Fabrication and electric measurements of nanostructures inside transmission electron microscope

Using manipulation holders specially designed for transmission electron microscope (TEM), nanostructures can be characterized, measured, modified and even fabricated in-situ. In-situ TEM techniques not only enable real-time study of structure-property relationships of materials at atomic scale, but also provide the ability to control and manipulate materials and structures at nanoscale. This review highlights in-situ electric measurements and in-situ fabrication and structure modification using manipulation holder inside TEM.     

Comparing electron tomography and HRTEM slicing methods as tools to measure the thickness of nanoparticles

Nanoparticles’ morphology is a key parameter in the understanding of their thermodynamical, optical, magnetic and catalytic properties. In general, nanoparticles, observed in transmission electron microscopy (TEM), are viewed in projection so that the determination of their thickness (along the projection direction) with respect to their projected lateral size is highly questionable. To date, the widely used methods to measure nanoparticles thickness in a transmission electron microscope are to use cross-section images or focal series in high-resolution transmission electron microscopy imaging (HRTEM “slicing”). In this paper, we compare the focal series method with the electron tomography method to show that both techniques yield similar particle thickness in a range of size from 1 to 5 nm, but the electron tomography method provides better statistics since more particles can be analyzed at one time. For this purpose, we have compared, on the same samples, the nanoparticles thickness measurements obtained from focal series with the ones determined from cross-section profiles of tomograms (tomogram slicing) perpendicular to the plane of the substrate supporting the nanoparticles. The methodology is finally applied to the comparison of CoPt nanoparticles annealed ex situ at two different temperatures to illustrate the accuracy of the techniques in detecting small particle thickness changes.     

Behaviour of TEM metal grids during in-situ heating experiments

The stability of Ni, Cu, Mo and Au transmission electron microscope (TEM) grids coated with ultra-thin amorphous carbon (α-C) or silicon monoxide film is examined by in-situ heating up to a temperature in the range 500–850 °C in a transmission electron microscope. It is demonstrated that some grids can generate nano-particles either due to the surface diffusion of metal atoms on amorphous film or due to the metal evaporation/redeposition. The emergence of nano-particles can complicate experimental observations, particularly in in-situ heating studies of dynamic behaviours of nano-materials in TEM. The most widely used Cu grid covered with amorphous carbon is unstable, and numerous Cu nano-particles start to form once the heating temperature reaches 600 °C. In the case of Ni grid covered with α-C film, a large number of Ni nano-crystals occur immediately when the temperature approaches 600 °C, accompanied by the graphitization of amorphous carbon. In contrast, both Mo and Au grids covered with α-C film exhibit good stability at elevated temperature, for instance, up to 680 and 850 °C for Mo and Au, respectively, and any other metal nano-particles are detected. Cu grid covered Si monoxide thin film is stable up to 550 °C, but Si nano-crystals appear under intensive electron beam. The generated nano-particles are well characterized by spectroscopic techniques (EDXS/EELS) and high-resolution TEM. The mechanism of nano-particle formation is addressed based on the interactions between the metal grid and the amorphous carbon film and on the sublimation of metal.     

Morphology visualization of irregular shape bacteria by electron holography and tomography

In the current work, irregular morphology of Staphylococcus aureus bacteria has been visualized by phase retrieval employing off‐axis electron holography (EH) and 3D reconstruction electron tomography using high‐angle annular dark field scanning transmission electron microscopy (HAADF‐STEM). Bacteria interacting with gold nanoparticles (AuNP) acquired a shrunken or irregular shape due to air dehydration processing. STEM imaging shows the attachment of AuNP on the surface of cells and suggests an irregular 3D morphology of the specimen. The phase reconstruction demonstrates that off‐axis electron holography can reveal with a single hologram the morphology of the specimen and the distribution of the functionalized AuNPs. In addition, EH reduces significantly the acquisition time and the cumulative radiation damage (in three orders of magnitude) over biological samples in comparison with multiple tilted electron expositions intrinsic to electron tomography, as well as the processing time and the reconstruction artifacts that may arise during tomogram reconstruction.     

纳米二氧化铈润滑油添加剂的摩擦学特性

用适当的表面活性剂对纳米二氧化铈粒子进行表面改性处理,采用透射电镜(TEM)和X-射线衍射法(XRD)观察与测量纳米二氧化铈粒子的形貌、结构和平均直径。将改性后的纳米二氧化铈粒子作为润滑油添加剂,采用四球摩擦磨损试验机测定添加纳米二氧化铈粒子的润滑油的摩擦学性能。利用扫描电镜(SEM)观察磨斑表面形貌以及纳米二氧化铈粒子在摩擦表面的形态等,并探讨了纳米二氧化铈粒子具有优良摩擦学性能的机制。结果表明,经表面改性的纳米二氧化铈在润滑油中具有良好的分散、稳定性;纳米二氧化铈粒子的添加量为0.6%(质量分数)左右时,润滑油在室温与较高温度下均具有优良的减摩、抗磨作用。     

Influence of nanostructure composition on its morphometric characterization by different techniques

Morphometric characterization of nanoparticles is crucial to determine their biological effects and to obtain a formulation pattern. Determining the best technique requires knowledge of the particles being analyzed, the intended application of the particles, and the limitations of the techniques being considered. The aim of this article was to present transmission (TEM) and scanning (SEM) electron microscopy protocols for the analysis of two different nanostructures, namely polymeric nanoemulsion and poly(lactic‐co‐glycolic acid) (PLGA) nanoparticles, and to compare these results with conventional dynamic light scattering (DLS) measurements. The mean hydrodynamic diameter, the polydispersity index, and zeta potential of the nanostructures of polymeric nanoemulsion were 370.5 ± 0.8 nm, 0.133 ± 0.01, and ?36.1 ± 0.15 mV, respectively, and for PLGA nanoparticles were 246.79 ± 5.03 nm, 0.096 ± 0.025, and ?4.94 ± 0.86 mV, respectively. TEM analysis of polymeric nanoemulsion revealed a mean diameter of 374 ± 117 nm. SEM analysis showed a mean diameter of 368 ± 69 nm prior to gold coating and 448 ± 70 nm after gold coating. PLGA nanoparticles had a diameter of 131 ± 41.18 nm in TEM and 193 ± 101 nm in SEM. Morphologically, in TEM analysis, the polymeric nanoemulsions were spherical, with variable electron density, very few showing an electron‐dense core and others an electron‐dense surface. PLGA nanoparticles were round, with an electron‐lucent core and electron‐dense surface. In SEM, polymeric nanoemulsions were also spherical with a rough surface, and PLGA nanoparticles were round with a smooth surface. The results show that the “gold standards” for morphometric characterization of polymeric nanoemulsion and PLGA nanoparticles were, respectively, SEM without gold coating and TEM with negative staining. Microsc. Res. Tech. 77:691–696, 2014. © 2014 Wiley Periodicals, Inc.     

Quantification of metallic nanoparticle morphology on TiO2 using HAADF-STEM tomography

Electron tomography is applied to photocatalytic gold/titanium oxide and gold/silver/titanium oxide samples. In order to obtain a tilt series for the electron tomography measurement, high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) is used under cryogenic conditions. Dedicated programs have been developed for measuring volume, surface area, thickness distribution and nearest-neighbour distance of metallic nanoparticles on samples. Using these quantification programs, the 3D morphology of gold and silver nanoparticles is accurately characterized. We paid particular attention to the quantitative measurement of surface area. The measurement error of the method and appropriate magnification are defined using spherical nanoparticle models. We measured the 3D morphology of gold nanoparticles supported on titanium oxide (total volume=6.5×10⁵ [nm³], surface area=1.4×10⁵ [nm²], and average nearest-neighbour distance=40 [nm]).     

Pawley and Rietveld refinements using electron diffraction from L1₂-type intermetallic Au₃Fe₁-x nanocrystals during their in-situ order-disorder transition

During the in-situ order-disorder transition of intermetallic L1₂-type Au₃Fe_1−x nanocrystals, structural information has been retrieved from their electron diffraction patterns based on the Pawley refinement that is unrelated to the electron kinematical or dynamical scattering nature as well as the Rietveld refinement using a kinematical approximation. At room temperature, it was found that the nanocrystals contain approximately x=40% vacancies at the Fe site. Based on in-situ heating this phase displayed an irreversible order-disorder transition, with the transition temperature between 553 and 593 K. A sudden increase in lattice parameter was detected during the first heating from the ordered phase, while the second heating of the disordered phase showed only a linear relationship with temperature. From the lattice parameter measurement of the disordered phase, the coefficient of thermal expansion was estimated as 1.462×10⁻⁵ K⁻¹. The long-range order parameter S was determined by the refined site occupancies, as well as the integrated intensities of the superlattice (1 0 0) and fundamental (2 2 0) reflections using the Pawley and Rietveld refinements during the order-disorder transition. Considering the dynamical scattering effect, Blackman two-beam approximation theory was applied to corrected S, which slightly attenuated after the correction. A comparison of the electron diffraction with X-ray diffraction data was made. It was demonstrated that elemental and structural information could be retrieved through quantitative electron diffraction studies of the nanomaterials. Since the Pawley refinement algorithm does not include the electron scattering event, it is especially useful to refine the electron diffraction data regardless of the sample thickness.     

Revealing local variations in nanoparticle size distributions in supported catalysts: a generic TEM specimen preparation method

The specimen preparation method is crucial for how much information can be gained from transmission electron microscopy (TEM) studies of supported nanoparticle catalysts. The aim of this work is to develop a method that allows for observation of size and location of nanoparticles deposited on a porous oxide support material. A bimetallic Pt‐Pd/Al₂O₃ catalyst in powder form was embedded in acrylic resin and lift‐out specimens were extracted using combined focused ion beam/scanning electron microscopy (FIB/SEM). These specimens allow for a cross‐section view across individual oxide support particles, including the unaltered near surface region of these particles. A site‐dependent size distribution of Pt‐Pd nanoparticles was revealed along the radial direction of the support particles by scanning transmission electron microscopy (STEM) imaging. The developed specimen preparation method enables obtaining information about the spatial distribution of nanoparticles in complex support structures which commonly is a challenge in heterogeneous catalysis.     

Calibration of the scanning (atomic) force microscope with gold particles

Scanning force microscopy (SFM) holds great promise for biological research. Two major problems that have confronted imaging with the scanning force microscope have been the distortion of the image and overestimation in measurements of lateral size due to the varying geometry and characteristics of the scanning tip. In this study, spherical colloidal gold particles (10, 20 and 40 nm in diameter) were used to determine (1) tip parameters (size, shape and semivertical angle); (2) the distortion of the image caused by the tip; and (3) the overestimation or broadening of lateral dimensions. These gold particles deviate little in size, are rigid and have a size similar to biological macromolecules. Images of the colloidal gold particles by SFM were compared with those obtained by electron microscopy (EM). The height of the gold particles as measured by SFM and EM was comparable and was little affected by the tip geometry. The measurements of the lateral dimensions of colloidal gold, however, showed substantial differences between SFM and EM in that SFM resulted in an overestimate of the lateral dimensions. Moreover, the distortion of images and broadening of lateral dimensions were specific to the SFM tip used. The calibration of the SFM tip with mica provided little clue as to the type of distortion and the amount of lateral broadening observed when the larger gold particles were scanned. The SFM image also depended on the orientation of the tip with respect to the specimen. Our results suggest that quantitative SFM imaging requires calibration to identify and account for both the distortions and the magnitude of lateral broadening caused by the cantilever tip. Calibration with gold particles is fast and nondestructive to the tip. The raw imaging data of the specimen can be corrected for the tip effect and true structural information can be derived. In summary, we present a simple and practical method for the calibration of the SFM tip using gold particles with a size in the range of biomacromolecules that allows: (1) selection of a cantilever tip that produces an image with minimal distortion; (2) quantitative determination of tip parameters; (3) reconstruction of the shape of the tip at different heights from the tip apex; (4) appreciation of the type of distortion that may be introduced by a specific tip and quantification of the overestimation of the lateral dimensions; and (5) calculation of the true structure of the specimen from the image data. The significance is that such calibration will permit quantitative and accurate imaging with SFM.     

Controlled Synthesis and Optical Properties of Pure Gold Nanoparticles

Abstract

Gold nanoparticles were synthesized by laser ablation of a gold metallic disc at wavelengths of 532 nm and 355 nm with 7 ns pulse duration in the pure water. The colloidal gold nanoparticles were characterized by ultraviolet-visible absorption spectroscopy, transmission electron microscopy, and fluorescence spectrometry. The presence of a surface plasmon resonance peak around ～ 524 nm indicates the formation of gold nanoparticles. The formation efficiencies of gold nanoparticles in colloids were found to increase when ablating the gold metallic disc with a laser having a longer wavelength. The size distributions of the gold nanoparticles thus produced were measured by transmission electron microscopy. A reduction in mean diameter of the particles was observed with a decrease in the laser wavelength under the irradiation at a high fluence of 25 mJ/pulse. The fluorescence spectroscopy demonstrated that these gold nanoparticles are fluorescent, showing a strong blue emission intensity at 458 nm.     

Preparation and characterization of TiO_2-SiO_2-Fe_3O_4 core-shell powders in nano scale

TiO2/SiO2/Fe3O4 nanoparticles have bigger specific area which can greatly increase the efficiency of photo-catalysis.The TiO2/SiO2/Fe3O4 particles in nano scale were prepared with reduction method at high temperature in this paper,and their morphology,particle size and magnetic property were characterized by transmission electron microscope(TEM),Xray diffraction(XRD) and magnetometer.The results show that the grain sizes of Fe3O4,SiO2-Fe3O4 and TiO2-SiO2-Fe3O4 particles were 50nm,70nm and 120nm,respectively.With the modification of SiO2,Fe3O4 magnetic cores are protected from oxidation.Moreover,by the addition of TiO2 function layer,TiO2-SiO2-Fe3O4 functional nanoparticles,with the saturation magnetization density of 34.1emu/g,is magnetically recoverable.The processes of this method are so simple that the nanoparticles can be produced in large quantity.     

On the interpretation of the forbidden spots observed in the electron diffraction patterns of flat Au triangular nanoparticles

In many cases nanostructures present forbidden spots in their electron diffraction patterns when they are observed by transmission electron microscopy (TEM). To interpret their TEM and high resolution transmission electron microscopy (HRTEM) images properly, an understanding of the origin of these spots is necessary. In this work we comment on the origin of the forbidden spots observed in the [111] and [112] electron diffraction patterns of flat gold triangular nanoparticles. The forbidden spots were successfully indexed as corresponding to the first laue Zone (FOLZ) and the HRTEM images presented a contrast produced by the interference of the zero-order Laue zone (ZOLZ) and FOLZ spots. We discuss the use of the forbidden spots in the study of the structure of nanoparticles and show that they are related to the shape and incompleteness of layers in the very thin particles.     

In-focus electron microscopy of frozen-hydrated biological samples with a Boersch phase plate

We report the implementation of an electrostatic Einzel lens (Boersch) phase plate in a prototype transmission electron microscope dedicated to aberration-corrected cryo-EM. The combination of phase plate, C_s corrector and Diffraction Magnification Unit (DMU) as a new electron-optical element ensures minimal information loss due to obstruction by the phase plate and enables in-focus phase contrast imaging of large macromolecular assemblies. As no defocussing is necessary and the spherical aberration is corrected, maximal, non-oscillating phase contrast transfer can be achieved up to the information limit of the instrument. A microchip produced by a scalable micro-fabrication process has 10 phase plates, which are positioned in a conjugate, magnified diffraction plane generated by the DMU. Phase plates remained fully functional for weeks or months. The large distance between phase plate and the cryo sample permits the use of an effective anti-contaminator, resulting in ice contamination rates of <0.6 nm/h at the specimen. Maximal in-focus phase contrast was obtained by applying voltages between 80 and 700 mV to the phase plate electrode. The phase plate allows for in-focus imaging of biological objects with a signal-to-noise of 5-10 at a resolution of 2-3 nm, as demonstrated for frozen-hydrated virus particles and purple membrane at liquid-nitrogen temperature.     

Are electron tweezers possible?

Positively answering the question in the title, we demonstrate in this work single electron beam trapping and steering of 20–300 nm solid Al nanoparticles generated inside opaque submicron-sized molten Al–Si eutectic alloy spheres. Imaging of solid nanoparticles and liquid alloy in real time was performed using energy filtering in an analytical transmission electron microscope (TEM). Energy-filtering TEM combined with valence electron energy-loss spectroscopy enabled us to investigate in situ nanoscale transformations of the internal structure, temperature dependence of plasmon losses, and local electronic and optical properties under melting and crystallization of individual binary alloy particles. For particles below 20 nm in size, enhanced vibrations of the dynamic solid–liquid interface due to instabilities near the critical threshold were observed just before melting. The obtained results indicate that focused electron beams can act as a tool for manipulation of metal nanoparticles by transferring linear and angular mechanical momenta. Such thermally assisted electron tweezers can be utilized for touchless manipulation and processing of individual nano-objects and potentially for fabrication of assembled nanodevices with atomic level sensitivity and lateral resolution provided by modern electron optical systems. This is by three orders of magnitude better than for light microscopy utilized in conventional optical tweezers. New research directions and potential applications of trapping and tracking of nano-objects by focused electron beams are outlined.     

超声诱导银纳米粒子的电化学制备及其表征

在络合剂EDTA、保护剂PVP存在的条件下,通过超声电沉积方法在硝酸银溶液中制备出形状不同的零维、一维银纳米材料。研究结果表明：当硝酸银浓度为0．0118mol／L、硝酸银与EDTA数量比为1：1时,银纳米粒子为类球形,直径约30nm。当加入2g／L的PVP时,可获得直径约30nm,长度不等的银纳米线。选区电子衍射和紫外可见吸收光谱表明,银纳米颗粒具有面心立方结构,其形貌和粒径影响微粒的光吸收特性。     

相转移法制备纳米CoFe_2O_4粉体

采用相转移法制备了纳米CoFe2O4前驱体.运用差示扫描量热仪(DSC)研究了纳米CoFe2O4前驱体的热分解特性.利用XRD、TEM研究了不同煅烧温度对生成的纳米CoFe2O4成分、形貌和粒度的影响,探讨了相转移法的制备机理.结果表明:相转移法可有效控制成核速度,油相的成膜有效地实现了阻聚作用,400℃为最佳煅烧温度,所得到的CoFe2O4粉体呈规则的立方形链状分布,无明显团聚体,平均粒径为30 nm,且粒径分布窄.     

4D ultrafast electron microscopy: Imaging of atomic motions,acoustic resonances,and moiré fringe dynamics

In four-dimensional (4D) ultrafast electron microscopy (UEM), timed-pulse electron imaging and selected-area diffraction are used to study structural dynamics with space- and time-resolutions that allow direct observation of transformations affecting the fundamental properties of materials. Only recently, the UEM studies have begun to reveal a variety of dynamic responses of nanoscale specimens to material excitation, on ultrafast time scales and up to microseconds. Here, we give an account of some of these results, including imaging and diffraction dynamics of gold and graphite single crystal films, revealing atomic motions and morphology change in the former and two forms of acoustic resonance in the latter. We also report, for the first time, dynamic changes upon lattice excitation of moiré fringes in graphite, recorded in bright- and dark-field images. Oscillations that are seen in moiré fringe spacing and other selected-area image properties have the same temporal period as observed in Bragg spot changes in diffraction patterns from the same specimen areas. This period is shown to vary linearly with the local thickness of the specimen, thus establishing that the oscillations are due to excitation of a resonant elastic modulation of the film thickness and allowing derivation of a value of the Young's modulus (c₃₃) of 36 GPa for the c-axis strain. The second form of resonance dynamics observed in graphite, on much longer time scales, corresponds to an out-of-plane drumming vibration of the film consistent with a 0.94 TPa elastic modulus for in-plane (a-axis) stretching. For the latter, the nanoscale membrane motion appears complicated (“chaotic”) at early time and builds up to a resonance at longer times. Finally, electron energy loss spectroscopy (EELS) in the UEM provides a unique domain of study of chemical bonding on the time scale of change (femtoseconds), and its application to graphite is discussed.     

Rationale for the application of thin,continuous metal films in high magnification electron microscopy

Various metal films of different thicknesses were deposited on to a particle test specimen and their effects on topographic contrast generation and specimen preservation were determined. Tobacco mosaic virus adsorbed on to thin carbon supports or silicon chips was imaged in TEM or high resolution SE-I SEM at a magnification of 350,000×. Tantalum films of 1–2 nm (average mass) thickness produced best contrasts and prevented volume loss of the particles from electron beam damage. Excessively thick films of 5–10 nm thickness blanketed fine structures and caused severe volume losses. Discontinuous 2 nm thick films of gold or platinum decorated the surfaces, caused a loss in topographic contrasts and induced very high volume losses. Thin continuous metal films were necessary to generate high topographic contrast and to prevent volume loss from beam damage by providing sufficient mechanical stability for small topographic features and increased thermal conductivity of the specimen surface.     

In Situ TEM Observation of the Behavior of an Individual Fullerene-Like MoS<Subscript>2</Subscript> Nanoparticle in a Dynamic Contact

Inorganic fullerene-(IF)-like nanoparticles made of metal dichalcogenides (IF-MoS₂, IF-WS₂) have been known to be effective as anti-wear and friction modifier additives under boundary lubrication. The lubrication mechanism of these nanoparticles has been widely investigated in the past and even if the exfoliation and third body transfer of molecular sheets onto the asperities constitute the prevalent mechanism for the improved tribological behavior of IF nanoparticles, it has also been suggested that a rolling friction process could also play a role for well crystallized and spherical particles. In this study, in situ Transmission Electron Microscopy (TEM) observations of the behavior of single IF-MoS₂ nanoparticles were conducted using a sample holder that combines TEM and Atomic Force Microscopy (AFM) which simultaneously can apply normal and shear loads. It was shown that depending on the test conditions, either a rolling process or a sliding of the fullerenes could be possible. These in situ TEM observations are the first carried out with IF nanoparticles.