期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 5, 期 22, 页码 11236-11245出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ta01457k
关键词
-
资金
- National Natural Science Foundation of China [21504012, 51125011, 51433001, 21501091]
- Fundamental Research Funds for the Central Universities [16D110617]
- Program of Shanghai Subject Chief Scientist [17XD1400100]
- Natural Science Foundation of Shanghai [17ZR1439900]
The combination of hierarchical porous transition-metal oxides with ultrathin two-dimensional (2D) transition-metal dichalcogenides (TMDs) with a favorable electrochemical performance beyond single-component materials is still very challenging. The present work demonstrates the general and targeted synthesis of hybrid heterostructures by the integration of porous transition-metal oxides (TMOs, e.g. NiO, Co3O4 and Fe2O3) and 2D MoS2 nanosheets. The as-prepared vertically aligned MoS2-NiO hybrids exhibit an excellent pseudocapacitive performance, such as a high specific capacitance of 1080.6 at 1 A g(-1) and long cycling durability with 101.9% capacitance retention after 9000 cycles at 2 A g(-1). This facile strategy using low-cost precursors is regarded as a general method to hybridize 2D MoS2 with other porous TMOs, such as Co3O4 and Fe2O3, with largely improved pseudocapacitive performances due to a favorable synergistic effect between MoS2 and TMOs with an enhanced electronic/ionic transport. Asymmetric supercapacitors using MoS2-TMO hybrids as both positive and negative electrodes are also demonstrated. As a proof-of-concept, the as-assembled MoS2-NiO//MoS2-Fe2O3 asymmetric supercapacitor operating within the potential window of 0-1.8 V delivers a high energy density of 39.6 W h kg(-1) with a long cycle life and excellent rate capability.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据