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Designing ultrastable P2/03-type layered oxides for sodium ion batteries by regulating Na distribution and oxygen redox chemistry

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Journal of Energy chemistry 2024年第7期94卷 466-476页

作者： Jieyou Huang Weiliang Li Debin Ye Lin Xu Wenwei Wu Xuehang Wu School of chemistry and Chemical Engineering Guangxi UniversityNanning 530004GuangxiChina Guangxi Key Laboratory for High-value Utilization of Manganese Resources Guangxi Normal University for NationalitiesChongzuo 532200GuangxiChina

P2/03-type Ni/Mn-based layered oxides are promising cathode materials for sodium-ion batteries(SIBs)owing to their high energy density.However,exploring effective ways to enhance the synergy between the P2 and 03 phases remains a necessity.Herein,we design a P2/03-type Na_(0.76)Ni_(0.31)Zn_(0.07)Mn_(0.50)Ti_(0.12)0_(2)(NNZMT)with high chemical/electrochemical stability by enhancing the coupling between the two phases.For the first time,a unique Na*extraction is observed from a Na-rich O3 phase by a Na-poor P2 phase and systematically investigated.This process is facilitated by Zn^(2+)/Ti^(4+)dual doping and calcination condition regulation,allowing a higher Na*content in the P2 phase with larger Na^(+)transport channels and enhancing Na transport kinetics.Because of reduced Na^(+)in the O3 phase,which increases the difficulty of H^(+)/Na^(+) exchange,the hydrostability of the O3 phase in NNZMT is considerably improved.Furthermore,Zn^(2+)/Ti^(4+)presence in NNZMT synergistically regulates oxygen redox chemistry,which effectively suppresses O_(2)/CO_(2) gas release and electrolyte decomposition,and completely inhibits phase transitions above 4.0 V.As a result,NNZMT achieves a high discharge capacity of 144.8 mA h g^(-1) with a median voltage of 3.42 V at 20 mA g^(-1) and exhibits excellent cycling performance with a capacity retention of 77.3% for 1000 cycles at 2000 mA g^(-1).This study provides an effective strategy and new insights into the design of high-performance layered-oxide cathode materials with enhanced structure/interface stability forSIBs.

关键词： Sodium-ion batteries P2/03-type layered oxides Na distribution oxygen redox chemistry Hydrostability

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oxygen redox chemistry in lithium-rich cathode materials for Li-ion batteries:Understanding from atomic structure to nano-engineering

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Nano Materials Science 2022年第4期4卷 322-338页

作者： Majid Farahmandjou Shuoqing Zhao Wei-Hong Lai Bing Sun Peter.H.L.Notten Guoxiu Wang Centre for Clean Energy Technology School of Mathematical and Physical SciencesFaculty of ScienceUniversity of Technology SydneySydneyNSW2007Australia Department of Chemical Engineering and chemistry Eindhoven University of Technology5600MBEindhoventhe Netherlands Fundamental Electrochemistry(IEK9) Forschungszentrum JülichD-52425JülichGermany

Lithium-rich oxide compounds have been recognized as promising cathode materials for high performance Li-ion batteries,owing to their high specific capacity.However,it remains a great challenge to achieve the fully reversible anionic redox reactions to realize high capacity,high stability,and low voltage hysteresis for lithiumrich cathode materials.Therefore,it is critically important to comprehensively understand and control the anionic redox chemistry of lithium-rich cathode materials,including atomic structure design,and nano-scale materials engineering technologies.Herein,we summarize the recent research progress of lithium-rich cathode materials with a focus on redox chemistry.Particularly,we highlight the oxygen-based redox reactions in lithium-rich metal oxides,with critical views of designing next generation oxygen redox lithium cathode materials.Furthermore,we purposed the most promising strategies for improving the performances of lithium-rich cathode materials with a technology-spectrum from the atomic scale to nano-scale.

关键词： oxygen redox chemistry Lithium-rich cathode Li-ion batteries Atomic structure Nano-engineering

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