Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/116980
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Physics | - |
| dc.contributor | Research Institute for Smart Energy | - |
| dc.creator | Li, F | en_US |
| dc.creator | Li, J | en_US |
| dc.creator | Hou, P | en_US |
| dc.creator | Lin, Z | en_US |
| dc.creator | Dong, M | en_US |
| dc.creator | Wang, LH | en_US |
| dc.creator | Zhang, H | en_US |
| dc.creator | Xu, X | en_US |
| dc.date.accessioned | 2026-01-21T03:54:32Z | - |
| dc.date.available | 2026-01-21T03:54:32Z | - |
| dc.identifier.issn | 2041-6520 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/116980 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.rights | © 2025 The Author(s). Published by the Royal Society of Chemistry | en_US |
| dc.rights | This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (http://creativecommons.org/licenses/by-nc/3.0/). | en_US |
| dc.rights | The following publication Li, F., Li, J., Hou, P., Lin, Z., Dong, M., Wang, L.-H., Zhang, H., & Xu, X. (2025). Stabilizing the oxygen anionic redox chemistry using a Li-deficient and Li-rich biphasic structure for high-energy Li-ion batteries [10.1039/D5SC04623H]. Chemical Science, 16(44), 20959-20967 is available at https://doi.org/10.1039/D5SC04623H. | en_US |
| dc.title | Stabilizing the oxygen anionic redox chemistry using a Li-deficient and Li-rich biphasic structure for high-energy Li-ion batteries | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.volume | 16 | en_US |
| dc.identifier.issue | 44 | en_US |
| dc.identifier.doi | 10.1039/d5sc04623h | en_US |
| dcterms.abstract | Li-rich layered oxides (LLOs) with a large specific capacity of ∼300 mAh g−1 show promise for developing high-energy Li-ion batteries (LIBs). However, the thermodynamic instability of the oxygen-anionic redox couple leads to lattice oxygen loss and structural transformation, resulting in a rapid decline in voltage and capacity. In this work, we rationally engineer Li-deficient phase formation in LLOs to stabilize oxygen-anionic redox chemistry and improve structural stability. The Li-deficient and Li-rich biphasic intergrowth composite is synthesized via ion exchange from the P3/O3 intermediate mixed-phase oxides. It is found that the incorporation of the Li-deficient phase makes the movement of the O 2p non-bonding energy band toward lower energy, which further alleviates the lattice oxygen release and stabilizes the oxygen-anionic redox chemistry upon Li+ de-intercalation. Consequently, the cycling stability is significantly enhanced in the biphasic LLOs, retaining superior capacity/voltage retention of ∼86%/88% after 400 cycles with a low capacity decay rate of 0.034% and voltage decline of 1.06 mV per cycle. The biphasic design offers a simple and feasible strategy for regulating the oxygen-anionic redox chemistry and boosting the structural stability of high-capacity LLOs. | - |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Chemical science, 28 Nov. 2025, v. 16, no. 44, 20959 | en_US |
| dcterms.isPartOf | Chemical science | en_US |
| dcterms.issued | 2025-11-28 | - |
| dc.identifier.eissn | 2041-6539 | en_US |
| dc.identifier.artn | 20959 | en_US |
| dc.description.validate | 202601 bcch | - |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | OA_Scopus/WOS | - |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | This work was funded by the National Natural Science Foundation of China (No. 22379052 and 22479112), the Taishan Scholars of Shandong Province (No. tsqn202507210 and tsqnz20221143), and the Tianjin Science & Technology Program (No. 22YFYSHZ00220). | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.oaCategory | CC | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| d5sc04623h.pdf | 1.53 MB | Adobe PDF | View/Open |
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