Nanopores employ a confined space for electrochemical seining of high-throughput individual biomolecules in solution.The most general mechanism of nanopore sensing is based on a volume exclusion effect.However,the increasing demands on revealing the single-molecule/particle chemistry and biophysics require the nanopores not only provide structural/conformational/sequencing information,but also directly read the dynamic functional properties of single molecules/particles.The traditional design ofnanopores (e.g.SiN,quartz nanopipette and biological nanopores) lacks an electrochemically active interface to detect both ionic flux and the accompanying faraday current.Given that,Ying and Long [1-3] proposed a new concept of electrochemically confined effects for the sophisticated design of a wireless nanopore electrode (WNE).The WNE possesses a metal layer on the inner wall of the asymmetric nanopipette,which is easy to be polarized under the electric field to provide a controllable electroactive interface (Figure 1).