Kalubarme Ramchandra S, Jadhav Sarika M, Kale Bharat B, Gosavi Suresh W, Terashima Chiaki, Fujishima Akira
Centre for Advanced Studies in Material Science, Department of Physics, Savitribai Phule Pune University, (Formerly University of Pune) Ganeshkhind, Pune-411007, India.
Nanotechnology. 2018 Jul 13;29(28):285705. doi: 10.1088/1361-6528/aac034. Epub 2018 Apr 26.
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 CoO (Mn-CoO@C) confirms the formation of nanoparticles (∼50 nm) with connected morphology, exhibiting spinel structure. The Mn-CoO@C electrode displays superior electrochemical performance as a Li-ion battery anode, delivering a specific capacity of 1250 mAh g. Mn-CoO@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-CoO@C and standard LiCoO electrode shows 90% capacity retention over 100 cycles.
氧化钴是一种过渡金属氧化物,因其高电荷存储能力而作为储能应用的电极材料得到了充分研究,尤其是在超级电容器和可充电电池领域。然而,它的导电性较低,这有效地阻碍了其长期稳定性。在本工作中,采用了一种简单的策略来提高氧化钴的导电性,通过简单可控的尿素辅助甘氨酸 - 硝酸盐燃烧过程,借助碳包覆和锰掺杂来实现稳定的电化学性能。对碳包覆锰掺杂的氧化钴(Mn-CoO@C)进行结构分析,证实形成了具有连通形态的纳米颗粒(约50纳米),呈现出尖晶石结构。Mn-CoO@C电极作为锂离子电池负极表现出优异的电化学性能,比容量为1250 mAh g。Mn-CoO@C在长期稳定性方面表现出色,由于富集的电子导电性提供的快速动力学协同效应,即使在高电流速率下电荷存储能力也能保持完整,这使得离子在氧化还原反应期间能够自由移动到活性位点,电子从反应位点移动到基底,同时高表面积与介孔结构相结合。使用Mn-CoO@C和标准LiCoO电极完全组装的电池装置在100次循环后容量保持率为90%。