A General Route for Encapsulating Monodispersed Transition Metal Phosphides into Carbon Multi‐Chambers toward High‐Efficient Lithium‐Ion Storage with Underlying Mechanism Exploration

Abstract

Abstract Transition metal phosphides (MP x ) with high theoretical capacities and low cost are regarded as the most promising anodes for lithium‐ion batteries (LIBs), but the large volume variations and sluggish kinetics largely restrict their development. To solve the above challenges, herein a generic but effective method is proposed to encapsulate various monodispersed MP x into flexible carbon multi‐chambers (MP x @NC, MNi, Fe, Co, and Cu, etc.) with pre‐reserved voids, working as anodes for LIBs and markedly boosting the Li + storage performance. Ni 2 P@NC, one representative example of MP x @NC anode, shows high reversible capacity (613 mAh g −1 , 200 cycles at 0.2 A g −1 ), and superior cycle stability (475 mAh g −1 , 800 cycles at 2 A g −1 ). Full cell coupled with LiFePO 4 displays a high reversible capacity (150.1 mAh g −1 at 0.1 A g −1 ) with stable cycling performance. In situ X‐ray diffraction and transmission electron microscope techniques confirm the reversible conversion reaction mechanism and robust structural integrity, accounting for enhanced rate and cycling performance. Theoretical calculations reveal the synergistic effect between MP x and carbon shells, which can significantly promote electron transfer and reduce diffusion energy barriers, paving ways to design high‐energy‐density materials for energy storage systems.