Search

Porous networks of Pt nanoparticles interlinked by bifunctional organic ligands have shown high potential as catalysts in micro‐machined hydrogen gas sensors. By varying the ligand among p‐phenylenediamine, benzidine, 4,4‘‘‐diamino‐p‐terphenyl, 1,5‐diaminonaphthalene, and trans‐1,4‐diaminocyclohexane, new variants of such networks were synthesized. Inter‐particle distances within the networks, determined via transmission electron microscopy tomography, varied from 0.8 to 1.4 nm in accordance with the nominal length of the respective ligand. While stable structures with intact and coordinatively bonded diamines were formed with all ligands, aromatic diamines showed superior thermal stability. The networks exhibited mesoporous structures depending on ligand and synthesis strategy and performed well as catalysts in hydrogen gas microsensors. They demonstrate the possibility of deliberately tuning micro‐ and mesoporosity and thereby transport properties and steric demands by choice of the right ligand also for other applications in heterogeneous catalysis., Pt nanocatalyst construction kit: variants of stable Pt nanoparticle networks were synthesized from the same Pt nanoparticle building block and 5 different aromatic and aliphatic diamines as joints. These ligand‐linked networks demonstrate the possibility of deliberately tuning their microporosity for applications in heterogeneous catalysis by choice of the right ligand.

Quantitative structural characterization of nanomaterials is important to tailor their functional properties. Corrosion of AgAu-alloy nanoparticles (NPs) results in porous structures, making them interesting for applications especially in the fields of catalysis and surface-enhanced Raman spectroscopy. For the present report, structures of dealloyed NPs were reconstructed three-dimensionally using scanning transmission electron microscopy tomography. These reconstructions were evaluated quantitatively, revealing structural information such as pore size, porosity, specific surface area, and tortuosity. Results show significant differences compared to the structure of dealloyed bulk samples and can be used as input for simulations of diffusion or mass transport processes, for example, in catalytic applications.

Dealloyed nanoporous metals hold great promise in the field of heterogeneous catalysis; however their tendency to coarsen at elevated temperatures or under catalytic reaction conditions sometimes limit further applications. Here, we report on a highly stable nanoporous gold catalyst (npAu) functionalized with praseodymia-titania mixed oxides as synthesized by a sol-gel method. Specifically, we used aberration-corrected transmission electron microscopy to study the morphology and the interface between the oxide deposits and the npAu substrate at the atomic level. Based on electron energy loss spectroscopy (EELS), it is concluded that Pr-TiOx mixed oxides form a solid solution. Flow reactor tests reveal that the Pr-TiOx functionalized nanoporous gold is not only highly active but also very stable for the water gas shift reaction in a large temperature range (180-400 °C). Our results demonstrate the potential of engineering the compositions of oxides coatings on npAu for advanced functional systems.

Nanoporous gold (npAu) fabricated from a AuCu alloy is a complex procedure mostly because of the passivated outer surface and the inhibited corrosion phenomena observed in those materials as a consequence of the formation of a Pm¯3m (AuCu3). To further deepen our understanding of the leaching of Cu in these materials, a series of experiments were performed to study the corrosion process and finally start giving an answer to this problem. Here we compare different corrosion methods, beginning with free corrosion (as the standard synthetic route for npAu) and finishing with an optimized potentiostatic dealloying (four-step method) procedure. In order to distinguish between the structural and chemical effects affecting the catalytic activity, a series of experiments employing scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM) coupled with Energy-dispersive X-ray spectroscopy (EDXS), and X-ray photoelectron spectroscopy (XPS) were performed before and after catalytic CO oxidation. The data reveals a clear influence in key synthetic steps in the master alloy synthesis (thermal treatment), as well as in the dealloying procedure.

The angle-resolved electron scattering is investigated in scanning-transmission electron microscopy (STEM) using a motorised iris aperture placed above a conventional annular detector. The electron intensity scattered into various angle ranges is compared with simulations that were carried out in the frozen-lattice approximation. As figure of merit for the agreement of experiment and simulation we evaluate the specimen thickness which is compared with the thickness obtained from position-averaged convergent beam electron diffraction (PACBED). We find deviations whose strengths depend on the angular range of the detected electrons. As possible sources of error we investigate, for example, the influences of amorphous surface layers, inelastic scattering (plasmon excitation), phonon-correlation within the frozen-lattice approach, and distortions in the diffraction plane of the microscope. The evaluation is performed for four experimental thicknesses and two angle-resolved STEM series under different camera lengths. The results clearly show that especially for scattering angles below 50 mrad, it is mandatory that the simulations take scattering effects into account which are usually neglected for simulating high-angle scattering. Most influences predominantly affect the low-angle range, but also high scattering angles can be affected (e.g. by amorphous surface covering).

4D-scanning transmission electron microscopy (4D-STEM) can be used to measure electric fields such as atomic fields or polarization-induced electric fields in crystal heterostructures. The paper focuses on effects occurring in 4D-STEM at interfaces, where two model systems are used: an AlN/GaN nanowire superlattice as well as a GaN/vacuum interface. Two different methods are applied: First, we employ the centre-of mass (COM) technique which uses the average momentum transfer evaluated from the intensity distribution in the diffraction pattern. Second, we measure the shift of the undiffracted disc (disc-detection method) in nano-beam electron diffraction (NBED). Both methods are applied to experimental and simulated 4D-STEM data sets. We find for both techniques distinct variations in the momentum transfer at interfaces between materials: In both model systems, peaks occur at the interfaces and we investigate possible sources and routes of interpretation. In case of the AlN/GaN superlattice, the COM and disc-detection methods are used to measure internal polarization-induced electric fields and we observed a reduction of the measured fields with increasing specimen thickness.

Properties of dealloyed nanoporous gold (npAu) in catalysis, sensing or actuation applications depend on its structure and chemical composition. NpAu is obtained by corrosion of alloys of gold and a less noble metal such as silver or copper. Structural parameters can be tuned by variations in the preparation process. Due to the large number of parameters that can be varied a direct comparison of results obtained with various samples is often difficult. In this report we compare structure and chemical composition of npAu dealloyed from AuAg and AuCu alloys keeping the number of different sample preparation parameters at a minimum.

Strain analyses from experimental series of nano-beam electron diffraction (NBED) patterns in scanning transmission electron microscopy are performed for different specimen tilts. Simulations of NBED series are presented for which strain analysis gives results that are in accordance with experiment. This consequently allows to study the relation between measured strain and actual underlying strain. A two-tilt method which can be seen as lowest-order electron beam precession is suggested and experimentally implemented. Strain determination from NBED series with increasing beam convergence is performed in combination with the experimental realization of a probe-forming aperture with a cross inside. It is shown that using standard evaluation techniques, the influence of beam convergence on spatial resolution is lower than the influence of sharp rings around the diffraction disc which occur at interfaces and which are caused by the tails of the intensity distribution of the electron probe. (C) 2018 Elsevier B.V. All rights reserved.

Reversible macroscopic length changes in nanoporous structures can be achieved by applying electric potentials or by exposing them to different gases or liquids. Thus, these materials are interesting candidates for applications as sensors or actuators. Macroscopic length changes originate from microscopic changes of crystal lattice parameters. In this report, we show spatially resolved measurements of crystal lattice strain in dealloyed nanoporous gold. The results confirm theory by indicating a compression of the lattice along the axis of cylindrically shaped ligaments and an expansion in radial direction. Furthermore, we show that curved npAu surfaces show inward relaxation of the surface layer. (Figure presented) IMPACT STATEMENT We show spatially resolved measurements of strain in nanoporous gold confirming theory: Crystal lattice is compressed along the axis of cylindrical ligaments and expanded in radial direction, surfaces relax inward.

In this paper we study the effect of lens aberrations (spherical aberration and astigmatism), beam tilt, contamination and shot noise on the accuracy and precision of position determination in imaging scanning transmission electron microscopy (ISTEM) on the example of BaTiO 3 . ISTEM images are simulated as a function of sample thickness and defocus starting from a nearly perfect microscope setting. A defocus range was identified, in which atom column positions were reliably visible and could be decently measured. By averaging over this defocus and thickness range a figure of merit was defined and used to study the influence of above mentioned disturbing effects as a function of their strength. It turned out that column positions might become inaccurate, but distances are measured accurately. These were used to obtain recommendations for the experimental setup to measure the atomic arrangement that induces ferroelectric switching of BaTiO 3 .

Methanol as a green and renewable resource can be used to generate hydrogen by reforming, i.e., its catalytic oxidation with water. In combination with a fuel cell this hydrogen can be converted into electrical energy, a favorable concept, in particular for mobile applications. Its realization requires the development of novel types of structured catalysts, applicable in small scale reactor designs. Here, three different types of such catalysts were investigated for the steam reforming of methanol (SRM). Oxides such as TiO2 and CeO2 and mixtures thereof (Ce1Ti2Ox) were deposited inside a bulk nanoporous gold (npAu) material using wet chemical impregnation procedures. Transmission electron and scanning electron microscopy reveal oxide nanoparticles (1–2 nm in size) abundantly covering the strongly curved surface of the nanoporous gold host (ligaments and pores on the order of 40 nm in size). These catalysts were investigated in a laboratory scaled flow reactor. First conversion of methanol was detected at 200 °C. The measured turn over frequency at 300 °C of the CeOx/npAu catalyst was 0.06 s−1. Parallel investigation by in situ infrared spectroscopy (DRIFTS) reveals that the activation of water and the formation of OHads are the key to the activity/selectivity of the catalysts. While all catalysts generate sufficient OHads to prevent complete dehydrogenation of methanol to CO, only the most active catalysts (e.g., CeOx/npAu) show direct reaction with formic acid and its decomposition to CO2 and H2. The combination of flow reactor studies and in operando DRIFTS, thus, opens the door to further development of this type of catalyst.

Strain has a strong effect on the properties of materials and the performance of electronic devices. Their ever shrinking size translates into a constant demand for accurate and precise measurement methods with very high spatial resolution. In this regard, transmission electron microscopes are key instruments thanks to their ability to map strain with sub-nanometer resolution. Here we present a novel method to measure strain at the nanometer scale based on the diffraction of electron Bessel beams. We demonstrate that our method offers a strain sensitivity better than $2.5 \cdot 10^{-4}$ and an accuracy of $1.5 \cdot 10^{-3}$, competing with, or outperforming, the best existing methods with a simple and easy to use experimental setup., This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Appl. Phys. Lett. 114, 243501 (2019) and may be found at https://aip.scitation.org/doi/abs/10.1063/1.5096245 Data available at: https://doi.org/10.5281/zenodo.2566137 and code available at: https://bitbucket.org/lutosensis/tem-thesis/src

Strain analysis by nano-beam electron diffraction allows for measurements of strain with nanometre resolution in a large field of view. This is done by evaluating distances between diffraction discs in diffraction patterns acquired while a focussed electron beam is scanned across the sample in a transmission electron microscope. The bottleneck of this method is a precise determination of diffraction disc positions, which suffers from the inner structure of the discs caused by dynamical diffraction. Electron beam precession is a tool that solves this problem but it is not commonly available in every microscope. Without precession significant progress has been reported recently by using patterned condenser apertures. The pattern of the aperture is reproduced in patterns of the diffraction discs allowing for a more precise position determination. In this report the accuracy of measured strain profiles using patterned apertures is investigated by evaluation of realistic simulations. This is done especially at interfaces between regions with different lattice plane spacing. It is found by evaluation of the simulations that measured strain profiles are more blurred and hence the accuracy at the interface is worse the more patterns are imprinted to the condenser aperture. An explanation of this effect is given and as a proof of principle a solution to this problem is provided applying geometric phase analysis ptychography.

Based on a sol–gel coating method, a series of nanoporous gold (npAu) catalysts functionalized with titania–ceria mixed oxides were prepared. Metal-oxides with different composition were formed inside the mesoporous material (ligaments and pores ∼45 nm) after thermal treatment at over 200 °C for 2 h. The water-gas shift (WGS) reaction (H2O + CO → H2 + CO2) was studied in a continuous flow reactor at ambient pressure using these Ce–TiOx/npAu catalytic materials. Formation of CO2 was observed at temperatures between 200 °C and 450 °C. The addition of CeO2 to TiO2 resulted in an strongly increased activity; the sample (with the molar ratio of Ce : Ti = 1 : 2 abbreviated as Ce1Ti2Ox/npAu) shows the highest activity which was nearly twice as high as the activity of all other samples at 300 °C. The loss of activity after 2 catalytic runs was only about 10% at 450 °C for the Ce1Ti2Ox/npAu sample and no coarsening was observed. Raman spectroscopic characterization of the materials indicates a dynamic correlation between the crystallization (oxygen storage) of the metal-oxides under oxidizing and reducing conditions.

Images acquired in transmission electron microscopes can be distorted for various reasons such as e.g. aberrations of the lenses of the imaging system or inaccuracies of the image recording system. This results in inaccuracies of measures obtained from the distorted images. Here we report on measurement and correction of elliptical distortions of diffraction patterns. The effect of this correction on the measurement of crystal lattice strain is investigated. We show that the effect of the distortions is smaller than the precision of the measurement in cases where the strain is obtained from shifts of diffracted discs with respect to their positions in images acquired in an unstrained reference area of the sample. This can be explained by the fact that diffraction patterns acquired in the strain free reference area of the sample are distorted in the same manner as the diffraction patterns acquired in the strained region of interest. In contrast, for samples without a strain free reference region such as nanoparticles or nanoporous structures, where we evaluate ratios of lattice plane distances along different directions, the distortions are usually not negligible. Furthermore, two techniques for the detection of diffraction disc positions are compared showing that for samples in which the crystal orientation changes over the investigated area it is more precise to detect the positions of many diffraction discs simultaneously instead of detecting each disc position independently.

Measurement of lattice strain is important to characterize semiconductor nanostructures. As strain has large influence on the electronic band structure, methods for the measurement of strain with high precision, accuracy and spatial resolution in a large field of view are mandatory. In this paper we present a theoretical study of precision and accuracy of measurement of strain by convergent nano-beam electron diffraction. It is found that the accuracy of the evaluation suffers from halos in the diffraction pattern caused by a variation of strain within the area covered by the focussed electron beam. This effect, which is expected to be strong at sharp interfaces between materials with different lattice plane distances, will be discussed for convergent-beam electron diffraction patterns using a conventional probe and for patterns formed by a precessing electron beam. Furthermore, we discuss approaches to optimize the accuracy of strain measured at interfaces. The study is based on the evaluation of diffraction patterns simulated for different realistic structures that have been investigated experimentally in former publications. These simulations account for thermal diffuse scattering using the frozen-lattice approach and the modulation-transfer function of the image-recording system. The influence of Poisson noise is also investigated.

Nanoporous gold (npAu) has attracted a lot of attention during the last decade as it has interesting applications particularly in the field of catalysis [1]. It is prepared by corrosion of a suitable gold master alloy, e.g. gold/silver. The remaining material forms a sponge-like structure built of ligaments and pores still preserving a crystalline structure over several tens of nanometres. A high surface to volume ratio, open porosity making it permeable for gases and liquids and a strongly curved ligament surface providing surface atoms of different coordination are only some properties which qualify npAu as catalytic material with well adjustable and reproducible structure. One important structural property that is expected to have strong influence on the catalytic activity is lattice strain, because strain affects the electronic states [2]. Here we present measurements of strain in npAu. A measurement of lattice strain by means of high-resolution TEM for example by the analysis of lattice plane distances is possible only in a very small field of view for npAu. As the positions of intensity maxima in the images depend on several experimental parameters, such as defocus, orientation, composition, lens aberrations and especially specimen thickness, maxima detection in TEM micrographs succeeds only in small parts of the sample, because thickness is varying strongly. This can be seen in Fig. 1. Close to the surface intensity maxima can be detected and thus strain can be measured, in this case tensile strain up to 5% has been found. But as the ligament gets thicker and defects become visible, contrast changes and strain analysis fails. A method that overcomes these problems is strain analysis using nano-beam electron diffraction (NBED) [3]. Here a focussed electron probe is scanned across the sample and at each position of the scanning beam the corresponding diffraction pattern is recorded. As distances between the non-overlapping diffraction discs depend basically on the local lattice parameter according to Bragg's law, strain can be measured by comparing distances between diffraction discs at different positions of the scanning beam. By an analysis of distances between diffraction discs in two linearly independent directions strain as well as shear-strain and rotation can be measured. A further advantage of strain analysis by NBED is its large field of view, because at first sight it is limited only by the size of the scanned part of the sample. Hence strain and rotation of neighbouring ligaments in npAu can be measured. On the other hand a large field of view requires the acquisition of a large number of diffraction patterns in a short time to avoid effects of sample drift, beam induced sample damage and contamination. Here we present strain and rotation maps of npAu measured using a delay-line detector for the acquisition of the diffraction patterns. With this detector strain maps at a scanning raster of e.g. 100x100 pixels can be recorded, allowing measurements in a field of view of several hundreds of nanometers (Fig. 2) still preserving a sampling limited spatial resolution of about 1.6 nm [4]. Furthermore we show by evaluation of simulations that two important aspects concerning the precision of the measurement have to be taken into account. As the precision of the measurement suffers from noise in the diffraction pattern, the precision degrades for shorter image integration times. On the other hand the precision can be increased using a precessing [5, 6] electron beam, as the diffraction discs are illuminated more homogeneously and hence their positions can be detected more precisely. In this way a compromise between precision and speed / size of the measurement has to be found. Keywords: nanoporous gold; strain measurement; NBED; precision