二硫化钼
介孔材料
超级电容器
化学
电极
钼
化学工程
二硫化碳
碳纤维
无机化学
电化学
催化作用
材料科学
有机化学
物理化学
复合材料
工程类
复合数
作者
Shiyi Yao,Songtao Zhang,Guangxun Zhang,Yijian Tang,Rongmei Zhu,Yi Peng,Yong Chen,Huan Pang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2023-09-18
卷期号:62 (39): 16038-16046
被引量:9
标识
DOI:10.1021/acs.inorgchem.3c02167
摘要
As the demand for fuel continues to increase, the development of energy devices with excellent performance is crucial. Supercapacitors (SCs) are attracting attention for their advantages of high specific energy and a long cycle life. At present, the development of high-performance electrode materials is the main point for research and development of SCs. Transition metal sulfides have the advantages of a large interlayer space and high theoretical capacity, making them promising electrode materials. Herein, we reported a series of ultrathin mesoporous iron family element (Fe, Co, Ni) molybdenum disulfide (MxMo1-xS2/C, M = Fe, Co, and Ni) by a template method. The original monolayer mesoporous structure of MoS2/C was maintained, and accumulation and agglomeration of MoS2/C were avoided. Based on our investigations, the best performance was that of CoxMo1-xS2/C nanohybrids. Furthermore, the concentrations of Co and Mo ions were modulated to obtain the best performance, in which Mo and Co ions were released at 1:1, 1:2, and 1:3 ratios and they were named CoxMo1-xS2/C-1, CoxMo1-xS2/C-2, and CoxMo1-xS2/C-3, respectively. Overall, these materials represent a significant improvement and show promise as high-performance SC electrode materials due to their enhanced capacitance and stability. At a current density of 0.5 A g-1, CoxMo1-xS2/C-2 has the optimal specific capacitance of 184 F g-1. CoxMo1-xS2/C-2 as an SC electrode exhibited better reversible capacity and cycling stability than MoS2/C, which is an improvement over MoS2/C regarding reversible capacity and cycling stability.
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