沉积(地质)
氯化物
材料科学
化学工程
纳米技术
无机化学
化学
冶金
工程类
地质学
古生物学
沉积物
作者
Dasol Jin,Héctor D. Abruña
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-05-14
标识
DOI:10.1021/acsnano.5c04497
摘要
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.
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