4.7 Article

Hydrogen bonding directed co-assembly of polyoxometalates and polymers to core-shell nanoparticles

期刊

MATERIALS CHEMISTRY FRONTIERS
卷 2, 期 11, 页码 2070-2075

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8qm00291f

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资金

  1. Program for Guangdong Introducing Innovative and Entrepreneurial Teams [2016ZT06C322]
  2. Thousand Talents Plan for Young Professionals from Chinese Government
  3. South China University of Technology
  4. NSF [CHE1607138]
  5. University of Akron
  6. DOE Office of Science, Argonne National Laboratory [DE-AC02-06CH11357]
  7. Laboratory Directed Research and Development (LDRD) from Argonne National Laboratory
  8. Office of Science, of the U.S. Department of Energy [DE-AC02-06CH11357]

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A general strategy has been developed here to co-assemble polyoxometalates (POMs) and polymers into core-shell hybrid nanoparticles via hydrogen bonding interaction. Due to the hydrogen bonds between the pyridine groups of poly(4-vinyl pyridine) (P4VP) and the hydrogen bonding donor groups on the POM surface, P4VP is stabilized by the POMs and dispersed as discrete hybrid core-shell nanoparticles in aqueous solution. For these thermodynamically stable nanoparticles, the P4VP cores are covered with hexagonal close-packed POMs. The size of the core-shell particles is controlled by the electrostatic repulsive interaction among the POMs. The introduction of extra salts screens the repulsive force among the POMs, thus increasing the size of the core-shell structures.

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