Lee Yoon Cheol, Han Dong-Wook, Park Mihui, Jo Mi Ru, Kang Seung Ho, Lee Ju Kyung, Kang Yong-Mook
Department of Energy and Materials Engineering, Dongguk University-Seoul , Seoul, 100-715, Republic of Korea.
ACS Appl Mater Interfaces. 2014 Jun 25;6(12):9435-41. doi: 10.1021/am5018122. Epub 2014 May 8.
We offer a brand new strategy for enhancing Li ion transport at the surface of LiFePO4/C nanofibers through noble Li ion conducting pathways built along reduced carbon webs by phosphorus. Pristine LiFePO4/C nanofibers composed of 1-dimensional (1D) LiFePO4 nanofibers with thick carbon coating layers on the surfaces of the nanofibers were prepared by the electrospinning technique. These dense and thick carbon layers prevented not only electrolyte penetration into the inner LiFePO4 nanofibers but also facile Li ion transport at the electrode/electrolyte interface. In contrast, the existing strong interactions between the carbon and oxygen atoms on the surface of the pristine LiFePO4/C nanofibers were weakened or partly broken by the adhesion of phosphorus, thereby improving Li ion migration through the thick carbon layers on the surfaces of the LiFePO4 nanofibers. As a result, the phosphidated LiFePO4/C nanofibers have a higher initial discharge capacity and a greatly improved rate capability when compared with pristine LiFePO4/C nanofibers. Our findings of high Li ion transport induced by phosphidation can be widely applied to other carbon-coated electrode materials.
我们提出了一种全新的策略,通过沿磷在还原碳网构建的贵金属锂离子传导途径,来增强磷酸铁锂/碳(LiFePO4/C)纳米纤维表面的锂离子传输。由一维(1D)磷酸铁锂纳米纤维组成、在纳米纤维表面带有厚碳涂层的原始磷酸铁锂/碳纳米纤维,是通过静电纺丝技术制备的。这些致密且厚的碳层不仅阻止了电解质渗透到内部的磷酸铁锂纳米纤维中,还阻碍了锂离子在电极/电解质界面的轻松传输。相比之下,原始磷酸铁锂/碳纳米纤维表面碳和氧原子之间现有的强相互作用因磷的附着而被削弱或部分破坏,从而改善了锂离子通过磷酸铁锂纳米纤维表面厚碳层的迁移。结果,与原始磷酸铁锂/碳纳米纤维相比,磷化的磷酸铁锂/碳纳米纤维具有更高的初始放电容量和大大提高的倍率性能。我们关于磷化诱导高锂离子传输的发现可广泛应用于其他碳包覆电极材料。