The size of the sensing region in solid-state nanopores is determined by the size of the pore and the thickness of the pore membrane, so ultrathin membranes such as graphene and single-layer molybdenum disulphide could potentially offer the necessary spatial resolution for nanopore DNA sequencing. However, the fast translocation speeds (3,000-50,000 nt ms -1 ) of DNA molecules moving across such membranes limit their usability. Here, we show that a viscosity gradient system based on room-temperature ionic liquids can be used to control the dynamics of DNA translocation through MoS 2 nanopores. The approach can be used to statistically detect all four types of nucleotide, which are identified according to current signatures recorded during their transient residence in the narrow orifice of the atomically thin MoS 2 nanopore. Our technique, which exploits the high viscosity of room-temperature ionic liquids, provides optimal single nucleotide translocation speeds for DNA sequencing, while maintaining a signal-to-noise ratio higher than 10.
Single nucleotide identification 1,2 and DNA sequencing 3 have already been demonstrated with biological nanopores. However, the fragility of such pores, together with difficulties related to measuring their pA-range ionic currents and their dependence on biochemical reagents, means that solid-state nanopores remain an attractive alternative 4 . In contrast to biological pores, solid-state nanopores can operate in various liquid media and pH conditions, their production is scalable and compatible with nanofabrication techniques 5 , and they do not require the excessive use of biochemical reagents. These advantages are expected to make solid-state nanopore sequencing cheaper than sequencing with biological pores.The basic sensing principle in sold-state nanopores is the same as in biological pores. A DNA molecule is threaded through a nanometre-sized pore under an applied potential and, ideally, the sequence of nucleotides is read by monitoring small changes in the ionic current flowing through the pore that are caused by individual nucleotides temporarily residing within the pore 6 . However, solid-state nanopores also allow a transverse detection scheme, which is based on detecting changes in the electrical conductivity of a thin semiconducting channel 4 . In both biological and solid-state nanopores, achieving an optimal translocation speed remains a significant challenge , ref. 8) and are also limited by their use of enzymes. Therefore, to achieve genome sequencing, thousands-or even millons-of biological pores need to be integrated into one sequencer. In solid-state nanopores, translocation speeds are on the order of 3,000-50,000 nt ms , the large range being a result of factors such as the pore size (1.5-25 nm) and the applied potential (100-800 mV) 9 . These fast speeds limit the ability of solid-state nanopores to reach single-nucleotide resolution, and are a major obstacle to the use of solid-state nanopores in the sequencing of DNA.Solid-state nanopores also face proble...