Quasi-two-dimensional (2D) sodium chloride (NaCl) crystals of various lateral sizes between graphene sheets were manufactured supersaturation from a saline solution. Aberration-corrected transmission electron microscopy was used for systematic investigations of the crystals and their decomposition under an 80 kV electron beam. Counterintuitively, bigger clusters were found to disintegrate faster under electron irradiation, but in general no correlation between crystal sizes and electron doses at which the crystals decompose was found. As for the destruction process, an abrupt decomposition of the crystals was observed, which can be described by a logistic decay function. Density-functional theory molecular dynamics simulations provide insights into the destruction mechanism, and indicate that even without account for ionization and electron excitations, free-standing NaCl crystals must quickly disintegrate due to the ballistic displacement of atoms from their surface and edges during imaging. However, graphene sheets mitigate damage development by stopping the displaced atoms and enable the immediate recombination of defects at the surface of the crystal. At the same time, once a hole in graphene appears, the displaced atoms escape, giving rise to the quick destruction of the crystal. Our results provide quantitative data on the stability of encapsulated quasi 2D NaCl crystals under electron irradiation and allow the conclusion that only high-quality graphene is suitable for protecting ionic crystals from beam damage in electron microscopy studies.
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http://dx.doi.org/10.1039/d1nr04792b | DOI Listing |
Nat Commun
January 2025
School of Physical Science and Technology, Ningbo University, Ningbo, China.
The two-dimensional (2D) "sandwich" structure composed of a cation plane located between two anion planes, such as anion-rich CrI, VS, VSe, and MnSe, possesses exotic magnetic and electronic structural properties and is expected to be a typical base for next-generation microelectronic, magnetic, and spintronic devices. However, only a few 2D anion-rich "sandwich" materials have been experimentally discovered and fabricated, as they are vastly limited by their conventional stoichiometric ratios and structural stability under ambient conditions. Here, we report a 2D anion-rich NaCl crystal with sandwiched structure confined within graphene oxide membranes with positive surface potential.
View Article and Find Full Text PDFACS Omega
December 2024
Department of Clinical Medicine, Macquarie University, Sydney, NSW 2109, Australia.
An aminoglycoside, tobramycin sulfate (TbS), was complexed with hexadecanoic acid (HdA), resulting in a TbS/HdA complex with a repeat unit of 5.3 nm of a lamellar nanostructure. The nanometer-sized TbS/HdA particles were produced using poloxamer 188 as a dispersing agent.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
School of Chemical Engineering and ARC Centre of Excellence for Enabling Eco-Efficient Beneficiation of Minerals (UQ Node), The University of Queensland, Brisbane, Queensland 4072, Australia. Electronic address:
Hypothesis: Ion-specific forces in concentrated salt solutions play critical roles in many applications, ranging from biology to engineering, e.g., separating water-soluble minerals in brines by flotation using air bubbles.
View Article and Find Full Text PDFSmall
December 2024
College of Chemistry and Chemical Engineering, Xi'an University of Science and Technology, Xi'an, 710054, China.
Unconventional fluorescent polymers are attracting increasing attention because of their excellent biocompatibility and wide applications. However, these polymers typically exhibit weak long-wavelength emission. Herein, three novel aliphatic linear polyphosphate esters are prepared via a one-pot polycondensation reaction.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Research School of Chemistry, Australian National University, Canberra, ACT, 2601, Australia.
Halogen-bonding (XB) interactions have been extensively studied in the preparation of crystalline frameworks, yet porous 3D framework materials built on XBs remain elusive. The donor-acceptor interactions are strengthened by use of anionic XB acceptors; however, the requisite charge-balancing cations typically disrupt the framework and occupy potential void space. In this work, we prepare a tetratopic XB donor bearing a crown ether moiety for sodium cation sequestration.
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