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Unlocking Ultralong Cycle Life and Temperature-Tolerable Secondary Batteries Using a Vacancy-Abundant
Xiaofei Huang1, Kehao Tao2, Kaifeng Huang3
1Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, Anhui 241002, PR China.
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Sodium-ion batteries face some critical anode-level barriers: sluggish Na+ transport, conversion-induced instability, and poor temperature adaptability. Here, we develop a vacancy-based synergy in Co9S8@ZnS/C synthesized by metal-organic framework-templated sulfidation. The Co-Zn-S system provides sodiophilic vacancies that lower Na+ diffusion barriers and further strengthen the interfacial field. This self-reinforcing synergy is validated through in situ X-ray diffraction and in situ Raman spectroscopy, demonstrating reversible conversion/alloying and interfacial reconstruction. The Co9S8@ZnS/C anode delivers exceptional performance, including a high capacity of 458.7 mAh g-1 after 400 cycles at 1.0 A g-1 and a remarkable ultralong stability of 249.1 mAh g-1 after 4000 cycles at 15.0 A g-1, with robust operation from -10 to 50 °C. Full cells paired with Na3V2(PO4)3 demonstrate excellent stability, validating their practical viability. This work establishes a generalizable vacancy-abundant design principle that deterministically links defect thermodynamics and electrostatics to long-term Na storage across diverse operating conditions.
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