Hetero-Phase MoO2/Cu2-x Se Nanocomposites Distributed in Porous Octahedral Carbon Networks for High-Performance Lithium Storage

被引:5
|
作者
Zhong, Ming [1 ,2 ,3 ,4 ]
Guo, Xue [1 ]
Li, Lingling [1 ]
Li, Yun-Wu [2 ,3 ]
Zhao, Kun [1 ]
Peng, Hui [4 ]
Zhang, Xiaobo [1 ]
机构
[1] Lanzhou Univ Technol, State Key Lab Adv Proc & Recycling Nonferrous Met, Lanzhou 730050, Peoples R China
[2] Liaocheng Univ, Collaborat Innovat Ctr Chem Energy Storage & Novel, Shandong Prov Key Lab, Liaocheng 252000, Peoples R China
[3] Liaocheng Univ, Sch Chem & Chem Engn, Liaocheng 252000, Peoples R China
[4] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Ecofunct Polymer Mat, Key Lab Ecoenvironm Polymer Mat Gansu Prov,Minist, Lanzhou 730070, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-organic framework; core-shell structure; heterophase nanocomposite; electrode material; lithium-ion battery; ELECTROCHEMICAL PERFORMANCE; FACILE SYNTHESIS; ANODE MATERIALS; ION STORAGE; CU2-XSE; MOO2; NANOCRYSTALS; COMPOSITE; GRAPHENE;
D O I
10.1021/acsanm.3c03824
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Owing to the mixed insertion and multielectron conversion reaction mechanisms, nonstoichiometric copper selenide (Cu2-xSe) has been known as a potential anode for lithium-ion batteries. However, huge volume changes during discharge and charge limit its ability for lithium-ion storage. Constructing heterophase nanocomposite uniformly distributed in the carbon network has been recognized as an effective approach to address the above issue. In this work, polyoxometalate-based metal-organic frameworks were used as the self-template to derive octahedral mesoporous carbon-coated heterophase copper selenide and molybdenum dioxide (MoO2/Cu2-xSe@C) nanocomposites, and the phase transformation of copper selenides from CuSe to Cu2-xSe can be achieved by tuning the pyrolysis temperature, thus optimizing the electrochemical performance. As a result, the optimized electrode delivers a high reversible specific capacity of 864.8 mAh g(-1) at 0.2 A g(-1) after 100 cycles, an excellent rate capability with a capacity of 480.9 mAh g(-1) at 2.0 A g(-1), and a long-term stability up to 500 cycles with a capacity decay rate per cycle of only 0.003%. Also, the reaction mechanism and structural stability after cycling were analyzed in detail.
引用
收藏
页码:20018 / 20027
页数:10
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