材料科学
阳极
锂(药物)
储能
化学工程
离子
电化学
热扩散率
分子
电极
无机化学
有机化学
物理化学
物理
工程类
内分泌学
医学
功率(物理)
化学
量子力学
作者
Xin Qi,Wenxin Xu,Chao Zhang,Yong-Qiang Miao,Yuting Xu,Songying He,Dong Zhang,Liang Li,Shin‐ichi Sasaki,Hitoshi Tamiaki,Xiaofeng Wang
标识
DOI:10.1016/j.mtcomm.2022.103465
摘要
The layered MoS2 is an attractive anode material for lithium-ion batteries (LIBs), which facilitates the deintercalation of lithium ions and possesses a relatively high theoretical capacity. Herein, we report a strategy of the organic/inorganic composite anode with widened interlayer distance, where zinc methyl 3-devinyl-3-hydroxymethyl-pyropheophorbide a (Chl) molecules self-aggregate among layered MoS2 or on its surface. The as-prepared electrodes exhibit better rate performance, higher reversible capacity, and higher retention and improve specific capacity at high current densities and faster Li+ diffusivity than pure MoS2. This work provides a potential idea for optimizing the energy storage performance of 2D MoS2 material by enlarging the interlayer space with some organic dye aggregates.
科研通智能强力驱动
Strongly Powered by AbleSci AI