Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/116980
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dc.contributorDepartment of Applied Physics-
dc.contributorResearch Institute for Smart Energy-
dc.creatorLi, Fen_US
dc.creatorLi, Jen_US
dc.creatorHou, Pen_US
dc.creatorLin, Zen_US
dc.creatorDong, Men_US
dc.creatorWang, LHen_US
dc.creatorZhang, Hen_US
dc.creatorXu, Xen_US
dc.date.accessioned2026-01-21T03:54:32Z-
dc.date.available2026-01-21T03:54:32Z-
dc.identifier.issn2041-6520en_US
dc.identifier.urihttp://hdl.handle.net/10397/116980-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© 2025 The Author(s). Published by the Royal Society of Chemistryen_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (http://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe 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.titleStabilizing the oxygen anionic redox chemistry using a Li-deficient and Li-rich biphasic structure for high-energy Li-ion batteriesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume16en_US
dc.identifier.issue44en_US
dc.identifier.doi10.1039/d5sc04623hen_US
dcterms.abstractLi-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.accessRightsopen accessen_US
dcterms.bibliographicCitationChemical science, 28 Nov. 2025, v. 16, no. 44, 20959en_US
dcterms.isPartOfChemical scienceen_US
dcterms.issued2025-11-28-
dc.identifier.eissn2041-6539en_US
dc.identifier.artn20959en_US
dc.description.validate202601 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis 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.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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