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Register a new userEmbedding a carbon nanotube across the diameter of a solid state nanopore
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A fabrication method for positioning and embedding a single-walled carbon nanotube (SWNT) across the diameter of a solid state nanopore is presented. Chemical vapor deposition (CVD) is used to grow SWNTs over arrays of focused ion beam (FIB) milled pores in a thin silicon nitride membrane. This typically yields at least one pore whose diameter is centrally crossed by a SWNT. The final diameter of the FIB pore is adjusted to create a nanopore of any desired diameter by atomic layer deposition (ALD), simultaneously embedding and insulating the SWNT everywhere but in the region that crosses the diameter of the final nanopore, where it remains pristine and bare. This nanotube-articulated nanopore is an important step towards the realization of a new type of detector for biomolecule sensing and electronic characterization, including DNA sequencing.
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Solid-state nanopores are single molecule sensors that measure changes in ionic current as charged polymers such as DNA pass through. Here, we present comprehensive experiments on the length, voltage and salt dependence of the frequency of double-stranded DNA translocations through conical quartz nanopores with mean opening diameter 15 nm. We observe an entropic barrier limited, length dependent translocation frequency at 4M LiCl salt concentration and a drift-dominated, length independent translocation frequency at 1M KCl salt concentration. These observations are described by a unifying convection-diffusion equation which includes the contribution of an entropic barrier for polymer entry.
The threading of a polymer chain through a small pore is a classic problem in polymer dynamics and underlies nanopore sensing technology. However important experimental aspects of the polymer motion in a solid-state nanopore, such as an accurate measurement of the velocity variation during translocation, have remained elusive. In this work we analysed the translocation through conical quartz nanopores of a 7 kbp DNA double-strand labelled with six markers equally spaced along its contour. These markers, constructed from DNA hairpins, give direct experimental access to the translocation dynamics. On average we measure a 5% reduction in velocity during the translocation. We also find a striking correlation in velocity fluctuations with a decay constant of 100s of {mu}s. These results shed light on hitherto unresolved problems in the dynamics of DNA translocation and provide guidance for experiments seeking to determine positional information along a DNA strand.
Defects with associated electron and nuclear spins in solid-state materials have a long history relevant to quantum information science going back to the first spin echo experiments with silicon dopants in the 1950s. Since the turn of the century, the field has rapidly spread to a vast array of defects and host crystals applicable to quantum communication, sensing, and computing. From simple spin resonance to long-distance remote entanglement, the complexity of working with spin defects is fast advancing, and requires an in-depth understanding of their spin, optical, charge, and material properties in this modern context. This is especially critical for discovering new relevant systems dedicated to specific quantum applications. In this review, we therefore expand upon all the key components with an emphasis on the properties of defects and the host material, on engineering opportunities and other pathways for improvement. Finally, this review aims to be as defect and material agnostic as possible, with some emphasis on optical emitters, providing a broad guideline for the field of solid-state spin defects for quantum information.
Solid-state or crystal acceleration has for long been regarded as an attractive frontier in advanced particle acceleration. However, experimental investigations of solid-state acceleration mechanisms which offer $rm TVm^{-1}$ acceleration gradients have been hampered by several technological constraints. The primary constraint has been the unavailability of attosecond particle or photon sources suitable for excitation of collective modes in bulk crystals. Secondly, there are significant difficulties with direct high-intensity irradiation of bulk solids, such as beam instabilities due to crystal imperfections and collisions etc. In this work, we model an experimentally practicable solid-state acceleration mechanism using collective electron oscillations in crystals that sustain propagating surface waves. These surface waves are driven in the wake of a submicron long particle beam in tube shaped nanostructured crystals with tube wall densities, $n_{rm tube}sim10^{22-24}rm cm^{-3}$. Particle-In-Cell (PIC) simulations carried out under experimental constraints demonstrate the possibility of accessing average acceleration gradients of several $rm TVm^{-1}$ using the solid-state tube wakefield acceleration regime. Furthermore, our modeling demonstrates the possibility that as the surface oscillations and resultantly the surface wave transitions into a nonlinear or crunch-in regime under $n_{rm beam}/n_{rm tube} gtrsim 0.05$, not only does the average gradient increase but strong transverse focusing fields extend down to the tube axis. This work thus demonstrates the near-term experimental realizability of Solid-State Tube Wakefield Accelerator (SOTWA). (truncated to comply with submission requirements)
Hybrid circuit quantum electrodynamics (QED) involves the study of coherent quantum physics in solid state systems via their interactions with superconducting microwave circuits. Here we present an implementation of a hybrid superconducting qubit that employs a carbon nanotube as a Josephson junction. We realize the junction by contacting a carbon nanotube with a superconducting Pd/Al bi-layer, and implement voltage tunability of the qubit frequency using a local electrostatic gate. We demonstrate strong dispersive coupling to a coplanar waveguide resonator via observation of a resonator frequency shift dependent on applied gate voltage. We extract qubit parameters from spectroscopy using dispersive readout and find qubit relaxation and coherence times in the range of $10-200~rm{ns}$.
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