Electric Field-Induced Specific Preconcentration to Enhance DNA-Based Electrochemical Sensing of Hg 2+ via the Synergy of Enrichment and Self-Cleaning.

Efficient preconcentration is critical for sensitive and selective electrochemical detection of metal ions, but rapid specific enrichment with depressed absorption of interfering ions at the electrode is challenging. Here, we proposed an electric field-induced specific preconcentration to boost the analytical performance of DNA-based electrochemical sensors for Hg 2+ detection. As for such preconcentration, a positive external electric field was first used to enrich Hg 2+ at an electrode assembled with T-rich DNA, thus boosting T-Hg 2+ -T recognitions. The following applied inverse electric field strips the nonspecifically absorbed Hg 2+ and other interfering ions, thus depressing matrix interferences via self-cleaning. Based on this principle, we designed a portable device to realize programmable control of electric fields; a T-Hg 2+ -T recognition-based electrochemical sensor was thus fabricated as a model platform to assess the feasibility of electric field-induced preconcentration. The experimental results revealed that such a strategy decreased the time of T-Hg 2+ -T-based recognition from 60 to 20 min and led to detection with better reproducibility by depressing the influence of free Hg 2+ as well as interfering ions. This strategy offered Hg 2+ detection limits of 0.01 pM─three-fold better than that without preconcentration─within 22 min. The proposed preconcentration strategy offers a new way to enhance the analytical performance of sensing at the solid-liquid interface.