Unlocking the origins of highly reversible lithium storage and stable cycling in a spinel high-entropy oxide anode for lithium-ion batteries
Creators
- 1. SEU‐FEI Nano‐Pico Center, Key Laboratory of MEMS of the Ministry of Education, Southeast University, Nanjing, 210096 (China)
- 2. School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore, 639798 (Singapore)
- 3. Electron Microscope Laboratory, Nanjing Forestry University, Nanjing, 210037 (China)
- 4. CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002 (China)
- 5. i‐Lab, CAS Center for Excellence in Nanoscience, Suzhou Institute of Nano‐Tech and Nano‐Bionics, Chinese Academy of Sciences, Suzhou, 215123 (China)
- 6. Key Laboratory of Multifunctional Nanomaterials and Smart Systems, Suzhou Institute of Nano‐Tech and Nano‐Bionics, Chinese Academy of Sciences, Suzhou, 215123 (China)
- 7. State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen, Fujian, 361005 (China)
Description
Developing high-capacity conversion-type anodes with superior durability substituting conventional graphite anodes is urgently desired to improve the energy density of lithium-ion batteries (LIBs). However, fatal capacity decay during cycling of the conversion-type anodes, which is primarily due to their inevitable structural degradation and continuous solid-electrolyte interphase reformation induced by drastic volume change, has highly restricted their commercialization. And, the interrelated effects of phase transformation, structural evolution, and electrochemical characteristics of the conversion-type anodes during cycling remain poorly understood. Herein, the findings on the fabrication and understanding of a previously unexplored entropy-stabilized spinel oxide, (CoMnVFeZn)O as a promising conversion anode for LIBs, exhibiting not only moderate volume change character but also highly reversible capacities of ≈900 mAh g for 500 cycles at 0.2 A g and ≈500 mAh g for 2000 cycles at 3 A g, respectively, are reported. Evidenced by in situ transmission electron microscopy coupled with theoretical calculations, its underlying mechanism underpinning highly reversible Li storage is explicitly revealed, which originates from reversible phase transformation and domain reconstruction during cycling. Moreover, the origin of small volume change is also clearly clarified. This work provides renewed mechanistic insights into designing high-capacity and durable conversion-type electrode materials for high-performance LIBs. (© 2023 Wiley‐VCH GmbH)
Additional details
Identifiers
Publishing Information
- Journal Title
- Advanced Functional Materials (Internet)
- Journal Volume
- 34
- Journal Issue
- 4
- Journal Page Range
- p. 1-13
- ISSN
- 1616-3028
- CODEN
- AFMDC6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 55022418
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S25: ENERGY STORAGE;
- Descriptors DEI
- ANODES; CAPACITY; COBALT OXIDES; ENTROPY; IRON OXIDES; LITHIUM ION BATTERIES; MANGANESE OXIDES; PHASE TRANSFORMATIONS; SPINELS; TRANSMISSION ELECTRON MICROSCOPY; VANADIUM OXIDES; ZINC OXIDES
- Descriptors DEC
- CHALCOGENIDES; COBALT COMPOUNDS; ELECTRIC BATTERIES; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTRON MICROSCOPY; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; IRON COMPOUNDS; MANGANESE COMPOUNDS; MICROSCOPY; MINERALS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHYSICAL PROPERTIES; THERMODYNAMIC PROPERTIES; TRANSITION ELEMENT COMPOUNDS; VANADIUM COMPOUNDS; ZINC COMPOUNDS
Optional Information
- Notes
- AID: 2307923