Dual‐Site Activation Coupling with a Schottky Junction Boosts the Electrochemiluminescence of Carbon Nitride

Author:

Wu Zhichao1,Wen Jing2,Qin Ying1,Ling Ling1,Jiao Lei1,Zhang Ruizhong3,Luo Zhen1,Xi Mengzhen1,Hu Liuyong2,Gu Wenling1,Zhu Chengzhou1ORCID

Affiliation:

1. National Key Laboratory of Green Pesticide International Joint Research Center for Intelligent Biosensing Technology and Health College of Chemistry Central China Normal University Wuhan 430079 P. R. China

2. Hubei Key Laboratory of Plasma Chemistry and Advanced Materials Hubei Engineering Technology Research Center of Optoelectronic and New Energy Materials Wuhan Institute of Technology Wuhan 430205 P. R. China

3. Tianjin Key Laboratory of Molecular Photoelectronic Sciences Department of Chemistry Tianjin University Tianjin 300072 P. R. China

Abstract

AbstractRobust electrochemiluminescence (ECL) of carbon nitride (CN) requires efficient electron‐hole recombination and the suppression of electrode passivation. In this work, Au nanoparticles and single atoms (AuSA+NP) loaded on CN serve as dual active sites that significantly accelerate charge transfer and activate peroxydisulfate. Meanwhile, the well‐established Schottky junctions between Au NPs and CN act as electron sinks, effectively trapping over‐injected electrons to prevent electrode passivation. As a result, the porous CN modified with AuSA+NP exhibits an enhanced and stable ECL emission, with a minimal relative standard deviation of 0.24 %. Furthermore, the designed ECL biosensor based on AuSA+NP‐CN shows a remarkable performance in detecting organophosphorus pesticides. This innovative strategy has the potential to offer new insights into strong and stable ECL emission for practical applications.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

Subject

General Chemistry,Catalysis

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