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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 721 records · Page 40
All sourcesNASA NTRSDOE OSTI
DOE OSTI2015

Chemical Free Surface Processing for High Gradient Superconducting RF Cavities

Chemical treatment such as buffered chemical polishing (BCP) or electro polishing (EP) followed by high pressure rinsing (HPR) of niobium (Nb) superconducting RF (SRF) cavities is expensive and complex multistep process. Furthermore, the cavity RF surfaces after the treatment still have numerous bubbles and pits that result from welding. These quench-producing weld defects together with the particulate contamination, result in significant scatter of the multi-cell Nb SRF cavities performance characteristics. This scatter is the major problem in the current manufacturing of the Nb SRF cavities. When developed the chemical free surafce processing using IEB will benefit first J-lab's CEBAF and Fermilab's Project X. Also, light sources, require 1.3 - 1.5 GHz SRF structures. Furthermore, IEB will produce much broader impact because it can be implemented into manufacturing of many other types of RF devices including both superconducting as well as normal conducting RF cavities. This program will develop a new process that will enhance quality of the superconducing radio-frequency cavities and allow acceleration of charged particles to much higher energies. The process also will improve the cavity manufacturing and result in substantial cost reduction of superconducting radio-frequency high-energy particle accelerators. Niobium samples were successfully processed by a DC electron beam to a degree that is suitable for the interior surface of an SRF cavity. To accomplish this, a complete system was developed from the ground up. A vacuum chamber system was acquired and adapted to act as the vessel for performing the Nb processing experiments. An extremely robust high voltage power supply was developed and manufactured to provide the power necessary to drive the multi-kW DC electron gun. A high voltage isolation filament transformer was also designed and manufactured to provide the necessary current to drive the filament within the electron gun. Finally, a beam melt characterization DC electron gun was created. This gun was used to explore the parameter space of interest for processing Nb SRF cavities. The beam melt characterization tests concluded that multiple quick passes at moderate beam power provided the most ideal melt zone characteristics Nb surfaces. It was also found that excellent melt and polish results could be achieved at lower voltages than originally conceived, getting the great results at a beam voltage of 20kV versus the 50kV used in the initial Phase I testing at Jefferson Laboratory. Operating at 20kV will also greatly reduce the challenges of designing a compact DC electron gun for processing of complete Nb SRF cavities, which will be done in Phase III. This final report is divided in eight parts which cover the major investigation work and results which have been performed and achieved. The first part addresses the design, fabrication and testing of the vacuum chamber. In the second part, the DC power supply output circuit design is presented for providing an operating space of 50-60kV with currents from 20-160mA and short and open circuit fault modes are considered and resolved. The third section covers testing and commissioning of the high voltage step up transformer and 150kV isolation transformer. Section four covers the design, construction and performance for a 100kV high voltage bushing. Section number five treats the filament design and load testing. Section number six covers electron gun design and simulation of electron beam melting. Section seven presents the beam target design, assembly and testing and test gun with solenoid magnet, design, fabrication and testing. Finally, section eight demonstrates electron beam melting and polishing of Nb, Cu and SS samples.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2014

Development of TRPN dendrimer-modified disordered mesoporous silica for CO{sub 2} capture

Highlights: • A novel series of TRPN dendrimers are synthesized. • Structurally disordered mesoporous silica was used to develop the CO{sub 2} adsorbent. • The CO{sub 2} adsorption capacity is relatively high. • The sorbent exhibits a high stability after 12 cycling runs. • The sorbent achieves complete desorption at low temperature (60 °C). - Abstract: A novel series of tri(3-aminopropyl) amine (TRPN) dendrimers were synthesized and impregnated on structurally disordered mesoporous silica (DMS) to generate CO{sub 2} adsorbents (TS). The physicochemical and adsorption properties of the adsorbents before and after dendrimer modification were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and N{sub 2} adsorption–desorption (N{sub 2}-BET) techniques. CO{sub 2} adsorption–desorption tests indicated that the sorbent demonstrates high CO{sub 2} adsorption capacity (138.1 mg g{sup −1} for G1 sample TS-G1-3CN-50 and 91.7 mg g{sup −1} for G2 sample TS-G2-6CN-50), and can completely desorb CO{sub 2} under vacuum at 60 °C. Its CO{sub 2} adsorption capacity at 25 °C increases with the amine loading, achieving the highest adsorption capacity (140.6 mg g{sup −1} for TS-G1-3CN) at 60%. The developed TS materials exhibited excellent cycling stability. After 12 consecutive adsorption–desorption runs, TS-G1-3CN-50 shows an adsorption capacity of 136.0 mg g{sup −1}, retaining 98.5% of its original value.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Dissipative time-dependent quantum transport theory: Quantum interference and phonon induced decoherence dynamics

A time-dependent inelastic electron transport theory for strong electron-phonon interaction is established via the equations of motion method combined with the small polaron transformation. In this work, the dissipation via electron-phonon coupling is taken into account in the strong coupling regime, which validates the small polaron transformation. The corresponding equations of motion are developed, which are used to study the quantum interference effect and phonon-induced decoherence dynamics in molecular junctions. Numerical studies show clearly quantum interference effect of the transport electrons through two quasi-degenerate states with different couplings to the leads. We also found that the quantum interference can be suppressed by the electron-phonon interaction where the phase coherence is destroyed by phonon scattering. This indicates the importance of electron-phonon interaction in systems with prominent quantum interference effect.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2013

Final Report: The Impact of Carbonate on Surface Protonation, Electron Transfer and Crystallization Reactions in Iron Oxide Nanoparticles and Colloids

This project addresses key issues of importance in the geochemical behavior of iron oxides and in the geochemical cycling of carbon and iron. For Fe, we are specifically studying the influence of carbonate on electron transfer reactions, solid phase transformations, and the binding of carbonate to reactive sites on the edges of particles. The emphasis on carbonate arises because it is widely present in the natural environment, is known to bind strongly to oxide surfaces, is reactive on the time scales of interest, and has a speciation driven by acid-base reactions. The geochemical behavior of carbonate strongly influences global climate change and CO 2 sequestration technologies. Our goal is to answer key questions with regards to specific site binding, electron transfer reactions, and crystallization reactions of iron oxides that impact both the geochemical cycling of iron and CO 2 species. Our work is focused on the molecular level description of carbonate chemistry in solution including the prediction of isotope fractionation factors. We have also done work on critical atmospheric species.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2021

Atomic Gradient Structure Alters Electronic Structure in 3D across the Bulk and Enhances Photoactivity

Abstract Understanding structure–function relationships enables the design of materials with tailored functionalities. The long‐standing challenge is to design materials with high active volume to improve efficiency. Tailored grain boundaries and lattice defects are traditionally used to tune the electronic structure near interfaces or defects to promote electron and hole separation. However, the active volume of point defect sites or interfaces in these traditional photocatalysts is extremely low. This study reports a structure with continuous atomic positional deformation across the bulk, altering the electronic structure in 3D and creating a significantly higher active volume. Such a structure in anatase is obtained and tuned by phase transformation during the heating process. Transmission electron microscopy and density functional theory results reveal that atomic deformations result in continuous band bending across the particles, facilitating electron–hole separation, inhibiting their recombination, and inducing dramatically enhanced photoactivity. These findings enable a different materials design paradigm that can potentially be harnessed for a broad range of applications.

Ren, Peng↗
DOE OSTI2019

Performance efficiency and kinetic studies of water purification using ZnO and MgO nanoparticles for potassium permanganate

Zinc oxide (ZnO) and Magnesium oxide (MgO) nanoparticles (NPs) have been synthesized by solid–solid reaction technique. X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier-transform infrared (FTIR) were used to investigate the structural properties of ZnO and MgO NPs. XRD indicates that structural of ZnO NPs has a hexagonal structure with space group P63mc. On the other hand, MgO NPs is cubic structure with space group Fm 3-bar m. The photocatalytic efficiency of both ZnO and MgO NPs as a catalyst was illustrated by studying the extreme quantity of potassium permanganate (KMnO{sub 4}) degradation rate in wastewater. KMnO{sub 4} achieved 17% and 25% degradation rate in 180 min for ZnO and MgO NPs, respectively. The experimental data were examined by the kinetic models of pseudo-first and second order as well as intra-particle diffusion. The obtained data is expressed well by the second-order kinetic model for both NPs. Moreover, according to the experimental results, MgO NPs has high-performance water purification as a comparison of ZnO NPs effect.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2016

Conditions and mechanisms for the formation of nano-sized Delafossite (CuFeO{sub 2}) at temperatures ≤90 °C in aqueous solution

In this study, we present the mechanism of CuFeO{sub 2} formation in aqueous solution at low temperatures ≤90 °C, using sulfate salts as reactants. Furthermore, we demonstrate the influence of experimental conditions (alkalization, reaction and ageing temperature and time) on the synthesized nanoparticles. In all cases, GR–SO{sub 4}, a Fe(II–III) layered double hydroxysulphate (Fe{sup 2+}{sub 4}Fe{sup 3+}{sub 2}(OH){sub 12}·SO{sub 4}) and Cu{sub 2}O precipitate first. During further OH{sup −} supply GR–SO{sub 4} oxidizes and forms Fe{sub 10}O{sub 14}(OH){sub 2}, Cu{sub 2}O and CuFeO{sub 2} crystals. Due to the high pH further CuFeO{sub 2} crystals grow at the cost of the unstable intermediate products. The reaction rate increases with increasing ageing temperature, reaction pH and, in particular, NaOH concentrations in the solution. As a result, highly crystalline CuFeO{sub 2} (3R and 2H polytypes) nanoparticles showing hexagonal morphology can be synthesized at 70 °C within 10 h or at 50 °C within 1 week. The formation of 2H polytype is favored by additional OH{sup −} supply during the pH-stat time and rather low temperatures. - Highlights: • We solve the formation mechanism of pure CuFeO{sub 2} using sulfates as reactants. • CuFeO{sub 2} nanoparticles crystallize on cost of green rust, Fe{sub 10}O{sub 14}(OH){sub 2} and Cu{sub 2}O. • The reaction rate increases with increasing temperature and OH- concentration. • CuFeO{sub 2} nanoparticles form at 50 °C within one week and at 70 °C within 10 h. • 2H-polytype of CuFeO{sub 2} is favored by additional NaOH supply during pH-stat-time.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2016

Effect of cobalt doping on structural and optical properties of ZnO nanoparticles

Cobalt doped ZnO nanoparticles of uniform sizes were prepared by a chemical method using ZnCl{sub 2} and NaOH as the source materials. The formation of Co-doped ZnO nanoparticles was confirmed by transmission electron microscopy (TEM), high resolution TEM (HR-TEM) and selected area electron diffraction (SAED) studies. The optical properties of obtained products were examined using room temperature UV-visible and FTIR spectroscopy. SAED of cobalt doped ZnO nanoparticles shows homogeneous distribution of nanoparticles with hexagonal structure. The HRTEM image of the Co-doped ZnO nanoparticles reveals a clear lattice spacing of 0.52 nm corresponding to the interplanar spacing of wurtzite ZnO (002) plane. The absorption band at 857 cm{sup −1} in FTIR spectra confirmed the tetrahedral coordination of Zn and a shift of absorption peak to shorter wavelength region and decrease in absorbance with Co doping.is observed in UV-Visible spectra.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2012

One step synthesis of monoclinic VO{sub 2} (B) bundles of nanorods: Cathode for Li ion battery

One of the metastable phases of vanadium dioxide, VO{sub 2}(B) bundles of nanorods and microspheres have been synthesized through a simple hydrothermal method by dispersing V{sub 2}O{sub 5} in aqueous quinol. The obtained products were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and electrochemical discharge-charge test for lithium battery. It was found that the morphologies of the obtained VO{sub 2}(B) can be tuned by manipulating the relative amount of quinol. The electrochemical test found that the bundles of nanorods exhibit an initial discharge capacity of 171 mAh g{sup -1} and its almost stabilized capacity was reached to 108 mAh g{sup -1} after 47 cycles at a current density of 0.1 mA g{sup -1}. The formation mechanism of the VO{sub 2}(B) bundles of nanorods and microspheres was also discussed. - Highlights: Black-Right-Pointing-Pointer VO{sub 2}(B) bundles of nanorods and microspheres were prepared by hydrothermal route at 180 Degree-Sign C for 1 day. Black-Right-Pointing-Pointer In this method for the synthesis of VO{sub 2}(B), we are the first to use quinol as a reducing agent. Black-Right-Pointing-Pointer Morphologies of the obtained VO{sub 2}(B) can be tuned by manipulating the relative amount of quinol. Black-Right-Pointing-Pointer VO{sub 2}(B) exhibits an initial capacity of 171 mAh g{sup -1} and reached to 108 mAh g{sup -1} after 47 cycles. Black-Right-Pointing-Pointer The formation mechanism of the VO{sub 2}(B) bundles of nanorods and microspheres is also discussed.

36 MATERIALS SCIENCE↗
DOE OSTI2024

Real-time tracking of structural evolution in 2D MXenes using theory-enhanced machine learning

In situ Electron Energy Loss Spectroscopy (EELS) combined with Transmission Electron Microscopy (TEM) has traditionally been pivotal for understanding how material processing choices affect local structure and composition. However, the ability to monitor and respond to ultrafast transient changes, now achievable with EELS and TEM, necessitates innovative analytical frameworks. Here, we introduce a machine learning (ML) framework tailored for the real-time assessment and characterization of in operando EELS Spectrum Images (EELS-SI). We focus on 2D MXenes as the sample material system, specifically targeting the understanding and control of their atomic-scale structural transformations that critically influence their electronic and optical properties. This approach requires fewer labeled training data points than typical deep learning classification methods. By integrating computationally generated structures of MXenes and experimental datasets into a unified latent space using Variational Autoencoders (VAE) in a unique training method, our framework accurately predicts structural evolutions at latencies pertinent to closed-loop processing within the TEM. This study presents a critical advancement in enabling automated, on-the-fly synthesis and characterization, significantly enhancing capabilities for materials discovery and the precision engineering of functional materials at the atomic scale.

47 OTHER INSTRUMENTATION↗
DOE OSTI2015

Structural, magnetic and electronic structure properties of Co doped ZnO nanoparticles

Highlights: • XRD and HR-TEM results show the single phase nature of Co doped ZnO nanoparticles. • XMCD and dc magnetization results indicate the RT-FM in Co doped ZnO nanoparticles. • Co L{sub 3,2} NEXAFS spectra infer that Co ions are in 2+ valence state. • O K edge NEXAFS spectra show that O vacancy increases with Co doping in ZnO. - Abstract: We reported structural, magnetic and electronic structure studies of Co doped ZnO nanoparticles. Doping of Co ions in ZnO host matrix has been studied and confirmed using various methods; such as X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy dispersed X-ray (EDX), high resolution transmission electron microscopy (HR-TEM), Fourier transform infrared spectroscopy (FT-IR), near edge X-ray absorption fine structure (NEXAFS) spectroscopy, magnetic hysteresis loop measurements and X-ray magnetic circular dichroism (XMCD). From the XRD and HR-TEM results, it is observed that Co doped ZnO nanoparticles have single phase nature with wurtzite structure and exclude the possibility of secondary phase formation. FE-SEM and TEM micrographs show that pure and Co doped nanoparticles are nearly spherical in shape. O K edge NEXAFS spectra indicate that O vacancies increase with Co doping. The Co L{sub 3,2} edge NEXAFS spectra revealed that Co ions are in 2+ valence state. DC magnetization hysteresis loops and XMCD results clearly showed the intrinsic origin of temperature ferromagnetism in Co doped ZnO nanoparticles.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Physicochemical, Antimicrobial and Cytotoxic Characteristics of Corn Starch Film Containing Propolis for Wound Dressing

Modern dressings increase the rate of wound healing rather than just covering them. Dressing can protect the injured skin and keep it appropriately moist to speed up the healing process. In this study, the ethanolic extract of propolis loaded with corn starch was successfully prepared using solvent casting. Characterizations of the samples performed in respect to their mechanical properties were examined by scanning electron microscopy, contact angle, and attenuated total reflectance—fourier transform infrared spectroscopy, as well as antimicrobial capacities. The MTT assay using fibroblast cells showed the cell viability of corn starch in the ethanolic extract of propolis wound dressing. The results showed that by increasing the amount of ethanolic propolis extract from 0.25 to 1%, the tensile strength and the Young’s modulus of the samples were decreased, the elongation at the break increased about 15% as compared to the control films, and the contact angle properties were detected by a slightly hydrophobic character of the films in the antibacterial activity against Escherichia coli and Staphylococcus aureus even at low ethanolic extract of propolis concentrations (1%), mainly due to its phenolic compounds. Therefore, ethanolic extract of propolis loaded with corn starch film will be a potential candidate for wound dressing and skin tissue engineering.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Visualizing heavy fermion confinement and Pauli-limited superconductivity in layered CeCoIn 5

Layered material structures play a key role in enhancing electron–electron interactions to create correlated metallic phases that can transform into unconventional superconducting states. The quasi-two-dimensional electronic properties of such compounds are often inferred indirectly through examination of bulk properties. Here we use scanning tunneling microscopy to directly probe in cross-section the quasi-two-dimensional electronic states of the heavy fermion superconductor CeCoIn 5 . Our measurements reveal the strong confined nature of quasiparticles, anisotropy of tunneling characteristics, and layer-by-layer modulated behavior of the precursor pseudogap gap phase. In the interlayer coupled superconducting state, the orientation of line defects relative to the d-wave order parameter determines whether in-gap states form due to scattering. Spectroscopic imaging of the anisotropic magnetic vortex cores directly characterizes the short interlayer superconducting coherence length and shows an electronic phase separation near the upper critical in-plane magnetic field, consistent with a Pauli-limited first-order phase transition into a pseudogap phase.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Rate and selectivity hysteresis during the carbon monoxide hydrogenation over promoted Co/MnO x catalysts

While cobalt-based catalysts have been used in industrial Fischer-Tropsch synthesis for decades, little is known about how the dynamics of the Co-Co 2 C phase transformation drive their performance. Here we report on the occurrence of hysteresis effects in the Fischer-Tropsch reaction over potassium promoted Co/MnO x catalyst. Both the reaction rate and the selectivity to chain-lengthened paraffins and terminally functionalized products (aldehydes, alcohols, olefins) show bistability when varying the hydrogen/carbon monoxide partial pressures back and forth from overall reducing to carbidizing conditions. While the carbon monoxide conversion and the selectivity to functionalized products follow clockwise hysteresis, the selectivity to paraffins shows counter-clockwise behavior. In situ X-ray diffraction demonstrates the activity/selectivity bistability to be driven by a Co-Co 2 C phase transformation. The conclusions are supported by High Resolution Transmission Electron Microscopy which identifies the Co-Co 2 C transformation, Mn 5 O 8 layered topologies at low H 2 /CO partial pressure ratios, and MnO at high such ratios.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Study on dielectric behavior and harvesting properties of new Ba0.5Sr0.4Ca0.1TiO3/poly(ether imide) composite films

Highlights: • 1% Nb{sub 2}O{sub 5} doped Ba{sub 0.5}Sr{sub 0.4}Ca{sub 0.1}TiO{sub 3} particles (BST) were prepared and characterized. • BST/poly(ether imide) composite films were prepared. • The composite films were flexible and exhibited high thermal stability. • The dielectric constant values of the films increased by introducing BST particles. • The films exhibit the ability to generate electrical energy from mechanical one. - Abstract: Barium strontium titanate particles with composition of Ba{sub 0.5}Sr{sub 0.4}Ca{sub 0.1}TiO{sub 3} were prepared by sol-gel method and doped with 1% Nb{sub 2}O{sub 5}. Poly(ether imide) composite films were obtained by mixing particles into a poly(amic acid) solution and casting onto glass plates followed by thermal treatment. The films were investigated by Fourier transform of infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy and broadband dielectric spectroscopy. They exhibited good thermal stability having the initial decomposition temperature above 773 K. The dielectric constant was in the range of 3.08–4.17 (room temperature and 1 kHz), and the dielectric loss maintained low values over a large interval of frequency and temperature. The subglass transitions γ and β, the α-relaxation corresponding to the glass transition and the conductivity process of the composite films were evidenced and correlated with the particle content. The ability to generate electrical energy on mechanical impulse was also evaluated.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Synthesis and Tuning of Hematite (α-Fe{sub 2}O{sub 3}) Iron Oxide Nanorods with Magnetism

In recent years, hematite (α-Fe{sub 2}O{sub 3}) iron oxide nanorods have attracted the attention of many researchers due to their wide applications in nanobiosensors, lithium batteries and nanomagnetism. In the present work, hematite nanorods with magnetic and optical properties were synthesized in desirable qualities via a fast and low-cost method. Features of these nanorods were determined using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), ultraviolet–visible (UV–vis) spectroscopy and vibrating sample magnetometry (VSM). Uniform nanorods with a length of between 20 and 30 nm were fabricated in a 0.05:1:3.4 molar ratio of cetyltrimethylammonium bromide (CTAB)/FeCl{sub 3}/NaOH. The VSM technique showed that the presence of the CTAB as a surfactant agent in 0.1, 0.05 and 0.025 mol L{sup − 1} concentrations can reduce the magnetization of nanorods with an increase in surface layers. The optical absorbance properties of the hematite nanorods demonstrated that the absorption peaks are well tuned in wavelengths of about 250 and 400 nm. The hematite nanorods with the tuned structure in terms of magnetic and optical properties can be proposed as a desirable option in future applications.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Effects of Nd, Er Doping on the Structure and Magnetic Properties of YFeO{sub 3}

Nd, Er co-doped YFeO{sub 3} compounds were synthesized by sol-gel method. The prepared compounds were characterized by powder x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive x-ray (EDX), and vibrating sample magnetometer (VSM) integrated in a physical property measurement system (PPMS-9), respectively. The results show that the compounds possess orthorhombic perovskite structure. The Y{sub 0.5}Er{sub 0.1}Nd{sub 0.4}FeO{sub 3} compound mainly consists of five elements (Er, Nd, Y, Fe, and O) and atom ratio matched well with the formula. With the increase of Nd{sup 3+} doping content in Y{sub 0.5}Er{sub 0.5−x}Nd{sub x}FeO{sub 3} (x = 0, 0.1, 0.2, 0.3, and 0.4), the coercivity increases gradually while the saturation magnetization and remanent magnetization decrease at the same time. Introducing Nd{sup 3+} and Er{sup 3+} ions into YFeO{sub 3} will make a change on a structure distortion, resulting in the decrease of the Fe–O–Fe angle and the consequent reduction of superexchange effect. From our research results, the relationship between the r (R{sup 3+}) and the superexchange bond angle is different from pure-phase orthoferrites R FeO{sub 3}.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2012

Evolution of surface morphology and electronic structure of few layer graphene after low energy Ar{sup +} ion irradiation

We report on co-existing dual anisotropy ripple formation, sp bonding transformation, and variation in the delocalized {pi} electron system in 1 keV Ar{sup +} ion irradiated few-layer graphene surfaces. Ripples in directions, perpendicular and parallel to the ion beam were found. The irradiation effect and the transition from the sp{sup 2}-bonding to sp{sup 3}-hybridized state were analyzed from the deconvolution of the C (1s) peak and from the shape of the derivative of the Auger transition spectra. The results suggest a plausible mechanism for tailoring of few-layer graphene electronic band structure with interlayer coupling tuned by the ion irradiation.

77 NANOSCIENCE AND NANOTECHNOLOGY↗