Regulation of Anion Redox Activity via Solid‐Acid Modification for Highly Stable Li‐Rich Mn‐Based Layered Cathodes

Author:

Wei Han‐xin12,Liu Yu‐ming12,Luo Yu‐hong12,Huang Ying‐de12,Tang Lin‐bo123,Wang Zhen‐yu12,Yan Cheng4,Mao Jing5,Dai Ke‐hua6,Wu Qing7,Zhang Xia‐hui12,Zheng Jun‐chao12ORCID

Affiliation:

1. School of Metallurgy and Environment Central South University Changsha Hunan 410083 P. R. China

2. Engineering Research Center of the Ministry of Education for Advanced Battery Materials Central South University Changsha Hunan 410083 P. R. China

3. Hunan Provincial Key Laboratory of Chemical Power Sources College of Chemistry and Chemical Engineering Central South University Changsha Hunan 410083 P. R. China

4. School of Mechanical Medical and Process Engineering Queensland University of Technology Brisbane Queensland 4001 Australia

5. School of Materials Science and Engineering Zhengzhou University Zhengzhou Henan 450001 P. R. China

6. College of Chemistry Tianjin Normal University Tianjin 300387 P. R. China

7. School of Information and Network Center Central South University Changsha Hunan 410083 P. R. China

Abstract

AbstractAnionic redox activity can trigger structural instability in Li‐rich Mn‐based cathodes. Lattice oxygen activity can be tuned through liquid acid‐induced spinel phases and oxygen vacancies. However, the liquid‐acid‐modified surface is still attacked by the electrolyte. Besides, the underlying mechanism of spinel phase suppression of lattice oxygen activity is controversial. Here, a solid acid strategy for modification is proposed and the underlying mechanism is investigated in detail. Unique solid acid can in situ generate an interface protection layer and remarkably stabilize the structure. Theoretical calculations and experimental characterizations reveal that the spinel phase suppresses the irreversible loss of lattice oxygen by decreasing the O 2p non‐bonding energy level and enriching electrons at the layered/spinel phase interface. The inert layer on the surface prevents highly active On− from being attacked by electrolytes. The obtained material exhibits significantly reduced irreversible lattice oxygen release and improved electrochemical performance. After 300 cycles, a slow capacity fading of 0.177 mAh g−1 per cycle and suppressed voltage fading are achieved. This study reveals the regulation method and mechanism for the anion activity of oxide cathodes in next‐generation Li‐ion batteries.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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