Chemo‑Electrochemical Tandem Catalysis Unlocking Sulfur Reaction in Practical Lithium–Sulfur Batteries
As next-generation high-energy batteries, lithium-sulfur (Li-S) batteries are promising solutions for long-range electric vehicles due to their ultrahigh theoretical energy density. However, they face fundamental challenges from low sulfur utilization, particularly under electrolyte-starved practical conditions that polysulfides are unable to dissolve. Here, we propose a chemo-electrochemical tandem catalyst, Li<sub>x</sub>TiS<sub>2</sub>, which chemically catalyzes the transformation of S<sub>8</sub>/Li<sub>2</sub>S<sub>8</sub> to Li<sub>2</sub>S<sub>4</sub> and subsequently catalyzes electrochemical reduction to lithium sulfide (Li<sub>2</sub>S). This tandem mechanism fundamentally alters the reaction kinetics from conventional first-order to zero-order behavior, overcoming the limitation imposed by the solubility of sulfur species. It thus enables efficient sulfur conversion and an ultralow activation energy of ∼0.3 eV (a 50% reduction compared to without catalysts) under a low electrolyte-to-sulfur (E/S) ratio (5 µL mg<sub>s</sub> <sup>-1</sup>), significantly improving battery performance in practical conditions. The coin cell shows an ultralow capacity decay of 0.028% per cycle over 1500 cycles, and a 2.0 Ah pouch cell achieves the high energy density of 550 Wh kg<sup>-1</sup> with good stability.
Authors
- Jiaqi Lan (ORCID: https://orcid.org/0000-0003-4687-9770)
- Ziqiang Wang (ORCID: https://orcid.org/0009-0000-7168-3070)
- Yaqi He (ORCID: https://orcid.org/0000-0001-5324-148X)
- Linkai Peng
- Yufei Zhao (ORCID: https://orcid.org/0000-0002-8653-8666)
- Jin Shi (ORCID: https://orcid.org/0009-0006-2337-201X)
- Chuannan Geng
- Yun Cao
- Wei Lv
Institutions
- University Town of Shenzhen (CN)
Publication Details
- Journal
- Advanced Materials
- Published
- 2026-01-06
- DOI
- https://doi.org/10.1002/adma.202521611
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.00