions in the germanate glass responsible for emission at 1.8 μm.     

A Coumarin-Based Fluorescent Chemosensor for Zn<Superscript>2+</Superscript> in Aqueous Ethanol Media

A coumarin-based fluorescent chemosensor 1 for Zn²⁺ was designed and synthesized. Compound 1 exhibits lower background fluorescence due to intramolecular photoinduced electron transfer. However, upon mixing with Zn²⁺ in 30% (v/v) aqueous ethanol, a “turn-on” fluorescence emission is observed. The fluorescence emission increases linearly with Zn²⁺ concentration in the range 0.5–10 μmol L⁻¹ with a detection limit of 0.29 μmol L⁻¹. No remarkable emission enhancement was, however, observed for other metal ions. The proposed chemosensor was applied to the determination of Zn²⁺ in water samples with satisfactory results.     

Infrared laser emission in two-photon pumped sodium vapour

We report infrared laser emission in the region of 3 to 5 μm from sodium vapour optically pumped by a pulsed dye laser with wavelengths ranging from 585 to 610nm. Twophoton excitation processes are believed to be responsible for the primary excitation. Both molecular transitions (4 to 5 μm) between high lying states, and atomic transitions (5² S _1/2−4² P _3/2,1/2 at 3.41 μm) have been identified.     

Morphological effects on the field emission characteristics of zinc oxide nanotetrapods films

The direct growth of a tetrapod-like ZnO nanostructure has been accomplished by using a thermal oxidation method without any catalysts. Studies on the field emission properties of the ordered ZnO nanotetrapods films found that the shape of the ZnO nanotetrapods has considerable effect on their field emission properties, especially the turn-on field and the emission current density. Compared with the rod-like legs ZnO nanotetrapods, the nanotetrapods with acicular legs have a lower turn-on field of 2.7 V/μm at a current density of 10 μA/cm², a high field enhancement factor of 1830, and an available stability. More importantly, the emission current density reached 1 mA/cm² at a field of 4.8 V/μm without showing saturation. The results could be valuable for using the ZnO nanostructure as a cold-cathode field-emission material.      

Vector meson study for the CBM experiment at FAIR/GSI

We have studied the possibility to detect vector mesons via their decay into μ⁺μ⁻ pairs in heavy-ion collisions at FAIR with a muon detection system as part of the Compressed Baryonic Matter (CBM) experiment. The text was submitted by the authors in English.     

Electron field emission from magnetic nanomaterial encapsulated multi-walled carbon nanotubes

The present work describes the field emission characteristics of nanoscale magnetic nanomaterial encapsulated multi-walled carbon nanotubes (MWNTs) fabricated over flexible graphitized carbon cloth. Ni/MWNTs, NiFe/MWNTs and NiFeCo/MWNTs have been synthesized by catalytic chemical vapor decomposition of methane over Mischmetal (Mm)-based AB₃ (MmNi₃, MmFe_1.5Ni_1.5 and MmFeCoNi) alloy hydride catalysts. Metal-encapsulated MWNTs exhibited superior field emission performance than pure MWNT-based field emitters over the same substrate. The results indicate that a Ni-filled MWNT field emitter is a promising material for practical field emission application with a lowest turn-on field of 0.6 V/μm and a high emission current density of 0.3 mA/cm² at 0.9 V/μm.     

Field emission from single-walled carbon nanotubes aligned on a gold plate using a self-assembly monolayer

Field emission from single-walled carbon nanotubes (SWNTs) aligned on a patterned gold surface is reported. The SWNT emitters were prepared at room temperature by a self-assembly monolayer technique. SWNTs were cut into sub-micron lengths by sonication in an acidic solution. Cut SWNTs were attached to the gold surface by the reaction between the thiol groups and the gold surface. The field-emission measurements showed that the turn-on field was 4.8 V/μm at an emission current density of 10 μA/cm². The current density was 0.5 mA/cm² at 6.6 V/μm. This approach provides a novel route for fabricating CNT-based field-emission displays. Received: 3 May 2002 / Accepted: 6 May 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +82-54/279-8298, E-mail: ce20047@postech.ac.kr     

Synthesis of Functionalized ZnSe Nanoparticles and Their Applications in the Determination of Bovine Serum Albumin

Luminescent quantum dots (QDs)-semiconductor nanocrystals were promising alternative to organic dyes for fluorescence-based applications. In this paper, we developed procedures to use mercaptoacetic acid (MAA) to modify ZnSe nanoparticles and made the nanoparticles to be soluble for the quantitative and selective determination of bovine serum albumin (BSA). Maximum fluorescence intensity was produced at pH 7.0, with excitation and emission wavelengths at 242 and 348 nm, respectively. Under optimal conditions, the straight line equation: ^△ F = 0.38 + 0.34 C (μg/ml) was found between the relative fluorescence intensity and the concentration of BSA in the range of 9.6–124.8 μg/ml, and the limit of detection was 2 μg/ml.     

Synthesis of LaB6 micro/nano structures using picosecond (Nd:YAG) laser and its field emission investigations

Micro/nano structures have been obtained by laser surface treatment on sintered LaB₆ pellets employing a picosecond pulsed Nd:YAG laser at a pressure of ∼1×10⁻³ mbar. The X-ray diffraction pattern of the laser treated pellet shows a set of well defined diffraction peaks, indexed to the cubic phase of LaB₆ only. The scanning electron microscope studies reveal formation of micro and nano structures upon laser treatment and the resultant surface morphology is found to be strongly influenced by the laser fluence. Field electron emission studies made on the LaB₆ pellet, treated with optimized laser fluence, have been performed in a planar diode configuration under ultra high vacuum conditions. The threshold field required to draw an emission current density of ∼10 μA/cm² has been found to be ∼2.3 V/μm and a current density of ∼530 μA/cm² has been drawn at an applied field of 5.2 V/μm. The Fowler-Nordheim plot is found to be linear in accordance with the quantum mechanical tunneling phenomenon, confirming the metallic nature of the emitter. The emission current at the pre-set value ∼10 μA shows very good stability over a period of more than 3 hours. The present results emphasize the effectiveness of a picosecond laser treatment towards fabrication of a nano metric LaB₆ emitter for high current density applications.     

Mid-Infrared Emission Characteristic and Energy Transfer of Ho<Superscript>3+</Superscript>-Doped Tellurite Glass Sensitized by Tm<Superscript>3+</Superscript>

We report on 2.0-μm emission characteristic and energy transfer of Ho³⁺-doped tellurite glass sensitized by Tm³⁺ upon excitation of a conventional 808 nm laser diode. The Judd-Ofelt strength parameters, spontaneous radiative transition probabilities and radiative lifetime of Ho³⁺ have been calculated from the absorption spectra by using the Judd-Ofelt theory. Significant enhancement of 2.0-μm emission of Ho³⁺ has been observed with increasing Tm³⁺ doping up to 0.7 mol%. The energy transfer coefficient of the forward Tm³⁺→Ho³⁺ is approximately 17 times larger than that of the backward Tm³⁺←Ho³⁺ energy transfer. Our result indicates that the maximum gain of 2.0-μm emission, assigned to the transition of ⁵I₇→⁵I₈ of Ho³⁺, might be achieved from the tellurite glass at the concentration of 0.5 mol% of Tm₂O₃ and 0.15 mol% of Ho₂O₃. The high gain coefficient and quantum efficiency (1.16) along with the large value of the product of the stimulated emission cross-section and the measured radiative lifetime (4.12×10⁻²⁷ m²s) of the Ho³⁺/Tm³⁺-codoped tellurite glasses might find potential applications in efficient 2.0-μm laser.     

Fiber optic evanescent field sensor for detection of explosives and CO<Subscript>2</Subscript> dissolved in water

A fiber optic approach for the determination of the carbon dioxide concentration in the gas or fluid phase during sequestration, as well as for the sensing of the explosive TNT is described. The sensor consists of a quartz glass multimode fiber with core diameter of 200 μm and is based on the evanescent field principle. Cladding and jacket of the fiber are removed in the sensing portion, therefore interaction between light within the fiber and the surrounding medium is possible. A single-mode distributed feedback (DFB) laser diode with an emission wavelength around λ= 1.57 μm and a frequency doubled passively Q-switched Cr⁴⁺:Nd³⁺:YAG microchip laser (λ= 1064 nm)are used as light sources. The experimental setup and the sensitivity of the evanescent field sensor are characterized. PACS 42.62.Fi; 42.79.Wc; 07.07.Df