Synthesis and characterization of nanoparticulate MnS within the pores of mesoporous silica.

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TY  - JOUR
  - Barry, L.,Copley, M.,Holmes, J. D.,Otway, D. J.,Kazakova, O.,Morris, M. A.
  - 2007
  - December
  - Journal of Solid State Chemistry
  - Synthesis and characterization of nanoparticulate MnS within the pores of mesoporous silica.
  - Validated
  - ()
  - 180
  - 12
  - 3443
  - 3449
  - Mesoporous silica was loaded with nanoparticulate MnS via a simple post-synthesis treatment. The mesoporous material that still contained surfactant was passivated to prevent MnS formation at the surface. The surfactant was extracted and a novel manganese ethylxanthate was used to impregnate the pore network. This precursor thermally decomposes to yield MnS particles that are smaller or equal to the pore size. The particles exhibit all three common polyrnorphs. The passivation treatment is most effective at lower loadings because at the highest loadings (SiO2:MnS molar ratio of 6:1) large particles (> 50 nm) form at the exterior of the mesoporous particles. The integrity of the mesoporous network is maintained through the preparation and high order is maintained. The MnS particles exhibit unexpected ferromagnetism at low temperatures. Strong luminescence of these samples is observed and this suggests that they may have a range of important application areas. (C) 2007 Elsevier Inc. All rights reserved.
  - 0022-4596
  - ://000251841100015
DA  - 2007/12
ER  - 
@article{V16860743,
   = {Barry,  L. and Copley,  M. and Holmes,  J. D. and Otway,  D. J. and Kazakova,  O. and Morris,  M. A. },
   = {2007},
   = {December},
   = {Journal of Solid State Chemistry},
   = {Synthesis and characterization of nanoparticulate MnS within the pores of mesoporous silica.},
   = {Validated},
   = {()},
   = {180},
   = {12},
  pages = {3443--3449},
   = {{Mesoporous silica was loaded with nanoparticulate MnS via a simple post-synthesis treatment. The mesoporous material that still contained surfactant was passivated to prevent MnS formation at the surface. The surfactant was extracted and a novel manganese ethylxanthate was used to impregnate the pore network. This precursor thermally decomposes to yield MnS particles that are smaller or equal to the pore size. The particles exhibit all three common polyrnorphs. The passivation treatment is most effective at lower loadings because at the highest loadings (SiO2:MnS molar ratio of 6:1) large particles (> 50 nm) form at the exterior of the mesoporous particles. The integrity of the mesoporous network is maintained through the preparation and high order is maintained. The MnS particles exhibit unexpected ferromagnetism at low temperatures. Strong luminescence of these samples is observed and this suggests that they may have a range of important application areas. (C) 2007 Elsevier Inc. All rights reserved.}},
  issn = {0022-4596},
   = {://000251841100015},
  source = {IRIS}
}
AUTHORSBarry, L.,Copley, M.,Holmes, J. D.,Otway, D. J.,Kazakova, O.,Morris, M. A.
YEAR2007
MONTHDecember
JOURNAL_CODEJournal of Solid State Chemistry
TITLESynthesis and characterization of nanoparticulate MnS within the pores of mesoporous silica.
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME180
ISSUE12
START_PAGE3443
END_PAGE3449
ABSTRACTMesoporous silica was loaded with nanoparticulate MnS via a simple post-synthesis treatment. The mesoporous material that still contained surfactant was passivated to prevent MnS formation at the surface. The surfactant was extracted and a novel manganese ethylxanthate was used to impregnate the pore network. This precursor thermally decomposes to yield MnS particles that are smaller or equal to the pore size. The particles exhibit all three common polyrnorphs. The passivation treatment is most effective at lower loadings because at the highest loadings (SiO2:MnS molar ratio of 6:1) large particles (> 50 nm) form at the exterior of the mesoporous particles. The integrity of the mesoporous network is maintained through the preparation and high order is maintained. The MnS particles exhibit unexpected ferromagnetism at low temperatures. Strong luminescence of these samples is observed and this suggests that they may have a range of important application areas. (C) 2007 Elsevier Inc. All rights reserved.
PUBLISHER_LOCATION
ISBN_ISSN0022-4596
EDITION
URL://000251841100015
DOI_LINK
FUNDING_BODY
GRANT_DETAILS