4.7 Article

Phase Progression of γ-Al2O3 Nanoparticles Synthesized in a Solvent-Deficient Environment

Journal

INORGANIC CHEMISTRY
Volume 52, Issue 8, Pages 4411-4423

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic302593f

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  2. U.S. Department of Energy [DE-FG02-05ER15666]
  3. National Science Foundation [CHE-0959862]

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Our simple and uniquely cost-effective solvent-deficient synthetic method produces 3-5 nm Al2O3 nanoparticles which show promise as improved industrial catalyst supports. While catalytic applications are sensitive to the details of the atomic structure, a diffraction analysis of alumina nanoparticles is challenging because of extreme size/rnicrostrain-related peak broadening and the similarity of the diffraction patterns of various transitional Al2O3 phases. Here, we employ a combination of X-ray pair-distribution function (PDF) and Rietveld methods, together with solid-state NMR and thermogravimetry/differential thermal analysis-mass spectrometry (TG/DTA-MS), to characterize the alumina phase-progression in our nanoparticles as a function of calcination temperature between 300 and 1200 degrees C. In the solvent-deficient synthetic environment, a boehmite precursor phase forms which transitions to gamma-Al2O3 at an extraordinarily low temperature (below 300 degrees C), but this gamma-Al2O3 is initially riddled with boehmite-like stacking-fault defects that steadily disappear during calcination in the range from 300 to 950 degrees C. The healing of these defects accounts for many of the most interesting and widely reported properties of the gamma-phase.

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