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WY
Verified CAS / Academic Author3 Decoded Studies

Prof. WU Yutiancheng

College of Electromechanical Engineering, Shandong Engineering Laboratory for Preparation and Application of High-performance Carbon-Materials, Qingdao University of Science & Technology, Qingdao 266061, P. R. China

Co-Affiliations:Not explicitly stated in the provided text; likely a Chinese university or research institute.School of Port and Coastal Engineering, Jimei University, Xiamen 361021, China; Xiamen Key Laboratory of Green and Smart Coastal Engineering, Xiamen 361021, China

Research Publications & English Decoded Briefs

Showing 3 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4369-1

Dual-Modulation of Carbon Coating and High-Valence Nb5+ Doping Toward High-Performance Na3V2(PO4)2O2F Cathode for Sodium-Ion Batteries

Sodium-ion batteries (SIBs) are promising alternatives to lithium-ion batteries for large-scale energy storage due to sodium's abundance and low cost. Among cathode materials, polyanionic compounds like Na3V2(PO4)2O2F (NVPOF) offer high energy density and dual voltage plateaus at ~3.6 and 4.0 V, but suffer from low electronic conductivity and sluggish Na+ diffusion. Here, we report a dual-modulation strategy combining high-valence Nb5+ doping and polydopamine-derived carbon coating to synthesize Na3V1.94Nb0.06(PO4)2O2F-C (NVPOF-Nb-C) via a hydrothermal route. X-ray diffraction and Rietveld refinement confirm that Nb5+ doping induces slight lattice expansion without altering the tetragonal I4/mmm framework. Density functional theory calculations reveal that Nb5+ doping optimizes the crystal structure and reduces the Na+ diffusion barrier, while the uniform carbon coating enhances electron transport. Consequently, NVPOF-Nb-C exhibits remarkably improved electrochemical performance, including high reversible capacity, excellent rate capability, and ultralong cycling stability. In a full cell with hard carbon anode, it delivers a high energy density of 487.2 Wh kg−1 at 1C and retains 91.51% capacity after 3000 cycles at 20C. This work provides a synergistic strategy to overcome the intrinsic limitations of polyanionic cathodes for practical SIB applications.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3746-x

Dual Regulation Strategy to Construct Robust and High-Conductivity Na3V2(PO4)2O2F for Ultra-Long-Life Sodium-Ion Full Cells

The polyanionic compound Na3V2(PO4)2O2F (NVPOF) possesses a stable three-dimensional framework, high theoretical specific capacity, and favorable operating voltage, yet its sluggish Na+ diffusion kinetics and low electronic conductivity impede industrial application. This study proposes a dual regulation strategy combining carbon coating and heat treatment temperature to synergistically enhance crystallinity and electrochemical performance. NVPOF@C-400 and NVPOF@C-600 were synthesized via in-situ dopamine hydrochloride coating followed by heat treatment at 400 °C and 600 °C, respectively. Carbon coating at 600 °C significantly improved crystallinity and increased electronic conductivity by three orders of magnitude through the carbon layer's conductive network. The ~4.5 nm carbon layer effectively suppressed abnormal grain growth and secondary crystallization aggregation at high temperatures, maintaining uniform particle size of approximately 0.36 μm, which shortens Na+ diffusion pathways and prevents ion transport obstruction. Consequently, NVPOF@C-600 delivered a high discharge capacity of 102.5 mAh g−1 at 20 C and retained 96.5% capacity after 10,000 cycles. In a full-cell configuration with hard carbon (HC), NVPOF@C-600//HC achieved an impressive 89.3% capacity retention after 9,000 cycles. This work provides critical insights for practical implementation of high-performance NVPOF cathodes in sodium-ion batteries.

Chinese Journal of Environmental Engineering2026DOI: 10.12030/j.cjee.202511062

Application and Mechanistic Study of Lactate Regulation and Microbial Immobilization Technology in Sediment Microbial Fuel Cell Systems

Sediment microbial fuel cells (SMFCs) are a green technology for simultaneous polluted sediment remediation and energy recovery, yet their performance is constrained by insufficient anodic microbial activity and low electron transfer efficiency. This study employed lactate addition combined with composite engineered microbial immobilization to synergistically optimize SMFC performance by enhancing microbial stability and carbon source supply. Results showed that lactate, as an easily utilized electron donor, promoted electrochemical activity, achieving a maximum power density of 22.06 mW·m−2 at 6 mmol·L−1, a 194% improvement over the blank group. Immobilization further enhanced electron transfer efficiency, with the highest output voltage (88.75 mV) being 2.09 times that of the non-immobilized group. For pollutant degradation, the 6 mmol·L−1 lactate group achieved TOC and TN removal rates of 29.02% and 28.4%, respectively, outperforming the control (22.41% and 21.42%). However, high lactate concentrations inhibited microbial metabolism, leading to TOC accumulation. 16S rRNA analysis revealed that the anodic microbial community was dominated by Bacillota and Pseudomonadota, both possessing electroactive and pollutant-degrading capabilities, indicating that lactate and immobilization exert a synergistic effect in SMFCs, simultaneously enhancing electricity generation and pollutant removal efficiency.