Oxide Deposition Research Articles

Effect of Metal Oxide Deposition on the Sensitivity and Resolution of E-Beam Photoresist.

Organic-inorganic hybrid resists offer a solution to the issue of low sensitivity in organic photoresists like poly(methyl methacrylate) (PMMA). In this study, an organic-inorganic hybrid resist (PMMA-Al2O3) with high sensitivity and resolution was prepared by depositing metal oxides into PMMA using sequential infiltration synthesis (SIS). PMMA-Al2O3 was prepared by precisely controlling the number of SIS cycles (<23) in various atomic layer deposition (ALD) processes to facilitate the growth of metal oxides within PMMA pores. The impact of different metal oxide contents and distributions on the sensitivity and resolution of electron beam exposure was investigated. Numerical simulations of the deposit formation within the PMMA pores were performed by solving the pore-scale ALD governing equations fed by the reactor-scale boundary conditions. The gradual pore constriction with SIS cycles was predicted and validated by the experimental charaterizations. The results demonstrated that PMMA-Al2O3 was prepared using 20 SIS cycles, which corresponds to the numerically predicted occurrence of the pore blockage at the upper region of the PMMA layer, exhibiting optimal electron beam (e-beam) resolution while enabling line exposure with a width of 50 nm. While the corresponding sensitivity was lower than those of the samples prepared using 5 and 10 SIS cycles, the degradation of the PMMA structure was affected under exposure. The pattern transfer results showed that the line width was well retained for 20 cycles of deposition because of the high etching resistance of Al2O3. This research is expected to provide an effective approach to developing next-generation high-performance photoresists.

Floating potential probes for process control during reactive magnetron sputtering

Long term deposition of aluminum oxide by reactive magnetron sputtering results in a drift of the discharge voltage. A similar drift of the floating potential is observed. The latter observation is further investigated and it is shown that the change of the floating potential can be linked to a change of the electric properties of the vacuum chamber walls. Optimization of the floating potential probe is performed to use the difference between the discharge voltage and the floating potential as a parameter for process control. The best results were obtained with a planar probe sufficiently far positioned opposite to the magnetron, and close enough to the chamber wall facing the magnetron. This choice can be understood in terms of the ability of the probe to sense the discharge while being protected from deposition. The usage of the aforementioned difference to control the process is demonstrated with the measurement of process curves, more specifically IV-characteristics and hysteresis experiments. The shown reproducibility of these measurements opens a pathway for more precise quantification of reactive sputter deposition simulations and enhanced process control.

A comprehensive study of gate-induced drain leakage current and electrical characteristics in nanosheet field-effect transistors due to variation in structural parameters and ambient temperature

Abstract IIn this paper, two substrate optimization approaches of triple stacked Nanosheet FET (SNSHFET), namely optimization of buried oxide and selective deposition of punch through stopper (PTS) substrate, have been examined and simulations have been carried out using Technology Computer-Aided (TCAD) software. A comprehensive study of leakage current and key electrical characteristics (I¬ON, VT, SS, DIBL) have also been extracted based on variation in temperature from 298 K to 450 K, sheet width, fin pitch, substrate width, and source/drain doping, as well as different substrates. When the ambient temperature of SNSHFET is varied from 298 K to 450 K, the gate-induced drain leakage (GIDL) current increases and degrades the VT and ION/IOFF ratio. GIDL current also increases with increased doping of the source and drain. Also, the impact of ultra-thin body substrate in SNSHFET is studied for the reduction in GIDL current and optimization in the performance. It is observed that a reduction in the substrate width and the nanosheet width decreases the GIDL current, while variation in Inter-fin pitch has no significant impact on the GIDL current and other electrical characteristics. The band-to-band tunneling rate and electric field profiles are observed at the channel-drain and gate-substrate overlap region for understanding the physical insights of leakage current in the SNSHFET. This work also answers the dependency of GIDL current on the gate and drain voltage supply respectively. In addition to that, how GIDL current responds to the variation in the source-drain doping and with different PTS doping has been explained. The 3 nm-based SNSHFET is designed and its electrical and GIDL characteristics are compared with novel devices like Forksheet FET and Complementary FET.

Molecular layer deposition of polyhydroquinone thin films for Li‐ion battery applications

AbstractMany next‐generation materials for Li‐ion batteries are limited by material instabilities. To stabilize these materials, ultrathin, protective coatings are needed that conduct both lithium ions and electrons. Here, we demonstrate a hybrid chemistry combining molecular layer deposition (MLD) of trimethylaluminum (TMA) and p‐hydroquinone (HQ) with oxidative molecular layer deposition (oMLD) of molybdenum pentachloride (MoCl5) and HQ to enable vapor‐phase molecular layer growth of poly(p‐hydroquinone) (PHQ)—a mixed electron and lithium ion conducting polymer. We employ quartz crystal microbalance (QCM) studies to understand the chemical mechanism and demonstrate controlled linear growth with a 0.5 nm/cycle growth rate. Spectroscopic characterization indicates that this hybrid MLD/oMLD chemistry polymerizes surface HQ monomers from the TMA‐HQ chemistry to produce PHQ. The polymerization to PHQ improves air stability over MLD TMA‐HQ films without crosslinking. Electrochemical measurements on hybrid MLD/oMLD films indicate electronic conductivity of ~10−9 S/cm and a Li‐ion conductivity of ~10−4 S/cm. While these coatings show promise for Li‐ion battery applications, this work focuses on establishing the coating chemistry and future studies are needed to examine the stability, structure, and cycling performance of these coatings in full Li‐ion cells.

The impact of aluminum oxide deposition on the high-temperature resistance of silica aerogels

The impact of aluminum oxide deposition on the high-temperature resistance of silica aerogels

Simulation and deposition of Tungsten oxide (WO3) films using DC sputtering towards UV photodetector for high responsivity

Tungsten trioxide (WO3) detects UV radiation with great sensitivity while disregarding visible light, and it also has excellent electron mobility, allowing for efficient charge transport and fast response times. This work aims to develop a highly sensitive UV photodetector using WO3 material by optimizing the deposition parameter partial oxygen pressure (PaO2) and annealing the samples at various temperatures to determine the best PaO2 and annealing temperature that results in an improvement in the UV photodetector's sensitivity. The material WO3 was coated on glass substrates using DC magnetron sputtering while altering the PaO2 as 6 × 10−2 Pa, 4 × 10−2 -2 Pa, and 2 × 10−2 Pa, and then each as-deposited sample from varied PaO2 was annealed at temperatures ranging from 100°C to 400°C. When the sample's responses were compared, it was observed that the sample deposited at PaO2 2 × 10−2 Pa and annealed at 400 °C exhibited good photodetection capabilities, as evidenced by several characterization techniques such as SEM, XRD, and IV characterization. The work was subsequently carried out by evaluating the sample deposited at PaO2 2 × 10−2 Pa and annealed at 700 °C, which produced a good result for UV photodetection with the device's responsivity of 1e+4 A/W.

Genesis of Devonian volcanic-associated Lahn-Dill-type iron ores – part II: trace element fractionation evidences diffuse fluid venting

The iron (Fe)-oxide deposits of the Lahn-Dill-type are composed of haematite-quartz and rare siderite-haematite ores. These ores formed as marine chemical sediments on top of volcaniclastic rocks near the Middle to Late Devonian boundary (∼ 380 Ma). As such, their trace element fractionation patterns provide key information on venting style, ocean chemistry, particle-solution interaction, and depositional environment at the time of ore formation. This study combines WDXRF and ICP-MS/OES whole-rock geochemistry with complementary in-situ LA-ICP-MS analysis, and TEM element mapping of ore samples from the Fortuna Mine (Rhenish Massif, Germany). In-situ measurments were conducted on quartz-haematite, haematite, and siderite-haematite microdomains. Bulk major element contents of the ores indicate (volcani)clastic contamination and post-depositional hydrothermal alteration. Microdomain trace element distributions reveal four different trace element signatures, which are related to: (1) syngenetic apatite formation due to sorption of P and REY from seawater; (2) Fe-(oxyhydr)oxide-specific trace element scavenging and fractionation within the seawater column; (3) diagenetic Fe(III) reduction and trace element mobilisation in pore water; and (4) simultaneous deposition of (volcani)clastic material and Fe-(oxyhydr)oxides. These results show that Lahn-Dill-type iron ore formation resulted from mixing of a low-temperature vent fluid with ambient seawater at high seawater to vent fluid ratios. This likely was related to an environment in which diffuse venting dominated over focused venting, and in which quick Fe-particle precipitation led to formation of haematite-quartz ores. Local diagenetic Fe(III) reduction resulted in post-depositional siderite-haematite ore formation during which trace elements were partially remobilised in pore water.

Stable and sustainable perovskite solar modules by optimizing blade coating nickel oxide deposition over 15 × 15 cm2 area

Perovskite solar cells have rapidly advanced, achieving over 26% power conversion efficiency on the laboratory scale. However, transitioning to large-scale production remains a challenge due to limitations in conventional fabrication methods like spin coating. Here, we introduce an optimized blade coating process for the scalable fabrication of large-area (15 cm × 15 cm) perovskite solar modules with a nickel oxide hole transport layer, performed in ambient air and utilizing a non-toxic solvent system. Self-assembled monolayers between the nickel oxide and perovskite layer improve the uniformity and morphology of the perovskite film. Perovskite solar modules with a 110 cm2 active area achieve a power conversion efficiency of 12.6%. Moreover, encapsulated modules retained 84% of their initial efficiency after 1,000 hours at 85 °C in air (ISOS-T-1). This study demonstrates progress in the large-scale production of perovskite solar cells that combine efficiency with long-term stability.

Electrophoretic deposition of graphene oxide modified carbon paper: Enhance the interface strength and decrease the interface resistance

The gas diffusion layer (GDL) is a key component of the proton exchange membrane fuel cell (PEMFC) with the central roles of transporting electrons, supporting the electrode structure and transporting protons. However, the traditional carbon paper for GDL greatly limits the large-scale commercial application of PEMFC due to shortcomings such as low mechanical strength and poor electrical conductivity. Based on this, in this paper, ultrasound-assisted electrophoretic deposition of graphene oxide process is used to modify the primary carbon fiber paper and simultaneously improve the interfacial bond strength and interfacial conductivity of the carbon fiber paper to realize the facile preparation of phenolic resin carbon/reduced graphene oxide/carbon fiber (CFP-GO250–25) carbon-carbon composites with high mechanical and electrical conductivity properties. Compared to the unmodified carbon paper, the prepared CFP-GO250–25 shows an increase in tensile strength of about 76.5 % to 5.4 Mpa, a decrease in resistivity from 24.00 mΩ·cm to 10.21 mΩ·cm, and also has an excellent air permeability of 7.58 L/min. This study provides a reference for the facile preparation of phenolic resin carbon/reduced graphene oxide/carbon fiber carbon/carbon composites and promotes the large-scale commercial application of carbon fiber paper for low-cost GDL.

Modeling the influence of the duration of water vapor pulses on the properties of hafnium oxide synthesized by atomic layer deposition method

The work experimentally and theoretically analyzes the process of atomic layer deposition of hafnium oxide with the participation of water vapor as an oxidizing agent. The study of infrared absorption, Auger spectroscopy and luminescence shows that with increasing water pulse duration, the concentration of oxygen vacancies decreases and the composition tends to stoichiometric, which is given by the formula HfO2. Modeling of gas dynamics and kinetics of film synthesis by atomic layer deposition was performed, which showed the dependence of the coverage of the film surface with oxygen on the pulse duration and deposition temperature. A comparison of calculations with experimental results made it possible to estimate the magnitude of the kinetic coefficients of the synthesis processes that describe the observed experimental dependences and to show that the larger of the two temperatures of the atomic layer deposition window is associated with water desorption.

Discovery of mafic dikes in northeastern Tibet plateau belonging to the Emeishan large igneous province: Implications for paleocontinental reconstruction and mineral exploration

Due to the lack of paleomagnetic data and paleoclimatic records, the paleocontinental belonging of the Yidun terrane in northeastern Tibet plateau is debated. In this paper, we use the distribution of the Emeishan large igneous province (ELIP) to put the issue to rest. The ELIP is the product of mantle plume activity, which took place at 260 ± 3 Ma in the western margin of the Yangtze craton. The Yangtze craton is the northern part of the South China paleocontinental block. Our new discovery of four mafic dikes in the Yidun terrane with ages and chemistry like the ELIP strongly supports a new interpretation that this terrane was an integral part of the Yangtze craton during the ELIP magmatic event. Baddeleyites from these mafic dikes yield the U–Pb ages of 257.1 ± 4.8, 259.8 ± 8.5, 260.2 ± 4.5 and 261.5 ± 6.8 Ma for each of these dikes, which are similar to the zircon U-Pb ages of the mafic–ultramafic intrusions of the ELIP within the Yangtze craton. The Yidun mafic dikes and some high-Ti basalts of the ELIP within the Yangtze craton have similar Sr-Nd isotope compositions and mantle-normalized incompatible trace element distribution patterns, indicating similar mantle source compositions. Mixing calculation using Sr-Nd isotope compositions shows that the parental magmas for the Yidun mafic dikes experienced only 2–3 % crustal contamination. Partial melting modelling shows that the primary magmas for the Yidun mafic dikes were produced by 5–6 % mantle partial melting at the depths > 85 km below surface, consistent with mantle plume-related magmatism in a continental setting. The Yidun terrane is a new exploration frontier for magmatic Fe-Ti-V oxide deposits that are present elsewhere in the ELIP.

Ultralong Bistable, Electrolytic MnO2-Based, Electrochromic Battery Enabled by Porous, Low-Barrier, Hydroxylated TiO2 Interface.

Electrochromic (EC)battery technology shows great potential in future "zero-energy building" by controlling outdoor solar transmission to tune heat gain as well as storing the consumed energy to reuse across other building systems. However, challenges still exist in exploring an electrochemical system to satisfy requirements on both ultra-long optical memory (also called bistability) without continuous power supply and high energy density. Herein, an ECbattery is proposed to demonstrate ultra-long bistability (>760h) based on the reversible deposition and dissolution of manganese oxide (MnO2) without the addition of any mediators. A porous low-barrier hydroxylated titanium dioxide (TiO2) interface is incorporated to synergistically enrich Mn2+-affinity active sites for deposition and effectively reduce the electron transport barrier of MnO2 for dissolution, thereby significantly improving the reversibility, high optical modulation (60.2% at 400nm), and energy density (352mAhm-2). The modification strategy is also verified on the cathode-less button cells with a much higher average coulombic efficiency (99.9%) compared to the batteries without the porous hydroxylated TiO2 interface (74.6%). These achievements lay a foundation for advancements in both electrochromism and Zn-Mn aqueous batteries.

Occurrence and enrichment of cobalt and nickel in the Yindongshan ultramafic–mafic intrusion-hosted iron deposit, western Hubei Province, China

The Yindongshan iron deposit in western Hubei Province of China is hosted within Ordovician ultramafic–mafic intrusions. Recent field geological surveys have detected cobalt (Co) and nickel (Ni) enrichment within the Yindongshan clinopyroxenite, suggesting good potential for subeconomic Co-Ni mineralization. This study investigated the occurrence modes and enrichment processes of Co and Ni in the Yindongshan deposit through field geology and in situ analysis of the rock texture, geochronology, and geochemistry of sulfides, Fe-Ti oxides, and silicate minerals. The Yindongshan clinopyroxenites were emplaced at 440.2 ± 7.2 Ma via titanite LA-ICP-MS U-Pb dating, and underwent extensive post-magmatic metamorphism at 401.2 ± 8.6 Ma via apatite U-Pb dating. This metamorphism led to the widespread formation of amphibole via the replacement of clinopyroxene. Subsequently, hydrothermal epidote-albite veins, calcite-pyrite veins, and later actinolite veins developed. Pyrites from both clinopyroxenites and calcite veins show limited δ34S variations from −5.4 ‰ to −1.2 ‰, suggesting a magmatic sulfur source. Late-vein actinolites display geochemical characteristics distinct from those of amphiboles, indicating possible involvement of external fluids. LA–ICP–MS trace element results reveal a general increase in Co and Ni contents from silicate minerals and Fe-Ti oxides to pyrite and from earlier-crystallized coarse-grained clinopyroxenite to later medium- to fine-grained clinopyroxenite. The highest Co and Ni contents observed in pyrite from coarse-grained clinopyroxenite suggest their preferential incorporation into early sulfide minerals and then progressively depleted through magmatic evolution such as fractional crystallization. The positive correlation between Co and Ni with Fe in pyrite, along with the consistent parallel time-resolved LA–ICP–MS depth profiles among different mineral phases, indicates that isomorphic substitution occurred in pyrite. In silicate minerals, the Co and Ni contents increase from pyroxene, amphibole, to actinolite, with almost no Co or Ni present in epidote. The elevated Co and Ni contents in metamorphic amphiboles are attributed to their remobilization from magmatic pyrite to newly formed amphiboles. During the late hydrothermal phase, external fluids might transport additional Co and Ni, contributing to higher concentrations in late actinolite veins. In general, Co and Ni in the Yindongshan iron deposit are primarily hosted in sulfide minerals and can be remobilized during regional metamorphism and metasomatism. Thus, magmatic iron or iron–titanium oxide deposits hosted by mafic–ultramafic intrusions with sulfide mineralization may serve as promising targets for further Co-Ni exploration.

Identification of Anthropogenic and Natural Inputs of Sulfate into River System of Carbonate Zn-Pb Mining Area in Southwest China: Evidence from Hydrochemical Composition, δ34SSO4 and δ18OSO4

The release of pollutants from lead-zinc mining areas poses a significant threat to the environment, making pollution tracing crucial for environmental protection. However, the complexity of carbonate mining areas makes tracing these pollutants challenging. This study used δ34SSO4 and δ18OSO4 isotopes combined with the Stable Isotope Mixing Models in R (SIMMR) to assess anthropogenic sulfate sources in the Daliangzi mining area. The river water types were mainly Ca2+-Mg2+-HCO3−, and SO42−, which are significantly influenced by dolomite dissolution. The δ34SSO4 values ranged from 6.47‰ to 17.96‰ and the δ18OSO4 values ranged from −5.66‰ to 13.98‰. The SIMMR results showed that evaporite dissolution in tributaries, driven by gypsum, contributed 31% of sulfate, while sulfide oxidation, sewage, and atmospheric deposition contributed 19%, 18%, and 24%, respectively. The tailings pond near Xincha Creek has a higher sulfate release potential than the processing plant near Cha Creek. In the mainstream, sulfide oxidation contributed 25%, primarily from mine drainage. Anthropogenic sources, including sulfide oxidation, fertilizers, and sewage, made up about 50% of the total sulfate, with sulfide oxidation accounting for half of this input. The strong correlation between the Zn and SO42− concentrations (R2 = 0.82) and between the Zn and the contribution from the sulfide oxidation (R2 = 0.67) indicates their co-release during sulfide oxidation, making SO42− a proxy for tracing Zn sources. This study highlights the utility of δ34SSO4 and δ18OSO4 with SIMMR in tracing anthropogenic inputs and underscores the significant impact of mining on river systems and the sulfur cycle.

Nanometer-thick molecular beam epitaxy Al films capped with in situ deposited Al2O3—High-crystallinity, morphology, and superconductivity

Achieving high material perfection in aluminum (Al) films and their associated Al/AlOx heterostructures is essential for enhancing the coherence time in superconducting quantum circuits. We grew Al films with thicknesses ranging from 3 to 30 nanometers (nm) epitaxially on sapphire substrates using molecular beam epitaxy (MBE). An integral aspect of our work involved electron-beam (e-beam) evaporation to directly deposit aluminum oxide (Al2O3) films on the freshly grown ultrathin epitaxial Al films in an ultra-high-vacuum (UHV) environment. This in situ oxide deposition is critical for preventing the oxidation of parts of the Al films, avoiding the formation of undesired native oxides, and thereby preserving the nm-thick Al films in their pristine conditions. The thicknesses of our Al films in the study were accurately determined; for example, coherence lengths of 3.0 and 20.2 nm were measured in the nominal 3.0 and 20 nm thick Al films, respectively. These Al films were epitaxially grown on sapphire substrates, showing an orientational relationship, denoted as Al(111)⟨21¯1¯⟩∥sapphire(0001)[21¯1¯0]. The Al/sapphire interface was atomically ordered without any interfacial layers, as confirmed by in situ reflection high-energy electron diffraction (RHEED) and cross-sectional scanning transmission electron microscopy (STEM). All sample surfaces exhibited smoothness with a roughness in the range of 0.1–0.2 nm. The Al films are superconducting with critical temperatures ranging from 1.23 to around 2 K, depending on the film thickness.

Occurrence and enrichment mechanism of Co in Fe-Ti oxide deposits: A case study of the world-class Panzhihua deposit in SW China

The Panzhihua deposit is the one of the largest Fe-Ti oxide deposits in the world and holds 10,000 to 20,000 tons of Co resource with grades varying from 0.01 % to 0.02 %. Detailed field geological investigations and major and trace element analyses, were conducted to reveal occurrence of Co and Ni and their enrichment mechanism. Co and Ni are predominantly enriched in massive magnetite ores (average 277 ppm Co, 281 ppm Ni) of the Lower zone in the Panzhihua intrusion. Co occurs as three types:(1) independent minerals such as cobalt pentlandite (Co3.96-6.98Ni0.85-2.62Fe1.36-2.53S8) and linnaeite (Co1.65-1.88Ni0.99-1.05Fe0.15-0.37S4); (2) isomorphic state substituting for Fe, Ni and/or Mg in pentlandite (Co0.53-0.55Ni4.57-4.65Fe3.80-3.83S8), Co-bearing pyrite (Co0.09-0.12Fe0.89-0.93S2), pyrrhotite (Co 111–1964 ppm), olivine (Co 161–184 ppm), pyrite (Co 3–272 ppm), titanomagnetite (Co 57–181 ppm), ilmenite (Co 57–110 ppm), clinopyroxeneclinopyroxene (Co 34–40 ppm); (3) microscopic sulfide inclusions in chalcopyrite. Sulfide segregation and crystallization are principal mechanisms of Co enrichment. The results offers valuable insights into understanding Co mineralization, resource assessment, and comprehensive utilization in magmatic Fe-Ti oxide deposits.

Stabilization of Metal Alloy Nanocatalysts by Encapsulation with a Metal Oxide

The threat of climate change motivates us to reduce our reliance on fossil fuels and transition to renewable energy infrastructure. Many clean energy technologies including hydrogen fuel cells, direct methanol fuel cells, and water electrolyzers utilize electrocatalysts to generate electricity from chemical energy or vice versa. One direction for increasing the catalytic performance and tolerance to contaminants of the catalyst layers is the development of metal alloy-based catalysts. For instance, ruthenium (Ru) can be alloyed with platinum (Pt) to increase the tolerance of Pt to carbon monoxide, a contaminant that can be found in hydrogen fuel. However, metal alloy catalysts have an additional route for degradation beyond the well-established Ostwald ripening, coalescence, and dissolution mechanisms that are an issue for nanoparticle electrocatalysts. Harsh fuel cell conditions can lead to a separation of the two metals that were originally alloyed in the nanocatalyst and, as a result, this leads to a loss in catalytic performance and tolerance to contaminants.1 This project focuses on the durability of alloyed PtRu electrocatalysts, which facilitate the methanol oxidation reaction in a direct methanol fuel cell and the hydrogen oxidation reaction in a hydrogen fuel cell.This project explored an encapsulation of electrodeposited PtRu nanoparticle catalysts with a porous niobium oxide as a method to stabilize the PtRu alloy. Niobium oxide was chosen due to its high corrosion resistance and previous studies showing its stabilization of Ru.2 PtRu alloyed nanoparticles were synthesized via electrodeposition on a glassy carbon electrode substrate and subsequently encapsulated by an electrophoretic deposition method adapted from Jha et al.3 The morphology and composition of the catalyst and encapsulating layer were characterized by scanning and transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, and optical microscopy. The activity and durability of pristine and encapsulated PtRu catalysts were evaluated by cyclic voltammetry, linear sweep voltammetry, chronoamperometry, and electrochemical impedance spectroscopy. Carbon monoxide stripping and the double layer capacitance methods were used to study changes in the electrochemically active surface area before and after deposition of the niobium oxide. Access to the electrocatalyst surfaces through the encapsulating layer was maximized by the addition of surfactants and through tuning the potentials applied during the deposition of the niobium oxide as a means to improve its porosity. The niobium oxide was shown to improve the stability of the PtRu alloy and maintain the CO tolerance of the alloy well beyond that of the un-encapsulated catalyst. The stabilization of PtRu imparted by the encapsulation of niobium oxide herein is promising for the stabilization of alloyed nanoparticle catalysts towards a wide range of electrocatalytic applications. Yang, Z.; Yu, X.; Zhang, Q. RSC Adv., 2016, 6, 114014-114018.Jha, G.; Tran, T.; Qiao, S.; Ziegler, J. M.; Ogata, A. F.; Dai, S.; Xu, M.; Thai, M. L.; Chandran, G. T.; Pan, X.; Penner, R. M. Mater. 2018, 30, 6549-6558.

(Invited) Near Field Photocatalysis for Site-Selective Reactions By Using ZnO Nanoplates

Nanofabrication is a technology for control of the morphology, orientation, and configuration of nanomaterials. When ordinary, propagating light is employed as a processing tool, subwavelength fabrication is difficult due to the diffraction limit. However, if optical near field, which is localized in a subwavelength region is used, nanofabrication beyond the diffraction limit is possible.We have demonstrated that subwavelength nanofabrication is possible by taking advantage of the optical near field. Since hot electron-hole pairs are generated at around the plasmonic resonance sites, the energetic carriers can be used to drive oxidative dissolution of Ag,1,2 oxidative deposition of PbO2,3,4 and reductive deposition of Ag,5 in a site-selective manner. These techniques have been applied to subwavelength photochromic data storage,1,2 fabrication of chiral nanoparticles,4-7 and site-selective modification of a plasmonic photocatalyst with a co-catalyst.8 Generation of optical near field is possible even at non-plasmonic, semiconducting or dielectric nanostructures. Here we employed In-doped ZnO (In:ZnO) as a semiconductor photocatalyst. Hexagonal In:ZnO nanoplates were synthesized and adsorbed onto a glass substrate, and irradiated with linearly polarized UV light in the presence of Ag ions for reductive deposition of Ag. The optical near field generated under polarized UV light gave rise to site-selective Ag deposition. Also, the sample exhibited linear dichroism (LD) signals, indicating that the nanoparticles have optical anisotropy. On the other hand, unpolarized UV light gave no optical anisotropy. Electromagnetic simulations successfully reproduced the LD spectra. We have also performed site-selective oxidation reactions by using the hexagonal In:ZnO nanoplates. Tanabe, I.; Tatsuma, T. Nano Lett. 2012, 12, 5418–5421. Saito, K.; Tanabe, I.; Tatsuma, T. J. Phys. Chem. Lett. 2016, 7, 4363–4368.Nishi, H.; Sakamoto, M.; Tatsuma, T. Chem. Commun. 2018, 54, 11741–11744.Saito, K.; Tatsuma, T. Nano Lett. 2018, 18, 3209–3212.Ishida, T.; Isawa, A.; Kuroki, S.; Kameoka, Y.; Tatsuma, T. Appl. Phys. Lett. 2023, 123, 061111.Morisawa, K.; Ishida, T.; Tatsuma, T. ACS Nano 2020, 14, 3603–3609.Shimomura, K.; Nakane, Y.; Ishida, T.; Tatsuma, T. Appl. Phys. Lett. 2023, 122, 151109.Kim, K.; Nishi, H.; Tatsuma, T. J. Chem. Phys. 2022, 157, 111101.

Effect of Graphene Oxide on the Electrothermal and Pressure-Sensitive Properties of Carbon Fiber Cementitious Composites.

The application of carbon fiber in cement matrix has some disadvantages, such as poor dispersion and poor interfacial adhesion. In order to improve the interaction between carbon fiber and cement matrix and improve the properties of cement-based composites, carbon fiber was modified by electrophoretic deposition of nano-graphene oxide (GO). In this paper, the effects of doping CF into the cement matrix before and after GO modification are studied comparatively in terms of electrical conductivity, electrothermal warming effect, and pressure-sensitive properties of the cement matrix. It was found that the GO-modified CF reduces both the electrical resistivity of cementitious composites and the required level of fiber incorporation compared to CF. The percolation threshold is 0.7 wt% for CF and 0.5 wt% for GO-CF. The GO-modified CF is more effective than CF as a conductive filler to enhance the electrothermal warming performance of the cement matrix. When the GO-CF doping rate is 0.5%, the specimen temperature increases most rapidly, and the temperature rise value reaches a maximum of up to 30.45 °C, which is twice that of the CF group. When the fiber content is 0.7%, the pressure sensitivity of the sample was the best. When the fiber content is 0.5%, GO-CF can improve the pressure sensitivity of cement mortar specimens, and increase the resistance change rate of the cement mortar specimens by 5.7%.

Exploring the machined surface characteristics of Haynes 25 superalloy: Cost mitigation and quality enhancement perspective

The current study investigates the surface characteristics and machining cost of electrical discharge machining (EDM) of Haynes 25 superalloy using tools made by additively manufactured CuCr1Zr, pure copper and graphite. Before assessing machinability, the workpiece and tool materials were characterized using Energy Dispersive Spectroscopy (EDS), X-ray Diffraction (XRD) and evaluations of tensile strength, micro-hardness, density and thermal conductivity. The effects of current (I), voltage (V), pulse duration (Ton), duty cycle (τ) and flushing pressure (Fp) is analyzed on surface characteristics viz. surface roughness (SR), surface crack density (SCD), recast layer thickness (RCT), heat-affected zone (HAZ), micro-hardness (MH) and machining cost (MC). Post machining XRD analysis revealed the formation of cobalt oxides like (CoO and Co3O4) affecting the micro-hardness of the machined surface. Alongside, a field emission scanning electron microscopy (FESEM) is carried out which confirms, the deposition of metal carbides and oxides on the EDMed surface. Current and pulse-on-time significantly influenced performance, with optimal EDM parameters identified and validated through confirmative experiments, resulting in a mean error of ∼2.84 %. It is seen that the use of additively manufactured CuCr1Zr tools resulted in improved machined surface characteristics and a more cost-effective approach for producing intricate profiles with minimal surface defects.