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Atomically Dispersed Tellurium‐Enabled Highly Stable Potassium Metal Batteries

Dandan YuCollege of Materials and Chemistry China Jiliang University Hangzhou Zhejiang ChinaJiawei LuoCollege of Materials and Chemistry China Jiliang University Hangzhou Zhejiang ChinaYing XiongState Key Laboratory for Environment‐Friendly Energy Materials Southwest University of Science & Technology Mianyang Sichuan ChinaM. M. AdilovInstitute of Ion Plasma Laser TechnologiesР. Х. АшуровInstitute of Ion Plasma Laser TechnologiesХ. Б. АшуровInstitute of Ion Plasma Laser TechnologiesJie YangHydrogen Energy Research Center PetroChina Petrochemical Research Institute Beijing ChinaHuayu ChenCollege of Materials and Chemistry China Jiliang University Hangzhou Zhejiang ChinaLaishun QinCollege of Materials and Chemistry China Jiliang University Hangzhou Zhejiang ChinaDong‐Liang PengCollege of Materials, State Key Laboratory for Physical Chemistry of Solid Surfaces, Fujian Key Laboratory of Materials Genome, Collaborative Innovation Center of Chemistry for Energy Materials Xiamen University Xiamen Fujian ChinaDa ChenCollege of Materials and Chemistry China Jiliang University Hangzhou Zhejiang China
Carbon Neutralizationjournal2026en
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ABSTRACT Potassium metal batteries hold great promise for grid‐scale energy storage. As a typical and widely used anode, Potassium (K) metal faces challenges of an unstable solid electrolyte interphase (SEI), notorious dendritic growth, and large volume change during K plating/stripping. Herein, atomic tellurium supported on nitrogen/phosphorus‐codoped porous carbon nanofibers (TeNPC) was designed as the host for accommodating metallic K. The uniformly dispersed Te atoms serve as potassiophilic sites, which can effectively reduce the nucleation energy barrier and guide K nuclei formation and growth. The atomic Te not only allows the homogeneous distribution of the electric field but also enhances the binding energy of the host to decrease K + concentration polarization, inducing smooth K deposition. Additionally, the hierarchical pore structure of TeNPC and the formation of SEI with a KF‐rich inner layer contribute to a dendrite‐free morphology of K@TeNPC. Consequently, TeNPC enables a low nucleation overpotential (~21 mV at 0.5 mA cm –2 and 1.0 mAh cm –2 ) and high Coulombic efficiency (~99.8% after 480 cycles) for K deposition/stripping. Furthermore, K@TeNPC shows favorable rate capability and cycle life in symmetric cells and potassium–sulfur batteries. This work presents a new insight into the development of highly efficient host materials for K metal anodes.

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