Nanofluidics has a very promising future owing to its numerous applications in many domains. It remains, however, very difficult to understand the basic physico-chemical principles that control the behavior of solvents confined in nanometric channels. Here, water and ion transport in carbon nanotubes is investigated using classical force field molecular dynamics simulations. By combining one single walled carbon nanotube (uniformly charged or not) with two perforated graphene sheets, we mimic single nanopore devices similar to experimental ones. The graphitic edges delimit two reservoirs of water and ions in the simulation cell from which a voltage is imposed through the application of an external electric field. By analyzing the evolution of the electrolyte conductivity, the role of the carbon nanotube geometric parameters (radius and chirality) and of the functionalization of the carbon nanotube entrances with OH or COO− groups is investigated for different concentrations of group functions.

Despite several decades of development, microfluidics lacks a sealing material that can be readily fabricated, leak-tight under high liquid water pressure, stable over a long time, and vacuum compatible. In this paper, we report the performances of a micro-scale processable sealing material for nanofluidic/microfluidics chip fabrication, which enables us to achieve all these requirements. We observed that micrometric walls made of SU-8 photoresist, whose thickness can be as low as 35 $μ$m, exhibit water pressure leak-tightness from 1.5 bar up to 5.5 bar, no water porosity even after 2 months of aging, and are able to sustain under $10^{-5}$ mbar vacuum. This sealing material is therefore reliable and versatile for building microchips, part of which must be isolated from liquid water under pressure or vacuum. Moreover, the fabrication process we propose does not require the use of aggressive chemicals or high-temperature or high-energy plasma treatment. It thus opens a new perspective to seal microchips where delicate surfaces such as nanomaterials are present.

In recent experiments, unprecedentedly large values for the conductivity of electrolytes through carbon nanotubes (CNTs) have been measured, possibly owing to flow slip and a high pore surface charge density whose origin is still unknown. By accounting for the coupling between the {quantum} CNT and the {classical} electrolyte-filled pore capacitances, we study the case where a gate voltage is applied to the CNT. The computed surface charge and conductivity dependence on reservoir salt concentration and gate voltage are intimately connected to the CNT electronic density of states. This approach provides key insight into why metallic CNTs have larger conductivities than semi-conducting ones.

Due to their atomically excellent structure and sp2-hybridization, carbon nanotubes (CNTs) have exceptional mechanical, thermal, and electrical properties. Single-walled CNTs (swCNTs) have recently gained interest as an intriguing host for the nanoscale confinement of fluids, with a variety of unexpected phenomena such as spontaneous filling, frictionless mass transport, unusual phase diagram etc[1]. The majority of these phenomena are still under debate and require experimental confirmation. However, it is challenging in this field to find experimental methods sensitive enough to carry out measurements at the level of individual nanotubes. The electronic properties of swCNTs are demonstrated to be sensitive to their diameter, defects, doping, adsorbates, and environment via swCNT field effect transistors (swCNT-FETs)[2], [3].In this contribution, we show that individual carbon nanotube field effect transistors (CNTFET) are the perfect tool for achieving this goal, enabling for the first time to accurate identification of water confined inside the nanotube. By investigating the electrical performances of several unopened and opened CNTFETs submitted to different atmosphere and temperature treatments, such as dry air, humidity, secondary vacuum, and current annealing, we demonstrate that it is possible to distinguish between water being outside and inside of the nanotube, just outside, or the nanotube free from water. Hence, we found that secondary vacuum and current annealing both shift the threshold gate voltage of opened swCNTs towards more negative values, however, the secondary vacuum had no effect on closed swCNTs compared to current annealing. In conclusion, the current annealing process is essential to distinguish water adsorbed outside from water confined inside swCNT. We demonstrate that this behavior is uniform across all devices’ metallicities, assuming that the nanotube’s surface has been pre-cleaned using current annealing. We will also discuss the mechanism behind the coupling of electronic transport and the presence of water.Our findings open up the possibility of using CNTFET to address long-standing issues in the nanofluidic community regarding the behavior of water confinement at the nanoscale, and also to use them for reliable, sensitive, and selective chemical and biological sensors.Reference:[1] T. A. Pascal, W. A. Goddard, and Y. Jung, “Entropy and the driving force for the filling of carbon nanotubes with water,” Proc. Natl. Acad. Sci., vol. 108, no. 29, pp. 11794–11798, 2011, doi: 10.1073/pnas.1108073108.[2] D. Cao et al., “Electronic sensitivity of carbon nanotubes to internal water wetting,” ACS Nano, vol. 5, no. 4, pp. 3113–3119, 2011, DOI: 10.1021/nn200251z.[3] I. Heller, A. M. Janssens, J. Männik, E. D. Minot, S. G. Lemay, and C. Dekker, “Identifying the mechanism of biosensing with carbon nanotube transistors,” Nano Lett., vol. 8, no. 2, pp. 591–595, 2008, DOI: 10.1021/nl072996i.