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Prof. YANG Deren

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering, Zhejiang University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3930-3

Stable precursor engineering for large and high-quality MAPbBr3 single crystal toward efficient high-energy radiation detection

Methylammonium lead tribromide (MAPbBr3) single crystals (SCs) are promising for room-temperature gamma-ray and X-ray detection, but scaling their size often compromises crystal quality. Here, we report a strategic precursor stoichiometry engineering approach to grow inch-sized, high-quality MAPbBr3 SCs via a constant-temperature evaporation method. We show that constructing a robust electrical double layer through organic cation modulation effectively stabilizes the colloidal precursor. This is achieved by synergistically suppressing MA+ deprotonation while promoting MA+ adsorption as counterions on the [PbBrn]2−n complexes, which collectively strengthens interparticle repulsion and raises the nucleation barrier. This multifaceted approach yields MAPbBr3 SCs with lateral dimensions up to 2 inches and an exceptional X-ray diffraction rocking curve full width at half maximum (FWHM) of 0.0093° at the (002) face. Consequently, the SCs enable spectroscopic-grade gamma-ray detection, achieving energy resolutions (ER) of 8.4% for the 57Co source (122 keV) and 11.1% for the 137Cs source (662 keV), along with a high X-ray sensitivity of 1.65 × 10^4 μC Gy−1 cm−2. This work paves the way for the practical application of MAPbBr3 SCs in high-performance gamma-ray and X-ray detection.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4070-2

Precise Modulation of Surface Pb-Rich Intermetallic Pd3Pb Nanocubes for Efficient Electrocatalytic CO2 Reduction

A series of ~20 nm intermetallic Pd3Pb nanocubes with tunable surface Pb exposure were synthesized via a facile one-step solvothermal approach, providing an ideal system to investigate the way in which the surface configurations of Pb-rich (Pd3Pb/Pb), Pd-rich (Pd3Pb/Pd), and standard Pd3Pb nanocubes influence the CO2 reduction reaction (CO2RR) mainly through the ligand effect while excluding geometric influences. Electrochemical measurement results indicate that the Pd3Pb/Pb catalyst delivered outstanding C1+ selectivity, achieving a high Faradaic efficiency of 96.88% at −0.72 V (vs. RHE), significantly outperforming the Pd3Pb/Pd (39.86%) and standard Pd3Pb (81.75%) counterparts. In situ FTIR together with DFT calculations further elucidated that Pb incorporation can modulate the electronic structure of Pd via p-d hybridization, leading to the upshift of the d-band center. This will, in return, strengthen the intermediate adsorption ability and lower the energy barriers of the C1+ pathways while effectively suppressing the competing hydrogen evolution reaction. This work establishes a precise surface engineering paradigm of intermetallic nanocrystals for designing high-performance electrocatalysts.