Screening high-performance anodic electrochemiluminescence
(ECL)
systems with low triggering potential is a promising way to broaden
their applications. In addition to electrochemiluminophore, co-reactant
also plays an important role in the ECL process, since the oxidation
of co-reactants is one of the most important steps in the anodic ECL
process. Herein, a novel co-reactant-mediated high-performance low-potential
Au nanocluster (AuNC)-based ECL system has been successfully developed.
Benefiting from the isopropyl substitution and hydroxyl addition to
the triethylamine (TEA), the BSA-AuNC/2-(diisopropylamino)ethanol
(DIPEA-OH) ECL system achieved higher energy efficiency at a lower
potential of 0.75 V. In addition, compared with the BSA-AuNC/TEA system,
the ECL intensity and quantum yield (Φ
ECL) with DIPEA-OH as a co-reactant increased 22.34-fold and
13-fold (as high as 68.17%), respectively. Based on the low potential,
high Φ
ECL of the AuNC/DIPEA-OH ECL
system, a sandwich-type immunosensor has been constructed for a highly
selective SARS-CoV-2 N protein assay. In the absence of any complex
signal amplification strategies, the ECL immunosensor for the SARS-CoV-2
N protein detection showed a linear range of 0.001–100 ng/mL
and a detection limit of 0.35 pg/mL. Moreover, the ECL platform had
good reproducibility and stability and exhibited acceptable detection
performance in the detection of actual serum samples. This work established
a framework for in-depth design and study of anode ECL co-reactants
for AuNCs and other luminophores, and expanded the potential application
of ECL sensors in the clinical diagnosis of COVID-19.