Quantitative 3D evolution of colloidal nanoparticle oxidation in solution

Author:

Sun Yugang1ORCID,Zuo Xiaobing2ORCID,Sankaranarayanan Subramanian K. R. S.3ORCID,Peng Sheng3,Narayanan Badri3ORCID,Kamath Ganesh3

Affiliation:

1. Department of Chemistry, Temple University, 1901 North 13th Street, Philadelphia, PA 19122, USA.

2. X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, USA.

3. Center for Nanoscale Materials, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439, USA.

Abstract

Watching nanomaterials transform in time Real-time analysis of chemical transformations of nanoparticles is usually done with electron microscopy of a few particles. One limitation is interference by the electron beam. Sun et al. monitored the oxidation of iron nanoparticles in solution by using small- and wide-angle x-ray scattering and molecular dynamics simulations (see the Perspective by Cadavid and Cabot). These methods revealed the formation of voids within the nanoparticles, diffusion of material into and out of the nanoparticles, and ultimately the coalescence of the voids. Science , this issue p. 303 ; see also p. 245

Funder

U.S. Department of Energy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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