Nanofluidic ionic and molecular transport through atomically
thin
nanopore membranes attracts broad research interest from both scientific
and industrial communities for environmental, healthcare, and energy-related
technologies. To mimic the biological ion pumping functions, recently,
light-induced and quantum effect-facilitated charge separation in
heterogeneous 2D-material assemblies is proposed as the fourth type
of driving force to achieve active and noninvasive transport of ionic
species through synthetic membrane materials. However, to date, engineering
versatile van der Waals heterostructures into 2D nanopore membranes
remains largely unexplored. Herein, we fabricate single nanopores
in heterobilayer transition metal dichalcogenide membranes with helium
ion beam irradiation and demonstrate the light-driven ionic transport
and molecular translocation phenomena through the atomically thin
nanopores. Experimental and simulation results further elucidate the
driving mechanism as the photoinduced near-pore electric potential
difference due to type II band alignment of the semiconducting WS2 and MoS2 monolayers. The strength of the photoinduced
localized electric field near the pore region can be approximately
1.5 times stronger than that of its counterpart under the conventional
voltage-driven mode. Consequently, the light-driven mode offers better
spatial resolution for single-molecule detection. Light-driven ionic
and molecular transport through nanopores in van der Waals heterojunction
membranes anticipates transformative working principles for next-generation
biomolecular sequencing and gives rise to fascinating opportunities
for light-to-chemical energy harvesting nanosystems.