Abstract
Lithium-sulfur (Li-S) batteries hold great promise as a next-generation energy storage system due to their high theoretical energy density (2600 W h kg-1), surpassing conventional lithium-ion batteries. However, their performance is often limited by the intrinsic transformation of soluble lithium polysulfides (LiPSs) into short-chain insoluble sulfur species (Li2S2/Li2S), which induces significant cell polarization, particularly under lean-electrolyte conditions. Through a galvanic replacement reaction (GRR), enabling precise tailoring of interfacial properties, AgCl-PVP nanocubes (NCs) were synthesized and utilized as sulfur host materials. These materials demonstrated effective entrapment of LiPSs, as confirmed by in situ electrochemical visualization. Furthermore, the AgCl-PVP NCs significantly reduced whole-cell polarization, particularly during the Li2S nucleation step, as validated by galvanostatic intermittent titration technique across the depth of discharge. Under lean-electrolyte conditions (5.6 μL mg-1), the AgCl-PVP NCs cathode exhibited high specific capacity (563.62 mA h g-1 at 0.2 C) with a low-capacity decay rate (1.81% per cycle). These results demonstrate the potential of GRR-engineered nanostructures as sulfur host material for enhancing the electrochemical performance and practical applicability of lean-electrolyte Li-S batteries.
| Original language | English |
|---|---|
| Pages (from-to) | 19454-19463 |
| Number of pages | 10 |
| Journal | ACS Nano |
| Volume | 19 |
| Issue number | 20 |
| DOIs | |
| State | Published - 2025.05.27 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- LiS nucleation
- Li−S Batteries
- galvanic replacement reaction
- galvanostatic intermittent titration technique
- polarization
- sulfur cathode
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