説明:
(abstract)Cation-disordered rocksalt oxides offer broad compositional flexibility and high theoretical capacities, but their electrochemical performance is often limited by uncontrolled competition between transition-metal and oxygen redox processes. In particular, controlling the balance between Mn and O redox activity remains a key challenge in Mn-based disordered oxides.
Here, a previously unexplored compositional space in the Li–Mn–Mo–O system is investigated, revealing that Mo incorporation systematically alters the electronic structure and redox behavior of Mn-based disordered rocksalt oxides. Mo doping lowers the average Mn oxidation state, thereby stabilizing a Mn-dominated charge compensation mechanism. Combined spectroscopic characterization and first-principles calculations reveal a shift in charge compensation from oxygen-centered to Mn-centered redox processes with Mo doping. As a result, Li1.25Mn0.5Mo0.25O2 delivers a reversible capacity exceeding 300 mAh g−¹ with enhanced electrochemical stability.
These findings demonstrate that targeted compositional and electronic-structure modulation enables effective control of redox pathways in cation-disordered oxides and offers design principles for stable, high-capacity Mn-based cathode materials.
権利情報:
キーワード: Manganese-Based Disordered Rocksalt Cathodes, Li-rich cathode materials, Cathode materials for Solid-state batteries
刊行年月日: 2026-06-09
出版者: American Chemical Society (ACS)
掲載誌:
研究助成金:
原稿種別: 出版者版 (Version of record)
MDR DOI:
公開URL: https://doi.org/10.1021/acs.chemmater.6c00304
関連資料:
その他の識別子:
連絡先:
更新時刻: 2026-07-10 10:06:40 +0900
MDRでの公開時刻: 2026-07-10 12:26:36 +0900
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Chem. Mater. 2026, 38, 5579-5587.pdf
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サイズ | 4.93MB | 詳細 |