SinoGreenTech Academic Portal
WZ
Verified CAS / Academic Author2 Decoded Studies

Prof. Wenli Zhou

Key Laboratory of Light Energy Conversion Materials of Hunan Province, College of Chemistry and Chemical Engineering, Hunan Normal University

Co-Affiliations:State Key Laboratory of Environmental-friendly Energy Materials, Southwest University of Science and Technology

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3969-9

Interface Reaction Inhibition in Phosphor-in-Silica Glass for High-Performance Laser Illumination

Phosphor-in-glass (PiG) materials are promising color converters for high-power laser illumination, yet suppressing interfacial reactions between phosphor and glass matrix at elevated sintering temperatures remains a critical challenge. Here, we report a Y3Al5O12:Ce3+ (YAG:Ce) phosphor-in-silica glass (PiSG) with high SiO2 content (>85 wt%) fabricated via a Cs2CO3 flux. Incorporation of Cs2O significantly inhibits SiO2-YAG:Ce reactions, preserving internal quantum efficiency (IQE) at 97.7% of pure YAG:Ce, and achieving 88.3% IQE even after calcination at 1400°C for 2 h. In contrast, smaller alkali ions (Li+, Na+) accelerate YAG:Ce decomposition. Mechanistic studies reveal that Cs+ with large ionic radius and weak interaction with oxygen suppresses non-bridging oxygen (NBO) formation, promoting a complete silica network that limits alkali ion diffusion. Leveraging the mixed alkali effect (10% Li2O + 5% Cs2O), the PiSG exhibits enhanced hydrothermal stability, withstanding 200°C treatment for 10 h. A PiG film-sapphire device delivers 3080 lm luminous flux and 213 lm W−1 efficiency under blue laser excitation. These findings establish YAG:Ce-PiSG as a highly promising color-conversion material for high-performance laser illumination.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-4185-6

Rapid Reconstruction of Commercial Bulk Niobium Oxide for Highly Stable Electrochemical Uranium Extraction in the Presence of Fluorine

Electrochemical uranium extraction from fluorine-containing nuclear wastewater is critical for nuclear fuel recovery, yet current electrode materials suffer from limited scalability and insufficient long-term stability. Here, we report a bulk monoclinic Nb2O5−x (H-Nb2O5−x) derived from commercial bulk niobium oxide via rapid reconstruction, exhibiting exceptional activity and robustness for electrochemical uranium extraction in fluorine-rich environments. The intrinsic active pairs of low-valent Nb4+ and compact oxygen structure strongly bind with dominant uranyl fluoride species (UO2F+, UO2F2, UO2F3−, UO2F4^2−), facilitating efficient separation. In a 30 g L−1 fluoride solution, H-Nb2O5−x achieved a uranium extraction efficiency of 99.1%. Notably, in a 10-L real nuclear wastewater test, the bulk material maintained stable performance over 40 days, reducing uranium concentration from 1372.3 mg L−1 to 0.93 mg L−1. This work demonstrates a scalable, durable electrode material for industrial electrochemical uranium extraction, addressing the bottlenecks of complexation and stability in fluoride-containing waste streams.