# In Situ Phase Separation Strategy to Construct Zinc Oxide Dots-Modified Vanadium Nitride Flower-like Heterojunctions as an Efficient Sulfur Nanoreactor for Lithium-Sulfur Batteries

**Authors:** Ningning Chen, Wei Zhou, Minzhe Chen, Ke Yuan, Haofeng Zuo, Aocheng Wang, Dengke Zhao, Nan Wang, Ligui Li

PMC · DOI: 10.3390/ma18112639 · Materials · 2025-06-04

## TL;DR

This paper introduces a new method to create efficient sulfur nanoreactors for lithium-sulfur batteries using zinc oxide and vanadium nitride heterojunctions.

## Contribution

A novel in situ phase separation strategy is introduced to construct ZnO dots-modified VN heterojunctions for improved LSB performance.

## Key findings

- Zn-QDs-VN heterojunctions show high initial specific capacity (1109.6 mAh g−1) and long cycle stability.
- The material performs well under high sulfur loading and lean electrolyte conditions.
- The interfacial synergistic effect enhances LiPS adsorption and reduces reaction energy barriers.

## Abstract

Exploring advanced sulfur cathode materials is important for the development of lithium-sulfur batteries (LSBs), but they still present challenges. Herein, zinc oxide dots-modified vanadium nitride flower-like heterojunctions (Zn-QDs-VN) as sulfur hosts are prepared by a phase separation strategy. Characterizations confirm that the flower structure with high specific surface area and pores improves active site exposure and electron/mass transfer. In situ phase separation enriches the Zn-QDs-VN interface, addressing the issues of uneven distribution and interface reduction of Zn-QDs-VN. Further theoretical computations reveal that ZnO-QDs-VN with optimized intermediate spin states can constitute a stable LiS* bond sequence, which can conspicuously facilitate the adsorption and conversion of LiPSs and reduce the battery reaction energy barrier. Therefore, the ZnO-QDs-VN@S cathode shows a high initial specific capacity of 1109.6 mAh g−1 at 1.0 C and long cycle stability (maintaining 984.2 mAh g−1 after 500 cycles). Under high S loading (8.5 mg cm−2) and lean electrolyte conditions (E/S = 6.5 μL mg−1), it also exhibits a high initial area capacity (10.26 mAh cm−2) at 0.2 C. The interfacial synergistic effect accelerates the adsorption and conversion of LiPSs and reduces the energy barriers in cell reactions. The study provides a new method for designing heterojunctions to achieve high-performance LSBs.

## Full-text entities

- **Chemicals:** LiPSs (-), S (MESH:D013455), ZnO (MESH:D015034), LiS (MESH:D008094)

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12156793/full.md

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