Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/100276
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Physics | - |
| dc.creator | Wang, S | en_US |
| dc.creator | Niu, S | en_US |
| dc.creator | Li, H | en_US |
| dc.creator | Lam, KK | en_US |
| dc.creator | Wang, Z | en_US |
| dc.creator | Du, P | en_US |
| dc.creator | Leung, CW | en_US |
| dc.creator | Qu, S | en_US |
| dc.date.accessioned | 2023-08-08T01:54:30Z | - |
| dc.date.available | 2023-08-08T01:54:30Z | - |
| dc.identifier.issn | 0957-4484 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/100276 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Institute of Physics Publishing | en_US |
| dc.rights | © 2019 IOP Publishing Ltd | en_US |
| dc.rights | This is the Accepted Manuscript version of an article accepted for publication in Nanotechnology. IOP Publishing Ltd is not responsible for any errors or omissions in this version of the manuscript or any version derived from it. The Version of Record is available online at https://doi.org/10.1088/1361-6528/ab27ce. | en_US |
| dc.rights | This manuscript version is made available under the CC-BY-NC-ND 4.0 license (https://creativecommons.org/licenses/by-nc-nd/4.0/). | en_US |
| dc.subject | Catalyst | en_US |
| dc.subject | Core shell | en_US |
| dc.subject | High efficiency | en_US |
| dc.subject | Nanowires | en_US |
| dc.subject | Recyclability | en_US |
| dc.title | Synthesis and controlled morphology of Ni@Ag core shell nanowires with excellent catalytic efficiency and recyclability | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.volume | 30 | en_US |
| dc.identifier.issue | 38 | en_US |
| dc.identifier.doi | 10.1088/1361-6528/ab27ce | en_US |
| dcterms.abstract | 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-1 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. | - |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Nanotechnology, 20 Sept. 2019, v. 30, no. 38, 385603 | en_US |
| dcterms.isPartOf | Nanotechnology | en_US |
| dcterms.issued | 2019-09-20 | - |
| dc.identifier.scopus | 2-s2.0-85069799156 | - |
| dc.identifier.pmid | 31174195 | - |
| dc.identifier.eissn | 1361-6528 | en_US |
| dc.identifier.artn | 385603 | en_US |
| dc.description.validate | 202308 bcvc | - |
| dc.description.oa | Accepted Manuscript | en_US |
| dc.identifier.FolderNumber | AP-0302 | - |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | The National Natural Science Foundation of China; The Zhejiang Provincial Natural Science Foundation | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.identifier.OPUS | 26960562 | - |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Lam_Synthesis_Controlled_Morphology.pdf | Pre-Published version | 709.15 kB | Adobe PDF | View/Open |
Page views
68
Citations as of Apr 14, 2025
Downloads
62
Citations as of Apr 14, 2025
SCOPUSTM
Citations
9
Citations as of Dec 19, 2025
WEB OF SCIENCETM
Citations
9
Citations as of Dec 18, 2025
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



