Radial distribution function imaging by STEM diffraction: Phase mapping and analysis of heterogeneous nanostructured glasses

Mu, Xiaoke; Wang, Di; Feng, Tao; Kübel, Christian

doi:10.1016/j.ultramic.2016.05.009

Cited by 59 publications

(55 citation statements)

References 35 publications

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“…The interatomic distances extracted from the e-PDF calculation are accurate, as the ED pattern calibration and the determination of the center of the ED pattern may cause an error smaller than ± 0.005 Å within the range of 1–5 Å [ 54 , 55 , 56 ]. To establish high accuracy of the observed peak positions, during our study, a proper calibration of the TEM camera length was carried out, and all the experiments were performed under similar microscope conditions.…”

Section: Resultsmentioning

confidence: 99%

Study of the Microstructure of Amorphous Silica Nanostructures Using High-Resolution Electron Microscopy, Electron Energy Loss Spectroscopy, X-ray Powder Diffraction, and Electron Pair Distribution Function

Khouchaf

Boulahya

Das³

et al. 2020

Materials

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Silica has many industrial (i.e., glass formers) and scientific applications. The understanding and prediction of the interesting properties of such materials are dependent on the knowledge of detailed atomic structures. In this work, amorphous silica subjected to an accelerated alkali silica reaction (ASR) was recorded at different time intervals so as to follow the evolution of the structure by means of high-resolution transmission electron microscopy (HRTEM), electron energy loss spectroscopy (EELS), and electron pair distribution function (e-PDF), combined with X-ray powder diffraction (XRPD). An increase in the size of the amorphous silica nanostructures and nanopores was observed by HRTEM, which was accompanied by the possible formation of Si–OH surface species. All of the studied samples were found to be amorphous, as observed by HRTEM, a fact that was also confirmed by XRPD and e-PDF analysis. A broad diffuse peak observed in the XRPD pattern showed a shift toward higher angles following the higher reaction times of the ASR-treated material. A comparison of the EELS spectra revealed varying spectral features in the peak edges with different reaction times due to the interaction evolution between oxygen and the silicon and OH ions. Solid-state nuclear magnetic resonance (NMR) was also used to elucidate the silica nanostructures.

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Section: Resultsmentioning

confidence: 99%

Study of the Microstructure of Amorphous Silica Nanostructures Using High-Resolution Electron Microscopy, Electron Energy Loss Spectroscopy, X-ray Powder Diffraction, and Electron Pair Distribution Function

Khouchaf

Boulahya

Das³

et al. 2020

Materials

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“…Local atomic PDFs were calculated from the 4D-STEM diffraction patterns according to the method described in refs. 45 , 46 .…”

Section: Methodsmentioning

confidence: 99%

Fast kinetics of multivalent intercalation chemistry enabled by solvated magnesium-ions into self-established metallic layered materials

et al. 2018

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Rechargeable magnesium batteries are one of the most promising candidates for next-generation battery technologies. Despite recent significant progress in the development of efficient electrolytes, an on-going challenge for realization of rechargeable magnesium batteries remains to overcome the sluggish kinetics caused by the strong interaction between double charged magnesium-ions and the intercalation host. Herein, we report that a magnesium battery chemistry with fast intercalation kinetics in the layered molybdenum disulfide structures can be enabled by using solvated magnesium-ions ([Mg(DME)x]2+). Our study demonstrates that the high charge density of magnesium-ion may be mitigated through dimethoxyethane solvation, which avoids the sluggish desolvation process at the cathode-electrolyte interfaces and reduces the trapping force of the cathode lattice to the cations, facilitating magnesium-ion diffusion. The concept of using solvation effect could be a general and effective route to tackle the sluggish intercalation kinetics of magnesium-ions, which can potentially be extended to other host structures.

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“…22,23 In addition, the radial distribution function can be computed from each diffraction pattern to map the local structure. 24 Here, we demonstrate that the dataset can be used to compute strain maps during deformation even in an amorphous material. The diffraction pattern of an amorphous material is characterized by a diffuse ring pattern.…”

mentioning

confidence: 83%

Local nanoscale strain mapping of a metallic glass during in situ testing

Gammer

Ophus

Pekin

et al. 2018

Applied Physics Letters

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The local elastic strains during tensile deformation in a CuZrAlAg metallic glass are obtained by fitting an elliptic shape function to the characteristic amorphous ring in electron diffraction patterns. Scanning nanobeam electron diffraction enables strain mapping with a resolution of a few nanometers. Here, a fast direct electron detector is used to acquire the diffraction patterns at a sufficient speed to map the local transient strain during continuous tensile loading in situ in the transmission electron microscope. The elastic strain in tensile direction was found to increase during loading. After catastrophic fracture, a residual elastic strain that relaxes over time was observed.

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Radial distribution function imaging by STEM diffraction: Phase mapping and analysis of heterogeneous nanostructured glasses

Cited by 59 publications

References 35 publications

Study of the Microstructure of Amorphous Silica Nanostructures Using High-Resolution Electron Microscopy, Electron Energy Loss Spectroscopy, X-ray Powder Diffraction, and Electron Pair Distribution Function

Study of the Microstructure of Amorphous Silica Nanostructures Using High-Resolution Electron Microscopy, Electron Energy Loss Spectroscopy, X-ray Powder Diffraction, and Electron Pair Distribution Function

Fast kinetics of multivalent intercalation chemistry enabled by solvated magnesium-ions into self-established metallic layered materials

Local nanoscale strain mapping of a metallic glass during in situ testing

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