Currently, cathodic photoelectrochemical (PEC) sensors, which could effectively reduce background interference, are urgently required for ultrasensitive environmental monitoring. Herein, porphyrin-based covalent organic framework (TAPP-COF) thin films were fabricated via a bottom-up growth approach on the liquid/liquid interface and applied as a photocathode material to "on-off-on" PEC sensing of Pb2+. Benefitting from the unique charge channels of COFs and the good photoelectric properties of porphyrin, the as-prepared TAPP-COF thin films presented an improved photocathodic current, with a strongly enhanced "signal-on" response with low background. Then, CdSe@SiO2 quantum dots (QDs), as a quenching agent, were introduced through a hybridization chain reaction (HCR) to obtain a "signal off" PEC response. Afterward, with the introduction of target Pb2+, CdSe@SiO2 QDs were detached from TAPP-COF thin films, and the PEC response transformed into a signal-on state. Benefiting from the multiple-quenching and steric hindrance effect of CdSe@SiO2 QDs and the photocathodic property of TAPP-COFs, accurate monitoring of Pb2+ in a wide detection range from 0.05 to 1000 nM with a lower detection limit of 0.012 nM was realized based on the proposed on-off-on PEC approach. Notably, the methodology provides an efficient platform for ultrasensitive determination of heavy metal ions, which would play a significant role in environmental monitoring and public safety fields.
Keywords: covalent organic frameworks; lead ion; photocathode; photoelectrochemical; porphyrin.