Morphology, studies transmission electron microscopy

Yakovlev, S., Balsara, N., Downing, K., Insights on the study of Nafion nanoscale morphology by transmission electron microscopy. Membranes 2013, 3 (4), 424-439. 

Thus, the interaction of the primary beam with the sample provides a wealth of information on morphology, crystallography and chemical composition. Using transmission electron microscopy to make a projection of the sample density is a routine way to study particle sizes in catalysts. 

SnC>2 nanoparticles have been successfully synthesized by chemical co-precipitation method using ethanol, acetone, tetrahydrofuran (THF) and ether as solvents. X-ray Diffraction (XRD), Field Emission Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM) have been used to study the crystallographic and morphological properties of synthesized SnC>2 nanoparticles, while their optical properties have been studied by UV-Visible absorption spectroscopy. UV-Vis absorption spectra shows a weak quantum confinement in all the synthesized SnCL samples. The photo-catalytic activity of as-synthesized SnC>2 nanoparticles under UV irradiation has been evaluated using Methylene Blue (MB) dye as a test contaminant in water. The results showed that solvents played a key role to control the morphology and photo-catalytic activity of SnCE nanoparticles. 

In contrast transmission electron microscopy (TEM) can in skilled hands yield detailed quantitative data on pore structure, and can even provide valuable information on the wet state of resins by plunge freezing such samples and microtom-ing on a cold stage [105]. To obtain quantitative information it is necessary to use advanced image analysis methodology which is extremely powerful [106]. Unfortunately the approach is time consuming and costly and can rarely be applied routinely in morphology studies. 

In 2008 Shin et al. used lETS and transmission electron microscopy (TEM) to characterize the chemical integrity and morphology of rubrene (C40H24) layers after deposition of an Fe top electrode [57]. The lETS spectra were consistent with the known IR- and Raman-active normal modes, which led the authors to conclude there were no chemical reactions with Fe. Cross-sectional TEM images showed continuous rubrene layers between the bottom Co layer and top Fe layer, with no evidence for small particle formation. Similar to the study by Santos et al., they found that the presence of an AI2O3 layer had a profound effect on the tunneling... 

In the author s opinion, the better approach to experimentally study the morphology of the silica surface is with the help of physical adsorption (see Chapter 6). Then, with the obtained, adsorption data, some well-defined parameters can be calculated, such as surface area, pore volume, and pore size distribution. This line of attack (see Chapter 4) should be complemented with a study of the morphology of these materials by scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning probe microscopy (SPM), or atomic force microscopy (AFM), and the characterization of their molecular and supramolecular structure by Fourier transform infrared (FTIR) spectrometry, nuclear magnetic resonance (NMR) spectrometry, thermal methods, and possibly with other methodologies. 

Changes in the morphological and structural characteristics of the carbon deposit resulting from pretreatment of the iron catalyst in H2S were determined from a combination of transmission electron microscopy techniques, X-ray diffraction, surface area measurements and controlled oxidation studies in CO2. Iron powder 200 mesh) was purchased from Johnson Matthey Inc. (99 99% purity) and had a BET surface area of 0.3 m2/g at -196°C, The gases used in this work CO (99 9%), hydrogen (99.999%), ethylene (99.999%), H2S/argon mixtures and helium (99,999%) were obtained from Alphagaz company and used without further purification. 

---