阳极
电化学
材料科学
电解质
电池(电)
阴极
锰
锌
化学工程
兴奋剂
充电周期
电极
电偶阳极
纳米技术
冶金
化学
光电子学
阴极保护
物理
物理化学
量子力学
涓流充电
工程类
功率(物理)
作者
Kaisheng Sun,Zemao Xiao,Yunfei Shen,Heng Lv,Jianpeng Zhu,Jianxiang Pang,Yang Zheng,Wenwen Kong,Long Chen
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-11-04
卷期号:17 (4): 2781-2789
被引量:49
标识
DOI:10.1007/s12274-023-6207-8
摘要
Mn-based zinc ion battery has the advantages of low cost and high performance, which makes it the promising energy storage system. However, the poor conductivity and the agglomeration in the synthesis process of manganese-based materials restrict the performance of batteries. Herein, the Se-doped MnS/Ti3C2Tx (Se-MnS/Ti3C2Tx) composite material derived from Mn-based metal-organic framework is reported. Electrochemical tests show that Se-doped could generate S defects and enhance the electrochemical activity of MnS. At the same time, the introduction of Ti3C2Tx substrate is conducive to exposing more sulfur defects and improving the utilization rate of defects. In the mechanism study, it is found that Se-MnS/Ti3C2Tx is transformed into S/Se co-doped Mn3O4 at the first charge, which innovatively elucidated the behavior of S/Se during activation. In the electrochemical performance test, the specific capacity can reach 74.7 mAh·g−1 at 5.0 A·g−1. In addition, the Zn-Ti3C2Tx membrane electrode is prepared by vacuum filtration as the zinc-poor anode, which is assembled into the rocking chair full battery to avoid dendrite growth and exhibit excellent rate performance. The addition of Zn2+ weakens the electrostatic repulsion between the interlayers of MXene, and the formation of the folded morphology aids the penetration of the electrolyte. At 1.0 A·g−1, the capacity can reach 50.6 mAh·g−1. This work is helpful to promote the research and development of the reaction mechanism of manganese based rocking chair batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI