Metal-organic framework-derived bimetallic oxides as anode materials for lithium-ion batteries: a mini review

被引:3
作者
Guan, Yingchun [1 ]
Guo, Zichen [1 ]
Zhou, Shengjun [1 ]
Chen, Zhanpeng [1 ]
Xu, Kang [1 ]
Zhang, Xiaoke [2 ]
Lin, Xiaoming [2 ]
Wu, Yongbo [3 ,4 ]
机构
[1] Hubei Energy Grp Renewables Dev Co Ltd, Wuhan 430077, Hubei, Peoples R China
[2] South China Normal Univ, Sch Chem, Guangzhou 510006, Guangdong, Peoples R China
[3] South China Normal Univ, Guangdong Basic Res Ctr Excellence Struct & Fundam, Key Lab Atom & Subatom Struct & Quantum Control, Sch Phys,Minist Educ, Guangzhou 510006, Peoples R China
[4] South China Normal Univ, Guangdong Prov Key Lab Quantum Engn & Quantum Mat, Guangdong Hong Kong Joint Lab Quantum Matter, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE ANODE; FACILE SYNTHESIS; ELECTROCHEMICAL PERFORMANCE; CONTROLLABLE SYNTHESIS; ELECTRODE MATERIALS; STORAGE PROPERTIES; EXCELLENT ANODE; NANOSHEETS; MICROSPHERES; NANOPARTICLES;
D O I
10.1039/d4nj02608j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic frameworks (MOFs) have received widespread attention for their large specific surface area, porous structure, and tunable particle size. MOFs can be utilized as precursors to prepare structurally diverse bimetallic oxides, which exhibit outstanding electrochemical properties as anode materials for lithium-ion batteries (LIBs). This paper introduces the study of MOF-derived bimetallic oxides as anode materials for LIBs, focusing on the application of MOF-derived manganese-, cobalt-, iron-, and vanadium-based bimetallic oxides in LIBs. MOF-derived bimetallic oxides, with the advantages of tunable compositions and nano-structures, are capable of further contributing to the enhancement of electrochemical performances. Finally, the problems of these derived materials in the application of LIBs are prospected, and reliable solutions and future development prospects are proposed. This review summarizes the MOF-derived bimetallic oxides as anode materials for lithium-ion batteries.
引用
收藏
页码:13466 / 13474
页数:9
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