Unlocking Deep and Fast Potassium-Ion Storage through Phosphorus Heterostructure

• Published in: Small (Weinheim an der Bergstrasse, Germany) Germany), 2023-09, Vol.19 (36), p.e2301750-e2301750
• Main Authors: Zhao, Xiaoju, Geng, Shitao, Zhou, Tong, Wang, Yan, Tang, Shanshan, Qu, Zongtao, Wang, Shuo, Zhang, Xiao, Xu, Qiuchen, Yuan, Bin, Ouyang, Zhaofeng, Peng, Huisheng, Tang, Shaochun, Sun, Hao
• Format: Article
• Language: English
• Subjects: Anodes; Density functional theory; Diffusion rate; Electrode materials; Energy storage; Heterostructures; Ion adsorption; Ion storage; Kinetics; Lithium-ion batteries; Nanotechnology; Phosphorus; Potassium; Rechargeable batteries; Renewable energy
• ISSN: 1613-6810; 1613-6829
• DOI: 10.1002/smll.202301750

Potassium-ion battery represents a promising alternative of conventional lithium-ion batteries in sustainable and grid-scale energy storage. Among various anode materials, elemental phosphorus (P) has been actively pursued owing to the ideal natural abundance, theoretical capacity, and electrode potential. However, the sluggish redox kinetics of elemental P has hindered fast and deep potassiation process toward the formation of final potassiation product (K P), which leads to inferior reversible capacity and rate performance. Here, it is shown that rational design on black/red P heterostructure can significantly improve K-ion adsorption, injection and immigration, thus for the first time unlocking K P as the reversible potassiation product for elemental P anodes. Density functional theory calculations reveal the fast adsorption and diffusion kinetics of K-ion at the heterostructure interface, which delivers a highly reversible specific capacity of 923 mAh g at 0.05 A g , excellent rate capability (335 mAh g at 1 A g ), and cycling performance (83.3% capacity retention at 0.8 A g after 300 cycles). These results can unlock other sluggish and irreversible battery chemistries toward sustainable and high-performing energy storage.