Sterilization efficacy of a homemade UV lamp system on ceramic and porcelain tiles.

Ultraviolet (UV) sterilization of Bacillus atrophaeus spores attached to eight types of tiles, consisting of combinations of ceramic and porcelain, white and black, and matte and glossy surfaces, was investigated using a homemade UV lamp system with different irradiation times (10 s, 30 s, and 60 s) and UV lamp-to-tile distances (32 mm, 76 mm, and 120 mm). The results demonstrated a reduction in colony numbers with increasing irradiation time and decreasing lamp-to-tile distance, with nearly complete sterilization observed for a 120 mm lamp-to-tile distance with 60 s UV irradiation and for a 32 mm lamp-to-tile distance with 10 s UV irradiation. Specifically, superior UV sterilization efficacy was observed on porcelain compared to ceramic tiles, on white compared to black tiles, and on matte compared to glossy tiles, consistent with the reflectance trend. In conclusion, among the tested tile surfaces, the white matte porcelain tile exhibited the most efficient UV sterilization, attributed to its highest UV reflectance.

Ultraviolet Light-Assisted Decontamination of Chemical Warfare Agent Simulant 2-Chloroethyl Phenyl Sulfide on Metal-Loaded TiO2 /Ti Surfaces.

The application of ultraviolet (UV) light for the decontamination of chemical warfare agents (CWAs) has gained recognition as an effective method, especially for treating hard-to-reach areas where wet chemical methods are impractical. In this study, TiO2 /Ti was employed as a model catalyst, which was contaminated with 2-chloroethyl phenyl sulfide (CEPS), and subjected to photocatalytic decontamination using both UVB and UVC light. Additionally, photocatalytic decontamination efficiency by introducing Au, Pt, and Cu onto the TiO2 /Ti surface was explored. During the photodecomposition process under UVC light, at least eight distinct secondary byproducts were identified. It was observed that the introduction of overlayer metals did not significantly enhance the photodecomposition under UVC light instead overlaid Au exhibited substantially improved activity under UVB light. Whereas, photodecomposition process under UVB light, only five secondary products were detected, including novel compounds with sulfoxide and sulfone functional groups. This novel study offers valuable insights into the generation of secondary products and sheds light on the roles of overlayer metals and photon wavelength in the photodecontamination process of CWA.

Opening Direct Electrochemical Fischer-Tropsch Synthesis Path by Interfacial Engineering of Cu Electrode with P-Block Elements.

The electrochemical synthesis of syngas (CO and H2) has garnered considerable attention in the context of Fischer-Tropsch (FT) synthesis employing thermal catalysts. Nonetheless, the need for a novel, cost-effective technique persists. In this investigation, we introduce a direct electrochemical (dEC) approach for FT synthesis that functions under ambient conditions by utilizing a p-block element (Sn and In) overlaid Cu electrode. Surface *CO and H* species were obtained in an electrolytic medium through the CO2 + H+ + e- → HOOCad → *CO (or direct CO adsorption) and H+ + e- → H* reactions, respectively. We have observed C2-7 long-chain hydrocarbons with a CnH2n+2/CnH2n ratio of 1-3, and this observation can be explained through the process of C-C coupling chain growth of the conventional FT synthesis, based on the linearity of the Anderson-Schulz-Flory equation plots. Thick Sn and In overlayers resulted in the dominant production of formate, while CO and C2H4 production were found to be proportional and inversely correlated to H2, C2H6, and C3-7 hydrocarbon production. The EC CO2/CO reduction used in dEC FT synthesis offers valuable insights into the mechanism of C2+ production and holds promise as an eco-friendly approach to producing long-chain hydrocarbons for energy and environmental purposes.

New reaction path for long-chain hydrocarbons by electrochemical CO2 and CO reduction over Au/stainless steel.

The Fischer-Tropsch (F-T) synthesis is recognized for its ability to produce long-chain hydrocarbons. In this study, we aimed to replicate F-T synthesis using electrochemical CO2 reduction and CO reduction reactions on a stainless steel (SS) support with a gold (Au) overlayer. Under CO2-saturated conditions, the presence of Au on the SS surface led to the formation of CH4 and a range of hydrocarbons (CnH2n and CnH2n+2, n = 2-7), while bare SS primarily produced hydrogen. The Au(10 nm)/SS exhibited the highest hydrocarbon production in CO2-saturated phosphate, indicating a synergistic effect at the Au-SS interface. In CO-saturated conditions, bare SS also produced long-chain hydrocarbons, but increasing Au thickness resulted in decreased production due to poor CO adsorption. Hydrocarbons were formed through both direct and indirect CO adsorption pathways. Anderson-Schulz-Flory analysis confirmed surface CO hydrogenation and C-C coupling polymerization following conventional F-T synthesis. The C2 hydrocarbons exhibited distinct behavior compared to C3-5 hydrocarbons, suggesting different reaction pathways. Despite low reduction product levels, our EC method successfully replicated F-T synthesis using the Au/SS electrode, providing valuable insights into C-C coupling mechanisms and electrochemical production of long-chain hydrocarbons. Depth-profiling X-ray photoelectron spectroscopy revealed significant changes in surface elemental compositions before and after EC reduction.

Electrochemical Performance of Layer-Structured Ni0.8Co0.1Mn0.1O2 Cathode Active Materials Synthesized by Carbonate Co-Precipitation.

The layered Ni-rich NiCoMn (NCM)-based cathode active material Li[NixCo(1-x)/2Mn(1-x)/2]O2 (x ≥ 0.6) has the advantages of high energy density and price competitiveness over an LiCoO2-based material. Additionally, NCM is beneficial in terms of its increasing reversible discharge capacity with the increase in Ni content; however, stable electrochemical performance has not been readily achieved because of the cation mixing that occurs during its synthesis. In this study, various layer-structured Li1.0[Ni0.8Co0.1Mn0.1]O2 materials were synthesized, and their electrochemical performances were investigated. A NiCoMnCO3 precursor, prepared using carbonate co-precipitation with Li2CO3 as the lithium source and having a sintering temperature of 850 °C, sintering time of 25 h, and metal to Li molar ratio of 1.00-1.05 were found to be the optimal parameters/conditions for the preparation of Li1.0[Ni0.8Co0.1Mn0.1]O2. The material exhibited a discharge capacity of 160 mAhg-1 and capacity recovery rate of 95.56% (from a 5.0-0.1 C-rate).

Interface Engineered V-Zn Hybrids: Electrocatalytic and Photocatalytic CO2 Reductions.

V-Zn hybrids have widely been used as catalyst materials in the environment and as energy. Herein, V-Zn hybrid electrodes were prepared by the hydrothermal and sputter-deposition methods using a Zn foil support. Their electrocatalytic CO2 reduction (EC CO2 RR) performances were tested under various applied potentials, different electrolytes, and concentrations before and after thermal treatment of the demonstrated electrode. Gas and liquid products were confirmed by gas chromatography and nuclear magnetic resonance spectroscopy, respectively. For V-Zn electrode by hydrothermal method produced mainly syngas (CO and H2) with tunable ratio by varying applied potential. Minor products include CH4, C2H4, and C2H6. A liquid product of formate showed a Faradaic efficiency (FE) of 2%. EC CO2 RR efficiency for CO, CH4, and formate was best in 0.2 M KHCO3 electrolyte condition. CO and formate were further increased by photoirradiation and Nafion-treated electrode. Formate and CH4 productions were significantly increased by thermal treatment of the V-Zn electrode. CO production was diminished for the V-Zn electrode by sputter deposition but was recovered by thermal treatment. Photocatalytic CO2 RR was tested to find that RR products include CH3OH, CO, CH4, C2H4, and C2H6. Interestingly long-chain hydrocarbons (CnH2n and CnH2n+2, where n = 3-6) were first observed under mild conditions. The long-chain formation was understood by Fisher-Tropsch (F-T) synthesis. Alkenes were observed to be more produced than alkanes unlike in the conventional F-T synthesis. The present new findings provide useful clues for the development of hybrid electro-and photo-catalysts tested under various experimental conditions in energy and environment.

Effective inactivation of Bacillus atrophaeus spores and Escherichia coli on disposable face masks using ultraviolet laser irradiation.

Due to the widespread emergence of COVID-19, face masks have become a common tool for reducing transmission risk between people, increasing the need for sterilization methods against mask-contaminated microorganisms. In this study, we measured the efficacy of ultraviolet (UV) laser irradiation (266 nm) as a sterilization technique against Bacillus atrophaeus spores and Escherichia coli on three different types of face mask. The UV laser source demonstrated high penetration of inner mask layers, inactivating microorganisms in a short time while maintaining the particle filtration efficiency of the masks. This study demonstrates that UV laser irradiation is an efficient sterilization method for removing pathogens from face masks.

Photoelectrochemical CO2 Reduction Products Over Sandwiched Hybrid Ga2O3:ZnO/Indium/ZnO Nanorods.

Recycled valuable energy production by the electrochemical CO2 reduction method has explosively researched using countless amounts of developed electrocatalysts. Herein, we have developed hybrid sandwiched Ga2O3:ZnO/indium/ZnO nanorods (GZO/In/ZnONR) and tested their photoelectrocatalytic CO2 reduction performances. Gas chromatography and nuclear magnetic spectroscopy were employed to examine gas and liquid CO2 reduction products, respectively. Major products were observed to be CO, H2, and formate whose Faradaic efficiencies were highly dependent on the relative amounts of overlayer GZO and In spacer, as well as applied potential and light irradiation. Overall, the present study provides a new strategy of controlling CO2 reduction products by developing a sandwiched hybrid catalyst system for energy and environment.

Sterilization effects of UV laser irradiation on Bacillus atrophaeus spore viability, structure, and proteins.

Bacillus spores are highly resistant to toxic chemicals and extreme environments. Because some Bacillus species threaten public health, spore inactivation techniques have been intensively investigated. We exposed Bacillus atrophaeus spores to a 266 nm Nd:YVO4 laser at a laser power of 1 W and various numbers of scans. As a result, the UV laser reduced the viability of Bacillus atrophaeus spores. Although the outer coat of spores remained intact after UV laser irradiation of 720 scans, damage inside the spores was observed. Spore proteins were identified by matrix-assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometry during the course of UV laser irradiation. Photochemical and photothermal processes are believed to be involved in the UV laser sterilization of Bacillus spores. Our findings suggest that a UV laser is capable of sterilizing Bacillus atrophaeus spores.

Photocatalytic and Electrocatalytic Properties of Cu-Loaded ZIF-67-Derivatized Bean Sprout-Like Co-TiO2/Ti Nanostructures.

ZIF-derivatized catalysts have shown high potential in catalysis. Herein, bean sprout-like Co-TiO2/Ti nanostructures were first synthesized by thermal treatment at 800 °C under Ar-flow conditions using sacrificial ZIF-67 templated on Ti sheets. It was observed that ZIF-67 on Ti sheets started to thermally decompose at around 350 °C and was converted to the cubic phase Co3O4. The head of the bean sprout structure was observed to be Co3O4, while the stem showed a crystal structure of rutile TiO2 grown from the metallic Ti support. Cu sputter-deposited Co-TiO2/Ti nanostructures were also prepared for photocatalytic and electrocatalytic CO2 reduction performances, as well as electrochemical oxygen reaction (OER). Gas chromatography results after photocatalytic CO2 reduction showed that CH3OH, CO and CH4 were produced as major products with the highest MeOH selectivity of 64% and minor C2 compounds of C2H2, C2H4 and C2H6. For electrocatalytic CO2 reduction, CO, CH4 and C2H4 were meaningfully detected, but H2 was dominantly produced. The amounts were observed to be dependent on the Cu deposition amount. Electrochemical OER performances in 0.1 M KOH electrolyte exhibited onset overpotentials of 330-430 mV (vs. RHE) and Tafel slopes of 117-134 mV/dec that were dependent on Cu-loading thickness. The present unique results provide useful information for synthesis of bean sprout-like Co-TiO2/Ti hybrid nanostructures and their applications to CO2 reduction and electrochemical water splitting in energy and environmental fields.

Thermal CO Oxidation and Photocatalytic CO2 Reduction over Bare and M-Al2O3 (M = Co, Ni, Cu, Rh, Pd, Ag, Ir, Pt, and Au) Cotton-Like Nanosheets.

Aluminum oxide (Al2O3) has abundantly been used as a catalyst, and its catalytic activity has been tailored by loading transition metals. Herein, γ-Al2O3 nanosheets were prepared by the solvothermal method, and transition metals (M = Co, Ni, Cu, Rh, Pd, Ag, Ir, Pt, and Au) were loaded onto the nanosheets. Big data sets of thermal CO oxidation and photocatalytic CO2 reduction activities were fully examined for the transition metal-loaded Al2O3 nanosheets. Their physicochemical properties were examined by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction crystallography, and X-ray photoelectron spectroscopy. It was found that Rh, Pd, Ir, and Pt-loading showed a great enhancement in CO oxidation activity while other metals negated the activity of bare Al2O3 nanosheets. Rh-Al2O3 showed the lowest CO oxidation onset temperature of 172 °C, 201 °C lower than that of bare γ-Al2O3. CO2 reduction experiments were also performed to show that CO, CH3OH, and CH4 were common products. Ag-Al2O3 nanosheets showed the highest performances with yields of 237.3 ppm for CO, 36.3 ppm for CH3OH, and 30.9 ppm for CH4, 2.2×, 1.2×, and 1.6× enhancements, respectively, compared with those for bare Al2O3. Hydrogen production was found to be maximized to 20.7 ppm during CO2 reduction for Rh-loaded Al2O3. The present unique pre-screening test results provided very useful information for the selection of transition metals on Al2O3-based energy and environmental catalysts.

Electrochemical Ce(III)/Ce(IV) Redox Behavior and Ce Oxide Nanostructure Recovery over Thio-Terpyridine-Functionalized Au/Carbon Paper Electrodes.

Understanding the electrochemical behaviors of Ce(III)/Ce(IV) ions is essential for better treatment, separation, and recycling of lanthanide (Ln) and actinide (An) elements. Herein, electrochemical redox behavior and interconversion of Ce(III)/Ce(IV) ions and their recoveries were demonstrated over newly developed thio-terpyridine-functionalized Au-modified carbon paper electrodes in acidic and neutral electrolytes. Cyclic voltammetry and amperometry were performed for the electrodes with and without thio-terpyridine functionalization. Ce oxide nanostructure recovery was successfully conducted by amperometry, and the electrodeposited nanostructured Ce materials were fully characterized by scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction crystallography, and X-ray photoelectron spectroscopy. Geometry optimization and the electronic energy state calculations were conducted by density functional theory at the B3LYP/GENECP level for the complexes of Ce(III) and Ce(IV) ions with the thio-terpyridine in an aqueous state. The present unique results provide valuable information on understanding redox behaviors of Ln and An ions for their recycling and treatment processes.

Electrochemical Recovery and Behaviors of Rare Earth (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Yb) Ions on Ni Sheets.

The electrochemical behaviors of rare earth (RE) ions have extensively been studied because of their high potential applications to the reprocessing of used nuclear fuels and RE-containing materials. In the present study, we fully investigated the electrochemical behaviors of RE(III) (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Yb) ions over a Ni sheet electrode in 0.1 M NaClO4 electrolyte solution by cyclic voltammetry between +0.5 and -1.5 V (vs. Ag/AgCl). Amperometry electrodeposition experiments were performed between -1.2 and -0.9 V to recover RE elements over the Ni sheet. The successfully RE-recovered Ni sheets were fully characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and photoluminescence spectroscopy. The newly reported recovery data for RE(III) ions over a metal electrode provide valuable information on the development of the treatment methods of RE elements.

Photocatalytic CO2 Reduction and Electrocatalytic H2 Evolution over Pt(0,II,IV)-Loaded Oxidized Ti Sheets.

Energy recycling and production using abundant atmospheric CO2 and H2O have increasingly attracted attention for solving energy and environmental problems. Herein, Pt-loaded Ti sheets were prepared by sputter-deposition and Pt4+-reduction methods, and their catalytic activities on both photocatalytic CO2 reduction and electrochemical hydrogen evolution were fully demonstrated. The surface chemical states were completely examined by X-ray photoelectron spectroscopy before and after CO2 reduction. Gas chromatography confirmed that CO, CH4, and CH3OH were commonly produced as CO2 reduction products with total yields up to 87.3, 26.9, and 88.0 µmol/mol, respectively for 700 °C-annealed Ti under UVC irradiation for 13 h. Pt-loading commonly negated the CO2 reduction yields, but CH4 selectivity was increased. Electrochemical hydrogen evolution reaction (HER) activity showed the highest activity for sputter-deposited Pt on 400 °C-annealed Ti with a HER current density of 10.5 mA/cm2 at -0.5 V (vs. Ag/AgCl). The activities of CO2 reduction and HER were found to be significantly dependent on both the nature of Ti support and the oxidation states (0,II,IV) of overlayer Pt. The present result could provide valuable information for designing efficient Pt/Ti-based CO2 recycle photocatalysts and electrochemical hydrogen production catalysts.

Pt Deposits on Bi/Pt NP Catalyst for Formic Acid Oxidation: Catalytic Enhancement and Longer Lifetime.

This work presents an improvement in the activity and catalytic lifetime of Pt deposits on Bi-modified Pt nanoparticles (Bi/Pt NP) toward formic acid oxidation (FAO). Using an irreversible adsorption method, Bi was deposited on Pt NP to form Bi/Pt NP and sequentially Pt was deposited on Bi/Pt NP to form Pt/Bi/Pt NP. Voltammetric studies of Pt NP, Bi/Pt NP, and Pt/Bi/Pt NPs supported that Pt deposits of Pt/Bi/Pt NPs provided quite a unique behavior: simultaneous surface oxidation of deposited Pt and Bi and significant resistance to the oxidative removal of Bi. Furthermore, combined spectroscopic investigations revealed that the concentration of the employed Pt precursor ion solution determined the amount of deposited Pt from ∼0.2 to ∼0.4 in coverage. The best Pt/Bi/Pt NP catalyst with a Pt coverage of ∼0.25 enhanced the dehydrogenation processes below ∼0.4 V by a factor of more than 2 and increased the FAO current at ∼0.8 V roughly by 15 times, referring to those of Bi/Pt NP. The lifetime measurement works revealed that after the 1000th voltammetric cycle to 0.4 V, the FAO currents of Pt/Bi/Pt NPs were 2 and 4 times higher than those of Bi/Pt NP and Pt NP, respectively. The Pt deposits on Bi/Pt NP were concluded to play two roles in FAO: the promotion of FAO processes to increase the activity and the retardation of Bi oxidative removal to maintain the activity much longer.

A novel RGO/N-RGO supercapacitor architecture for a wide voltage window, high energy density and long-life via voltage holding tests.

Here, we demonstrated a unique symmetric supercapacitor (SSC) device architecture based on reduced graphene oxide (RGO) and nitrogen-doped RGO (N-RGO) electrodes. The RGO/N-RGO SSC shows a wide voltage window (2.2 V), high energy density (106.3 W h kg-1), and ultra-high power density (15184.8 W kg-1). The RGO/N-RGO SSC also delivers outstanding stability of 95.5% over 10 000 galvanostatic charging-discharging tests and 90.5% over 8 h of voltage holding tests. Additionally, this work explores a better understanding of leakage current and self-discharge mechanisms, which justifies the excellent state of health of the RGO/N-RGO SSC device.

Plasmonic Ag-Decorated Few-Layer MoS2 Nanosheets Vertically Grown on Graphene for Efficient Photoelectrochemical Water Splitting.

A controllable approach that combines surface plasmon resonance and two-dimensional (2D) graphene/MoS2 heterojunction has not been implemented despite its potential for efficient photoelectrochemical (PEC) water splitting. In this study, plasmonic Ag-decorated 2D MoS2 nanosheets were vertically grown on graphene substrates in a practical large-scale manner through metalorganic chemical vapor deposition of MoS2 and thermal evaporation of Ag. The plasmonic Ag-decorated MoS2 nanosheets on graphene yielded up to 10 times higher photo-to-dark current ratio than MoS2 nanosheets on indium tin oxide. The significantly enhanced PEC activity could be attributed to the synergetic effects of SPR and favorable graphene/2D MoS2 heterojunction. Plasmonic Ag nanoparticles not only increased visible-light and near-infrared absorption of 2D MoS2, but also induced highly amplified local electric field intensity in 2D MoS2. In addition, the vertically aligned 2D MoS2 on graphene acted as a desirable heterostructure for efficient separation and transportation of photo-generated carriers. This study provides a promising path for exploiting the full potential of 2D MoS2 for practical large-scale and efficient PEC water-splitting applications.

Photoluminescence imaging of europium (III)-doped γ-Al2 O3 nanofiber structures.

Aluminium oxide (Al2 O3 ) has widely been used for catalysts, insulators, and composite materials for diverse applications. Herein, we demonstrated if γ-Al2 O3 was useful as a luminescence support material for europium (Eu) (III) activator ion. The hydrothermal method and post-thermal treatment at 800°C were employed to synthesize Eu(III)-doped γ-Al2 O3 nanofibre structures. Luminescence characteristics of Eu(III) ions in Al2 O3 matrix were fully understood by taking 2D and 3D-photoluminescence imaging profiles. Various sharp emissions between 580 to 720 nm were assigned to the 5 D0 →7 FJ (J = 0, 1, 2, 3, 4) transitions of Eu(III) activators. On the basis of X-ray diffraction crystallography, Auger elemental mapping and the asymmetry ratio, Eu(III) ions were found to be well doped into the γ-Al2 O3 matrix at a low (1 mol%) doping level. A broad emission at 460 nm was substantially increased upon higher (2 mol%) Eu(III) doping due to defect creation. The first 3D photoluminescence imaging profiles highlight detailed understanding of emission characteristics of Eu(III) ions in Al oxide-based phosphor materials and their potential applications.

Blue-Light-Emitting Photostable Hybrid Films for High-Efficiency Large-Area Light Converter and Photonic Applications.

A blue fluorophore of Schiff base zinc complex is prepared by a hydrolysis-free solution-based synthetic method. Under ultraviolet (UV) excitation, the complex produces blue emission with a quantum yield ( Q) of 42.6% in methylene chloride and 24.0% in standalone powder form. Quantum mechanical calculations show that the blue emission is generated by the change in the chemical state of the ligand associated with the complexation with Zn cations. Thin films of Zn complexes incorporated in polymethylmethacrylate (PMMA) and cellulose acetate butyrate (CAB) polymers are also prepared by dispersing the complexes into the polymer matrices. These hybrid polymer films exhibit several notable features, particularly enhanced luminescence efficiency (with maximum Q of 85.8% for PMMA and 30.0% for CAB) and scalability for fabrication over a large area while retaining the original properties of the host polymers. Light-emitting diodes are also fabricated using the CAB hybrid thin films, and they show a Q of 43.2% with excellent photostability. The complex and its hybrid films demonstrate their great potential for such applications as UV-to-blue conversion devices in photoelectronics, solar-cell concentrators, solid-state lighting and display, and greenhouse agriculture.

Bimetallic Au@M (M = Ag, Pd, Fe, and Cu) Nanoarchitectures Mediated by 1,4-Phenylene Diisocyanide Functionalization.

Hybridization with gold has attracted a lot of attention in many application areas such as energy, nanomedicine, and catalysts. Here, we demonstrate electrochemical hybridization of two different metals by using bare and 1,4-phenylene diisocyanide (PDI) functionalized gold nanoislands (GNIs) supported on a Si substrate. As pristine GNIs are not tightly locked on the Si surface, bimetallic Au@M (M = Ag, Pd, Fe, and Cu) core-shell type nanostructures are produced by an electric-field-induced clustering of GNIs and metal deposition. On the other hand, upon functionalization of GNIs by PDI, 3D island growth on the functionalized GNI template is observed as PDI acts as a protector against the electric-field-induced clustering. Depth-profiling X-ray photoelectron spectroscopy reveals no discernible difference in the interfacial electronic structures of hybrid metals prepared by using pristine and PDI-functionalized GNI templates. This work demonstrates a new approach to produce a secured template and to manipulate growth of hybrid nanoparticles on this template supported on a Si substrate by using electrodeposition and organic functionalization.