Direct Atomic Resolution Imaging Research Articles

Subsurface oxygen at transition metal surfaces: Its direct atom-resolved imaging and role in metal oxidation

Clarifying how oxygen is incorporated into the subsurface region of metal surfaces is a crucial step towards a robust understanding of the initial oxidation of metals. Due to lack of direct atomic-resolution imaging of subsurface oxygen, the atomistic mechanisms of oxygen-metal interactions and the role of subsurface oxygen remain elusive. Here, by state-of-the-art transmission electron microscopy, we demonstrate a direct atom-resolved imaging of subsurface oxygen that is dissolved in the subsurface region of the Fe (001) and Ti (0001) surfaces. It is found that subsurface oxygen occupies the octahedral sites of the Fe and Ti lattices, rather than the tetrahedral sites. First-principles calculations reveal that the octahedral-site occupancy of subsurface oxygen is energetically more favorable compared to the tetrahedral-site occupancy and will facilitate the process of metal oxidation by reducing the formation energy of metal oxides. Our findings clarify the atomistic mechanism of how oxygen attacks metal surfaces for the initiation of oxidation that occurs everywhere in nature.

Chirality reversal of magnetic solitons in chiral Cr1/3TaS2

Ferromagnetism in two-dimensional (2D) materials provides an ideal platform to study emergent electromagnetic phenomena in low dimensions for future spintronics. In magnetic-element intercalated transition metal dichalcogenides, topologically nontrivial spin textures, such as chiral helimagnetic spin states and chiral soliton lattices, are realized due to the chiral lattice distortions induced by intercalated magnetic ions. Consequently, the magnetic chirality is predictably determined by the sign of antisymmetric exchange interaction (or Dzyaloshinskii–Moriya interaction, DMI) vector that is coupled to the underlying crystal chirality. Here, using cryogenic Lorentz phase microscopy, we directly observed the chirality reversal behavior of the chiral soliton lattices in Cr1/3TaS2 across the structural defects. We show that a partial 1 T stacking in 2H-TaS2 locally reduces DMI, leading to magnetic chirality reversal with direct atomic resolution imaging. Our experimental results show that manipulation of stacking sequence provides a viable way to control the chirality of topologically nontrivial soliton lattices in 2D magnets.

A dislocation core in titanium dioxide and its electronic structure

We provide a direct atomic-resolution imaging of the core structure of a dislocation in technologically important TiO2 and predict that every individual impurity-free dislocation exhibits electric conductivity in an otherwise insulating TiO2.

Atomic-scale observation of migration and coalescence of Au nanoclusters on YSZ surface by aberration-corrected STEM.

Unraveling structural dynamics of noble metal nanoclusters on oxide supports is critical to understanding reaction process and origin of catalytic activity in heterogeneous catalysts. Here, we show that aberration-corrected scanning transmission electron microscopy can provide direct atomic-resolution imaging of surface migration, coalescence, and atomic rearrangement of Au clusters on an Y:ZrO2 (YSZ) support. The high resolution enables us to reveal migration and coalescence process of Au clusters at the atomic scale, and to demonstrate that the coalesced clusters undergo a cooperative atomic rearrangement, which transforms the coherent into incoherent Au/YSZ interface. This approach can help to elucidate atomistic mechanism of catalytic activities and to develop novel catalysts with enhanced functionality.

Fluorine in Shark Teeth: Its Direct Atomic‐Resolution Imaging and Strengthening Function

Atomic-resolution imaging of beam-sensitive biominerals is extremely challenging, owing to their fairly complex structures and the damage caused by electron irradiation. Herein, we overcome these difficulties by performing aberration-corrected electron microscopy with low-dose imaging techniques, and report the successful direct atomic-resolution imaging of every individual atomic column in the complex fluorapatite structure of shark tooth enameloid, which can be of paramount importance for teeth in general. We demonstrate that every individual atomic column in shark tooth enameloid can be spatially resolved, and has a complex fluorapatite structure. Furthermore, ab initio calculations show that fluorine atoms can be covalently bound to the surrounding calcium atoms, which improves understanding of their caries-reducing effects in shark teeth.

Intrinsic Structural Defects in Monolayer Molybdenum Disulfide

Monolayer molybdenum disulfide (MoS2) is a two-dimensional direct band gap semiconductor with unique mechanical, electronic, optical, and chemical properties that can be utilized for novel nanoelectronics and optoelectronics devices. The performance of these devices strongly depends on the quality and defect morphology of the MoS2 layers. Here we provide a systematic study of intrinsic structural defects in chemical vapor phase grown monolayer MoS2, including point defects, dislocations, grain boundaries, and edges, via direct atomic resolution imaging, and explore their energy landscape and electronic properties using first-principles calculations. A rich variety of point defects and dislocation cores, distinct from those present in graphene, were observed in MoS2. We discover that one-dimensional metallic wires can be created via two different types of 60° grain boundaries consisting of distinct 4-fold ring chains. A new type of edge reconstruction, representing a transition state during growth, was also identified, providing insights into the material growth mechanism. The atomic scale study of structural defects presented here brings new opportunities to tailor the properties of MoS2 via controlled synthesis and defect engineering.

In Situ Real-time Environmental High Resolution Electron Microscopy of Nanometer Size Novel Xerogel Catalysts for Hydrogenation Reactions in Nylon 6,6

AbstractIn situ real-time environmental high resolution electron microscopy (EHREM) under controlled reaction environments permits direct atomic resolution imaging of dynamic surface and sub-surface microstructures of reacting catalysts. Using the EHREM and complementary microscopy methods, we have investigated selective hydrogenation reaction mechanisms over novel xerogel catalysts of ruthenium and Ru with Co and Au promoters on titania supports, and report an alternative heterogeneous catalytic process for the hydrogenation of adiponitrile (ADN) in the manufacture of Nylon 6,6. The direct EHREM observations are supported by ultra-high resolution low voltage scanning electron microscope (SEM) of spatial distributions of the highly dispersed nanometer-size catalyst particles and parallel chemical studies. The results demonstrate the important role of in situ EHREM in the design of heterogeneous catalytic hydrogenation processes on the nanoscale.

In Situ Real-time Environmental High Resolution Electron Microscopy of Nanometer Size Novel Xerogel Catalysts for Hydrogenation Reactions in Nylon 6,6

Abstract In situ real-time environmental high resolution electron microscopy (EHREM) under controlled reaction environments permits direct atomic resolution imaging of dynamic surface and sub-surface microstructures of reacting catalysts. Using the EHREM and complementary microscopy methods, we have investigated selective hydrogenation reaction mechanisms over novel xerogel catalysts of ruthenium and Ru with Co and Au promoters on titania supports, and report an alternative heterogeneous catalytic process for the hydrogenation of adiponitrile (ADN) in the manufacture of Nylon 6,6. The direct EHREM observations are supported by ultra-high resolution low voltage scanning electron microscope (SEM) of spatial distributions of the highly dispersed nanometer-size catalyst particles and parallel chemical studies. The results demonstrate the important role of in situ EHREM in the design of heterogeneous catalytic hydrogenation processes on the nanoscale.