Issue 27, 2025

Dual-interface engineered SnO2/Sn4P3@C heterojunctions: built-in electric field-driven fast kinetics for highly reversible lithium storage

Abstract

The practical application of SnO2 anodes in lithium-ion batteries is fundamentally constrained by cascading challenges of structural degradation and kinetic limitations. We demonstrate a dual-interface engineering strategy through precisely controlled gas-phase phosphorization, constructing SnO2/Sn4P3 heterojunctions tightly encapsulated within hierarchical carbon frameworks (SnO2/Sn4P3@C, SOPC). The SnO2/Sn4P3 heterojunction generates a built-in electric field, reducing charge transfer resistance and activation energy (UPS work function: 2.91 eV) and guides LiF-rich SEI formation, while the dual-carbon confinement buffers mechanical strain and ensures the structural stability with long-term cycling at high current density. These features enable hybrid storage kinetics with capacitive dominance at high rates and stable faradaic reactions at low currents. The SOPC anode achieves exceptional cyclability with capacities of 954.8 mA h g−1 after 600 cycles at 1 A g−1 and 118.9 mA h g−1 after 3000 cycles at 20 A g−1. Full cells paired with LiFePO4 demonstrate practical viability. This work establishes a universal interfacial engineering strategy for high-performance alloying/conversion anodes, bridging atomic-scale electronic modulation to scalable battery systems.

Graphical abstract: Dual-interface engineered SnO2/Sn4P3@C heterojunctions: built-in electric field-driven fast kinetics for highly reversible lithium storage

Supplementary files

Article information

Article type
Paper
Submitted
18 Apr 2025
Accepted
16 Jun 2025
First published
17 Jun 2025

Phys. Chem. Chem. Phys., 2025,27, 14589-14596

Dual-interface engineered SnO2/Sn4P3@C heterojunctions: built-in electric field-driven fast kinetics for highly reversible lithium storage

Z. Huang, Z. Wu, W. Miao, Z. Yu, H. Jia, Q. Chen, X. Huang, Z. Lin and S. Ying, Phys. Chem. Chem. Phys., 2025, 27, 14589 DOI: 10.1039/D5CP01495F

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