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The oriented attachment (OA) of nanoparticles is an important mechanism for the synthesis of the crystals of inorganic functional materials, and the formation of natural minerals. For years it has been generally acknowledged that OA is a physical process, i.e., particle alignments and interface fusion via mass diffusion, not involving the formation of new substances. Hence, the obtained crystals maintain identical crystallographic structures and chemical constituents to those of the precursor particles. Here we report a chemical reaction directed OA growth, through which Y2(CO3)3.2H2O nanoparticles are converted to single-crystalline double-carbonates (e.g., NaY(CO3)2.6H2O). The dominant role of OA growth is supported by our first-principles calculations. Such a new OA mechanism enriches the aggregation-based crystal growth theory.
Oriented attachment (OA) has become a well-recognized mechanism for the growth of metal, ceramic, and biomineral crystals. While many computational and experimental studies of OA have shown that particles can attach with some misorientation then rota
Photoluminescence spectra of YVO$_{4}$:Eu$^{3+}$ nanoparticles are presented,with and without the attachment of of organic linker molecules that are proposed for linking to biomolecules. YVO$_{4}$:Eu$^{3+}$ nanoparticles with 5% dopant concentration
The ability to synthesis well-ordered two-dimensional materials under ultra-high vacuum and directly characterize them by other techniques in-situ can greatly advance our current understanding on their physical and chemical properties. In this paper,
We perform a systematic first-principles study of phosphorene in the presence of typical monovalent (hydrogen, fluorine) and divalent (oxygen) impurities. The results of our modeling suggest a decomposition of phosphorene into weakly bonded one-dimen
Cobalt carbide nanoparticles were processed using polyol reduction chemistry that offers high product yields in a cost effective single-step process. Particles are shown to be acicular in morphology and typically assembled as clusters with room tempe