# Designing with Li2S in Lithium–Sulfur Batteries: From Fundamental Chemistry to Practical Architectures

**Authors:** Hyeona Park, Arcangelo Celeste, Shulin Wang, Chaiwon Lee, Yul Yang, Kaizhao Wang, Aleksandar Matic, Sergio Brutti, Shivam Kansara, Shizhao Xiong, Marco Agostini, Jang‐Yeon Hwang

PMC · DOI: 10.1002/smll.202513644 · 2026-01-25

## TL;DR

This paper explores how Li2S can be used to design better lithium-sulfur batteries with higher energy and easier manufacturing.

## Contribution

The paper introduces multiscale strategies for Li2S activation and integration into anode-free battery designs.

## Key findings

- Li2S-based cathodes enable lithium-free and anode-free battery architectures.
- Hierarchical carbon frameworks and electrolyte co-design improve Li2S performance.
- Redox mediators and machine learning aid in scaling Li2S battery technology.

## Abstract

Lithium‐sulfur (Li‐S) batteries deliver gravimetric energy densities considerably higher than those of conventional lithium‐ion systems while relying on low‐cost, earth‐abundant materials. Despite decades of progress, their commercialization remains hindered by intrinsic challenges such as the insulating nature of sulfur and lithium sulfide (Li2S), formation and dissolution of soluble polysulfides, and instability of lithium‐metal anodes. Among these, the use of Li2S as a pre‐lithiated cathode has redefined the landscape of Li─S chemistry by offering a pathway toward lithium‐free and anode‐free architectures that are compatible with the existing manufacturing infrastructure. This perspective revisits the Li2S electrochemistry from a conceptual and design standpoint. The perspective emphasizes multiscale strategies for atomic‐level catalytic engineering, mesoscale electrode architectures, and electrolyte–interface control, which collectively determine Li2S activation and reversibility. The perspective also examines emerging approaches that integrate Li2S cathodes with graphite, silicon, and solid‐state configurations to enable safe, high‐energy, and manufacturable Li─S technologies. Finally, this perspective discusses the evolving roles of redox mediators, machine learning‐based discovery, and sustainable synthesis in bridging the gap between laboratory breakthroughs and industrial viability. Collectively, these insights frame Li2S not only as an alternative, cathode, but also as a platform for reimagining Li─S electrochemistry in the post‐lithium‐metal era.

This perspective highlights the design evolution of Li2S‐based lithium‐batteries, illustrating sulfur redox chemistry and Li2S activation. Emphasis is placed on catalytic interfaces, hierarchical carbon frameworks, and electrolyte‐solvation co‐design, enabling lithium‐free, anode‐free, and solid‐state Li‐S architectures for high‐energy, manufacturable systems.

## Linked entities

- **Chemicals:** Li2S (PubChem CID 64734), sulfur (PubChem CID 5362487)

## Full-text entities

- **Chemicals:** Li-S (-), metal (MESH:D008670), sulfur (MESH:D013455), Li S (MESH:D008094), lithium sulfide (MESH:C550775), polysulfides (MESH:C032915), silicon (MESH:D012825), graphite (MESH:D006108)

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12895229/full.md

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Source: https://tomesphere.com/paper/PMC12895229