4.8 Article

Cluster defects in gibbsite nanoplates grown at acidic to neutral pH

Journal

NANOSCALE
Volume 13, Issue 41, Pages 17373-17385

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nr01615f

Keywords

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Funding

  1. IDREAM (Interfacial Dynamics in Radioactive Environments and Materials), an Energy Frontier Research Center - U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES)
  2. Office of Biological and Environmental Research at Pacific Northwest National Laboratory (PNNL) [grid.436923.9]
  3. DOE by Battelle Memorial Institute operating [DE-AC05-76RL0-1830]
  4. BES Chemical Sciences, Geosciences, & Biosciences (CSGB) Division
  5. DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]

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Gibbsite is a common mineral phase with many industrial applications, serving as the solubility limiting phase for aluminum over a wide pH range. By examining defects in gibbsite nanoplates and recrystallizing them in highly alkaline solutions, it has been shown that the crystallinity can be gradually improved and most defects eliminated, highlighting a possible cluster-mediated growth mechanism.
Gibbsite [alpha-Al(OH)(3)] is the solubility limiting phase for aluminum across a wide pH range, and it is a common mineral phase with many industrial applications. The growth mechanism of this layered-structure material, however, remains incompletely understood. Synthesis of gibbsite at low to circumneutral pH yields nanoplates with substantial interlayer disorder. Here we examine defects in this material in detail, and the effects of recrystallization in highly alkaline sodium hydroxide solution at 80 degrees C. We employed a multimodal approach, including scanning electron microscopy, magic-angle spinning nuclear magnetic resonance (MAS-NMR), Raman and infrared spectroscopies, X-ray diffraction (XRD), and X-ray total scattering pair distribution function (XPDF) analysis to characterize the ageing of the nanoplates over several days. XRD and XPDF indicate that gibbsite nanoplates precipitated at circumneutral pH contain dense, truncated sheets imparting a local difference in interlayer distance. These interlayer defects appear well described by flat Al-13 aluminum hydroxide nanoclusters nearly isostructural with gibbsite sheets present under synthesis conditions and trapped as interlayer inclusions during growth. Ageing at elevated temperature in alkaline solutions gradually improves crystallinity, showing a gradual increase in H-bonding between interlayer OH groups. Between 7 to 8 vol% of the initial gibbsite nanoparticles exhibit this defect, with the majority of differences disappearing after 2-4 hours of recrystallization in alkaline solution. The results not only identify the source of disorder in gibbsite formed under acidic/neutral conditions but also point to a possible cluster-mediated growth mechanism evident through inclusion of relict oligomers with gibbsite-like topology trapped in the interlayer spaces.

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