Hierarchical mesoporous urchin-like Mn3O4/carbon microspheres with highly enhanced lithium battery performance by in-situ carbonization of new lamellar manganese alkoxide (Mn-DEG)

被引:98
作者
Huang, Shao-Zhuan [1 ]
Cai, Yi [1 ]
Jin, Jun [1 ]
Liu, Jing [1 ]
Li, Yu [1 ]
Yu, Yong [1 ]
Wang, Hong-En [1 ]
Chen, Li-Hua [1 ]
Su, Bao-Lian [1 ,2 ,3 ,4 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Lab Living Mat, Wuhan 430070, Hubei, Peoples R China
[2] Univ Namur, Lab Inorgan Mat Chem CMI, B-5000 Namur, Belgium
[3] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[4] Univ Cambridge, Clare Hall Coll, Cambridge CB2 1EW, England
基金
美国国家科学基金会;
关键词
Lamellar manganese alkoxide; Carbonization; Hierarchically porous Mn3O4/carbon microspheres; Anode materials; Li battery; IMPROVED REVERSIBLE CAPACITY; ANODE MATERIAL; FACILE SYNTHESIS; ION BATTERIES; ENERGY-CONVERSION; CYCLIC STABILITY; METAL-OXIDES; MN3O4; GRAPHENE; MN2O3;
D O I
10.1016/j.nanoen.2015.01.040
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two types of hierarchical mesoporous urchin-like Mn3O4/carbon microspheres (HM-MO/C-MS) have been prepared via the in situ carbonization of the newly synthesized lamellar manganese alkoxide (Mn-DEG) along with the crystallization of Mn3O4 in air (MO-A) and nitrogen (MO-N), respectively. Such unique HM-MO/C-MS with high surface area provides obvious advantages including a large contact area with electrolyte, a short transport path for Li+ ions, a low resistance for charge transfer, and a superior structural stability. When used as an anode material for lithium ion batteries in the voltage range of 0.01-3 V, the HM-MO/C-MS obtained in nitrogen (MO-N) exhibits high lithium storage capacity (915 mA h g(-1) at 100 mA g(-1) for 50 cycles), great cycling stability (94.5% capacity retention versus the second cycle) and excellent rate capability (510 mA h g(-1) at 1000 mA g(-1)). In particular, when cycling at a high current density of 1500 mA g(-1), the reversible capacity of the MO-N sample can still be maintained as high as 480 mA h g(-1) with a high capacity retention of 93.7% after 200 cycles. Even in a narrower voltage range of 0.01-1.5 V, the lithium storage capacity of the MO-N sample can reach 556 mA h g(-1) at 100 mA g(-1) with a very good cycling stability (over 91% capacity retention from the second cycle) and have an excellent rate capability of 269 mA h g(-1) at 1000 mA g(-1). Both MO-N and MO-A samples present a very high volumetric capacity of 741.2 mA h cm(-3) and 647.4 mA h cm(-3) at 100 mA g(-1), respectively. Such high performances both in the voltage ranges of 0.01-3 V and 0.01-1.5 V are among the highest reported. Ex-situ SEM images showed clearly the excellent morphological and structural stability of our materials. The results demonstrate that the unique hierarchical mesoporous microspheres/ carbon structure is favorable for improving the cyclability and rate capability in energy storage applications. Our effective synthesis strategy can be broadened to construct other mesoporous metal oxides/carbon composites for high-performance lithium ion batteries. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:833 / 844
页数:12
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