CDs assembled metal-organic framework: Exogenous coreactant-free biosensing platform with pore confinement-enhanced electrochemiluminescence

Despite the various synthesis approachs to obtain luminous carbon dots (CDs), it is still quite challenging to construct the efficient electrochemiluminescence (ECL) owing to their low ECL reactivity and easy agglomeration. Herein, an efficient and concise ECL system was skillfully constructed by taking advantage of the nitrogen and sulfur co-doped CDs (N,S-CDs) with surfaces rich in hydrazide groups as luminophors to emit intense ECL, and metal-organic framework (MOF) as the matrix to confine CDs in its nanospace. Surprisingly, the proposed CDs assembled MOF (CDs/ZIF-8) enhanced anodic ECL signal up to 250% of pure CDs under the exogenous coreactant-free condition. As a proof of concept, the highly sensitive detection of uric acid (UA) was realized by the constructed ECL platform with a low detection limit of 3.52 nmol/L ranging from 10 nmol/L to 50 µmol/L. This work expanded ideas for the application of pore confinement effect, and provided references for the detection of disease biomarkers of gout and hyperuricemia. Herein, an efficient ECL nanoluminophor of the CDs assembled MOF was skillfully prepared by taking advantage of the nitrogen and sulfur co-doped CDs (N,S-CDs) with surfaces rich in hydrazide groups as luminophors and MOF as matrix. Due to the pore confinement-enhanced ECL, the anodic ECL signal rose up to 250% of the pure CDs under the exogenous coreactant-free condition.