Atomic Force Microscopy Measurements Research Articles

Alterations in paraffin wax crystal networks induced by asphaltenes and pour point depressants, investigated by atomic force microscopy

Wax crystallization in pipelines in cold environments is a key factor affecting flow assurance during crude oil production. Polar crude oil components, such as asphaltenes, and polymeric pour point depressants (PPDs) have been demonstrated to interact with wax during gelation and crystallization through complex formation during nucleation or crystal growth alteration which leads to co-crystallization. This study introduces a methodology based on atomic force microscopy (AFM) to characterize features of solid surfaces precipitated from model wax, wax-PPD, wax-asphaltene and asphaltene systems. Height data collected from AFM measurements enabled the quantification of modifications in crystal sizes and shapes induced by the presence of asphaltenes and PPDs. The 2D Fourier transform of the height was used to generate statistics for the frequency of height amplitude, revealing information about the pore size and the height patterns. A stiffness/elasticity analysis was used to calculate the Young Modulus of the upper layers. In wax and wax-asphaltene systems, two nano-scale layers with different Young Modulus profiles emerged. The nano-scale layer on the top was softer and corresponded to more amorphous wax crystal networks with trapped dissolved wax. The nano-scale layer on the bottom was stiffer, comprising of more crystalline structures, corresponding to wax crystals with lower deviations from full crystallinity, with properties independent of asphaltene concentration. A bilayer did not form in the presence of PPD, which prevented the formation of amorphous phases with trapped dissolved wax or gel. After a methodology for model systems was established, the focus moved to systems based on production wax i.e. recovered from deposits. This was complemented by a comparison between model precipitation conditions and precipitation by cold finger, resembling industrial processes. Results highlighted the effect of change in chemical composition on topography, elasticity and adhesion of the surface. AFM provided new insights into wax crystallization patterns in the presence of inhibitors, which can be used to quantify the extent of wax-inhibitor interactions and project it on production systems. The method could be used to explain macro-scale rheological properties of oils during flow assurance in the future.

Development of a microcantilever-based biosensor for detecting Programmed Death Ligand 1

The ongoing global concern of cancer worldwide necessitates the development of advanced diagnostic and therapeutic strategies. The majority of recent detection strategies involve the employment of biomarkers. A critical biomarker for cancer immunotherapy efficacy and patient prognosis is Programmed Death Ligand 1 (PD-L1), which is a key immune checkpoint protein. PD-L1 can be particularly linked to cancer progression and therapy response. Current detection methods, such as enzyme-linked immunosorbent assay (ELISA), face limitations like high cost, time consumption, and complexity. This study introduces a microcantilever-based biosensor designed for the detection of soluble PD-L1 (sPD-L1), which has a specific association with PD-L1. The biosensor utilizes anti-PD-L1 as the sensing layer, capitalizing on the specific binding affinity between anti-PD-L1 and sPD-L1. The presence of the sensing layer was confirmed through Atomic Force Microscopy (AFM) and contact angle measurements. Binding between sPD-L1 and anti-PD-L1 induces a shift in the microcantilever's resonance frequency, which is proportional to the PD-L1 concentration. Notably, the resonance frequency shift demonstrates a robust linear relationship with the increasing biomarker concentration, ranging from 0.05 ng/ml to 500 ng/ml. The detection limit of the biosensor was determined to be approximately 10 pg/ml. The biosensor demonstrates excellent performance in detecting PD-L1 with high specificity even in complex biological matrices. This innovative approach not only provides a promising tool for early cancer diagnosis but also holds potential for monitoring immunotherapy efficacy, paving the way for personalized and effective cancer treatments.

Abstract 6394: Tissue nanomechanical signature predicts response to neoadjuvant chemotherapy in patients with breast cancer

Abstract Background: Neoadjuvant chemotherapy (NACT) is increasingly used in patients with breast cancer. However, predicting response to NACT remains a challenge in everyday clinical practice. Increasing (pre)- and clinical evidence demonstrate the importance of cancer biomechanics in mediating therapy response. We and others have previously demonstrated that complex biomechanical alterations in cancer tissues, can be measured by the Atomic Force Microscopy (AFM) at the nanoscale level. Incorporating AFM measurements of clinical biopsies within standard of care is thus a promising avenue to leverage tissue mechanics as prognostic and predictive biomarker for solid cancers. Methods: Fresh clinical biopsy samples from 545 breast cancer patients were measured using the AFM-based Automated and Reliable Tissue Diagnostics (ARTIDIS) investigational device - ART-1. Measurements were performed on baseline biopsies within routine clinical workflow in the Breast Clinic, University Hospital Basel. This cohort comprises 30 patients who received NACT including: anthracycline and/or taxane based chemo (n=17), and anthracycline and/or taxane with platinum chemo (n=13). Study endpoints were radiological complete response (rCR) prior and pathological complete response (pCR) after surgery. Multiparametric nnanomechanical signature data has been analyzed in an automated manner using the proprietary ARTIDISNET software platform. Results: From the 30 patients who received NACT, 12 patients presented with rCR, 17 patients presented with rPR, and 1 patient presented with rNR. pCR has been achieved only in 9 patients. In this study, he ARTIDIS nanomechanical signature of response to NACT in breast cancer showed 100% negative predictive value (NPV) and 89% positive predictive value (PPV), with 93% of accuracy for patients receiving chemotherapy, independent of molecular subtype or treatment regimen. Sensitivity was 100% and specificity was 85% (AUC=0.91). Conclusion: ARTIDIS nanomechanical signature can be seamlessly integrated within clinical settings to predict response to standard of care NACT in patients with breast cancer in a prospective manner. These results are currently being validated in a global, multicentre prospective study in breast cancer (ANGEL, NCT06085833), enrolling in total 2706 patients, with the aim to support implementation of the ARTIDIS nanomechanical signature into routine clinical practice. Citation Format: Mariam Gachechiladze, Sara Nizzero, Tobias Appenzeller, Leonie Briner, Rosemarie Burian, Sabine Schädelin, Simone Muenst-Soysal, Tatjana Vlaijnic, Ellen Obermann, Sophie Dellas, Serafino Forte, Zlatko Marušić, Ahmed Jizawi, Papa Diogop Ndiaye, Philipp Oertle, Gregory Zaugg, Marko Loparic, Marija Plodinec. Tissue nanomechanical signature predicts response to neoadjuvant chemotherapy in patients with breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 6394.

Digital Alloy-Grown InAs/GaAs Short-Period Superlattices with Tunable Band Gaps for Short-Wavelength Infrared Photodetection.

The InGaAs lattice-matched to InP has been widely deployed as the absorption material in short-wavelength infrared photodetection applications such as imaging and optical communications. Here, a series of digital alloy (DA)-grown InAs/GaAs short-period superlattices were investigated to extend the absorption spectral range. The scanning transmission electron microscopy, high-resolution X-ray diffraction, and atomic force microscopy measurements exhibit good material quality, while the photoluminescence (PL) spectra demonstrate a wide band gap tunability for the InGaAs obtained via the DA growth technique. The photoluminescence peak can be effectively shifted from 1690 nm (0.734 eV) for conventional random alloy (RA) InGaAs to 1950 nm (0.636 eV) for 8 monolayer (ML) DA InGaAs at room temperature. The complete set of optical constants of DA InGaAs has been extracted via the ellipsometry technique, showing the absorption coefficients of 398, 831, and 1230 cm-1 at 2 μm for 6, 8, and 10 ML DA InGaAs, respectively. As the period thickness increases for DA InGaAs, a red shift at the absorption edge can be observed. Furthermore, the simulated band structures of DA InGaAs via an environment-dependent tight binding model agree well with the measured photoluminescence peaks, which is advantageous for a physical understanding of band structure engineering via the DA growth technique. These investigations and results pave the way for the future utilization of the DA-grown InAs/GaAs short-period superlattices as a promising absorption material choice to extend the photodetector response beyond the cutoff wavelength of random alloy InGaAs.

Correlation between morphology and transport properties of Au/Co/Au/Si wedge ultra-thin film

We report the thermoelectric power (TEP) and electrical resistivity characterization supported by structural and surface morphological properties on a wedge shaped ultra-thin sample of Au/Co/Au/Si (100) with Co have varying thickness from 0.5 nm to 4 nm across the sample. The sample was prepared by Ion Beam Sputtering method, with an ultrathin layer of Co sandwiched between two layers of Au (3 nm thicknesses each). The observed TEP results showed that the system is semiconductor in nature and the concentration of the charge carrier is inversely proportional to the Seebeck coefficient (S) and also concentration of charge carrier modifies with the film thickness leading to a change in thermo power, which is found to be higher at lower thicknesses of Co sandwiched layer. The type of charge carrier was also determined to be electrons in this system. The observed results are in good agreement with the resistivity measurement carried out as a function of film thickness indicating a decrease in resistivity as a function of film thickness due to enhancement in charge carrier mobility. The thermal activation energy was seen to increase from ∼29.5 meV to ∼280.3 meV as the film thickness increased from the minimum to the highest. Corresponding Atomic Force Microscopy (AFM) measurement revealed island type grain growth with the introduction of a significant amount of roughness, while Magnetic Force Microscopy (MFM) experiments exhibit randomly oriented magnetic domain structures. The overall results suggest that lowest thickness film shows semiconducting nature, while variable range hopping phenomena due to some localized energy levels near the valence and conduction band is observed in the highest thickness film. This result is also well supported by XRD measurement, which revealed crystalline nature of the films. Such low cost, easy to fabricate materials may find applications in Peltier cooling or energy harvesting applications without the harmful carbon dioxide emission. For this, advance experiments will be done in future.

Etching and Compositional Ratio Effect on the Surface Properties of Bismuth Telluride Thin Films

Bismuth telluride has garnered considerable attention owing to its versatile properties applicable in thermoelectric and antibacterial domains, as well as its intriguing topological insulating properties. In this work, our group fabricated bismuth telluride thin films with various ratios using radio frequency magnetron sputtering. The surface properties of these thin films were thoroughly analyzed by employing a diverse array of analytical techniques, including X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), four-point probe and contact angle (CA) measurements. Specifically, our XPS findings indicated that Bi is more susceptible to oxidation than Te following Ar+-ion etching. Pure Te thin films exhibited the highest Rq value of 31.2 nm based on AFM and SEM results due to their larger grain sizes. The XRD patterns revealed a peak at 27.75° for thin films with 20% Te, attributed to its rhombohedral structure. Moreover, thin films with 30% Te yielded the highest weighted average work function with a value of 4.95 eV after etching. Additionally, pristine Bi and Te thin films demonstrated the most robust hydrophobic properties compared to intermediate-composition thin films, as determined by CA measurements.

From environmental issue to purification aid: Novel positively charged functionalized algal biochar as robust modifier of composite nanofiltration membranes

Robust membrane modifiers were achieved for the first time by functionalizing the algal biochar of unique porous structure. The biochar was prepared through the pyrolysis of Cladophora glomerata, the most widespread freshwater macroalga, functionalized by diethylenetriamine and dendrimer poly(amidoamine), and employed to fabricate positively charged composite nanofiltration membranes. The presence of hydrophilic functionalizers of positive charge on the membrane was verified through Fourier transform infrared and energy dispersive X-ray analyses and atomic force microscopy and zeta potential measurements were performed to determine surface roughness and confirm positive charge of the modified membranes. Dispersion of modifiers on the surface and morphology of the were also revealed through field-emission scanning electron microscopy images. It has shown that, compared to the pristine membrane, pure water fluxes were increased by 214% and 185%, and water contact angles were reduced from 66.1° to 39.5° and 43.3° in those modified by biochar functionalized with dendrimer poly(amidoamine) and diethylenetriamine, respectively. More than 90% dye rejections and salt and heavy metals removals were recorded for the membranes possessed 0.6 wt% of modifiers. Finally, a comparative study conducted between the novel modifier introduced in this study and those reported in the literature, indicated that C. glomerata biochar decorated with amine functional groups could be considered as a robust and practical alternative to the common modifiers used to manipulate nanocomposite membranes characteristics.

In situ differential atomic force microscopy (AFM) measurement for ultra-thin Thiol SAM patterns by area-selective deposition technique

Developing novel characterization methods is crucial to enhancing the accuracy and precision of measurements in semiconductor ultrathin films. By combining "bottom-up" and "top-down" patterning techniques, we successfully fabricated five uniform alkyl thiol-derived self-assembled monolayer (SAM) patterns. Employing the innovative in situ differential Atomic Force Microscopy (AFM) Measurement, we analyzed the thickness, morphology, and mechanical properties of the thiol films. This method greatly reduced errors caused by uneven substrates, resulting in more precise measurements compared to large-area measurements. It is shown that as the thiol chain length increased, the variation in SAM film thickness aligned consistently with the thickness of a single Atomic Layer Deposition (ALD) cycle, and the surface roughness of the SAM surface mirrored that of ALD. Consequently, the experiment affirms the effectiveness of the SAM film in simulating ALD, providing validation for the precision and feasibility of the in situ differential results. Furthermore, adhesion measurement results revealed a diminishing passivation effect of SAM as the chain length increased. This suggests that an appropriate SAM could be selected as a passivation material through real-time monitoring of the mechanical properties of the mask surface during the Area-Selective Deposition (ASD) process.

Self‐assembly of supramolecular monomers into 2D twinned crystals on mica surface

AbstractDespite the widespread use of microscopy techniques to characterize supramolecular polymers, the role of surfaces in the formation of these structures is unclear. Here we describe the epitaxial growth of intriguing 2D crystals of alkyl benzene‐1,3,5‐triscarboxamides formed by competitive attractive interactions with the mica surface. In contrast to the fibrous structure observed in apolar diluted solution, five‐fold twinned crystals or ribbon‐like structures are obtained on the mica surface. Moreover, these structures are still dynamic on the surface, being able to reorganize during the atomic force microscopy measurements. This work demonstrates that surface‐monomer interactions can be exploited to modulate the structure of 1D supramolecular polymers into 2D crystals.

Evaluating the optoelectronic properties of individual CsPbBr3 microcrystals by electric AFM techniques

All-inorganic perovskite materials are attracting the attention of researchers owing to the good performance that they exhibit in optoelectronic device applications. In particular, cesium lead halide single crystals are of interest for their electric conductivity. However, the conductive properties of these materials are still far from being fully understood. In this work, we used several scanning probe microscopy techniques to investigate different properties of CsPbBr3 single crystals, namely their topography, electric conductivity, electric surface potential and ferroelectricity. We observed heterogeneity in conductance and work function of the different facets by using conductive atomic force microscopy and Kelvin probe force microscopy measurements. Additionally, piezo-response force microscopy was carried out to gain insight on the origin of the hysteresis in our microcrystals. Our results show the absence of ferroelectric domains and we attribute the I–V hysteresis to ionic migration within the crystal.

Localized compaction of collagen hydrogels using acoustic droplet vaporization promotes osteogenic differentiation of mesenchymal stem cells

The lineage specification of mesenchymal stem cells (MSCs) is dependent on matrix stiffness, with osteogenesis promoted on or within stiff microenvironments. Unlike native extracellular matrix, conventional hydrogels have relatively static and uniform mechanical properties, thereby limiting the study of how spatiotemporally controlled mechanical cues impact MSC behavior. Here, we spatiotemporally control MSC differentiation in 3D hydrogels by actively modulating matrix stiffness using acoustic droplet vaporization (ADV). An acoustically responsive scaffold (ARS) was generated by co-encapsulating MSCs and perfluorohexane-based emulsion (13 μm) within type I collagen. ADV was used to generate bubbles within the ARS. Bubble diameter and the width of the compacted matrix region increased over time following ADV. Atomic force microscopy measurements demonstrated that the hydrogel region proximal to the bubble was significantly stiffer than the distal regions. Significantly greater levels of Runx2 and osteocalcin expression were observed in MSCs proximal to bubbles compared to distal on days 7 and 14. Higher alkaline phosphatase activity also validated the above findings. The significant upregulation of these osteogenic biomarkers suggests ADV-induced, mechanical changes in ARSs were sufficient to enhance osteogenic differentiation of MSCs. This approach is a significant step towards controlling the 3D differentiation of MSCs in a spatially localized, non-invasive, and on-demand manner.

Topological Structure Realized in Cove-Edged Graphene Nanoribbons via Incorporation of Periodic Pentagon Rings.

Cove-edged zigzag graphene nanoribbons are predicted to show metallic, topological, or trivial semiconducting band structures, which are precisely determined by their cove offset positions at both edges as well as the ribbon width. However, due to the challenge of introducing coves into zigzag-edged graphene nanoribbons, only a few cove-edged graphene nanoribbons with trivial semiconducting bandgaps have been realized experimentally. Here, we report that the topological band structure can be realized in cove-edged graphene nanoribbons by embedding periodic pentagon rings on the cove edges through on-surface synthesis. Upon noncontact atomic force microscopy and scanning tunneling spectroscopy measurements, the chemical and electronic structures of cove-edged graphene nanoribbons with periodic pentagon rings have been characterized for different lengths. Combined with theoretical calculations, we find that upon inducing periodic pentagon rings the cove-edged graphene nanoribbons exhibit nontrivial topological structures. Our results provide insights for the design and understanding of the topological character in cove-edged graphene nanoribbons.

Avalanches and Extreme Value Statistics of a Mesoscale Moving Contact Line.

We report direct atomic force microscopy measurements of pinning-depinning dynamics of a circular moving contact line (CL) over the rough surface of a micron-sized vertical hanging glass fiber, which intersects a liquid-air interface. The measured capillary force acting on the CL exhibits sawtoothlike fluctuations, with a linear accumulation of force of slope k (stick) followed by a sharp release of force δf, which is proportional to the CL slip length. From a thorough analysis of a large volume of the stick-slip events, we find that the local maximal force F_{c} needed for CL depinning follows the extreme value statistics and the measured δf follows the avalanche dynamics with a power law distribution in good agreement with the Alessandro-Beatrice-Bertotti-Montorsi (ABBM) model. The experiment provides an accurate statistical description of the CL dynamics at mesoscale, which has important implications to a common class of problems involving stick-slip motion in a random defect or roughness landscape.

Atomic Defect Quantification by Lateral Force Microscopy.

Atomic defects in two-dimensional (2D) materials impact electronic and optoelectronic properties, such as doping and single photon emission. An understanding of defect-property relationships is essential for optimizing material performance. However, progress in understanding these critical relationships is hindered by a lack of straightforward approaches for accurate, precise, and reliable defect quantification on the nanoscale, especially for insulating materials. Here, we demonstrate that lateral force microscopy (LFM), a mechanical technique, can observe atomic defects in semiconducting and insulating 2D materials under ambient conditions. We first improve the sensitivity of LFM through consideration of cantilever mechanics. With the improved sensitivity, we use LFM to locate atomic-scale point defects on the surface of bulk MoSe2. By directly comparing LFM and conductive atomic force microscopy (CAFM) measurements on bulk MoSe2, we demonstrate that point defects observed with LFM are atomic defects in the crystal. As a mechanical technique, LFM does not require a conductive pathway, which allows defect characterization on insulating materials, such as hexagonal boron nitride (hBN). We demonstrate the ability to observe intrinsic defects in hBN and defects introduced by annealing. Our demonstration of LFM as a mechanical defect characterization technique applicable to both conductive and insulating 2D materials will enable routine defect-property determination and accelerate materials research.

Sulfate Doping Promotes Agglomeration of Calcium Fluoride Crystals.

Calcium salt precipitation is an effective solution to wastewater fluoride pollution. The purity and precipitation efficiency of calcium fluoride is critical for its removal and recovery. This study aimed to reveal the role of coexisting sulfates in the precipitation of calcium fluoride. A low sulfate concentration promoted calcium fluoride precipitation. The size of calcium fluoride-aggregated particle clusters increased from 750 to 2000 nm when the molar ratio of sulfate to fluoride was increased from 0 to 3:100. Sulfate doped in the calcium fluoride crystals neutralized the positive charge of the calcium fluoride. Online atomic force microscopy measurements showed that sulfate reduced the repulsive force between calcium fluoride crystals and increased the adhesion force from 1.62 to 2.46 nN, promoting the agglomeration of calcium fluoride crystals. Sulfate improved the precipitation efficiency of calcium fluoride by promoting agglomeration; however, the purity of calcium fluoride was reduced by doping. Sulfate reduced the induction time of calcium fluoride crystallization and improved the nucleation rate of calcium fluoride. Sulfate should be retained to improve the precipitation of calcium fluoride and to avoid its loss from the effluents. However, it is necessary to separate sulfate from fluoride to obtain high-purity calcium fluoride. Therefore, sulfate concentration regulation in high-fluoride wastewater is key to achieving the efficient removal and recovery of fluoride ions.

Gutless Helper-Dependent and First-Generation HAdV5 Vectors Have Similar Mechanical Properties and Common Transduction Mechanisms.

Delivering vectorized information into cells with the help of viruses has been of high interest to fundamental and applied science, and bears significant therapeutic promise. Human adenoviruses (HAdVs) have been at the forefront of gene delivery for many years, and the subject of intensive development resulting in several generations of agents, including replication-competent, -defective or retargeted vectors, and recently also helper-dependent (HD), so-called gutless vectors lacking any viral protein coding information. While it is possible to produce HD-AdVs in significant amounts, physical properties of these virus-like particles and their efficiency of transduction have not been addressed. Here, we used single-cell and single virus particle assays to probe the effect of genome length on HAdV-C5 vector transduction. Our results demonstrate that first-generation C5 vectors lacking the E1/E3 regions of the viral genome as well as HD-AdV-C5 particles with a wild type (wt) ∼36 kbp or an undersized double-strand DNA genome are similar to human adenovirus C5 (HAdV-C5) wt regarding attachment to human lung epithelial cells, endocytic uptake, endosome penetration and dependency on the E3 RING ubiquitin ligase Mind Bomb 1 for DNA uncoating at the nuclear pore complex. Atomic force microscopy measurements of single virus particles indicated that small changes in the genome length from 94% to 103% of HAdV-C5 have no major impact on physical and mechanical features of AdV vectors. In contrast, an HD-AdV-C5 with ∼30 kbp genome was slightly stiffer and less heat-resistant than the other particles, despite comparable entry and transduction efficiencies in tissue culture cell lines, including murine alveolar macrophage-like Max-Planck-Institute (MPI)-2 cells. Together, our in vitro studies reinforce the use of HD-AdV vectors for effective single round gene delivery. The results illustrate how physical properties and cell entry behavior of single virus particles can provide functional information for anticipated therapeutic vector applications.

Wavelet-based information theory in quantitative assessment of AFM images’ quality

The quantitative assessment of the image quality produced by atomic force microscopy (AFM) is an ongoing and challenging task. In our study, we demonstrate Shannon’s application of information theory for measuring image quality. Specifically, we propose quantifying the loss of image information due to the various distortion processes by exploring the relationship between image information based on the information channel capacity (ICC), spectral image representation, and visual quality. Since the ideal image is unavailable, the power and noise spectrum, the critical input information for the image quality evaluation, must be robustly estimated in the proposed method. The classical, most popular Welch method for spectral estimation uses an average of several windowed periodograms and can produce biased spectrum estimates. Therefore, in our work, we discuss an alternative technique based on the wavelet transform that can be applied to solve this challenging problem, specifically in the case of noisy, uncertain AFM measurements. Finally, we validate the performance of the enhanced ICC-wavelet-based algorithm with noisy measurement AFM data.

Boosted carbon electrocatalytic effect towards sensing and green energy applications by tailoring the catalyst-support interface on a nature-inspired solution

Carbon electrodes are widely accepted as very versatile platforms, with applications ranging from electrocatalysis to sensors and other devices, like fuel cells and water electrolyzers. However, there are still difficulties given that over time, at high potentials, the oxidation of carbon materials (as a catalyst and/or catalyst support) can play a detrimental role, undermining the efficiency and stability of the electrochemical processes and devices performance. In this paper, it is reported the research work followed by resourcing to electrochemical analytical techniques, like cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), along with complementary atomic force microscopy (AFM) and water contact angle (WCA) measurements. These techniques were used to characterise glass-type and paper-based carbon electrodes. On a nature-inspired solution, we took advantage of the different interfacial carbon-support hierarchical porous structures to boost the carbon electrocatalytic effect towards sensing the ferri/ferrocyanide redox couple ([Fe(CN)6]3-/4−) in aqueous solution. It is shown that the best results were achieved with carbon paper electrodes without wet proofing, given its hierarchical porous structure and absence of the insulating binder. This research endeavors to contribute to the ongoing advancements in the field of electrochemical green energy conversion by exploring innovative approaches and materials, with the ultimate aim of developing carbon substrates that not only enhance performance but also promote environmental sustainability.

The Effect of Deposition Temperature on Structural, Morphological, and Dielectric Properties of Yttria-Doped Zirconia Thin Films

The aim of this study was to investigate the effect of deposition temperature on the structural, optical, morphological, and dielectric properties of yttria-stabilised zirconia (YSZ) films prepared by sol-gel spin-coating method. X-ray diffraction (XRD) measurements of YSZ films showed that the peaks of the cubic phase were prominent and the peak intensities increased with deposition temperature. The crystallite size, dislocation density, and microstrain of the thin films were identified by XRD. It was observed that the crystal size of the YSZ thin films increased from 16 nm to 22 nm with the deposition temperature. The surface roughness of the thin films was found to have changed as revealed by Atomic Force Microscopy (AFM) measurements. The roughness increased from 7.72 nm to 11.92 nm with increasing temperature. The optical transmittance of the YSZ thin films was investigated in the wavelength range 200-900 nm and was found to increase slightly with increasing deposition temperature. Metal-Oxide-Semiconductor (MOS) devices were fabricated from these YSZ materials for dielectric characterization. The dielectric properties of the Ag/YSZ/n-Si MOS structure were investigated. It was found that the capacitance, conductivity and other dielectric parameters of these structures are strongly frequency dependent.

High pressure induced formation of carbon nanorods from tetracosane

Morphology control of carbon structures is essential for improving their performance in many applications. Direct pyrolysis of organic precursors, however, usually yields bulk amorphous carbon. Therefore, traditional methods for controlling the morphology of carbon structures involve multistep processes and complex precursor molecules. While various methods have been developed under ambient pressure, the impact of pressure on the morphology of the resulting carbon structures remains unexplored. Herein, we present the synthesis of carbon nanorods by direct pyrolysis of the low-cost aliphatic hydrocarbon tetracosane under high pressure conditions. The diameters of the carbon nanorods are adjusted by simply varying the synthetic pressures. High pressure allows controlling both the nanorod morphology as well as the degree of order, and local conductivity of the thus prepared nanorods has been confirmed by conductive atomic force microscopy measurements. Our method promises a convenient strategy to synthesize carbon structures with controlled morphology and high ordered chemical structure, which opens opportunities for potential electronic and electrochemical applications.