Improved electrochemical detection of levofloxacin in diverse aquatic samples using 3D flower-like Co@CaPO4 nanospheres.

The misuse of antibiotics has become a concerning environmental issue, posing a significant threat to public health. Levofloxacin (LFX), a fluoroquinolone antibiotic, is particularly worrisome due to its detrimental impact on human health and the ecosystem. Therefore, the selective and accurate identification of LFX is of utmost importance. In this study, we have developed an electrochemical sensor based on cobalt-doped calcium phosphate (Co@CaHPO) for the sensitive and selective detection of LFX in various water samples. Under optimized conditions, the Co@CaHPO-modified glassy carbon electrode (GCE) exhibited exceptional electrochemical activity, low charge transfer resistance, and a fast electron transfer rate, outperforming the unmodified GCE. The proposed Co@CaHPO-modified GCE demonstrated remarkable electrochemical characteristics, including a wide linear range (0.3-460 µM) and a lower detection limit (0.151 µM) with high sensitivity (0.676 µAµM-1 cm2). This detection approach may enable the direct detection of LFX in the pharmaceutical environment. Furthermore, the resulting sensor exhibited good selectivity, excellent cyclic and storage stability, reproducibility, and repeatability. The practical application of this LFX sensor can be extended to various water samples, yielding reliable and satisfactory results.

Efficient photoelectrocatalytic degradation of amoxicillin using nano-TiO2 photoanode thin films: A comparative study with photocatalytic and electrocatalytic methods.

Excessive utilization of antibiotics in human, animal, and aquaculture poses a substantial threat to human health and the environment. Photoelectrochemical processes are increasingly applied for water remediation because they generate oxidizing species and mineralize organic pollutants, making even small water quantities more amenable for utilization. Thus, this study presents the fabrication of an efficient nano-TiO2 photoanode thin film (PATF) specifically designed for the photoelectrocatalytic (PEC) degradation of amoxicillin (AMX). The TiO2 PATFs were deposited on fluorine-doped tin oxide (FTO) substrate using an ultrasonic spray pyrolysis process with various titanium isopropoxide (TTIP) acetylacetone (AcacH) molar ratios (1:1 to 1:10). The PEC oxidation of AMX was investigated using various molar ratios of TTIP:AcacH TiO2 PATF/FTO by linear sweep voltammetry, and a 1:8 M ratio of PATF exhibited superior PEC oxidation activity than other TiO2 PATFs. Subsequently, the PEC degradation efficiency of AMX was compared with that of photocatalytic (PC) and electrocatalytic (EC) methods. The results demonstrated that the PEC process effectively eliminated 76.2% of AMX within 120 min at 0.8 V, outperforming the removal rates attained by the EC (32.3%) and PC (52.6%). Notably, increasing the voltage to 1.0 V accelerated the PEC degradation of AMX, attaining a removal efficiency of 91.2% within 90 min and exceeding 95% within 120 min.

Quantification of van der Waals forces in bimodal and trimodal AFM.

The multifrequency formalism is generalized and exploited to quantify attractive forces, i.e., van der Waals interactions, with small amplitudes or gentle forces in bimodal and trimodal atomic force microscopy (AFM). The multifrequency force spectroscopy formalism with higher modes, including trimodal AFM, can outperform bimodal AFM for material property quantification. Bimodal AFM with the second mode is valid when the drive amplitude of the first mode is approximately an order of magnitude larger than that of the second mode. The error increases in the second mode but decreases in the third mode with a decreasing drive amplitude ratio. Externally driving with higher modes provides a means to extract information from higher force derivatives while enhancing the range of parameter space where the multifrequency formalism holds. Thus, the present approach is compatible with robustly quantifying weak long range forces while extending the number of channels available for high resolution.

Gender inequality and self-publication are common among academic editors.

Scientific editors shape the content of academic journals and set standards for their fields. Yet, the degree to which the gender makeup of editors reflects that of scientists, and the rate at which editors publish in their own journals, are not entirely understood. Here, we use algorithmic tools to infer the gender of 81,000 editors serving more than 1,000 journals and 15 disciplines over five decades. Only 26% of authors in our dataset are women, and we find even fewer women among editors (14%) and editors-in-chief (8%). Career length explains the gender gap among editors, but not editors-in-chief. Moreover, by analysing the publication records of 20,000 editors, we find that 12% publish at least one-fifth, and 6% publish at least one-third, of their papers in the journal they edit. Editors-in-chief tend to self-publish at a higher rate. Finally, compared with women, men have a higher increase in the rate at which they publish in a journal soon after becoming its editor.

Rational design of Nd2O3 decorated functionalized carbon nanofiber composite for selective electrochemical detection of carbendazim fungicides in vegetables, water, and soil samples.

Abuse of carbendazim (CBZ) leaves excessive pesticide residues on agricultural products, which endangers human health because of the residues' high concentrations. Hence, a composite consisting of functionalized carbon nanofibers (f-CNF) with neodymium oxide (Nd2O3) was fabricated to monitor CBZ at trace levels. The Nd2O3/f-CNF composite-modified electrode displays higher electro-oxidation ability towards CBZ than Nd2O3 and f-CNF-modified electrodes. The combined unique properties of Nd2O3 and f-CNF result in a substantial specific surface area, superior structural stability, and excellent electrocatalytic activity of the composite yielding enhanced sensitivity to detecting CBZ with a detection limit of 4.3 nM. Also, the fabricated sensor electrode can detect CBZ in the linear concentration range of up to 243.0 µM with high selectivity, appropriate reproducibility, and stability. A demonstration of the sensing capability of CBZ in vegetables, water, and soil samples was reported paving the way for its use in practical applications.

Rapid Colorimetric pH-Responsive Gold Nanocomposite Hydrogels for Sensing Applications.

Surface functionalization of metallic nanoparticles (NPs) with external groups can be engineered to fabricate sensors that are responsive to various stimuli like temperature, pH, and numerous ions. Herein, we report the synthesis of gold nanoparticles (GNPs) functionalized with 3-mercaptopropionic acid (GNPs-MPA) and the doping of these nanoparticles into hydrogel materials using the breathing-in/breathing-out (BI-BO) method. MPA has a carboxyl group that becomes protonated and, thus, ionized at a pH below its pKa (4.32); hence, the GNPs-MPA solutions and gels were mostly pH-responsive in the range of 3-5. Optical properties were assessed through ultraviolet-visible (UV-Vis) spectroscopy, namely: transmission and absorption, and the parameters used to quantify the pH changes were the full width at half maximum (FWHM) and position of surface plasmon resonance (SPR). The solutions and gels gradually changed their colors from red to indigo with pH decrementation from 5 to 3, respectively. Furthermore, the solutions' and doped gels' highest FWHM sensitivities towards pH variations were 20 nm and 55 nm, respectively, while the SPR's position sensitivities were 18 nm and 10 nm, respectively. Also, transmission and scanning electron microscopy showed synchronized dispersion and aggregation of NPs with pH change in both solution and gel forms. The gel exhibited excellent repeatability and reversibility properties, and its response time was instantaneous, which makes its deployment as a colorimetric pH-triggered sensor practical. To the best of our knowledge, this is the first study that has incorporated GNPs into hydrogels utilizing the BI-BO method and demonstrated the pH-dependent optical and colorimetric properties of the developed nanocomposites.

A user-friendly FIB lift-out technique to prepare plan-view TEM sample of 2D thin film materials.

Plan-view transmission electron microscopy (TEM) or electron diffraction imaging of a bulk or 2D material can provide detailed information about the structural or atomic arrangement in the material. A systematic and easily implementable approach to preparing site-specific plan-view TEM samples for 2D thin film materials using FIB is discussed that could be routinely used. The methodology has been successfully applied to prepare samples from 2D materials such as, MoS2 thin film, vertically oriented graphene film (VG), as well as heterostructure material SnTiS3. It is worth mentioning that in contrast to planar conventional graphene, VG grows vertically from the substrate and takes nanosheet arrays. Samples prepared using this methodology provide a simple, faster, and precise course in obtaining valuable structural information. The top-view imaging offers various information about the growth nature of the materials suggesting the efficiency of the sample preparation process.

Hydration Dynamics and the Future of Small-Amplitude AFM Imaging in Air.

Here, we discuss the effects that the dynamics of the hydration layer and other variables, such as the tip radius, have on the availability of imaging regimes in dynamic AFM-including multifrequency AFM. Since small amplitudes are required for high-resolution imaging, we focus on these cases. It is possible to fully immerse a sharp tip under the hydration layer and image with amplitudes similar to or smaller than the height of the hydration layer, i.e., ~1 nm. When mica or HOPG surfaces are only cleaved, molecules adhere to their surfaces, and reaching a thermodynamically stable state for imaging might take hours. During these first hours, different possibilities for imaging emerge and change, implying that these conditions must be considered and reported when imaging.

A review of focused ion beam applications in optical fibers.

Focused ion beam (FIB) technology has become a promising technique in micro- and nano-prototyping due to several advantages over its counterparts such as direct (maskless) processing, sub-10 nm feature size, and high reproducibility. Moreover, FIB machining can be effectively implemented on both conventional planar substrates and unconventional curved surfaces such as optical fibers, which are popular as an effective medium for telecommunications. Optical fibers have also been widely used as intrinsically light-coupled substrates to create a wide variety of compact fiber-optic devices by FIB milling diverse micro- and nanostructures onto the fiber surface (endfacet or outer cladding). In this paper, the broad applications of the FIB technology in optical fibers are reviewed. After an introduction to the technology, incorporating the FIB system and its basic operating modes, a brief overview of the lab-on-fiber technology is presented. Furthermore, the typical and most recent applications of the FIB machining in optical fibers for various applications are summarized. Finally, the reviewed work is concluded by suggesting the possible future directions for improving the micro- and nanomachining capabilities of the FIB technology in optical fibers.

Random lasers from photonic crystal wings of butterfly and moth for speckle-free imaging.

Several biological membranes have been served as scattering materials of random lasers, but few of them include natural photonic crystals. Here, we propose and demonstrate a facile approach to fabricating high-performance biological photonic crystal random lasers, which is cost-effective and reproducible for mass production. As a benchmark, optical and lasing properties of dye-coated Lepidoptera wings, including Papilio ulysses butterfly and Chrysiridia rhipheus moth, are characterized and show a stable laser emission with a superior threshold of 0.016 mJ/cm2, as compared to previous studies. To deploy the proposed devices in practical implementation, we have applied the as-fabricated biological devices to bright speckle-free imaging applications, which is a more sustainable and more accessible imaging strategy.

Study of laser actions by bird's feathers with photonic crystals.

Random lasers had been made by some biomaterials as light scattering materials, but natural photonic crystals have been rarely reported as scattering materials. Here we demonstrate the ability of natural photonic crystals to drive laser actions by sandwiched the feathers of the Turquoise-Fronted Amazon parrot and dye between two plastic films. Parrot feathers comprise abundant photonic crystals, and different color feathers compose of different ratios of the photonic crystal, which directly affect the feather reflectance. In this study, the multi-reflection scattering that occurred at the interface between the photonic crystal and gain media efficiently reduce the threshold; therefore, the more photonic crystal constitutes in the feathers; the lower threshold can be obtained. The random lasers can be easily made by the integration of bird feather photonic crystals and dye with a simple and sustainable manufacturing approach.

Rapid discrimination of chemically distinctive surface terminations in 2D material based heterostructures by direct van der Waals identification.

We demonstrate that surfaces presenting heterogeneous and atomically flat domains can be directly and rapidly discriminated via robust intensive quantifiables by exploiting one-pass noninvasive methods in standard atomic force microscopy (AFM), single ∼2 min passes, or direct force reconstruction, i.e., ∼103 force profiles (∼10 min collection time), allowing data collection, interpretation, and presentation in under 20 min, including experimental AFM preparation and excluding only sample fabrication, in situ and without extra experimental or time load. We employ a misfit SnTiS3 compound as a model system. Such heterostructures can be exploited as multifunctional surface systems and provide multiple support sites with distinguishable chemical, mechanical, or opto-electronic distinct properties. In short, they provide an ideal model system to exemplify how current AFM methods can significantly support material discovery across fields.

Explaining doping in material research (Hf substitution in ZnO films) by directly quantifying the van der Waals force.

Non-monotonic behavior has been observed in the optoelectronic properties of ZnO thin films as doped with Hf (HZO). Here we propose that two competing mechanisms are responsible for such behaviour. Specifically, we propose that provided two crystal orientations dominate film growth, only one of them might be responsible for direct Hf substitution. Nonmonotonic behaviour is expected at once by considering that preferential growth of the crystal that allows for direct Hf substitution is inhibited by Hf concentration in the manufacturing process. This inhibition would also be a thermodynamic consequence of Hf substitution. Maxima in Hf substitution is thus reached at a point where enough crystals exhibit the preferential orientation, and where enough Hf is present on the surface for substitution. Outside this optimum scenario, Hf substitution can only decrease. We interpret the surface phenomena by discussing surface energy and the van der Waals forces as measured experimentally by means of atomic force microscopy.

Hybrid graphene metasurface for near-infrared absorbers.

We experimentally demonstrated an amorphous graphene-based metasurface yielding near-infrared super absorber characteristic. The structure is obtained by alternatively combining magnetron-sputtering deposition and graphene transfer coating fabrication techniques. The thickness constraint of the physical vapor-deposited amorphous metallic layer is unlocked and as a result, the as-fabricated graphene-based metasurface absorber achieves near-perfect absorption in the near-infrared region with an ultra-broad spectral bandwidth of 3.0 µm. Our experimental characterization and theoretical analysis further point out that the strong light-matter interaction observed is caused by localized surface plasmon resonance of the metal film's particle-like surface morphology. In addition to the enhanced light absorption characteristics, such an amorphous metasurface can be used for surface-enhanced Raman scattering applications. Meanwhile, the proposed graphene-based metasurface relies solely on CMOS-compatible, low cost and large-area processing, which can be flexibly scaled up for mass production.

Insights into graphene wettability transparency by locally probing its surface free energy.

In this work, we study the surface energy of monolayer, bilayer and multilayer graphene coatings, produced through exfoliation of natural graphite flakes and chemical vapor deposition. We employ bimodal atomic force microscopy and micro-Raman spectroscopy for high spatial resolution and large area scanning of force of adhesion on the regions of the graphene/SiO2 surface with different graphene layers. Our measurements show that the interface conditions between graphene and SiO2 dominate the experimentally observed graphene surface energy. This finding sheds new light on the controversy surrounding graphene transparency studies. By separating the surface energy into polar and non-polar interactions, our findings suggest that monolayer graphene is nearly van der Waals opaque but partially transparent (near 60%) to polar interactions, which is further supported by characterizing graphene on the copper surface and two levels of density functional theory simulation. In addition to providing quantitative insight into the surface interactions of complicated graphene coatings, this work demonstrates a new route to nondestructively monitor the interface between graphene and coated substrates.

Direct Measurement of the Magnitude of the van der Waals Interaction of Single and Multilayer Graphene.

Vertical stacking of monolayers via van der Waals (vdW) assembly is an emerging field that opens promising routes toward engineering physical properties of two-dimensional materials. Industrial exploitation of these engineering heterostructures as robust functional materials still requires bounding their measured properties so as to enhance theoretical tractability and assist in experimental designs. Specifically, the short-range attractive vdW forces are responsible for the adhesion of chemically inert components and are recognized to play a dominant role in the functionality of these structures. Here, we reliably quantify the strength of ambient vdW forces in terms of an effective Hamaker coefficient for chemical vapor deposition-grown graphene and show how it scales by a factor of two or three from single to multiple layers on standard supporting surfaces such as copper or silicon oxide. Furthermore, direct measurements on freestanding graphene provide the means to discern the interplay between the vdW potential of graphene and its supporting substrate. Our results demonstrated that the underlying substrates could be controllably exploited to enhance or reduce the vdW force of graphene surfaces. We interpret the physical phenomena in terms of a Lifshitz theory-based analytical model.

The evolution in graphitic surface wettability with first-principles quantum simulations: the counterintuitive role of water.

The surface wettability of graphite has gained a lot of interest in nanotechnology and fundamental studies alike, but the types of adsorptions that dominate its time resolved surface property variations in ambient environment are still elusive. Prediction of the intrinsic surface wettability of graphite from first-principles simulations offers an opportunity to clarify the overall evolution. In this study, by combining experimental temporal Fourier transform infrared spectroscopy, atomic force microscopy (AFM), and static contact angle measurements with density functional theory (DFT)-predicted contact angles and DFT AFM force simulations, we provide conclusive evidence to demonstrate the role played by water adsorption in the evolution of surface properties of aged graphite in ambient air. Moreover, this study has the merit of linking DFT-predicted adhesive energy at the solid/liquid interface and cohesive energy at the liquid/liquid interface with the DFT AFM-predicted force of adhesion through the Young-Dupre equation. This establishes the basis of the quantum surface wettability theory by combining two independent atomic-level quantum physics simulation methodologies.

Surface aging investigation by means of an AFM-based methodology and the evolution of conservative nanoscale interactions.

The divergence in physical properties of surfaces exposed to airborne contaminants in the atmosphere has been widely investigated in recent years, but agreement regarding the role that airborne hydrocarbons and water contamination have on surface property evolution remains elusive. Here we investigate the evolution of a freshly grown highly oriented pyrolytic graphite (HOPG) surface exposed to a controlled environment solely containing airborne water contamination, i.e. water vapor. Our approach combines standard electromagnetic spectrum-based spectrometry methods and atomic force microscopy based techniques to provide a holistic view of the surface properties. We provide evidence of the affect that water adsorption kinetics has on surface properties, interpreting time dependent force-distance profiles and force of adhesion maps directly obtained from the standard observables in a bimodal AFM. To demonstrate the generality of our approach we also apply it to aged calcite surfaces, proving its advantages in providing comprehensive transient characterization of surfaces with sufficient spatial resolution.

Discerning the Contribution of Morphology and Chemistry in Wettability Studies.

The wetting behavior of homogeneous systems is now well understood at the macroscopic scale. However, this understanding offers little predictive power regarding wettability when mesoscopic chemical and morphological heterogeneities come into play. The fundamental interest in the effect of heterogeneity on wettability is derived from its high technological relevance in several industries, including the petroleum industry where wettability is recognized as a key determinant of the overall efficiency of the water-flooding-based enhanced oil recovery process. Here, we demonstrate the use of the atomic force microscopy force curve measurements to distinguish the roles of chemistry and morphology in the wetting properties of rock formations, thus providing a clear interpretation and deeper insight into the wetting behavior of heterogeneous formations. Density functional theory calculations further prove the versatility of our approach by establishing benchmarks on ideal surfaces that differ in chemistry and morphology in a predefined manner.

Water wettability of graphene: interplay between the interfacial water structure and the electronic structure.

Wetting phenomena are ubiquitous and impact a wide range of applications. Simulations so far have largely relied on classical potentials. Here, we report the development of an approach that combines density-functional theory (DFT)-based calculations with classical wetting theory that allows practical but sufficiently accurate determination of the water contact angle (WCA). As a benchmark, we apply the approach to the graphene and graphite surfaces that recently received considerable attention. The results agree with and elucidate the experimental data. For metal-supported graphene where electronic interactions play a major role, we demonstrate that doping of graphene by the metal substrate significantly alters the wettability. In addition to theory, we report new experimental measurements of the WCA and the force of adhesion that corroborate the theoretical results. We demonstrate a correlation between the force of adhesion and WCA, and the use of the atomic force microscope (AFM) technique as an alternative measure for wettability at the nanoscale. The present work not only provides a detailed understanding of the wettability of graphene, including the role of electrons, but also sets the stage for studying the wettability alteration mechanism when sufficiently accurate force fields may not be available.