材料科学
电极
介孔材料
锂(药物)
化学工程
纳米技术
碳纤维
离子
储能
纳米复合材料
吸附
复合材料
复合数
催化作用
医学
化学
物理
功率(物理)
有机化学
物理化学
量子力学
工程类
内分泌学
作者
Xiue Zhang,Chao Shen,Huayu Wu,Yue Han,Xiaoyu Wu,Weiran Ding,Lubin Ni,Guowang Diao,Ming Chen
标识
DOI:10.1016/j.ensm.2019.11.019
摘要
A facile and feasible spatial confinement strategy is proposed for the preparation of ultrathin ReS2 nanosheets confined in hollow mesoporous carbon spheres (HMCSs), forming nanosheets filled hollow carbon spheres (NSFHCSs) ReS2@C. Based on the spatially confined growth, the as-synthesized ReS2@C nanocomposites achieve novel filled-structure and well-defined heterogeneous interfaces. In the excellent architecture, the porous carbon framework precisely constrains ultrathin ReS2 nanosheets within its void space, which can generate essential electrical contacts, buffer volume expansion, and prohibit the loss of active materials during the pulverization process. For lithium-ion batteries, the NSFHCSs ReS2@C display high adsorption energy of Li in the heterogenous interface by the first-principle calculation, and achieve superior reversible capacity of 578 mA h g−1 after 1000 cycles at 1 A g−1. Research shows that the capacitive behavior plays a major role in specific capacity contribution of ReS2@C electrode. For sodium-ion batteries, the NSFHCSs ReS2@C demonstrate reversible discharge capacity of 319 mA h g−1 at 0.2 A g−1 after 400 cycles. The enlarged interlayer spacing and few layer structure of ReS2 nanosheets are conducive to enhance the Li+/Na+ mobility and improve the dynamic characteristic of electrode material.
科研通智能强力驱动
Strongly Powered by AbleSci AI