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Polypyrrole Modified MoS2 Nanorod Composites as Durable Pseudocapacitive Anode Materials for Sodium-Ion Batteries
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As a typical two-dimensional layered metal sulfide, MoS2 has a high theoretical capacity and large layer spacing, which is beneficial for ion transport. Herein, a facile polymerization method is employed to synthesize polypyrrole (PPy) nanotubes, followed by a hydrothermal method to obtain flower-rod-shaped MoS2/PPy (FR-MoS2/PPy) composites. The FR-MoS2/PPy achieves outstanding electrochemical performance as a sodium-ion battery anode. After 60 cycles under 100 mA g−1, the FR-MoS2/PPy can maintain a capacity of 431.9 mAh g−1. As for rate performance, when the current densities range from 0.1 to 2 A g−1, the capacities only reduce from 489.7 to 363.2 mAh g−1. The excellent performance comes from a high specific surface area provided by the unique structure and the synergistic effect between the components. Additionally, the introduction of conductive PPy improves the conductivity of the material and the internal hollow structure relieves the volume expansion. In addition, kinetic calculations show that the composite material has a high sodium-ion transmission rate, and the external pseudocapacitance behavior can also significantly improve its electrochemical performance. This method provides a new idea for the development of advanced high-capacity anode materials for sodium-ion batteries.
Title: Polypyrrole Modified MoS2 Nanorod Composites as Durable Pseudocapacitive Anode Materials for Sodium-Ion Batteries
Description:
As a typical two-dimensional layered metal sulfide, MoS2 has a high theoretical capacity and large layer spacing, which is beneficial for ion transport.
Herein, a facile polymerization method is employed to synthesize polypyrrole (PPy) nanotubes, followed by a hydrothermal method to obtain flower-rod-shaped MoS2/PPy (FR-MoS2/PPy) composites.
The FR-MoS2/PPy achieves outstanding electrochemical performance as a sodium-ion battery anode.
After 60 cycles under 100 mA g−1, the FR-MoS2/PPy can maintain a capacity of 431.
9 mAh g−1.
As for rate performance, when the current densities range from 0.
1 to 2 A g−1, the capacities only reduce from 489.
7 to 363.
2 mAh g−1.
The excellent performance comes from a high specific surface area provided by the unique structure and the synergistic effect between the components.
Additionally, the introduction of conductive PPy improves the conductivity of the material and the internal hollow structure relieves the volume expansion.
In addition, kinetic calculations show that the composite material has a high sodium-ion transmission rate, and the external pseudocapacitance behavior can also significantly improve its electrochemical performance.
This method provides a new idea for the development of advanced high-capacity anode materials for sodium-ion batteries.
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