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In-situ construction of binder-free MnO2/MnSe heterostructure membrane for high-performance energy storage in pseudocapacitors

假电容器 电容 硒化物 电解质 电导率 化学 化学工程 材料科学 无机化学 超级电容器 冶金 电极 工程类 物理化学
作者
Qasim Abbas,Abdul Mateen,Sajid Hussain Siyal,Najam Ul Hassan,Asma A. Alothman,Mohamed Ouladsmane,Sayed M. Eldin,Mohd Zahid Ansari,Muhammad Sufyan Javed
出处
期刊:Chemosphere [Elsevier]
卷期号:313: 137421-137421 被引量:15
标识
DOI:10.1016/j.chemosphere.2022.137421
摘要

Manganese (Mn)-based oxides are considered suitable positive electrode materials for supercapacitors (SCs). However, their cycle stability and specific capacitance are significantly hindered by key restrictions such as structural instability and low conductivity. Herein, we demonstrated a novel nanorod (NR)-shaped heterostructured manganese dioxide/manganese selenide membrane (MnO2/MnSe) on carbon cloth (CC) (denoted as MnO2/MnSe-NR@CC) with a high aspect ratio by a straightforward and facile hydrothermal process. Experiments have demonstrated that doping selenium atoms to oxygen sites reduce electronegativity, increasing the intrinsic electronic conductivity of MnO2, decreasing electrostatic interactions with electrolyte ions, and thus boosting the reaction kinetics. Further, the selenium doping results in an amorphous surface with extensive oxygen defects, which contributed to the emergence of additional charge storage sites with pseudocapacitive characteristics. As expected, novel heterostructured MnO2/MnSe-NR@CC as an electrode for SC exhibits a high capacitance of 740.63 F/g at a current density of 1.5 A/g, with excellent cycling performance (93% capacitance retention after 5000 cycles). The MnO2/MnSe-NR@CC exhibited outstanding charge storage capability, dominating capacitive charge storage (84.6% capacitive at 6 mV/s). To examine the practical applications of MnO2/MnSe-NR@CC-ASC as a positive electrode, MnO2/MnSe-NR@CC//AC device was fabricated. The MnO2/MnSe-NR@CC//AC-ASC device performed exceptionally well, with a maximum capacitance of 166.66 F/g at 2 A/g, with a capacitance retention of 94%, after 500 GCD cycles. Additionally, it delivers an energy density of 75.06 Wh/kg at a power density of 1805.1 W/kg and maintains 55.044 Wh/kg at a maximum power density of 18,159 W/kg. This research sheds fresh information on the anionic doping method and has the potential to be applied to the synthesis of positive electrode materials for energy storage applications.

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