Advances in nanomaterials have led to tremendous progress in different areas with the development of high performance and multifunctional platforms. However, a relevant gap remains in providing the mass-production of these nanomaterials with reproducible surfaces. Accordingly, the monitoring of such materials across their entire life cycle becomes mandatory to both industry and academy. In this paper, we use a microfluidic electronic tongue (e-tongue) as a user-friendly and cost-effective method to classify nanomaterials according to their surface chemistry. The chip relies on a new single response e-tongue with association of capacitors in parallel, which consisted of stainless steel microwires coated with SiO, NiO, AlO, and FeO thin films. Utilizing impedance spectroscopy and a multidimensional projection technique, the chip was sufficiently sensitive to distinguish silica nanoparticles and multiwalled carbon nanotubes dispersed in water in spite of the very small surface modifications induced by distinct functionalization and oxidation extents, respectively. Flow analyses were made acquiring the analytical readouts in a label-free mode. The device also allowed for multiplex monitoring in an unprecedented way to speed up the tests. Our goal is not to replace the traditional techniques of surface analysis, but rather propose the use of libraries from e-tongue data as benchmark for routine screening of modified nanomaterials in industry and academy.
Electronic tongues (e-tongues) are promising analytical devices for a variety of applications to address the challenges of quality control in water monitoring and industries of foods, beverages, and pharmaceuticals. A crucial drawback in the current e-tongues is the need to recalibrate the device when one or more sensing units (usually with modified surface) are replaced. Another downside is the necessity to perform subsequent surface modifications and analyses to each of the diverse sensing units, undermining the simplicity and velocity of the method. These features have prevented widespread commercial use of the e-tongues. In this paper, we introduce a microfluidic e-tongue that overcomes all such limitations. The key principle of global selectivity of the e-tongue was achieved by recording only a single response, namely, the equivalent admittance spectrum of an association of resistors in parallel. Such resistors consisted of five nonfunctionalized stainless steel microwires (sensing units), which were short-circuited and coated with gold, platinum, nickel, iron, and aluminum oxide films. The microwires were inserted in a chip composed of a single piece of polydimethylsiloxane (PDMS). Using impedance spectroscopy, the e-tongue was successfully applied in classification of basic tastes at a concentration below the threshold for the human tongue. In addition, our chip allowed the distinction of various chemicals used in oil industry. Finally, our cleanroom-free prototyping allows the mass production of chips with easily replaceable and reproducible sensing units. Hence, one can now envisage the widespread dissemination of e-tongues with fast and reproducible data.
The theoretical description of the external degrees of freedom of atoms trapped inside a magnetooptical trap (MOT) often relies on the decoupling of the evolution of the internal and external degrees of freedom. That is possible thanks to much shorter timescales typically associated with the first ones. The electronic structure of alkaline-earth atoms, on the other hand, presents ultra-narrow transitions and metastable states that makes such an approximation invalid in the general case. In this article, we report on a model based on open Bloch equations for the evolution of the number of atoms in a magneto-optical trap. With this model we investigate the loading of the strontium blue magnetooptical trap under different repumping schemes, either directly from a Zeeman slower, or from an atomic reservoir made of atoms in a metastable state trapped in the magnetic quadrupolar field. The fluorescence observed on the strong 461 nm transition is recorded and quantitatively compared with the results from our simulations. The comparison between experimental results and calculations within our model allowed to identify the existence of the decay paths between the upper level of the repumping transition and the dark strontium metastable states, which could not be explained by electric dipole transition rates calculated in the literature. Moreover, our analysis pinpoints the role of the atomic movement in limiting the efficiency of the atomic repumping of the Sr metastable states.
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