Abstract
The performance of the lithium-sulfur battery at harsh conditions of lean electrolyte and low temperature is impeded by nanometric clustering of lithium polysulfides (LiPSs), which inherently hinders sulfur reaction kinetics. Here we describe a cluster-disrupting strategy wherein a fluorinated borane anion acceptor, tris(perfluorophenyl)borane, is exploited to regulate the LiPSs solvation structure and to promote their reactions under harsh conditions. The electron-deficient anion acceptor molecules bond with the electron-rich LiPSs via soft Lewis acid-base interactions, which disrupts LiPSs’ clustering and promotes Li2S solvation, facilitating a three-dimensional Li2S growth via solution-mediated mechanism at low temperatures. With the borane anion acceptor, the cell shows a significantly improved capacity at −25 °C. Impressively, this strategy enables stable cycling of a 1.83 Ah pouch cell at 0 °C retaining 96.0% capacity over 50 cycles. Our study provides a general methodology for manipulating the fundamental electrolyte chemistry to regulate LiPSs clustering and improve sulfur batteries at harsh conditions.
Original language | English |
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Pages (from-to) | 3029-3037 |
Number of pages | 9 |
Journal | Nano Letters |
Volume | 25 |
Issue number | 8 |
DOIs | |
State | Published - 26 Feb 2025 |
Externally published | Yes |
Keywords
- Li−S battery
- anion acceptor
- coordination structure
- lithium polysulfides
- nanometric clustering