Near-infrared electrochemiluminescence of defect-rich molybdenum disulfide quantum dots for sensitive bioanalysis

Developing high-efficiency near-infrared (NIR) electrochemiluminescence (ECL) active transition metal dichalcogenides quantum dots (TMDs QDs) for spectroscopic multiplex analysis and biological imaging poses a significant challenge in versatile bioanalysis. In this work, we report a facile one-step hydrothermal method for the synthesis of defect-rich molybdenum disulfide quantum dots (MoS 2 QDs). Because of the defect effect on the nanocrystalline surface, the MoS 2 QDs exhibit enhanced fluorescence (quantum yield is 7.7%) in comparison with those from top-down physical approaches. Moreover, the defect-rich MoS 2 QDs exhibit remarkable ECL performance using K 2 S 2 O 8 as a coreactant, with a maximum emission at ∼810 nm. The ECL mechanisms of potential-dependent emission from MoS 2 QDs were elucidated based on electrochemistry, photoluminescence, and spooling ECL spectroscopy. Leveraging the good biocompatibility and defect-induced ECL enhancement of MoS 2 QDs, a sandwich ECL immunosensor was developed for carcinoembryonic antigen (CEA) detection. Without any signal amplification techniques, the proposed biosensor demonstrated a detection limit of 0.005 ng/mL CEA with a linear range from 0.005 ng/mL to 400 ng/mL, and a good selectivity and potential for real human serum analysis. The defect engineering of MoS 2 QDs in this study provides guidance for regulating their optical properties and exploring new bioanalysis applications.