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YW
Verified CAS / Academic Author2 Decoded Studies

Prof. Yuping Wu

Fudan University

Co-Affiliations:School of Chemical Engineering, Nanjing University of Science and Technology

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3599-5

Tellurium vacancy-rich Bi2Te3 as a high-performance cathode material for aqueous zinc ion storage

Layered transition metal tellurides (TMTs) are promising cathode materials for aqueous zinc ion batteries (AZIBs) due to their graphite-like layered structure and weak van der Waals interactions, which facilitate rapid ion transport. However, their holistic performance—specific capacity, rate capability, and cycling stability—remains insufficient for practical applications. Here, we report a straightforward NaBH4-assisted chemical etching method to introduce abundant Te vacancies on the surface of Bi2Te3 (denoted H-Bi2Te3). Experimental and theoretical analyses reveal that these Te vacancies refine the band structure, enhance electrical conductivity, and significantly reduce the diffusion barrier for Zn2+ ions. Additionally, the vacancies provide increased storage sites for Zn ions. Consequently, H-Bi2Te3 exhibits superior zinc storage performance: a high Zn2+ diffusion coefficient of 3.98×10−11 cm2 s−1, a specific capacity of 325 mAh g−1 at 0.1 A g−1, a rate capability of 217 mAh g−1 at 1 A g−1, and exceptional cycling stability with 70 mAh g−1 retained after 10,000 cycles at 1 A g−1. This work introduces a novel vacancy defect engineering strategy for TMT-based cathodes in AZIBs and expands the potential applications of vacancy-rich TMT materials.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3944-9

Dual-Functional Chemical Pre-Sodiation of Carbon-Coated Hard Carbon Anodes with Initial Coulombic Efficiency up to 99.5% for Sodium-Ion Batteries

Hard carbon (HC) is a promising anode material for sodium-ion batteries (SIBs) but suffers from low initial Coulombic efficiency (ICE) and unstable solid electrolyte interphase (SEI). Here, we report a dual-functional strategy combining surface engineering and solution chemical pre-sodiation. A graphitic carbon coating on HC acts as a conductive buffer network and shields surface defects, while sodium biphenyl (Na-Bp) pre-sodiation drives sodium ions into the material via a potential difference, inducing a pre-SEI layer that matures into a thin, dense, NaF-rich inorganic SEI during cycling. This approach compensates for irreversible sodium loss and enhances cycling stability. The pre-sodiated electrode (pCH4-HC) achieves an ICE of 99.5% and a reversible capacity of 321.7 mAh g−1, compared to 54.2% for untreated HC. Long-term cycling shows 74.0% capacity retention after 1000 cycles at 300 mA g−1. In full-cells with NaNi1/3Fe1/3Mn1/3O2 (NFM) cathode, pCH4-HC||NFM delivers 81.9 mAh g−1 after 100 cycles, demonstrating excellent stability and rate performance. This dual-strategy approach validates the adaptability of pre-sodiation technology for high-performance SIBs.