Abstract
High-energy-density lithium–sulfur batteries exhibit obvious kinetics differences involving multistep reactions, making it hard to realize constantly high-efficient polysulfide conversion during the full charging/discharging Herein, we propose a concept of Li+-respiration-effect-induced cascade catalysis through taking full advantage of dynamic active sites from in situ potential-modulated TiNb2O7. The Li+ respiration effect activates the lattice O atom and regulates the antibonding orbitals filling, triggering an electrochemical-dominated switchable catalytic for sequential conversion of intermediates. As a result, the Li–S cell displays a good cycling stability and wide-temperature ability from −30 to +60 °C. A flexible pouch cell maintains a capacity retention of 94.6% after 120 cycles. Our discovery provides a fire-new perspective in electrochemically reconstructed catalysis for wide-temperature-tolerant Li − S batteries.
| Original language | English |
|---|---|
| Article number | e24645 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 65 |
| Issue number | 5 |
| DOIs | |
| State | Published - 28 Jan 2026 |
| Externally published | Yes |
Keywords
- Cascade catalysis
- High cathode utilization
- Li respiration effect
- Lithium–sulfur batteries
- Wide temperature adaption
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