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Engineering the metathesis and oxidation-reduction reaction in solid state at room temperature for nanosynthesis
It is a long-standing goal to explore convenient synthesis methodology for functional materials. Recently, several multiple-step approaches have been designed for photocatalysts Ag(n)X@Ag (X = Cl(−), PO(4)(3−), etc.), mainly containing the ion-exchange (metathesis) reaction followed by photoreductio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948356/ https://www.ncbi.nlm.nih.gov/pubmed/24614918 http://dx.doi.org/10.1038/srep04153 |
Sumario: | It is a long-standing goal to explore convenient synthesis methodology for functional materials. Recently, several multiple-step approaches have been designed for photocatalysts Ag(n)X@Ag (X = Cl(−), PO(4)(3−), etc.), mainly containing the ion-exchange (metathesis) reaction followed by photoreduction in solution. But they were obsessed by complicated process, the uncontrollability of composition and larger sizes of Ag particles. Here we show a general solid-state route for the synthesis of Ag(n)X@Ag catalysts with hierarchical structures. Due to strong surface plasmon resonance of silver nanoparticles with broad shape and size, the Ag(n)X@Ag showed high photocatalytic activity in visible region. Especially, the composition of Ag(n)X@Ag composites could be accurately controlled by regulating the feed ratio of (NH(2)OH)(2)·H(2)SO(4) to anions, by which the performance were easily optimized. Results demonstrate that the metathesis and oxidation-reduction reactions can be performed in solid state at room temperature for nanosynthesis, greatly reducing the time/energy consumption and pollution. |
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