Triple‐Shell Hollow FeS/MoS2 Heterostructure Anodes: Synergistic Effects of Built‐In Electric Field on Ultra‐Stable Sodium Storage

MoS2 as anode material for SIBs usually suffers from slow Na⁺ diffusion and low conductivity. In this work, triple‐shell FeS/MoS2@NC structured material as anode are designed, where the FeS/MoS2 heterostructure interface introduced internal electric field and spin‐polarized surface capacitance could boost Na⁺ diffusion dynamics and further enhance Na⁺ storage, ensuring excellent long‐cycle stability (451.5 mAh g−1 for 9 000 cycles). Abstract Metal sulfides are intensively pursed as promising anode materials for sodium‐ion batteries (SIBs) owing to their high theoretical capacities, abundant and inexpensive raw materials, however, challenges remain in designing their structures, particularly due to the slow Na⁺ storage kinetics in individual sulfide, and unshaped and inefficient heterostructure persists the issue of low intrinsic ion conductivity. Herein, hollow triple‐shell FeS/MoS2@NC structure by integrating molecular and microstructural engineering is constructed. The intimate connection between FeS and MoS2 in FeS/MoS2@NC arises from the simultaneous sulfidation of Fe2(MoO4)3. This hollow multi‐shell structure, along with the high effective built‐in electric field between the sulfides, effectively mitigates the volume expansion and propelled Na⁺ storage kinetics. Additionally, superparamagnetic Fe0 nanodots appeared from FeS reduction at low voltage during charge–discharge cycles facilitate Na+ storage. As a result, the hollow triple‐shell FeS/MoS2@NC presented high reversible capacity (611.8 mAh g−1 at 0.1 A g−1) and ultra‐stable cycling span‐life (451.5 mAh g−1 after 9000 cycles at 5 A g−1). In addition, the assembled Na3V2(PO4)3@rGO//FeS/MoS2@NC coin‐type full cell exhibited remarkable electrochemical performance (322.2 mAh g−1 after 400 cycles at 1 A g−1). This work will stimulate the further development of metal sulfide heterostructure and also provide new perspectives on high performance SIBs anodes. MoS 2 as anode material for SIBs usually suffers from slow Na⁺ diffusion and low conductivity. In this work, triple-shell FeS/MoS 2 @NC structured material as anode are designed, where the FeS/MoS 2 heterostructure interface introduced internal electric field and spin-polarized surface capacitance could boost Na⁺ diffusion dynamics and further enhance Na⁺ storage, ensuring excellent long-cycle stability (451.5 mAh g −1 for 9 000 cycles). Abstract Metal sulfides are intensively pursed as promising anode materials for sodium-ion batteries (SIBs) owing to their high theoretical capacities, abundant and inexpensive raw materials, however, challenges remain in designing their structures, particularly due to the slow Na⁺ storage kinetics in individual sulfide, and unshaped and inefficient heterostructure persists the issue of low intrinsic ion conductivity. Herein, hollow triple-shell FeS/MoS 2 @NC structure by integrating molecular and microstructural engineering is constructed. The intimate connection between FeS and MoS 2 in FeS/MoS 2 @NC arises from the simultaneous sulfidation of Fe 2 (MoO 4 ) 3. This hollow multi-shell structure, along with the high effective built-in electric field between the sulfides, effectively mitigates the volume expansion and propelled Na⁺ storage kinetics. Additionally, superparamagnetic Fe0 nanodots appeared from FeS reduction at low voltage during charge–discharge cycles facilitate Na+ storage. As a result, the hollow triple-shell FeS/MoS 2 @NC presented high reversible capacity (611.8 mAh g −1 at 0.1 A g −1 ) and ultra-stable cycling span-life (451.5 mAh g −1 after 9000 cycles at 5 A g− 1 ). In addition, the assembled Na 3 V 2 (PO 4 ) 3 @rGO//FeS/MoS 2 @NC coin-type full cell exhibited remarkable electrochemical performance (322.2 mAh g −1 after 400 cycles at 1 A g −1 ). This work will stimulate the further development of metal sulfide heterostructure and also provide new perspectives on high performance SIBs anodes. Advanced Science, Volume 12, Issue 43, November 20, 2025.