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Abstract
A comprehensive nanoscale understanding of layered double hydroxide (LDH) thermal evolution is critical for their current and future applications as catalysts, flame retardants and oxygen evolution performers. In this report, we applied in situ transmission electron microscopy (TEM) to extensively characterise the thermal progressions of nickel-iron containing (Ni-Fe) LDH nanomaterials. The combinative approach of TEM and selected area electron diffraction (SAED) yielded both a morphological and crystallographic understanding of such processes. As the Ni-Fe LDH nanomaterials are heated in situ, an amorphization occurred at 250 °C, followed by a transition to a heterogeneous structure of NiO particles embedded throughout a NiFe2O4 matrix at 850 °C, confirmed by high-resolution TEM and scanning TEM. Further electron microscopy characterisation methodologies of energy-filtered TEM were utilised to directly observe these mechanistic behaviours in real time, showing an evolution and nucleation to an array of spherical NiO nanoparticles on the platelet surfaces. The versatility of this characterisation approach was verified by the analogous behaviours of Ni-Fe LDH materials heated ex situ as well as parallel in situ TEM and SAED comparisons to that of an akin magnesium-aluminium containing (Mg-Al) LDH structure. The in situ TEM work hereby discussed allows for a state-of-the-art understanding of the Ni-Fe material thermal evolution. This is an important first, which reveals pivotal information, especially when considering LDH applications as catalysts and flame retardants.
Layered double hydroxides: in situ TEM uncovers thermal evolution pathways
In situ transmission electron microscopy unveils the thermal evolution of Ni-Fe and Mg-Al containing layered double hydroxides (LDH). A team led by Valeria Nicolosi at Trinity College Dublin combined transmission electron microscopy with selected area electron diffraction to provide in-depth morphological and crystallographic understanding of the thermal processes occurring when LDH nanomaterials are heated in situ. In Ni-Fe LDH, after an initial amorphisation stage occurring at 250 °C, a transition to NiO particles arranged within a NiFe2O4 trevorite matrix was detected. Larger NiO particles tended to form on the central sections of the platelets, with smaller NiO crystallites arranged on the platelet edge regions. Conversely, Mg-Al containing LDH evolved into Al2O3 and MgAl2O4 structures, with the development of a porous matrix as opposed to the generation of spherical particles.
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1 Trinity College Dublin (TCD), School of Physics, Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705); Trinity College Dublin (TCD), Advanced Materials and Bioengineering Research Centre (AMBER) and Centre for Research of Adaptive Nanostructures and Nanodevices (CRANN), Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705); Trinity College Dublin (TCD), The Advanced Microscopy Laboratory, CRANN, Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705)
2 Trinity College Dublin (TCD), Advanced Materials and Bioengineering Research Centre (AMBER) and Centre for Research of Adaptive Nanostructures and Nanodevices (CRANN), Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705); Trinity College Dublin (TCD), School of Chemistry, Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705)
3 Trinity College Dublin (TCD), Advanced Materials and Bioengineering Research Centre (AMBER) and Centre for Research of Adaptive Nanostructures and Nanodevices (CRANN), Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705); Trinity College Dublin (TCD), The Advanced Microscopy Laboratory, CRANN, Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705)
4 IWKS, Fraunhofer-Project Group Materials Recycling and Resource Strategies, Hanau, Germany (GRID:grid.8217.c)
5 Trinity College Dublin (TCD), School of Physics, Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705); Trinity College Dublin (TCD), The Advanced Microscopy Laboratory, CRANN, Dublin, Ireland (GRID:grid.8217.c) (ISNI:0000 0004 1936 9705)
6 TNO, Department of Materials Solutions, Eindhoven, The Netherlands (GRID:grid.4858.1) (ISNI:0000 0001 0208 7216)
7 ISC, Fraunhofer Institute for Silicate Research, Würzburg, Germany (GRID:grid.424644.4) (ISNI:0000 0004 0495 360X); Julius-Maximilians University Würzburg, Chair of Chemical Technology of Materials Synthesis, Department Chemistry and Pharmacy, Würzburg, Germany (GRID:grid.8379.5) (ISNI:0000 0001 1958 8658)