To improve the accuracy and reliability of the detection system, this study combined the exonuclease-assisted autocatalytic target cycling fluorescence strategy with an electrochemical platform to establish a dual-mode fluorescence-electrochemical aptasensor for the ultra-sensitive quantification of lead ion (Pb2+). In the fluorescence detection strategy, ssDNA could hybridize with the aptamer to form double-stranded DNA. With the addition of Pb2+, the aptamer dissociated from the double-stranded DNA to capture Pb2+ and trigger the enzymatic digestion process, leading to the target recirculation to achieve the first signal amplification. The free ssDNA could then hybridize with S1, and the released S2 was able to trigger a hybridization chain reaction (HCR) in the electrochemical system, achieving the second signal amplification. The quantification of Pb2+ was realized by measuring both the fluorescence and the differential pulse voltammetry signals with detection limits of 0.028ng/mL and 0.788pg/mL, respectively. This fluorescence-electrochemical dual-mode aptasensor overcame the limitations of complex matrices and environmental interference, and provided a valuable reference for the development of reliable multi-signal sensors in water, tea and vegetable safety monitoring.