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用于先进锂离子电池的由配位驱动自组装聚集体生成的多孔纳米结构Co3O4阳极材料。

Porous nano-structured Co3O4 anode materials generated from coordination-driven self-assembled aggregates for advanced lithium ion batteries.

作者信息

Ge Danhua, Geng Hongbo, Wang Jiaqing, Zheng Junwei, Pan Yue, Cao Xueqin, Gu Hongwei

机构信息

Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215123, China.

出版信息

Nanoscale. 2014 Aug 21;6(16):9689-94. doi: 10.1039/c4nr01978d. Epub 2014 Jul 4.

Abstract

A simple and scalable coordination-derived method for the synthesis of porous Co3O4 hollow nanospheres is described here. The initially formed coordination-driven self-assembled aggregates (CDSAAs) could act as the precursor followed by calcination treatment. Then the porous hollow Co3O4 nanospheres are obtained, in which the primary Co3O4 nanoparticles are inter-dispersed. When the nanospheres are used as anode materials for lithium storage, they show excellent coulombic efficiency, high lithium storage capacity and superior cycling performance. In view of the facile synthesis and excellent electrochemical performance obtained, this protocol to fabricate special porous hollow frameworks could be further extended to other metal oxides and is expected to improve the practicality of superior cycle life anode materials with large volume excursions for the development of the next generation of LIBs.

摘要

本文描述了一种简单且可扩展的基于配位的方法来合成多孔Co3O4空心纳米球。最初形成的配位驱动自组装聚集体(CDSAAs)可作为前驱体,随后进行煅烧处理。然后获得多孔空心Co3O4纳米球,其中初级Co3O4纳米颗粒相互分散。当这些纳米球用作锂存储的负极材料时,它们表现出优异的库仑效率、高锂存储容量和卓越的循环性能。鉴于所获得的简便合成方法和优异的电化学性能,这种制备特殊多孔空心框架的方案可进一步扩展到其他金属氧化物,并有望提高具有大体积变化的优异循环寿命负极材料的实用性,以推动下一代锂离子电池的发展。

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