Department of Materials Science and Engineering , Korea Advanced Institute of Science and Technology (KAIST) , Daejeon 34141 , Republic of Korea.
ACS Appl Mater Interfaces. 2018 Jun 20;10(24):20540-20549. doi: 10.1021/acsami.8b04968. Epub 2018 Jun 11.
Facile synthesis of rationally designed nanostructured electrode materials with high reversible capacity is highly critical to meet ever-increasing demands for lithium-ion batteries. In this work, we employed defect engineering by incorporating metal organic framework (MOF) templates into one-dimensional nanostructures by simple electrospinning and subsequent calcination. The introduction of Co-based zeolite imidazole frameworks (ZIF-67) resulted in abundant oxygen vacancies, which induce not only more active sites for Li storage but also enhanced electrical conductivity. Moreover, abundant mesoporous sites are formed by the decomposition of ZIF-67, which are present both inside and outside the resultant SnO-CoO nanofibers (NFs). Attributed to the creation of vacancy sites along with the synergistic effects of SnO and CoO, SnO-CoO NFs exhibit an excellent reversible capacity for 300 cycles (1287 mA h g at a current density of 500 mA g) along with superior rate capabilities and improved initial Coulombic efficiency compared with pristine SnO NFs. This is an early report on utilizing MOF structures as the defect formation platform into one-dimensional nanostructures, which is expected to result in superior electrochemical performances required for advanced electrodes.
为满足锂离子电池日益增长的需求,设计合理的具有高可逆容量的纳米结构电极材料的简便合成方法至关重要。在这项工作中,我们采用缺陷工程,通过简单的静电纺丝和随后的煅烧,将金属有机骨架(MOF)模板引入一维纳米结构中。Co 基沸石咪唑酯骨架(ZIF-67)的引入导致了丰富的氧空位,这不仅为 Li 存储提供了更多的活性位点,而且提高了电导率。此外,ZIF-67 的分解形成了丰富的介孔位,这些介孔位存在于 SnO-CoO 纳米纤维(NFs)的内外。由于空位位的形成以及 SnO 和 CoO 的协同作用,SnO-CoO NFs 在 500 mA g 的电流密度下循环 300 次后(在 500 mA g 的电流密度下,其可逆容量为 1287 mA h g)表现出优异的可逆容量,具有优异的倍率性能和改进的初始库仑效率,优于原始 SnO NFs。这是早期关于利用 MOF 结构作为缺陷形成平台引入一维纳米结构的报道,有望获得先进电极所需的优异电化学性能。