As an emerging semiconductor, graphite-phase polymeric carbon nitride (GPPCN) has drawn much attention not only in photocatalysis but also in optical sensors such as electrochemiluminescence (ECL) sensing of metal ions. However, when the concentrations of interfering metal ions are several times higher than that of the target metal ion, it is almost impossible to distinguish which metal ion changes the ECL signals in real sample detection. Herein, we report that the dual-ECL signals could be actuated by different ECL reactions merely from GPPCN nanosheets at anodic and cathodic potentials, respectively. Interestingly, the different metal ions exhibited distinct quenching/enhancement of the ECL signal at different driven potentials, presumably ascribed to the diversity of energy-level matches between the metal ions and GPPCN nanosheets and catalytic interactions of the intermediate species in ECL reactions. On this basis, without any labeling and masking reagents, the accuracy and reliability of sensors based on the ECL of GPPCN nanosheets toward metal ions were largely improved; thus, the false-positive result caused by interferential metal ions could be effectively avoided. As an example, the proposed GPPCN ECL sensor with a detection limit of 1.13 nM was successfully applied for the detection of trace Ni(2+) ion in tap and lake water.
Keywords: carbon nitride nanosheets; dual-signal sensing; electrochemiluminescence; potential resolved; single luminophor.