Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Ultrathin two-dimensional (2D) nanomaterials have attracted intense research efforts due to their extraordinary optoelectronic properties. However, the nucleation and growth mechanisms of 2D colloidal nanosheets are still poorly understood. Here, we follow the formation of ultrathin colloidal Cu 2– x S nanosheets by in situ small-angle X-ray scattering. While thermal decomposition of copper–dodecanethiolates produces spheroidal Cu 2–x S nanocrystals, the addition of chloride to the reaction mixture results in 2 nm thick Cu 2–x S nanosheets with well-defined shape and size. Our results show that chloride stabilizes stacks of lamellar copper–thiolate supramolecular complexes, so that they remain intact beyond the onset of Cu 2– x S nucleation at 230 °C, leading to 2D-constrained stack-templated nucleation and growth. The face-to-face stacking of the nanosheets reinforces the 2D constraints imposed by the lamellar soft template, since it prevents internanosheet mass transport and nanosheet coalescence, thereby inhibiting growth in the thickness direction and allowing only for lateral growth. Our work thus provides novel insights into soft-templating formation mechanisms of ultrathin colloidal nanosheets, which may be exploited for other metal sulfide compositions.
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Affiliations
Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Post Office Box 80000, 3508 TA Utrecht, The Netherlands
Beamline ID02, European Synchrotron Radiation Facility, 71 avenue des Martyrs, 38000 Grenoble, France
Physical and Colloid Chemistry, Debye Institute for Nanomaterials Science, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands
Laboratory of Physical Chemistry, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, Post Office Box 513, 5600 MB Eindhoven, The Netherlands
Funding
Nederlandse Organisatie voor Wetenschappelijk Onderzoek