Layered oxides based on manganese (Mn), rich in lithium (Li), and free of cobalt (Co) are the most promising cathode candidates used for lithium-ion batteries due to their high capacity, high voltage and low cost. These types of material can be written as xLiMnO·(1 - x) LiTMO (TM = Ni,Mn,etc.). Though, LiMnO is known to have poor cycling stability and low capacity, which hinder its industrial application commercially. In this work, LiNiMnO materials with different amounts of structural defects was successfully synthesized using powder metallurgy followed by different cooling processes in order to improve its electrochemical properties. Microstructural analyses and electrochemical measurements were carried out on the study samples synthesized by a combination of X-ray diffraction, transmission electron microscopy, and cyclic voltammetry. It is found that the disorder of the transition metal layer in LiMnO promotes its electrochemical activity, whereas the Li/Ni antisites of the Li layer maintain the stability of its local structure. The material with optimal amount of structural defects had an initial capacity of 188.2 mAh g, while maintaining an excellent specific capacity of 144.2 mAh g after 500 cycles at 1C. In comparison, LiNiMnO without structural defect only gives a capacity of 40.8 mAh g after cycling. This microstructural control strategy provides a simple and effective route to develop high-performance Co-free, Li-rich Mn-based cathode materials and scale-up manufacturing.
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http://dx.doi.org/10.1016/j.jcis.2022.10.105 | DOI Listing |
Chem Asian J
January 2025
University of Queensland, School of Chemical Engineering, AUSTRALIA.
The activation mechanism of Li-rich cathode has been discussed for many years, yet there is still debate on different theories. Potassium doping can assist the investigation on activation mechanism through its unique function in terms of blocking TM migration during activation. K-doping works by occupying Li sites even after Li has been extracted, increasing stability by blocking transition metals from migrating into these sites, which can help us distinguish the pathway of activation.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
December 2024
Institute of Advanced Battery Materials and Devices, College of Materials Science and Engineering, Beijing University of Technology, Beijing 100124, China.
Adv Mater
November 2024
College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, Zhejiang Province, 310027, China.
Despite extensive investigation on the lattice oxygen redox (LOR) in Li-rich cathodes, significant challenges remain in utilizing LOR activity without compromising structural and electrochemical stability. Related breakthroughs are hindered by the lack of understanding regarding how different LOR activity influences the structural evolution and electrochemical stability, and what is the optimal LOR activity. Herein, the degree of LOR activity is successfully regulated from 22% to 92% in Co-free Li-rich cathodes (LiMnNiO) by controlling local chemical disorder, and the relationship between LOR activity and cycling stability is revealed.
View Article and Find Full Text PDFSmall Methods
October 2024
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL, 60439, USA.
J Colloid Interface Sci
January 2025
College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China; Institute of Zhejiang University-Quzhou, Zheda Road 99, Quzhou 324000, China. Electronic address:
Cobalt (Co)-free lithium (Li)-rich layered oxides (LLOs) have emerged as promising cathode materials for the next generation of Li-ion batteries, attributed to their competitive market positioning and high energy density. Nevertheless, challenges arise from surface oxygen loss due to irreversible anionic redox reactions, leading to severe voltage and capacity decay that hinder the large-scale adoption of LLOs. Herein, we present an innovative, facile, and environmentally friendly hydrothermal approach to induce surface reconstruction of LiMnNiO material.
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