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@ARTICLE{Vegso:207257,
      author       = {Vegso, Karol and Siffalovic, Peter and Jergel, Matej and
                      Weis, Martin and Majkova, Eva and Luby, Stefan and Capek,
                      Ignac and Buffet, Adeline and Roth, Stephan V.},
      title        = {{A} {N}on-{E}quilibrium {T}ransient {P}hase {R}evealed by
                      in {S}itu {GISAXS} {T}racking of the {S}olvent-{A}ssisted
                      {N}anoparticle {S}elf-{A}ssembly},
      journal      = {Journal of nanoparticle research},
      volume       = {16},
      number       = {8},
      issn         = {1572-896X},
      address      = {Dordrecht [u.a.]},
      publisher    = {Springer Science + Business Media B.V},
      reportid     = {PUBDB-2015-01240},
      pages        = {2536},
      year         = {2014},
      note         = {(c) Springer Science+Business Media Dordrecht},
      abstract     = {We report on a time-resolved study of the colloidal
                      nanoparticle self-assembly into a high-quality nanoparticle
                      crystal with the face-centered cubic crystallographic
                      symmetry. In particular, the grazing-incidence small-angle
                      X-ray scattering technique was employed to track kinetics of
                      the solvent evaporation driven self-assembly on casting a
                      drop of plasmonic Ag nanoparticles on a silicon substrate.
                      The short-range (cumulative) disorder typical for
                      paracrystal structures before the complete solvent
                      evaporation at 300–350 s from the drop casting was found
                      with the exception of the time window of 125–150 s where a
                      highly regular transient phase with the long-range order was
                      observed. This temporary improvement of the nanoparticle
                      crystal perfection occurring shortly before the complete
                      solvent evaporation is the main message of the paper. It is
                      attributed to interaction between the surfactant shells of
                      the neighboring nanoparticles getting into contact in the
                      presence of solvent residua to the end of the solvent
                      evaporation which results in a larger nanoparticle
                      hydrodynamic diameter with a smaller dispersion and
                      improvement of the crystallization. This process has direct
                      impact on the quality of the resulting nanoparticle crystal
                      and tailoring its properties.},
      cin          = {DOOR / FS-PE},
      ddc          = {570},
      cid          = {I:(DE-H253)HAS-User-20120731 / I:(DE-H253)FS-PE-20120731},
      pnm          = {PETRA Beamline P03 (POF2-54G14)},
      pid          = {G:(DE-H253)POF2-P03-20130405},
      experiment   = {EXP:(DE-H253)P-P03-20150101},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000339338800001},
      doi          = {10.1007/s11051-014-2536-6},
      url          = {https://bib-pubdb1.desy.de/record/207257},
}