SinoGreenTech Academic Portal
SL
Verified CAS / Academic Author2 Decoded Studies

Prof. Shisheng Li

College of Materials, Xiamen University

Co-Affiliations:College of Science, Nanjing University of Aeronautics and Astronautics

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4315-2

Ultra-high-crystallinity transparent glass-ceramic scintillators for high-temperature X-ray imaging

High-temperature X-ray imaging demands scintillators with high crystallinity, efficient scintillation, and robust thermal stability, yet suitable materials remain scarce. Here, we report an ultra-high-crystallinity transparent glass-ceramic (GC) scintillator strategically designed via controllable heat-treatment-induced crystallization. A sequential precipitation method is employed, where cubic CaF2 nanocrystals initially form, subsequently promoting heterogeneous nucleation and growth of hexagonal BaAl2Si2O8. Intrinsic nanoscale phase separation into F-rich and O-rich domains significantly reduces atomic diffusion distances, yielding an unprecedented crystallinity of up to 97.6%. Notably, defect traps (oxygen vacancy defects, likely located within the lattice or at crystalline/amorphous interfaces) enable efficient carrier capture and thermally stimulated release, contributing to remarkable resistance to thermal quenching. Consequently, the GC scintillator maintains 90.6% of its integrated X-ray excited luminescence (XEL) intensity at 300 °C, with the integrated XEL intensity reaching 94.2% of commercial Bi4Ge3O12 (BGO) at room temperature. This enables stable high-temperature X-ray imaging with a spatial resolution of ~10.4 lp mm−1 up to 225 °C. This work provides a versatile pathway for developing high-sensitivity scintillators for extreme-environment X-ray imaging.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-4097-3

Stress-Guided Anisotropic Etching of MoS2 Nanostructures with Spatial Control over Edge Structure and Morphology

The on-demand patterning of two-dimensional transition metal dichalcogenides (TMDs) with tailored edges is critical for electronic and optoelectronic applications but remains technically challenging. Here, we report a stress-guided anisotropic etching strategy for producing large-area, well-ordered MoS2 nanostructures, including nano-ribbons and nano-squares, without templates. By applying uniaxial cumulative stress followed by selective thermal etching, MoS2 monolayers are statistically etched into ribbon-like structures whose width inversely correlates with applied stress magnitude. The newly etched edges are macroscopically straight or serrated, predominantly Mo-zigzag terminated, and enhance photoluminescence by a factor of ~8.0. The edge type depends on the angle between stress direction and crystallographic orientation, corroborated by theoretical calculations. Biaxial stressing generates well-defined nano-squares, offering a scalable, versatile patterning route for engineering 2D materials with tailored functional edges, promising for electrocatalytic and optoelectronic applications.