4.8 Article

Formation of Single-Walled Aluminosilicate Nanotubes from Molecular Precursors and Curved Nanoscale Intermediates

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 133, 期 14, 页码 5397-5412

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja111055q

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资金

  1. NSF [CBET-0846586]
  2. DFG [SCHE 524/9]
  3. Div Of Chem, Bioeng, Env, & Transp Sys
  4. Directorate For Engineering [0846586] Funding Source: National Science Foundation

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We report the identification and elucidation of the mechanistic role of molecular precursors and nanoscale (1-3 nm) intermediates with intrinsic curvature in the formation of single-walled aluminosilicate nanotubes. We characterize the structural and compositional evolution of molecular and nanoscale species over a length scale of 0.1-100 nm by electrospray ionization mass spectrometry, nuclear magnetic resonance spectroscopy (Al-27 liquid-state, Al-27 and Si-29 solid-state MAS), and dynamic light scattering. Together with structural optimization of key experimentally identified species by solvated density functional theory calculations, this study reveals the existence of intermediates with bonding environments, as well as intrinsic curvature, similar to the structure of the final nanotube product. We show that proto-nanotube-like intermediates with inherent curvature form in aqueous synthesis solutions immediately after initial hydrolysis of reactants, disappear from the solution upon heating to 95 degrees C due to condensation accompanied by an abrupt pH decrease, and finally form ordered single-walled aluminosilicate nanotubes. Detailed quantitative analysis of NMR and ESI-MS spectra from the relevant aluminosilicate, aluminate, and silicate solutions reveals the presence of a variety of monomeric and polymeric aluminate and aluminosilicate species (Al1Six-Al13Six), such as Keggin ions [AlO4Al12(OH)(24)(H2O)(12)](7+) and polynuclear species with a six-membered Al oxide ring unit. Our study also directly reveals the complexation of aluminate and aluminosilicate species with perchlorate species that most likely inhibit the formation of larger condensates or nontubular structures. Integration of all of our results leads to the construction of the first molecular-level mechanism of single-walled metal oxide nanotube formation, incorporating the role of monomeric and polymeric aluminosilicate species as well as larger nanoparticles.

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