Synthesis and characterization of hierarchically structured mesoporous MnO2 and Mn2O3

被引:57
作者
Liu, Mi [1 ,2 ]
Zhang, Gui-Jun [1 ,2 ]
Shen, Zhu-Rui [1 ,2 ]
Sun, Ping-Chuan [1 ,2 ]
Ding, Da-Tong [3 ]
Chen, Tie-Hong [1 ,2 ]
机构
[1] Nankai Univ, Key Lab Energy Mat Chem Tianjin, Inst New Catalyt Mat Sci, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Chem, Engn Res Ctr Energy Storage & Convers MOE, Tianjin 300071, Peoples R China
[3] Nankai Univ, Coll Phys, Tianjin 300071, Peoples R China
关键词
Mesoporous; Amorphous; Manganese dioxide; L-Lysine; Hierarchical structure; ELECTRODE MATERIAL; MOLECULAR-SIEVES; AMORPHOUS MNO2; LITHIUM; TEMPLATE; BATTERIES; CRYSTALS; OXIDES; SUPERCAPACITOR; PERFORMANCE;
D O I
10.1016/j.solidstatesciences.2008.05.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Hierarchically structured mesoporous MnO2 with high surface area was prepared by a facile precursor route. Well-defined morphological manganese oxalate, synthesized by adding L-Lysine via a hydrothermal method, was used as precursor. Mesoporous amorphous MnO2 with high Brunauer-Emmett-Teller (BET) surface area (340 m(2)/g) and mesoporous Mn2O3 composed of nano-crystals (BET surface area 188 m(2)/g) were obtained by selective calcination of the oxalate precursor at 330 degrees C and 400 degrees C, respectively. Thermogravimetric and differential thermal analyses (TG-DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N-2-sorption analysis and X-ray photoelectron spectroscopy (XPS) were used to characterize the structure and property of products. Cyclic voltammetry (CV) and charge-discharge measurements were used to preliminarily stud), the electrochemical performance of the products. The range of pH value (about 5.0-7.0) in the synthesis process is apt to prepare the hierarchical structured manganese dioxide. Other types of amino acids were also employed as the crystallization modifiers and different morphologies of manganese dioxides were obtained. (c) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:118 / 128
页数:11
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