No Arabic abstract
Advances in atomic resolution in situ environmental transmission electron microscopy for direct probing of gas-solid reactions, including at very high temperatures are described. In addition, recent developments of dynamic real time in situ studies at the Angstrom level using a hot stage in an aberration corrected environment are presented. In situ data from Pt and Pd nanoparticles on carbon with the corresponding FFT (optical diffractogram) illustrate an achieved resolution of 0.11 nm at 500 C and higher in a double aberration corrected TEM and STEM instrument employing a wider gap objective pole piece. The new results open up opportunities for dynamic studies of materials in an aberration corrected environment.
For quantitative electron microscopy high precision position information is necessary so that besides an adequate resolution and sufficiently strong contrast of atoms, small width of peaks which represent atoms in structural images is needed. Size of peak is determined by point spread (PS) of instruments as well as that of atoms when point resolution reach the subangstrom scale and thus PS of instruments is comparable with that of atoms. In this article, relationship between PS with atomic numbers, sample thickness, and spherical aberration coefficients will be studied in both negative Cs imaging (NCSI) and positive Cs imaging (PCSI) modes by means of dynamical image simulation. Through comparing the peak width with different thickness and different values of spherical aberration, NCSI mode is found to be superior to PCSI considering smaller peak width in the structural image.
In this work, an optic fiber based $textit{in situ}$ illumination system integrated into an aberration-corrected environmental transmission electron microscope (ETEM) is designed, built, characterized and applied. With this illumination system, the dynamic responses of photoactive materials to photons can be directly observed at the atomic level, and other stimuli including heating and various gases can also be applied simultaneously. Either a broadband light source or a high power laser source aiming to expedite photoreactions can be utilized, fitting different application needs. The optic fiber enters the ETEM through the objective aperture port, with a carefully designed curvature and a 30{deg} cut at the tip to orient the emitted light upwards onto the TEM specimen. The intensity distributions striking the sample from the broadband and laser sources are both measured, and due to the non-uniform distributions, an alignment procedure has been developed to align the bright spot with the electron optical axis of the TEM. The imaging and spectroscopy performances of the ETEM are proved to be maintained after incorporating this illumination system. Furthermore, Langmuir evaporation is observed when in situ laser light is applied to GaAs, demonstrating the phenomenon of optical heating on suitable semiconductor materials.
Incommensurate modulated structure (IMS) in Bi2Sr1.6La0.4CuO6+{delta} (BSLCO) has been studied by aberration corrected transmission electron microscopy in combination with high-dimensional (HD) space description. Two images in the negative Cs imaging (NCSI) and passive Cs imaging (PCSI) modes were deconvoluted, respectively. Similar results as to IMS have been obtained from two corresponding projected potential maps (PPMs), but meanwhile the size of dots representing atoms in the NCSI PPM is found to be smaller than that in PCSI one. Considering that size is one of influencing factors of precision, modulation functions for all unoverlapped atoms in BSLCO were determined based on the PPM obtained from the NCSI image in combination with HD space description.
An environmental cell high resolution electron microscope (EHREM) has been developed for in situ studies of dynamic chemical reactions on the atomic scale. It allows access to metastable intermediate phases of catalysts and to sequences of reversible microstructural and chemical development associated with the activation, deactivation and poisoning of a catalyst. Materials transported through air can be restored or recreated and samples damaged, e.g. by dehydration, by the usual vacuum environment in a conventional electron microscope can be preserved. A Philips C M30 HRTEM and STEM system has been extensively modified in our laboratory to add facilities for in situ gas-solid reaction studies in controlled atmospheres of gas or vapor at pressures of 0 to 50 mbar, instead of the regular TEM high vacuum environment. The integrated new environmental cell capability is combined with the original 0.23 nm TEM resolution, STEM imaging (bright field and annular dark field) and chemical and crystallographic microanalyses. Regular sample holders are used and include hot stages to higher than 1000 C. Examples of applications include direct studies of dynamic reactions with supported metal particle catalysts, the generation of defects and structural changes in practical complex oxide catalyst systems under operating conditions and carbon microstructures.
Lithium (Li) is the simplest metal and the lightest solid element. Here we report the first demonstration of controlled growth of two-dimensional (2D) ultrathin Li nanosheets with large lateral dimensions up to several hundreds of nanometres and thickness limited to just a few nanometres by in-situ transmission electron microscopy (TEM). The nanoscale dynamics of nanosheets growth were unravelled by real-time TEM imaging, which, in combination with density function theory (DFT) calculations indicates that the growth of bcc structured Li into 2D nanosheets is a consequence of kinetic control as mediated by preferential oxidization of the (111) surfaces due to the trace amount of O2 (~10-6 Pa) within TEM chamber. The plasmonic optical properties of the as-grown Li nanosheets were probed by cathodoluminescence (CL) spectroscopy equipped within TEM, and a broadband visible emission was observed that contains contributions of both in-plane and out-of-plane plasmon resonance modes.