Timescale correlation of shallow trap states increases electrochemiluminescence efficiency in carbon nitrides
Yanfeng Fang,
Hong Yang,
Yuhua Hou,
Wang Li,
Yanfei Shen (),
Songqin Liu and
Yuanjian Zhang ()
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Yanfeng Fang: School of Chemistry and Chemical Engineering
Hong Yang: School of Chemistry and Chemical Engineering
Yuhua Hou: School of Chemistry and Chemical Engineering
Wang Li: School of Chemistry and Chemical Engineering
Yanfei Shen: Southeast University
Songqin Liu: School of Chemistry and Chemical Engineering
Yuanjian Zhang: School of Chemistry and Chemical Engineering
Nature Communications, 2024, vol. 15, issue 1, 1-13
Abstract:
Abstract Highly efficient interconversion of different types of energy plays a crucial role in both science and technology. Among them, electrochemiluminescence, an emission of light excited by electrochemical reactions, has drawn attention as a powerful tool for bioassays. Nonetheless, the large differences in timescale among diverse charge-transfer pathways from picoseconds to seconds significantly limit the electrochemiluminescence efficiency and hamper their broad applications. Here, we report a timescale coordination strategy to improve the electrochemiluminescence efficiency of carbon nitrides by engineering shallow electron trap states via Au-N bond functionalization. Quantitative electrochemiluminescence kinetics measurements and theoretic calculations jointly disclose that Au-N bonds endow shallow electron trap states, which coordinate the timescale of the fast electron transfer in the bulk emitter and the slow redox reaction of co-reagent at diffusion layers. The shallow electron trap states ultimately accelerate the rate and kinetics of emissive electron-hole recombination, setting a new cathodic electrochemiluminescence efficiency record of carbon nitrides, and empowering a visual electrochemiluminescence sensor for nitrite ion, a typical environmental contaminant, with superior detection range and limit.
Date: 2024
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DOI: 10.1038/s41467-024-48011-y
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