Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/98950
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Physics | en_US |
| dc.contributor | Research Institute for Smart Energy | en_US |
| dc.creator | Wang, J | en_US |
| dc.creator | Guo, X | en_US |
| dc.creator | Du, X | en_US |
| dc.creator | Liang, J | en_US |
| dc.creator | Wu, J | en_US |
| dc.creator | Zhao, G | en_US |
| dc.creator | Li, X | en_US |
| dc.creator | Gui, S | en_US |
| dc.creator | Zheng, F | en_US |
| dc.creator | Zhao, J | en_US |
| dc.creator | Xu, C | en_US |
| dc.creator | Wang, D | en_US |
| dc.creator | Yang, H | en_US |
| dc.creator | Zhang, B | en_US |
| dc.creator | Zhu, Y | en_US |
| dc.date.accessioned | 2023-06-06T00:55:16Z | - |
| dc.date.available | 2023-06-06T00:55:16Z | - |
| dc.identifier.issn | 2405-8297 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/98950 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier | en_US |
| dc.rights | © 2022 Elsevier B.V. All rights reserved. | en_US |
| dc.rights | © 2022. 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.rights | The following publication Wang, J., Guo, X., Du, X., Liang, J., Wu, J., Zhao, G., ... & Zhu, Y. (2022). Revealing the complex lithiation pathways and kinetics of core-shell NiO@ CuO electrode. Energy Storage Materials, 51, 11-18 is available at https://doi.org/10.1016/j.ensm.2022.06.022. | en_US |
| dc.subject | Ex/in situ electron microscopy | en_US |
| dc.subject | Lithium ion batteries | en_US |
| dc.subject | Lithium pathways | en_US |
| dc.subject | Nickel/copper oxides electrodes | en_US |
| dc.subject | Reaction kinetics | en_US |
| dc.title | Revealing the complex lithiation pathways and kinetics of core-shell NiO@CuO electrode | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 11 | en_US |
| dc.identifier.epage | 18 | en_US |
| dc.identifier.volume | 51 | en_US |
| dc.identifier.doi | 10.1016/j.ensm.2022.06.022 | en_US |
| dcterms.abstract | Nanostructured composite electrodes with multiple active phases offer extraordinary performance that can be harnessed in future batteries. However, it is difficult to disclose the complicated reaction pathways. In this work, NiO@CuO core-shell nanocomposites are prepared and used as anodes for lithium-ion batteries, with superior rate and stability performance compared with single-phase CuO and NiO. Using a combination of in situ and ex situ electron microscopy, a two-stage lithiation reaction pathway on NiO@CuO is identified, with CuO reduced to Cu2O first and followed by the simultaneous reduction of both Cu2O and NiO to metals, resolving the existing inconsistency in literature. Chemomechanical simulation further discloses the key role of the core-shell structure in high cycling stability of NiO@CuO, which decreases the probability of cracking during the discharge-charge process. This work provides new insights to explore lithiation mechanisms and kinetics in novel electrodes, which contribute to further development of various electrode materials. | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Energy storage materials, Oct. 2022, v. 51, p. 11-18 | en_US |
| dcterms.isPartOf | Energy storage materials | en_US |
| dcterms.issued | 2022-10 | - |
| dc.identifier.scopus | 2-s2.0-85132836553 | - |
| dc.identifier.eissn | 2405-8289 | en_US |
| dc.description.validate | 202306 bcww | en_US |
| dc.description.oa | Accepted Manuscript | en_US |
| dc.identifier.FolderNumber | a2076 | - |
| dc.identifier.SubFormID | 46473 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Wang_Revealing_Complex_Lithiation.pdf | Pre-Published version | 3.43 MB | Adobe PDF | View/Open |
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