Nanoprober-Based Pick-and-Place Process for Site-Specific Characterization of Individual Carbon Nanotubes

2008 ◽  
Vol 1081 ◽  
Author(s):  
Thomas Hantschel ◽  
Peter Ryan ◽  
Saku Palanne ◽  
Oliver Richard ◽  
Kai Arstila ◽  
...  

AbstractThe potential use of carbon nanotubes (CNT) as interconnects requires also new characterization approaches as the existing ones are optimized for three-dimensional materials and do not work for inherently one-dimensional structures like CNTs. Therefore, we have developed a so-called pick-and-place process which allows to remove an individual CNT from a specific site and to place it at another location for further analysis. The approach is based on nanomanipulation combined with scanning electron microscopy (SEM). This paper presents the pick-and-place concept and explains the different steps required for its successful application. We further demonstrate its power by characterizing individual CNTs using transmission electron microscopy (TEM) and atomic force microscopy (AFM). The developed pick-and-place approach overcomes the challenge of site-specific analysis of CNT interconnects and strongly facilitates the routine analysis of CNTs.

2017 ◽  
Vol 23 (3) ◽  
pp. 661-667 ◽  
Author(s):  
Yue Li ◽  
Di Zhang ◽  
Ilker Capoglu ◽  
Karl A. Hujsak ◽  
Dhwanil Damania ◽  
...  

AbstractEssentially all biological processes are highly dependent on the nanoscale architecture of the cellular components where these processes take place. Statistical measures, such as the autocorrelation function (ACF) of the three-dimensional (3D) mass–density distribution, are widely used to characterize cellular nanostructure. However, conventional methods of reconstruction of the deterministic 3D mass–density distribution, from which these statistical measures can be calculated, have been inadequate for thick biological structures, such as whole cells, due to the conflict between the need for nanoscale resolution and its inverse relationship with thickness after conventional tomographic reconstruction. To tackle the problem, we have developed a robust method to calculate the ACF of the 3D mass–density distribution without tomography. Assuming the biological mass distribution is isotropic, our method allows for accurate statistical characterization of the 3D mass–density distribution by ACF with two data sets: a single projection image by scanning transmission electron microscopy and a thickness map by atomic force microscopy. Here we present validation of the ACF reconstruction algorithm, as well as its application to calculate the statistics of the 3D distribution of mass–density in a region containing the nucleus of an entire mammalian cell. This method may provide important insights into architectural changes that accompany cellular processes.


2006 ◽  
Vol 12 (4) ◽  
pp. 302-310 ◽  
Author(s):  
Yung-Ching Chien ◽  
Alfonso Mucci ◽  
Jeanne Paquette ◽  
S. Kelly Sears ◽  
Hojatollah Vali

The bulk morphology and surface features that developed upon precipitation on micrometer-size calcite powders and millimeter-size cleavage fragments were imaged by three different microscopic techniques: field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) of Pt-C replicas, and atomic force microscopy (AFM). Each technique can resolve some nanoscale surface features, but they offer different ranges of magnification and dimensional resolutions. Because sample preparation and imaging is not constrained by crystal orientation, FE-SEM and TEM of Pt-C replicas are best suited to image the overall morphology of microcrystals. However, owing to the decoration effect of Pt-C on the crystal faces, TEM of Pt-C replicas is superior at resolving nanoscale surface structures, including the development of new faces and the different microtopography among nonequivalent faces in microcrystals, which cannot be revealed by FE-SEM. In conjunction with SEM, Pt-C replica provides the evidence that crystals grow in diverse and face-specific modes. The TEM imaging of Pt-C replicas has nanoscale resolution comparable to AFM. AFM yielded quantitative information (e.g., crystallographic orientation and height of steps) of microtopographic features. In contrast to Pt-C replicas and SEM providing three-dimensional images of the crystals, AFM can only image one individual cleavage or flat surface at a time.


2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Xiaozhou Su ◽  
Lei Li ◽  
Weihan Huang

Complex nanomicelles were prepared by sericin and type A gelatin with molecular weight of 5789 Da and 128664 Da separately. The assembling conditions were as follows: mass ratio (sericin/gelatin) was 1 : 1, protein concentration was 0.5%, temperature was 35°C, and assembling time was 18 hours. Scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and dynamic light scattering (DLS) were conducted to observe and characterize the complex nanomicelles. Results showed that the complex sericin/gelatin micelles was a kind of nanospindle micelles. The micelles had high electrochemical stability, thermal stability, antidilution stability, and storage stability.


2012 ◽  
Vol 16 (07n08) ◽  
pp. 713-740 ◽  
Author(s):  
José H. Zagal ◽  
Sophie Griveau ◽  
Mireya Santander-Nelli ◽  
Silvia Gutierrez Granados ◽  
Fethi Bedioui

We discuss here the state of the art on hybrid materials made from single (SWCNT) or multi (MWCNT) walled carbon nanotubes and MN4complexes such as metalloporphyrins and metallophthalocyanines. The hybrid materials have been characterized by several methods such as cyclic voltammetry (CV), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and scanning electrochemical microscropy (SECM). The materials are employed for electrocatalysis of reactions such as oxygen and hydrogen peroxide reduction, nitric oxide oxidation, oxidation of thiols and other pollutants.


1998 ◽  
Vol 536 ◽  
Author(s):  
G. F. Grom ◽  
L. Tsybeskov ◽  
K. D. Hirschman ◽  
P. M. Fauchet ◽  
J. P. McCaffrey ◽  
...  

AbstractThe morphology of nanocrystalline (nc)-Si/amorphous (a)-SiO2 superlattices (SLs) is studied using Raman spectroscopy in the acoustic and optical phonon ranges, transmission electron microscopy (TEM), and atomic force microscopy (AFM). It is demonstrated that high temperature annealing (up to 1100°C) and oxidation in O2/H2O ambient do not destroy the SL structure, which retains its original periodicity and nc-Si/a-SiO2 interface abruptness. It is found that oxidation at high temperatures reduces the defect density in nc-Si/a-SiO2 SLs and induces the lateral coalescence of Si nanocrystals (NCs). The size, shape, packing density, and crystallographic orientation of the Si nanocrystals are studied as a function of the oxidation time.


2014 ◽  
Vol 887-888 ◽  
pp. 161-166
Author(s):  
Xiao Jun Liu ◽  
Li Yun Song ◽  
Zong Cheng Zhan ◽  
Hong He ◽  
Xue Hong Zi ◽  
...  

The two-dimensional (2D) assembly of the palladium nanoparticles (Pd NPs) was studied in this work. The cubic Pd NPs were successfully synthesized and assembled on mica and silicon wafer in the dip-coating way. The morphology of the Pd NPs and the topography of the Pd NPs assembly on the substrates were characterized with transmission electron microscopy (TEM) and atomic force microscopy (AFM). In the process of the fabrication, the excess cetyltrimethylammonium bromide (CTAB) was removed with the deposition-redispersion strategy, the UV-vis spectra and zeta-potential of the Pd NPs colloid were measured. It was found that the assembly and AFM characterization of the Pd NPs were affected negatively by the presence of excess CTAB. The hydrophilic property of the substrate is the crucial factor to control the 2D assembly of the Pd NPs. Compared with the washed silicon wafer, mica is ultra-hydrophilic and can attract more Pd NPs.


2002 ◽  
Vol 740 ◽  
Author(s):  
Oxana V. Kharissova ◽  
Israel Nieto Lopez ◽  
Ubaldo Ortiz Méndez ◽  
Juan A. Aguilar ◽  
Moisés Hinojosa Rivera

ABSTRACTThis work is devoted to microwave heating of graphite for studying the processing of carbon nanotubes (CNTs) by graphite vaporization. We have applied heating by microwaves (MW) (power 800W, frequency 2.45 GHz) in air at 20–90 min. The oven temperature was approximately 1200°C. The condensed material was collected on a fused silica target. After deposition, the morphology of carbon nanotubes was studied by Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), and Transmission Electron Microscopy (TEM). The samples were found to contain nanotubes, nanoparticles and fibers (at 1.30–2.80 micrometers to 6–11 micrometers) which appeared to be highly graphitized. It was observed that multi-walled nanotubes (MWNT's) were produced by this method.


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