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Updated: Oct 25, 2026

Elemental-sensitive Detection of the Chemistry in Batteries through Soft X-ray Absorption Spectroscopy and Resonant Inelastic X-ray Scattering
Published on: April 17, 2018
Dual-Defects Engineering and Fe-S-Ga Bridging Synergy in Secondary Battery Anode Enable Fast-Charging and Durable
Xiaofei Huang1, Tianli Han1, Haohan Song1
1Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui241002, PR China.
Abstract:
Defect-engineering commonly enables improved energy-storage performance; however, how it synergizes with interfacial bond bridging to boost fast-charging capacity remains a challenge. Here, we develop a FeS2@Ga2S3 heterostructure as sodium-ion battery anode that integrates dual-phase vacancies with Fe-S-Ga bonds. Peak-force atomic force microscopy and insitu characterizations reveal that Fe-S-Ga bonds enable structural stability. Density functional theory (DFT) calculations and kinetic analyses demonstrate the tailored heterointerface exhibits moderate Na+ adsorption energy and reduced diffusion barrier. The FeS2@Ga2S3 anode delivers a capacity of 468.5 mAh g-1 after 1000 cycles at 10.0 A g-1 with nearly 100% Coulombic efficiency, an exceptional rate-performance keeping 416.8 mAh g-1 at 20.0 A g-1, and stable performance over wide temperatures from -15 to 50 °C. FeS2@Ga2S3||Na3V2(PO4)3 full cell retains 442.4 mAh g-1 after 500 cycles at 1.0 A g-1, exhibiting a good potential for applications. This dual-defects and chemical bond-bridging design could be applied for developing a broad set of battery systems.
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