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Prof. Ke Gao

Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University

Co-Affiliations:Shandong University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3666-2

Blue-emitting ionic multi-resonance emitters for efficient narrowband light-emitting electrochemical cells

Light-emitting electrochemical cells (LECs) are promising for low-cost, solution-processed display and lighting applications, yet achieving high efficiency and color purity remains challenging. Here, we report two ionic multi-resonance (MR) emitters with narrowband blue emission for high-color-purity LECs. By covalently bonding an imidazolium functional group into a boron/nitrogen-doped polycyclic skeleton, the emitters retain the narrowband emission and high photoluminescence quantum yield (PLQY) of the MR core while gaining ionic character. The design exploits two types of nitrogen atoms in the imidazolium unit: the pyrrolic N at the 1-position forms a para-B-π-N linkage, elevating excited-state energy levels and blue-shifting emission; the pyridinic N at the 3-position provides a quaternization site, yielding intrinsically ionic emitters compatible with ionic hosts. The emitters exhibit blue emission with narrow full-width at half-maximum of 26–27 nm and high PLQYs of 95%–97% in solid-state films. LECs based on these emitters achieve narrowband blue electroluminescence with CIE coordinates of (0.12, 0.26) and a maximum external quantum efficiency (EQE) of 4.6%, representing the first narrowband blue LECs based on intrinsically ionic MR emitters. This work demonstrates a viable molecular design strategy for high-color-purity LECs, addressing the long-standing trade-off between efficiency and color purity in this technology.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3497-6

Functional graphdiyne based on perylene diimide units facilitating boosted performance of photothermal catalytic hydrogen evolution

Graphdiyne (GDY) possesses a tunable intrinsic bandgap, high charge carrier mobility, and broad-spectrum absorption, making it a candidate for photocatalytic hydrogen evolution. However, GDY/wide-band semiconductor photocatalysts are constrained by low doping concentrations and insufficient absorption in the visible-to-near-infrared (Vis-NIR) region, which limits full-spectrum energy utilization. To address these limitations, functional graphdiyne quantum dots (PG-QDs) incorporating perylene diimide (PDI) units were designed and synthesized. The PG-QDs exhibit tailored spectral absorption, reducing competition with wide-band semiconductors for UV light while enhancing Vis-NIR absorption and photothermal conversion. The PG-QDs overcome the doping concentration limitations of conventional GDY-based photocatalysts, achieving an optimal doping ratio of 15% without suppressing hydrogen evolution activity. The pronounced photothermal effect effectively suppresses the recombination of photogenerated carriers and enhances charge carrier separation efficiency. The hydrogen evolution rate reached 12.69 mmol g−1 h−1, over thirty times higher than that of P25. This study presents a strategy for improving the full-spectrum energy utilization of GDY-based photocatalysts.