FIB/SEM Characterization of Paper Materials

3D microscopy is of interest for structural characterization of paper materials to study the use of cellulose nanofibrils as a paper additive. Focused ion beam (FIB) tomography is a promising microscopy technique for this application, combining scanning electron microscopy (SEM) with serial sectioning by ion beam, potentially with nanoscale resolution. In this work, FIB tomography is demonstrated for paper samples, showing that the technique is applicable to this class of materials. Volume reconstructions with voxel resolution down to 13x13x 15nm3 for volumes of up to approximately 10x10x2 μm3 are obtained. The latter is limited by the acquisition time, and can therefore be extended. A working protocol is developed, from sample preparation and image acquisition to processing and volume reconstruction. The method is discussed in comparison to established 3D methods for paper materials, and suggestions are made for improving the resolution and increasing the volume

FIB/SEM Characterization of Paper Materials

3D microscopy is of interest for structural characterization of paper materials to study the use of cellulose nanofibrils as a paper additive. Focused ion beam (FIB) tomography is a promising microscopy technique for this application, combining scanning electron microscopy (SEM) with serial sectioning by ion beam, potentially with nanoscale resolution. In this work, FIB tomography is demonstrated for paper samples, showing that the technique is applicable to this class of materials. Volume reconstructions with voxel resolution down to 13x13x 15nm3 for volumes of up to approximately 10x10x2 μm3 are obtained. The latter is limited by the acquisition time, and can therefore be extended. A working protocol is developed, from sample preparation and image acquisition to processing and volume reconstruction. The method is discussed in comparison to established 3D methods for paper materials, and suggestions are made for improving the resolution and increasing the volume

Characterization of ferroelectric domain walls by scanning electron microscopy

Ferroelectric domain walls are a completely new type of functional interface, which have the potential to revolutionize nanotechnology. In addition to the emergent phenomena at domain walls, they are spatially mobile and can be injected, positioned, and deleted on demand, giving a new degree of flexibility that is not available at conventional interfaces. Progress in the field is closely linked to the development of modern microscopy methods, which are essential for studying their physical properties at the nanoscale. In this article, we discuss scanning electron microscopy (SEM) as a powerful and highly flexible imaging technique for scale-bridging studies on domain walls, continuously covering nano- to mesoscopic length scales. We review seminal SEM experiments on ferroelectric domains and domain walls, provide practical information on how to visualize them in modern SEMs, and provide a comprehensive overview of the models that have been proposed to explain the contrast formation in SEM. Going beyond basic imaging experiments, recent examples for nano-structuring and correlated microscopy work on ferroelectric domain walls are presented. Other techniques, such as 3D atom probe tomography, are particularly promising and may be combined with SEM in the future to investigate individual domain walls, providing new opportunities for tackling the complex nanoscale physics and defect chemistry at ferroelectric domain walls

Fluorescent Nanocomposites: Hollow Silica Microspheres with Embedded Carbon Dots

Intrinsically fluorescent carbon dots may form the basis for a safer and more accurate sensor technology for digital counting in bioanalytical assays. This work presents a simple and inexpensive synthesis method for producing fluorescent carbon dots embedded in hollow silica particles. Hydrothermal treatment at low temperature (160 °C) of microporous silica particles in presence of urea and citric acid results in fluorescent, microporous and hollow nanocomposites with a surface area of 12 m2/g. High absolute zeta potential (−44 mV) at neutral pH demonstrates the high electrosteric stability of the nanocomposites in aqueous solution. Their fluorescence emission at 445 nm is remarkably stable in aqueous dispersion under a wide pH range (3–12) and in the dried state. The biocompatibility of the composite particles is excellent, as the particles were found to show low genotoxicity at exposures up to 10 μg/cm2.publishedVersio

Fluorescent Nanocomposites: Hollow Silica Microspheres with Embedded Carbon Dots

Intrinsically fluorescent carbon dots may form the basis for a safer and more accurate sensor technology for digital counting in bioanalytical assays. This work presents a simple and inexpensive synthesis method for producing fluorescent carbon dots embedded in hollow silica particles. Hydrothermal treatment at low temperature (160 °C) of microporous silica particles in presence of urea and citric acid results in fluorescent, microporous and hollow nanocomposites with a surface area of 12 m2/g. High absolute zeta potential (−44 mV) at neutral pH demonstrates the high electrosteric stability of the nanocomposites in aqueous solution. Their fluorescence emission at 445 nm is remarkably stable in aqueous dispersion under a wide pH range (3–12) and in the dried state. The biocompatibility of the composite particles is excellent, as the particles were found to show low genotoxicity at exposures up to 10 μg/cm2

Contact-free reversible switching of improper ferroelectric domains by electron and ion irradiation

Focused ion beam (FIB) and scanning electron microscopy (SEM) are used to reversibly switch improper ferroelectric domains in the hexagonal manganite ErMnO3. Surface charging is achieved by local ion (positive charging) and electron (positive and negative charging) irradiation, which allows controlled polarization switching without the need for electrical contacts. Polarization cycling reveals that the domain walls tend to return to the equilibrium configuration obtained in the as-grown state. The response of sub-surface domains is studied by FIB cross-sectioning, enabling imaging in the direction perpendicular to the applied electric field. The results clarify how the polarization reversal in hexagonal manganites progresses at the level of domains, resolving both domain wall movements and the nucleation and growth of new domains. Our FIB-SEM based switching approach is applicable to all ferroelectrics where a sufficiently large electric field can be built up via surface charging, facilitating contact-free high-resolution studies of the domain and domain wall response to electric fields in 3D

Fluorescent Nanocomposites: Hollow Silica Microspheres with Embedded Carbon Dots

Intrinsically fluorescent carbon dots may form the basis for a safer and more accurate sensor technology for digital counting in bioanalytical assays. This work presents a simple and inexpensive synthesis method for producing fluorescent carbon dots embedded in hollow silica particles. Hydrothermal treatment at low temperature (160 °C) of microporous silica particles in presence of urea and citric acid results in fluorescent, microporous and hollow nanocomposites with a surface area of 12 m2/g. High absolute zeta potential (−44 mV) at neutral pH demonstrates the high electrosteric stability of the nanocomposites in aqueous solution. Their fluorescence emission at 445 nm is remarkably stable in aqueous dispersion under a wide pH range (3–12) and in the dried state. The biocompatibility of the composite particles is excellent, as the particles were found to show low genotoxicity at exposures up to 10 μg/cm2

Fluorescent Nanocomposites: Hollow Silica Microspheres with Embedded Carbon Dots

Intrinsically fluorescent carbon dots may form the basis for a safer and more accurate sensor technology for digital counting in bioanalytical assays. This work presents a simple and inexpensive synthesis method for producing fluorescent carbon dots embedded in hollow silica particles. Hydrothermal treatment at low temperature (160 °C) of microporous silica particles in presence of urea and citric acid results in fluorescent, microporous and hollow nanocomposites with a surface area of 12 m2/g. High absolute zeta potential (−44 mV) at neutral pH demonstrates the high electrosteric stability of the nanocomposites in aqueous solution. Their fluorescence emission at 445 nm is remarkably stable in aqueous dispersion under a wide pH range (3–12) and in the dried state. The biocompatibility of the composite particles is excellent, as the particles were found to show low genotoxicity at exposures up to 10 μg/cm2

Fluorescent Nanocomposites: Hollow Silica Microspheres with Embedded Carbon Dots

Intrinsically fluorescent carbon dots may form the basis for a safer and more accurate sensor technology for digital counting in bioanalytical assays. This work presents a simple and inexpensive synthesis method for producing fluorescent carbon dots embedded in hollow silica particles. Hydrothermal treatment at low temperature (160 °C) of microporous silica particles in presence of urea and citric acid results in fluorescent, microporous and hollow nanocomposites with a surface area of 12 m2/g. High absolute zeta potential (−44 mV) at neutral pH demonstrates the high electrosteric stability of the nanocomposites in aqueous solution. Their fluorescence emission at 445 nm is remarkably stable in aqueous dispersion under a wide pH range (3–12) and in the dried state. The biocompatibility of the composite particles is excellent, as the particles were found to show low genotoxicity at exposures up to 10 μg/cm2

Fluorescent Nanocomposites: Hollow Silica Microspheres with Embedded Carbon Dots

Intrinsically fluorescent carbon dots may form the basis for a safer and more accurate sensor technology for digital counting in bioanalytical assays. This work presents a simple and inexpensive synthesis method for producing fluorescent carbon dots embedded in hollow silica particles. Hydrothermal treatment at low temperature (160 °C) of microporous silica particles in presence of urea and citric acid results in fluorescent, microporous and hollow nanocomposites with a surface area of 12 m2/g. High absolute zeta potential (−44 mV) at neutral pH demonstrates the high electrosteric stability of the nanocomposites in aqueous solution. Their fluorescence emission at 445 nm is remarkably stable in aqueous dispersion under a wide pH range (3–12) and in the dried state. The biocompatibility of the composite particles is excellent, as the particles were found to show low genotoxicity at exposures up to 10 μg/cm2