Effect of sandblasting and acid surface pretreatment on the specific capacitance of CuO nanostructures grown by hot water treatment for supercapacitor electrode applications.

Crystalline copper oxide (CuO) nanostructures with micro, nano, and micro-nano surface roughness were grown on Cu sheet substrates by a facile, scalable, low-cost, and low-temperature hot water treatment (HWT) method that simply involved immersing Cu sheet in DI water at 75 °C for 24 h without any chemical additives. Various morphological features and sizes of CuO nanostructures were tuned by using different surface pretreatment techniques including acid treatment, sandblasting, or a combination of those two. The surface morphology of the prepared samples was analyzed by scanning electron microscopy. The crystal structure of the CuO nanostructures was investigated by x-ray diffraction XRD and Raman spectroscopy. To study the pseudocapacitive behavior, their potential supercapacitor performance, and equivalent series resistance, electrochemical analysis was done by cyclic voltammetry and electrochemical impedance spectroscopy for all the CuO/Cu samples in 1 M of Na2SO4electrolyte. Among all, the best supercapacitive performance was achieved for CuO/Cu samples pretreated with Sandblasting followed by Acid treatment resulting in a specific capacitance of about 104 F g-1. The electrode with the sandblasted + acid pretreated sample showed a maximum of ∼69% capacitive retention after 2000 consecutive cycles. Our results indicate that CuO nanostructures on Cu substrates prepared with different surface pretreatment conditions and grown by HWT can be promising electrodes for supercapacitor device applications.

Enhancing the antibacterial efficacy of aluminum foil by nanostructuring its surface using hot water treatment.

Bacterial biofilm has become one of the most frequent health problems as it contributes to persistent chronic infections. Therefore, it is vital to find alternatives to currently used bactericidal agents to prevent bacterial contamination on surfaces effectively and prevent the biofilms formation. Several metallic materials are well known for their antimicrobial activity; this includes copper, copper alloys, silver, gold, titanium, and zinc. On the other hand, some metals, such as aluminum, do not have noteworthy antimicrobial properties. In this study, we demonstrate that the antibacterial activity of household aluminum foil can be enhanced by nanostructuring the foil's surface by a simple hot water treatment (HWT) process. Cultures ofEscherichia coliandStaphylococcus aureuswere grown on nutrient agar while exposed to the samples of treated and untreated Al foils and left for 24 h. Our results indicate that treated Al foil can more effectively inhibit the bacteria growth compared to the regular untreated Al foil. This enhancement in antibacterial property might be due to a combination of chemical and morphological changes that the cell undergoes once it encounters nanofeatures of HWT-Al foil surface.

CuO/Cu core/shell nanostructured photoconductive devices by hot water treatment and high pressure sputtering techniques.

This work demonstrates the fabrication of simple photoconductive devices based on CuO/Cu core/shell nanostructured heterojunction that performs notable photocurrent response. Copper oxide (CuO) nanoleaf structures (NLs) have been successfully grown on ITO-coated glass substrate via a simple hot water treatment (HWT) method. A conformal Cu shell was fabricated by high pressure sputtered (HIPS) deposition technique on the CuO nanoleaves to produce NLs-core/metal shell photoconductive devices. For comparison, CuO thin film (TF) was prepared by the thermal oxidation method to manufacture the conventional planar thin film devices. Results showed that the HWT method resulted in the formation of dense 3D CuO nanoleaves on ITO/glass substrate with a high surface area. CuO NLs showed higher optical absorption than CuO TF in the ultraviolet and visible spectrum. Further, the optical band gaps of CuO NLs and TF samples have been estimated from Touc's plot to be 1.45 ± 0.10 eV and 1.63 ± 0.20 eV, respectively. Current density-voltage measurements' result revealed that core/shell devices have superior photocurrent response compared to TF devices. The average photocurrent density at zero-bias for the NLs devices was 23.5 ± 2.0 µA cm-2 and for TF devices was 6.7 ± 1.0 µA cm-2. Besides, NLs core/shell photoconductive devices exhibit a remarkable increase in photocurrent response values with increasing bias voltage compared to the increased values in TF devices. The results demonstrate that the devices based on HWT-NLs-core/HIPS-shell design showed a significant enhancement on the photoconductivity response compared with the conventional TF design. The performance enhancement can be attributed to improving light trapping, photocarriers generation-recombination times and carrier collection by introducing an alternative radial interface in core/shell design. Also, HWT CuO NLs geometry feature with the high surface area has worked to enhance light absorption that enables the design of high efficiency, functional and commercial photoconductive detectors.

Self-anti-reflective density-modulated thin films by HIPS technique.

A critical factor for an efficient light harvesting device is reduced reflectance in order to achieve high optical absorptance. In this regard, refractive index engineering becomes important to minimize reflectance. In this study, a new fabrication approach to obtain density-modulated CuIn x Ga(1-x)Se2 (CIGS) thin films with self-anti-reflective properties has been demonstrated. Density-modulated CIGS samples were fabricated by utilizing high pressure sputtering (HIPS) at Ar gas pressure of 2.75 × 10-2 mbar along with conventional low pressure sputtering (LPS) at Ar gas pressure of 3.0 × 10-3 mbar. LPS produces conventional high density thin films while HIPS produces low density thin films with approximate porosities of ∼15% due to a shadowing effect originating from the wide-spread angular atomic of HIPS. Higher pressure conditions lower the film density, which also leads to lower refractive index values. Density-modulated films that incorporate a HIPS layer at the side from which light enters demonstrate lower reflectance thus higher absorptance compared to conventional LPS films, although there is not any significant morphological difference between them. This result can be attributed to the self-anti-reflective property of the density-modulated samples, which was confirmed by the reduced refractive index calculated for HIPS layer via an envelope method. Therefore, HIPS, a simple and scalable approach, can provide enhanced optical absorptance in thin film materials and eliminate the need for conventional light trapping methods such as anti-reflective coatings of different materials or surface texturing.

Hierarchical Multi-Diameter Single-Crystal Silicon Nanowires by Successive Wet Chemical Etching.

A simple and low cost top­down wet chemical etching method was developed to fabricate hierarchical multi-diameter well-ordered single-crystal silicon nanowires. The procedure starts with forming single diameter silicon nanowire arrays by using nanosphere lithography and metal-assisted chemical etching of single crystal silicon wafer, which is followed by anisotropic radial etching of the wires. Successive repetitions of these etching steps result in arrays of multi-diameter single crystal nanowires. This technique can allow engineering nanowires in a hierarchical three-dimensional geometry for the development of advanced nano devices.

Influence of Substrate Location and Temperature Variation on the Growth of ZnO Nanorods Synthesized by Hot Water Treatment.

Hot water treatment (HWT) is a versatile technique for synthesizing metal oxide nanostructures (MONSTRs) by immersing metal substrates in hot water, typically in glass beakers. The proximity of substrates to the heat source during HWT can influence the temperature of the substrate and subsequently impact MONSTR growth. In our study, zinc (Zn) substrates underwent HWT at the base of a glass beaker in contact with a hot plate and at four different vertical distances from the base. While the set temperature of deionized (DI) water was 75.0 °C, the substrate locations exhibited variations, notably with the base reaching 95.0 °C. Scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and Raman spectroscopy showed stoichiometric and crystalline zinc oxide (ZnO) nanorods. ZnO rods on the base, exposed to higher temperatures, displayed greater growth in length and diameter, and higher crystallinity. Nanorods with increasing vertical distances from the base exhibited a logarithmic decrease in length despite identical temperatures, whereas their diameters remained constant. We attribute these findings to crucial HWT growth mechanisms like surface diffusion and "plugging", influenced by temperature and water flow within the beaker. Our results provide insights for optimizing synthesis parameters to effectively control MONSTR growth through HWT.

Hydrophobic metallic nanorods with Teflon nanopatches.

Introducing a hydrophobic property to vertically aligned hydrophilic metallic nanorods was investigated experimentally and theoretically. The platinum nanorod arrays were deposited on flat silicon substrates using a sputter glancing angle deposition technique (GLAD). Then a thin layer of Teflon (nanopatch) was partially deposited on the tips of platinum nanorods at a glancing angle of theta(dep) = 85 degrees for different deposition times. Teflon deposition on Pt nanorods at normal incidence (theta(dep) = 0 degrees) was also performed for comparison. Morphology and elemental analysis of Pt/Teflon nanocomposite structures were carried out using scanning electron microscopy (SEM) and energy dispersive x-ray analysis (EDAX), respectively. It was found that the GLAD technique is capable of depositing ultrathin isolated Teflon nanostructures on selective regions of nanorod arrays due to the shadowing effect during obliquely incident deposition. Contact angle measurements on nanocomposite Pt nanorods with Teflon nanopatches exhibited contact angle values as high as 138 degrees, indicating a significant increase in the hydrophobicity of originally hydrophilic Pt nanostructures that had an angle of about 52 degrees. The enhanced hydrophobicity of the Pt nanorod/Teflon nanopatch composite is attributed to the presence of nanostructured Teflon coating, which imparted a low surface energy. Surface energy calculations were performed on Pt nanorods, Teflon thin film, and Pt/Teflon composite using the two-liquid method to confirm the contact angle measurements. Furthermore, a new contact angle model utilizing Cassie and Baxter theory for heterogeneous surfaces was developed in order to explain the enhanced hydrophobicity of Pt/Teflon nanorods. According to our model, it is predicted that the solid-liquid interface is mainly at the Teflon tips when the composite nanorods are in contact with water.

Size control of Cu nanorods through oxygen-mediated growth and low temperature sintering.

Control of the size of Cu nanorods vapor-deposited at an oblique angle (approximately 85 degrees) by oxygen-mediated growth was investigated using scanning electron microscopy (SEM) and x-ray diffraction (XRD). It was observed that exposure of Cu nanorods to the oxygen ambient periodically resulted in a reduction in the diameter of the nanorods as well as an increase in the areal density of the nanorods. This oxygen-induced modification to the nanorod growth is attributed to the higher energy barrier for Cu adatom migration on the oxide surface at room temperature; this reduces the rod diameter. At a low annealing temperature of approximately 300 degrees C, the SEM images show that the nanorods have densified and formed a continuous film structure, which is consistent with the sintering phenomenon. The XRD and SEM analyses show that the coalescent/grain growth rate for Cu nanorods with smaller diameters is enhanced due to the size effect. This low temperature sintering characteristic of the Cu nanorod array has great potential for being utilized in wafer bonding for three-dimensional integration of devices.

Metal oxide nanostructures by a simple hot water treatment.

Surfaces with metal oxide nanostructures have gained considerable interest in applications such as sensors, detectors, energy harvesting cells, and batteries. However, conventional fabrication techniques suffer from challenges that hinder wide and effective applications of such surfaces. Most of the metal oxide nanostructure synthesis methods are costly, complicated, non-scalable, environmentally hazardous, or applicable to only certain few materials. Therefore, it is crucial to develop a simple metal oxide nanostructure fabrication method that can overcome all these limitations and pave the way to the industrial application of such surfaces. Here, we demonstrate that a wide variety of metals can form metal oxide nanostructures on their surfaces after simply interacting with hot water. This method, what we call hot water treatment, offers the ability to grow metal oxide nanostructures on most of the metals in the periodic table, their compounds, or alloys by a one-step, scalable, low-cost, and eco-friendly process. In addition, our findings reveal that a "plugging" mechanism along with surface diffusion is critical in the formation of such nanostructures. This work is believed to be of importance especially for researchers working on the growth of metal oxide nanostructures and their application in functional devices.

Enhanced photocurrent and dynamic response in vertically aligned In2S3/Ag core/shell nanorod array photoconductive devices.

Enhanced photocurrent values were achieved through a semiconductor-core/metal-shell nanorod array photoconductive device geometry. Vertically aligned indium sulfide (In2S3) nanorods were formed as the core by using glancing angle deposition technique (GLAD). A thin silver (Ag) layer is conformally coated around nanorods as the metallic shell through a high pressure sputter deposition method. This was followed by capping the nanorods with a metallic blanket layer of Ag film by utilizing a new small angle deposition technique combined with GLAD. Radial interface that was formed by the core/shell geometry provided an efficient charge carrier collection by shortening carrier transit times, which led to a superior photocurrent and gain. Thin metal shells around nanorods acted as a passivation layer to decrease surface states that cause prolonged carrier lifetimes and slow recovery of the photocurrent in nanorods. A combination of efficient carrier collection with surface passivation resulted in enhanced photocurrent and dynamic response at the same time in one device structure. In2S3 nanorod devices without the metal shell and with relatively thicker metal shell were also fabricated and characterized for comparison. In2S3 nanorods with thin metal shell showed the highest photosensitivity (photocurrent/dark current) response compared to two other designs. Microstructural, morphological, and electronic properties of the core/shell nanorods were used to explain the results observed.

High optical absorption of indium sulfide nanorod arrays formed by glancing angle deposition.

Indium(III) sulfide has recently attracted much attention due to its potential in optical sensors as a photoconducting material and in photovoltaic applications as a wide band gap material. On the other hand, optical absorption properties are key parameters in developing photosensitive photodetectors and efficient solar cells. In this work, we show that indium sulfide nanorod arrays produced by the glancing angle deposition technique have superior absorption and low reflectance properties compared to conventional flat thin film counterparts. We observed an optical absorption value of approximately 96% for nanorods at wavelengths <500 nm in contrast to 79% for conventional thin films of indium sulfide. A superior photoconductivity (PC) response as high as about 40% (change in resistance upon illumination) was also observed in nanorod samples. This is mainly believed to be due to their high optical absorption, whereas only less than 1% PC change was detected in conventional thin films. We give a preliminary description of the enhanced light absorption properties of the nanorods by using the Shirley-George model, which predicts diffusion of light as a function of the roughness of the surface.