材料科学
氧化钴
阳极
超级电容器
氧化物
化学工程
电化学
钴
介孔材料
尖晶石
纳米复合材料
电极
电导率
电池(电)
无机化学
纳米技术
催化作用
化学
生物化学
功率(物理)
物理
物理化学
量子力学
工程类
冶金
作者
Ramchandra S. Kalubarme,Sarika Jadhav,Bharat B. Kale,Suresh Gosavi,Chiaki Terashima,Akira Fujishima
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2018-04-26
卷期号:29 (28): 285705-285705
被引量:22
标识
DOI:10.1088/1361-6528/aac034
摘要
Cobalt oxide is a transition metal oxide, well studied as an electrode material for energy storage applications, especially in supercapacitors and rechargeable batteries, due to its high charge storage ability. However, it suffers from low conductivity, which effectively hampers its long-term stability. In the present work, a simple strategy to enhance the conductivity of cobalt oxide is adopted to achieve stable electrochemical performance by means of carbon coating and Mn doping, via a simple and controlled, urea-assisted glycine-nitrate combustion process. Structural analysis of carbon coated Mn-doped Co3O4 (Mn-Co3O4@C) confirms the formation of nanoparticles (∼50 nm) with connected morphology, exhibiting spinel structure. The Mn-Co3O4@C electrode displays superior electrochemical performance as a Li-ion battery anode, delivering a specific capacity of 1250 mAh g-1. Mn-Co3O4@C demonstrates excellent performance in terms of long-term stability, keeping charge storage ability intact even at high current rates due to the synergistic effects of fast kinetics-provided by enriched electronic conductivity, which allows ions to move freely to active sites and electrons from reaction sites to substrate during redox reactions-and high surface area combined with mesoporous architecture. The fully assembled battery device using Mn-Co3O4@C and standard LiCoO2 electrode shows 90% capacity retention over 100 cycles.
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