Xiaojun Zhao, Zhen Yang, Yizhuo Song, Panqing Bai, Youlin Yang, Wenqing Zhou, Zhenyu Dong, Wangzi Li, Hongzhou Ma, Xu Wang, Fei Li, Jiannong Wang, Anjun Hu, Wei Wang
ABSTRACT The practical application of lithium−sulfur (Li−S) batteries is hindered by the shuttle effect of soluble lithium polysulfides and sluggish sulfur redox kinetics, resulting in rapid capacity fading and limited cycle life. Here, we present a rationally engineered yolk–shell nanoreactor architecture that integrates dual confinement and catalytic functionality to address these challenges. The nanoreactor comprises a polar, catalytically active core encapsulated within a conductive nitrogen‐doped carbon shell, offering synergistic physical restriction of polysulfides and accelerated multistep sulfur conversion. Density functional theory calculations reveal uniformly low‐energy barriers along the Li 2 S 8 ‐to‐Li 2 S pathway, with no evident rate‐limiting step. Benefiting from this cooperative design, the sulfur host achieves a ultralow capacity decay (0.028% per cycle over 1000 cycles at 2 C) and enables a high areal capacity (493 mAh g −1 at 4.3 mg cm −2 sulfur loading) with 76.3% retention after 100 cycles at 0.3 C. This work offers a versatile strategy for constructing catalysis‐integrated sulfur hosts and highlights the potential of yolk–shell nanoreactors in advancing practical Li−S energy storage systems.