Abstract
Lithium–sulfur batteries, owing to their excellent advantages (including low cost and high theoretical energy density), might be the next-generation energy storage devices. However, the low S contents in their electrodes and the shuttling effect of soluble polysulfides can significantly deteriorate their capacities and cycle lives. Herein, we demonstrate a uniquely structured composite electrode, named porous polymerized vinyl acetate (p-PVAc) thin films, to break through the “trade-off” between the energy density and rate capability. S nanoparticles were encapsulated by porous p-PVAc layers and then anchored on graphene (p-PVAc/S/G), facilitating ion exchange and electron transfer during electrochemical operations. Consequently, p-PVAc/S/G delivered a high specific capacity of 719 mAh g−1 at 0.1 A g−1 and exceeded even 350 mAh g−1 at a high current density of 5 A g−1, whereas the average Coulombic efficiency was preserved to be higher than 98.50% when repeated for more than 300 cycles at 1 A g−1.
| Original language | English |
|---|---|
| Article number | 149199 |
| Journal | Applied Surface Science |
| Volume | 547 |
| DOIs | |
| State | Published - 1 May 2021 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Instant polymerization
- Ion transfer channel
- Lithium–sulfur batteries
- Partial evaporation
- Porous polymer thin film
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