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Prof. Ting Xiang

Sun Yat-sen University

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SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3906-2

Dual-mode Förster resonance energy transfer for color-tunable and stimulus-responsive organic afterglow

Achieving flexible polymer-based organic afterglow materials with color-tunable and stimulus-responsive capabilities is significant in diverse optoelectronic fields, especially in next-generation wearable full-color display applications, yet remains a great challenge. Here, we report polymer-based dual-mode afterglow systems that realize long-lived color-tunable afterglow with full-color gamut of blue, green, orange, red, and even white-light emissions with ultralong lifetimes up to 2.42 s. This unique performance is enabled by a universal strategy of dual-mode afterglow-assisted Förster resonance energy transfer (FRET) that utilizes seconds-long dual-mode afterglow materials as energy donors and permits efficient synchronous transfer of singlet and triplet excitons from energy donors to the fluorescent dye acceptors. More impressively, the dual-mode afterglow-assisted FRET efficiency reaches up to 99%, with the lifetime of the energy acceptor reaching 1.55 s. Associated with the abundant hydrogen-bonding interactions within the polymer system, the doped afterglow films exhibit water/thermal stimulus responsiveness and recyclability. Furthermore, these full-color dual-mode afterglow materials are employed for multicolor screen-printing, optical anti-counterfeiting, and high-level information encryption, demonstrating considerable application potential in advanced anti-counterfeiting technologies.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3480-1

Highly dispersed Cu/WO3 heterojunctions featuring a promoted hydrogen radical-mediated pathway for efficient nitrate reduction to ammonia

Electrochemical nitrate reduction to ammonia (NRA) offers a sustainable route for wastewater denitrification and decentralized ammonia synthesis, but its practical deployment is constrained by sluggish reaction kinetics and the competing hydrogen evolution reaction (HER). Monometallic Cu electrocatalysts, despite favorable nitrate adsorption and tunable electronic structure, exhibit weak H* adsorption, limiting the hydrogen radical-mediated pathway that suppresses HER at low overpotentials. Here, highly dispersed Cu/WO3 heterojunctions supported on carbon fiber were synthesized via carbothermal shock reduction, which reaches ultra-high temperatures within seconds and prevents active-site accumulation. The optimal Cu/WO3 heterojunction achieves an ammonia yield rate of 158.66 μmol h−1 cm−2 and a Faradaic efficiency of 98.27%. Electron paramagnetic resonance and density functional theory calculations reveal a synergistic mechanism: Cu sites preferentially adsorb NO3−, while adjacent WO3 sites accelerate water dissociation to generate hydrogen radicals (H*), which drive the continuous hydrogenation of nitrate to ammonia. This spatial separation of functions promotes the H*-mediated pathway and suppresses HER. The work establishes a heterojunction design strategy for non-precious-metal NRA electrocatalysts, enabling high-rate, high-selectivity ammonia production under mild conditions.