自催化
硫黄
锂(药物)
材料科学
自催化反应
化学工程
接口(物质)
纳米技术
化学
生物化学
催化作用
吸附
有机化学
物理
冶金
生物
统计物理学
吉布斯等温线
工程类
内分泌学
作者
Zhen Wu,Mingliang Liu,Wenfeng He,Tong Guo,Wei Tong,Erjun Kan,Xiaoping Ouyang,Fen Qiao,Junfeng Wang,Xueliang Sun,Xin Wang,Junwu Zhu,Ali Coskun,Yongsheng Fu
标识
DOI:10.1038/s41467-024-53797-y
摘要
Electrocatalysts are extensively employed to suppress the shuttling effect in lithium-sulfur (Li-S) batteries. However, it remains challenging to probe the sulfur redox reactions and mechanism at the electrocatalyst/LiPS interface after the active sites are covered by the solid discharge products Li2S/Li2S2. Here, we demonstrate the intrinsic autocatalytic activity of the Li2S (100) plane towards lithium polysulfides on single-atom nickel (SANi) electrocatalysts. Guided by theoretical models and experimental data, it is concluded that LiPS dissociates into Li2S2 and short-chain LiPS on the Li2S (100) plane. Subsequently, Li2S2 undergoes further lithiation to Li2S on the Li2S (100) surface, generating a new Li2S (100) layer, thus enabling the autocatalytic formation of a new Li2S (100) surface. Benefiting from the autocatalytic growth of Li2S, the concentration of LiPS in the electrolyte remains at a lower level, enabling Li-S batteries under high loading and low electrolyte conditions to exhibit superior electrochemical performance. This study reveals the autocatalytic growth of Li2S crystals at the solid-liquid interface in lithium-sulfur batteries enabling good electrochemical performance under high loading and low electrolyte conditions.
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