Embedding Heterostructured α-MnS/MnO Nanoparticles in S-Doped Carbonaceous Porous Framework as High-Performance Anode for Lithium-Ion Batteries

被引:25
|
作者
Ma, Yuan [1 ,2 ]
Ma, Yanjiao [1 ,2 ]
Diemant, Thomas [3 ]
Cao, Kecheng [4 ]
Kaiser, Ute [4 ]
Behm, R. Juergen [1 ,3 ]
Varzi, Alberto [1 ,2 ]
Passerini, Stefano [1 ,2 ]
机构
[1] Helmholtz Inst Ulm HIU Electrochem Energy Storage, Helmholtzstr 11, D-89081 Ulm, Germany
[2] Karlsruhe Inst Technol KIT, POB 3640, D-76021 Karlsruhe, Germany
[3] Ulm Univ, Inst Surface Chem & Catalysis, Albert Einstein Allee 47, D-89081 Ulm, Germany
[4] Ulm Univ, Grp Electron Microscopy Mat Sci, Cent Facil Electron Microscopy, Albert Einstein Allee 11, D-89081 Ulm, Germany
关键词
heterostructure; in situ XRD/lithium storage mechanism; lithium-ion batteries; S-doped carbonaceous frameworks; α-MnS/MnO nanoparticles;
D O I
10.1002/celc.202100110
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work, the synthesis of alpha-MnS/MnO/S-doped C micro-rod composites via a simple sulfidation process is demonstrated, starting from a Mn-based metal-organic framework. The resulting heterostructured alpha-MnS/MnO nanoparticles (8 +/- 2 nm) are uniformly embedded into the S-doped carbonaceous porous framework with hierarchical micro-/meso-porosity. The combination of structural and compositional characteristics results in the promising electrochemical performance of the as-obtained composites as anode materials for lithium-ion batteries, coupled with high reversible capacity (940 mAh g(-1) at 0.1 A g(-1)), excellent rate capability as well as long cycling lifespan at high rate of 2.0 A g(-1) for 2000 cycles with the eventual capacity of similar to 300 mAh g(-1). Importantly, in situ X-ray diffraction studies clearly reveal mechanistic details of the lithium storage mechanism, involving multistep conversion processes upon initial lithiation.
引用
收藏
页码:918 / 927
页数:10
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