Wet Chemistry Research Articles

Planar and Curved π-Extended Porphyrins by On-Surface Cyclodehydrogenation.

Recent advancements in on-surface synthesis have enabled the reliable and predictable preparation of atomically precise low-dimensional materials with remarkable properties, which are often unattainable through traditional wet chemistry. Among these materials, porphyrins stand out as a particularly intriguing class of molecules, extensively studied both in solution and on surfaces. Their appeal lies in the ability to fine-tune their unique chemical and physical properties through central metal exchange or peripheral functionalization. However, the synthesis of π-extended porphyrins featuring unsubstituted anthracenyl groups has remained elusive. Herein, we report an in vacuo temperature-controlled cyclodehydrogenation of bis- and tetraanthracenyl Zn(II) porphyrins on a gold(111) surface. By gradually increasing the temperature, sequential dehydrogenation leads to the formation of fused anthracenyl porphyrin products. Notably, at high molecular coverage, the formation of bowl-shaped porphyrins occurs, along with transmetalation of Zn with Au. These findings open the door to a variety of π-extended anthracenyl-containing porphyrin products via cyclodehydrogenation and transmetalation, offering significant potential in the fields of molecular (photo/electro)catalysis, (opto)electronics, and spintronics.

Enhanced carbon fiber interface with thermoplastics via nanostructure surface modification: failure, morphology and wettability analysis

Improving the fiber-matrix adhesion in thermoplastic composites remains a significant challenge due to the lack of chemical bonding between thermoplastics and common reinforcing fibers. This study investigates the effectiveness of carbon fibers enhanced with nanostructure surface modification for strengthening the interfacial adhesion to thermoplastic matrices. The fiber surface was modified with graphene nanoplatelets (GNP) through the facile coating method, and the apparent interfacial shear strength (IFSS) was determined by the single-fiber pullout test. GNP-coated fiber improved IFSS by 74% with neat high-density polyethylene (HDPE-Neat) and 28% with maleic anhydride-grafted HDPE (HDPE-8MA), while reduced by 27% with polyamide 6 (PA6) due to different failure mechanisms. Morphology, chemical, and wettability analysis were conducted on the nano-enhanced carbon fibers to quantitatively elucidate these findings on micro/nanoscale, combining machine learning-based image segmentation, X-ray photoelectron spectroscopy (XPS), and contact-angle measurements of intermittent beading on fibers.

Investigation of Cr2SiC Ceramic MAX Phase Coated Metallic Bipolar Plates in Ex-situ Conditions for Proton Exchange Membrane Fuel Cells

Essential for compact and lightweight proton exchange membrane fuel cell (PEMFC) stacks, metallic bipolar plates (MBPs) suffer from durability and conductivity issues due to surface corrosion and passivation. This study conducts ex-situ characterization of Cr2SiC ceramic MAX phase coatings on stainless steel (SS) 316 L substrates to evaluate their suitability for MBP application. The investigation encompasses coating structure, surface morphology, corrosion resistance, surface wettability, in-plane electrical conductivity, and interfacial contact resistance. X-ray diffraction and X-ray photoelectron spectroscopy confirm the presence of Cr2SiC coatings on SS316L, while energy-dispersive X-ray spectroscopy verifies uniform coverage and elemental weight percentage. Corrosion resistance is evaluated using potentiostatic and potentiodynamic polarization tests, showing excellent resistance with low corrosion current density (Icorr) at both 25 °C (3.29E-03 μA/cm2) and 80 °C (4.32E-02 μA/cm2), meeting US Department of Energy (DOE) technical targets. Potentiodynamic polarization reveals large corrosion potential and small Icorr values at both temperatures, outperforming uncoated samples. Electrochemical impedance spectroscopy post-accelerated corrosion tests show high charge transfer resistance at 25 °C (3.68E+05 Ω cm2) and 80 °C (3.02E+05 Ω cm2), indicating stability in acidic environments. Surface wettability analysis indicates low water affinity with a large contact angle (75°) and low surface free energy (28.92 mJ/m2) for the coated samples as compared to the uncoated samples. Electrical conductivity meets DOE targets with an in-plane conductivity of 4.59E+05 S/m and interfacial contact resistance of 8.04 mΩcm2 after 5-h accelerated corrosion tests at 80 °C. These results suggest that Cr2SiC coated SS316L exhibits excellent corrosion resistance, surface wettability, and electrical characteristics, making them viable for PEMFC applications.

Enhanced adhesion strength of copper deposited epoxy composite films for chip substrates by tuning copper oxide and internal stress

Copper oxides and internal stress have an obvious influence on adhesion strength of copper deposited polymer composites. However, the effect of the evolution behavior of copper oxides and internal stress on adhesion force of chip substrates is no clear and rare far. Herein, the copper deposited epoxy-phenolic/silica composite film with different desmear time was fabricated by using wet chemistry and electrochemistry methods. The chemical structure, surface roughness, morphology, surface chemical state, crystal structure and adhesion strength of copper and epoxy resin substrate were characterized by scanning electron microscope (SEM), interference microscope, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The adhesion strength of samples is increased from 3 N/cm to 4.7 N/cm. The effect of the evolution behavior of copper oxides and internal stress on adhesion strength of copper deposited epoxy resin composite films at the interfaces was systematically investigated, the mechanisms and reason of increasing adhesion strength and interfacial adhesion failure for copper deposited epoxy resin composite substrates were revealed. This work will provide a guidance in theory and experiment to enhance interfacial adhesion force of epoxy resin composite films for advanced substrate in the future.

Enhancing anti-icing efficacy in hybrid polyurethane coatings: Evaluating the significance of molecular weight, chemical structure, and content of PEG/PDMS

This study investigates the advantages of adding polydimethyl siloxane/polyethylene glycol (PEG/PDMS) copolymers to polyurethane coatings, with a particular focus on optimizing anti-icing efficacy. A range of characterization techniques are applied, including attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) analysis, surface roughness measurements, wettability analysis, tensile testing, and ice adhesion measurements, to elucidate the intricate relationships between copolymer molecular weight, chemical structure, and content and their collective effect on the anti-icing properties of the developed coatings. Tailored PEG/PDMS copolymers significantly reduce ice nucleation temperatures and enhance the anti-icing properties of polyurethane coatings. Adding PEG/PDMS copolymers to polyurethane alters the surface roughness, wettability, and mechanical properties of the coatings to improve anti-icing performance. The presence of copolymers decreases ice adhesion strength (<50 kPa), attributed to the formation of a quasi-liquid layer that acts as a lubricant between the ice and the coatings, and delays ice formation. Furthermore, the enhanced durability of copolymer-containing coatings ensures a long-lasting anti-icing effect after multiple icing/de-icing cycles, although some degradation was observed over time. The tailored PEG/PDMS copolymers demonstrate potential for maximizing the anti-icing properties of polyurethane coatings and advancing anti-icing technologies.

Preparation of Nonfouling Zwitterionic Coatings by Plasma-Enhanced Chemical Vapor Deposition under Ambient Pressure.

Nonspecific protein adsorption significantly impacts the performance of biomedical devices in both hemocompatibility and tissue compatibility. Polyzwitterionic coatings are a promising solution. However, conventional zwitterionic coatings always have to rely on sophisticated wet chemistry methods, leading to low controllability and high cost. In this work, zwitterionic coatings were prepared by nitrogen plasma-enhanced chemical vapor deposition (PECVD) of precursors for 90 s under ambient pressure followed by hydrolysis. The results showed that the PECVD-coated thermoplastic polyurethane (TPU), Tecoflex, effectively resists nonspecific protein adsorption, platelet adhesion, and bacterial adhesion without changing the mechanic properties of TPU. This approach simplified the zwitterionic coating process with highly controllability, showing a promising potential for the surface modification of biomedical devices.

Glucose electrooxidation on carbon supported NiAu electrocatalysts

NiAu/C nanomaterials are synthesised using a wet chemistry method with targeted Au atomic ratios of 10 %, 20 % and 30 %. Physicochemical characterisations indicate that the materials have mean compositions close to the nominal ones but ca. 20 at% Au richer in average than expected (Au ratios of 13.6 at%, 23.1 at% and 35.9 at%, respectively). The NiAu/C materials are composed of Au-rich spherical-like Janus particles of several tenths nm and of a phase of very small Ni-rich nanoparticles and Ni(OH2) clusters. The electrochemical measurements in a 0.1 M NaOH/0.1 M glucose electrolyte indicate that the NiAu20/C catalyst is the most active for the glucose oxidation reaction, leading to a mass activity at +0.6 V vs RHE >1.5 times higher than that with a pure Au/C catalyst, although the Au content is almost 5 times lower. The chronoamperometry measurements for 900 s at +0.6 V vs RHE confirm the activity gain with the NiAu20/C catalyst. The electrolysis measurement at a cell voltage of + 0.6 V for 6 h shows that the NiAu20/C catalyst is selective towards the production of gluconic acid, with a faradaic efficiency higher than 100 %, indicating the occurrence of a 1-electron reaction with anodic hydrogen coproduction. At +0.8 V, the faradaic efficiency is lower than 100 %, indicating the formation of other products than gluconic acid, but at a very low extent (not detectable by HPLC) guarantying a very high selectivity towards gluconic acid.

Experimental investigation of pool boiling on Ti-Cu composite coated surfaces prepared using Electric Discharge Coating

Boiling heat transfer has become a very potent two-phase heat transfer mechanism for cooling high heat-producing devices such as microelectronic devices, fusion reactors or turbine blades. Increasing research has shown that micro/nano-structures on surfaces increase the number of nucleation sites for bubble formation, which ultimately results in a major improvement in boiling performance. This led to studies on developing various coated surfaces in order to generate micro/nano-structures on surfaces. In the current study, microstructured boiling surfaces were prepared using the Electric Discharge Coating (EDC) process. Titanium-copper (Ti-Cu) composite microparticles were coated on copper surface under reverse polarity in the Electric Discharge Machine. Four surfaces were prepared by using current settings of 3 A, 4 A, 5 A and 6 A. It was followed by characterisation of the surfaces which included, wettability analysis, porosity, pore size estimation, mean roughness measurement and elemental analysis, in order to better understand the boiling results on the surfaces. The surfaces formed were hydrophilic in nature, with contact angles varying from 47° to 65°. Pool boiling were performed with the developed surfaces and critical heat flux (CHF) and nucleate boiling heat transfer coefficient (NBHTC) improvement of 37.17 % and 172 % respectively were observed with the best performing surface compared to the bare surface. The best performing surface was also compared with relevant published literature to determine its standing against the present state of the art.

NIR spectroscopy prediction model for capsaicin content estimation in chilli: A rapid mining tool for trait-specific germplasm screening

Chilli is a widely produced crop, highly valued for its capsaicin content, a key economic trait. Traditional wet chemistry methods for estimating capsaicin are time-taking and laborious, while non-destructive methods like NIRS coupled with chemometrics, offer efficient alternatives, simplifying and accelerating biochemical assessments. This study is the first to develop and validate and tested for applicability of NIRS-based prediction model for capsaicin content in Indian chilli germplasm using MPLS regression. Various mathematical treatments were performed, and the most suited model was selected based on high RSQexternal, RPD and lower SEP values in the external validation set, indicating strong prediction accuracy and minimal error. The model achieved high RSQexternal value of 0.808, RPD value of 2.088 and low SEP value of 3.415 for capsaicin content, demonstrating excellent prediction performance. A paired sample t-test p-value of 0.757 (p > 0.05) showed non-significant difference between wet lab and predicted values, confirming the model’s accuracy. The applicability of the model was validated on fresh harvest germplasm the following year, showing a higher reliability score of 0.949, further confirming model’s reliability. This model would aid in high-throughput, accurate screening of chilli germplasm for capsaicin, accelerating chilli crop improvement programs and the development of new high-capsaicin varieties.

Techno-Economic Analysis of Near-Infrared (NIR) Systems at Feed Millsas a Low-Cost, High-Speed Alternative to Feed Ingredient Testing

Improperly balanced diets not only impact the quality of animal production but also the profits of a livestock operation. Typically, the nutrient and chemical content of feed ingredients and forages are determined using well-established wet chemistry tests. However, these tests can be expensive and time-consuming. Moreover, the increasing use of various by-products which are known to have large variations in chemical and nutrient content warrants a real-time on-site feed and forage testing system. Near infrared (NIR) spectroscopy systems are quick and effective on-site testing tools. While NIR systems are being adopted for on-farm or at feed mill ingredient and forage testing, little is known about the economic impacts of such an investment for a livestock or feed mill operator. This study developed a baseline model and an Excel based spreadsheet application for performing Return on Investment (ROI) analysis to determine the feasibility of using an on-farm or at feed mill NIR testing system. ROI was calculated based on the nutrient cost saved or spent determined from the difference of estimated nutrient content and actual calculated value. The findings from this study will promote low-cost alternatives for onfarm or at feed mill ingredient testing, positively impacting quality of animal products and minimizing costs.

High entropy alloys mediated formation of multi-oxide nanoparticles on carbon fiber cloths and their synergistic effects in electrochemical performance

A wet chemistry technique is developed to produce high entropy alloy nanoparticles on carbon fibers. Coatings display solution phase and can be aerially oxygenated into multi-oxides. Electrochemical measurements confirm the generation of high specific capacitance from multi-oxide coatings where individual components show redox reactions at different potentials thus producing large loops of charge–discharge. Comparative study confirms synergistic effects arising from individual oxides in coatings.

An experimental and theoretical investigation of the enhanced effect of Ni atom-functionalized MXene composite on the mechanism for hydrogen storage performance in MgH2

The deposition of ultrafine single-atom nickel particles on Nb2C (MXene) was successfully achieved using a wet chemistry method to synthesize Ni@Nb2C composite. This study explored the effect of Ni@Nb2C on the hydrogen absorption and desorption properties of MgH2 through theoretical calculations and experimental investigations. Under the catalytic action of Ni@Nb2C, the initial dehydrogenation temperature of MgH2 was reduced by 121°C, with approximately 4.26 wt.% of H2 desorbed at 225°C in 100 min. The dehydrogenation activation energy of the MgH2 + Ni@Nb2C composite dropped to 86.7 kJ∙mol−1, a reduction of 60.5 kJ∙mol−1 compared to pure MgH2. Density functional theory calculations indicated that the incorporation of Ni@Nb2C enhanced the performance of MgH2 performance by improving interactions among Nb2C, Ni, Mg, and H atoms. In the Ni@Nb2C + MgH2 system, the lengths of Mg-H bonds (1.91–1.99 Å) were found to be longer than those observed in pure MgH2 (1.71 Å). The dehydrogenation energy for this system (1.08 eV) was lower than that for Nb2C (1.52 eV). These findings suggest that the synergistic effect of Ni and Nb2C significantly enhances the hydrogenation/dehydrogenation kinetics of MgH2, thereby introducing a novel approach for catalytic modification of solid hydrogen storage materials through synergistic actions.

Thickness dependent crystallinity, hydrophilicity, and surface microtexture in CaF2 thin films deposited via thermal evaporation method

This study investigates the deposition and characterization of CaF₂ thin films with thicknesses ranging from 40 to 320 nm, fabricated via thermal evaporation onto glass substrates. X-ray diffractometry (XRD) revealed that increased film thickness leads to enhanced crystallinity, with larger crystallite sizes and reduced lattice strain. Wettability analysis demonstrated a transition from hydrophobic behavior (contact angle ∼70° for 40 nm) to hydrophilic behavior (contact angle ∼52° for 320 nm) as film thickness increased. Surface morphology, examined via atomic force microscopy (AFM), showed a significant reduction in surface roughness in thicker films, with smoother, more coalesced surfaces observed for films over 160 nm. Monofractal analysis further confirmed the evolution of surface microtexture, with thicker films exhibiting higher uniformity and reduced surface complexity. These findings provide critical insights into optimizing CaF₂ thin films for applications in optics, electronics, and surface coatings, where improved crystallinity and surface properties are essential.

Opal‐Inspired SiO2‐Mediated Carbon Dot Doping Enables the Synthesis of Monodisperse Multifunctional Afterglow Nanocomposites for Advanced Information Encryption

AbstractDespite recent advancements in inorganic and organic phosphors, creating monodisperse afterglow nanocomposites (NCs) remains challenging due to the complexities of wet chemistry synthesis. Inspired by nanoinclusions in opal, we introduce a novel SiO2‐mediated carbon dot (CD) doping method for fabricating monodisperse, multifunctional afterglow NCs. This method involves growing a SiO2 shell matrix on monodisperse nanoparticles (NPs) and doping CDs into the SiO2 shell under hydrothermal conditions. Our approach preserves the monodispersity of the parent NP@SiO2 NCs while activating a green afterglow in the doped CDs with an impressive lifetime of 1.26 s. Additionally, this method is highly versatile, allowing for various core and dopant combinations to finely tune the afterglow through core‐to‐CD or CD‐to‐dye energy transfer. Our findings significantly enhance the potential of SiO2 coatings, transforming them from merely enhancing the biocompatibility of NCs to serving as a versatile matrix for emitters, facilitating afterglow generation and paving the way for new applications.

Opal-Inspired SiO2-Mediated Carbon Dot Doping Enables the Synthesis of Monodisperse Multifunctional Afterglow Nanocomposites for Advanced Information Encryption.

Despite recent advancements in inorganic and organic phosphors, creating monodisperse afterglow nanocomposites (NCs) remains challenging due to the complexities of wet chemistry synthesis. Inspired by nanoinclusions in opal, we introduce a novel SiO2-mediated carbon dot (CD) doping method for fabricating monodisperse, multifunctional afterglow NCs. This method involves growing a SiO2 shell matrix on monodisperse nanoparticles (NPs) and doping CDs into the SiO2 shell under hydrothermal conditions. Our approach preserves the monodispersity of the parent NP@SiO2 NCs while activating a green afterglow in the doped CDs with an impressive lifetime of 1.26 s. Additionally, this method is highly versatile, allowing for various core and dopant combinations to finely tune the afterglow through core-to-CD or CD-to-dye energy transfer. Our findings significantly enhance the potential of SiO2 coatings, transforming them from merely enhancing the biocompatibility of NCs to serving as a versatile matrix for emitters, facilitating afterglow generation and paving the way for new applications.

Metal-Free Wet Chemistry for the Fast Gram-Scale Synthesis of γ-Graphyne and its Derivatives.

γ-Graphyne (GY), an emerging carbon allotrope, is envisioned to offer various alluring properties and broad applicability. While significant progress has been made in the synthesis of GY over recent decades, its widespread application hinges on developing efficient, scalable, and accessible synthetic methods for the production of GY and its derivatives. Here we report a facile metal-free nucleophilic crosslinking method using wet chemistry for fast gram-scale production of GY and its derivatives. This synthesis method involves the aromatic nucleophilic substitution reactions between fluoro-(hetero)arenes and alkynyl silanes in the presence of a catalytic amount of tetrabutylammonium fluoride, where the fluoride plays a crucial role in removing protective groups from alkynyl silanes and generating reactive alkynylides. Our comprehensive analysis of the as-prepared GY reveals a layered structure, characterized by the presence of the C(sp)-C(sp2) bond. The synthetic strategy shows remarkable tolerance to various functional groups and enables the preparation of diverse F-/N-rich GY derivatives, using electron-deficient fluoro-substituted (hetero)arenes as precursors. The feasibility of producing GY and derivatives from fluorinated (hetero)arenes through the metal-free, scalable, and cost-effective approach paves the way for broad applications of GY and may inspire the development of new carbon materials.

Seasonal and Climatic Drivers of Wet Deposition Organic Matter at the Continental Scale

AbstractDissolved organic matter (DOM) concentrations and composition within wet deposition are rarely monitored despite contributing a large input of bioavailable dissolved organic carbon (DOC) and nitrogen (DON) to the Earth's surface. Lacking from the literature are spatially comprehensive assessments of simultaneous measurements of wet deposition DOC and DON chemistry and their dependencies on metrics of climate and environmental factors. Here, we use archived precipitation samples from the US National Atmospheric Deposition Program collected in 2017 to 2018 from 17 sites across six ecoregions to investigate variability in the concentration and composition of depositional DOM. We hypothesize metrics of DOM chemistry vary with ecoregion, season, large‐scale climate drivers, and precipitation geographic source. Findings indicate differences in DOC and DON concentrations and loads among ecoregions. The highest wet deposition concentrations are from sites in the Northern Forests and lowest concentrations from sites in Marine West Coast Forests. Summer and autumn samples contained the highest DOC concentrations and DON concentrations that were consistently above detection limit, corresponding with seasonality of peak air temperatures and the phenology of the growing season in the northern hemisphere. Compositional trends suggest lighter DOM molecules in autumn and winter and heavier molecules in spring and summer. Climate drivers explain 51% of variation in DOM chemistry, revealing differing drivers on the concentrations and loads of DOC versus DON in wet deposition. This study highlights the necessity of incorporating DOC and DON measurements into national deposition monitoring networks to understand spatial and temporal feedbacks between climate change, atmospheric chemistry and landscape biogeochemistry.

Effects of long-term nitrogen and phosphorus fertilization on soil phosphorus forms and dynamics under continuous wheat production in Saskatchewan, Canada

Many agricultural crops require both nitrogen (N) and phosphorus (P) fertilizers to sustain crop yields. However, long-term application of NH4–N fertilizers can cause soil acidification, which alters soil abiotic and biotic processes, including soil P dynamics. Long-term continuous wheat plots in Saskatchewan, Canada, were used to assess effects of N and P fertilization from 1967 and P fertilizer cessation in subplots from 1995. General soil chemical properties and soil P pools and forms were determined and then correlated with soil pH, total N (TN), and total P (TP) concentrations to show the relative importance on soil P dynamics of (a) crop nutrition (TN and TP); (b) soil acidification (pH); or (c) P fertilization/cessation. Fertilization with NH4–N decreased soil pH and altered exchangeable cation concentrations; however, long-term crop growth was poor in no-N plots and was best with both N and P fertilizers, in turn increasing soil carbon and organic matter. Applying P fertilizers without N increased soluble phosphates and the risk of P losses in runoff. Soil organic P (TPo) concentrations were correlated negatively to pH and positively to TN, but the concentrations of P compounds were not correlated to pH. This suggests that TPo accumulation may be from increased long-term crop residue inputs from crops with N and P fertilizers, rather than increased sorption from reduced pH. However, soil pH will continue to decrease with continued NH4–N fertilization, affecting soil chemistry and future P cycling; monitoring with a suite of wet chemistry and spectroscopic techniques is recommended.

Relationship between Xylene Solubles and Crystallization Elution Fractionation of Polypropylene.

The Xylene Soluble (XS) is one of the most important parameters closely related to the performance of polypropylene (PP) materials. In order to obtain precise and accurate XS data, ASTM D 5492-17, based on the wet chemistry separation mechanism, strictly specifies each and every step of the procedure, such as a glassware setup, heating and cooling rates, etc. Meanwhile, crystallization elution fractionation (CEF), a newly developed technique, is capable of quantifying polyolefin structural regularity and comonomer distribution in a fast and automated manner. There have been a few pieces of preliminary work aiming to provide XS value from the CEF test with a limited number of samples. It is important to gain deep insights into the relationship between XS and the purge fraction of CEF by studying a large number of diverse polypropylene materials. In this paper, close to 300 commercial polypropylene and/or homemade polypropylene, both homopolypropylene (hPP) and propylene-ethylene copolymers (P/E) made with various catalysts under different conditions, were employed. XS values were obtained via CRYSTEX QC calibration. It was found that XS and the soluble fraction (SF) from CEF yielded a linear relationship with R 2 = 0.9942. This linearity is applicable regardless of polymer types, which can differ significantly in terms of molecular weight distribution, tacticity, chemical composition, and melt flow rate. One of the prominent advantages of using the CEF test instead of ASTM D 5492-17 is the elimination of the time-consuming procedure for much-improved precision and high productivity. In addition, the catalytic system was found to have an influence on SF and crystalline fractions of copolymers.

Growth of zinc oxide nanowires by a hot water deposition method.

Recently, various methods have been developed for synthesizing zinc oxide (ZnO) nanostructures, including physical and chemical vapor deposition, as well as wet chemistry. These common methods require either high temperature, high vacuum, or toxic chemicals. In this study, we report the growth of zinc oxide ZnO nanowires by a new hot water deposition (HWD) method on various types of substrates, including copper plates, foams, and meshes, as well as on indium tin oxide (ITO)-coated glasses (ITO/glass). HWD is derived from the hot water treatment (HWT) method, which involves immersing piece(s) of metal and substrate(s) in hot deionized water and does not require any additives or catalysts. Metal acts as the source of metal oxide molecules that migrate in water and deposit on the substrate surface to form metal oxide nanostructures (MONSTRs). The morphological and crystallographic analyses of the source-metals and substrates revealed the presence of uniformly crystalline ZnO nanorods after the HWD. In addition, the growth mechanism of ZnO nanowires using HWD is discussed. This process is simple, inexpensive, low temperature, scalable, and eco-friendly. Moreover, HWD can be used to deposit a large variety of MONSTRs on almost any type of substrate material or geometry.