Ni@Ag core shell nanowires (NWs) were prepared by in situ chemical reduction of Ag around NiNWs as the inner core. Different Ni@Ag NWs with controllable morphologies were achieved through the layer-plus-island growth mode and this mechanism was confirmed by scanning electron microscopy, X-ray fluorescence, and X-ray photoelectron spectroscopy analyses. When used as a catalyst, the synthesized Ni@Ag NWs exhibited high reduction efficiency by showing a high reaction rate constant k of 0.408 s in reducing 4-nitrophenol at room temperature. Besides, combining the magnetic property, including high saturation magnetization and low coercivity, the magnetic NiNW core contributes to excellent recyclability and long-term stability with only a 2.2% performance loss after 10 recycles by magnets. The Ni@Ag NWs proposed here show unprecedentedly high potential in applications requiring high efficiency and a recyclable catalyst.
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http://dx.doi.org/10.1088/1361-6528/ab27ce | DOI Listing |
Nanotechnology
September 2019
State Key Lab of Silicon Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, Zhejiang province, 310027, People's Republic of China.
Ni@Ag core shell nanowires (NWs) were prepared by in situ chemical reduction of Ag around NiNWs as the inner core. Different Ni@Ag NWs with controllable morphologies were achieved through the layer-plus-island growth mode and this mechanism was confirmed by scanning electron microscopy, X-ray fluorescence, and X-ray photoelectron spectroscopy analyses. When used as a catalyst, the synthesized Ni@Ag NWs exhibited high reduction efficiency by showing a high reaction rate constant k of 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2016
Department of Chemistry, Duke University, Durham, North Carolina 27708-0354, United States.
We demonstrate a one-pot, low-cost, and scalable method for fast synthesis of superfine and uniform core-shell Cu nanowires (NWs) coated with optional metals and/or alloy. Cu NWs in high aspect ratio (>3000) were synthesized through an oleylamine-mediated solution method, and tunable shell coating was performed by injecting metal-organic precursors at the last stage of reaction. Superfine Cu@metal NWs (Ti, Zn, V, Ni, Ag, NiZn, etc) were achieved in diameter of ∼30 nm and length of ∼50 μm.
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