Recent Developments in the Application of Inorganic Nanomaterials and Nanosystems for the Protection of Cultural Heritage Organic Artifacts

Cultural heritage (CH) represents human identity and evidence of the existence and activities that people have left over time. In response to the action of aggressive degrading factors, different materials have been developed and used to protect cultural heritage artifacts. The discovery of optimal materials for this purpose also raises several problems, mainly related to their compatibility with the support material, the most important aspect being that they must preserve their aesthetic characteristics. In this context, the present review paper aims to provide a critical discussion about the possibilities of using different inorganic nanomaterials and recipes for the conservation of cultural heritage objects of organic nature (such as paper, wood, and other support materials). In addition, also are covered different aspect concerning protection mechanisms and application methods as well as future perspectives in this area.

Feasibility test of STEM at home prototype kit as science project-based learning media for Junior High School students

To promote the application of the STEM approach in science learning, it is necessary to provide cheap, easy-to-obtain, and effective STEM project support materials. In addition, science teachers should try to plan and implement STEM in their teaching, even for simple projects. To overcome the problem of the length of time on projects in science teaching, we propose "STEM at Home", a term which means that STEM projects are carried out by students at home under the supervision of parents or families. In order for this home project-based learning to be effective, we have prepared a STEM at Home Kit and Worksheet for Junior High Schools students. We chose the topic Simple . The STEM at Home Kit and Worksheet that have been developed, have received expert approval as learning media that are suitable for use. One-to-one evaluation with 3 participants, and small group evaluation with 14 participants, were carried out to obtain feedback on students’ difficulties in using the product, their perceptions of the product, and their perceptions of the potential impact produced by the instructional product. The results of these evaluation showed that the STEM at Home Project Kit and Worksheet are valid and practically used in science learning, especially on the topic of Simple Machines

Electrochemical Passivation Properties of Valve Transition Metal Carbides

Transition metal carbides have the potential to be employed as corrosion protective coating for a variety of applications such as e.g. steel based bipolar plates, porous transport layers or as catalyst support in polymer electrolyte membrane fuel cells and water electrolyzers. Yet, little is known of their fundamental, intrinsic corrosion and passivation properties. Herein, we conducted a detailed electrochemical passivation study of various valve transition metal carbides such as titanium carbide, tantalum carbide or tungsten carbide. Via flow cell measurements coupled to an inductively coupled plasma mass spectrometer, the in-situ transition metal dissolution was monitored, and the faradaic dissolution efficiency was calculated. Together with the determination of the grown oxide layer via X-ray photoelectron spectroscopy, a thorough evaluation of the passivation efficiency was conducted. Moreover, it was shown that a beneficial stabilization effect can be achieved through alloying of different carbides, which paves the way towards tailor-made coatings or catalyst support materials.

PARTICIPACE STUDENTŮ NA TVORBĚ PODPŮRNÝCH VÝUKOVÝCH MATERIÁLŮ V PŘEDMĚTU NĚMČINA PRO BANKOVNICTVÍ

The students of bachelor’s degree programmes at the Faculty of Economics of the University of West Bohemia in Pilsen have the opportunity to broaden their knowledge and skills acquired in specialized subjects through additional specialized courses taught in German. The language courses in question aim to prepare students adequately for their professional career as well as to provide them with practical competences. This paper focuses on the students’ participation in creating the support materials in the German for Banking course. The graphics online tool called Canva was chosen to present the students’ projects. The individual students’ presentations were created in the form of interactive videos using EdPuzzle, another online tool. The popularity of online tools was also verified using a questionnaire.

Recent Advancements in the Synthesis and Application of Carbon-Based Catalysts in the ORR

Fuel cells are a promising alternative to non-renewable energy production industries such as petroleum and natural gas. The cathodic oxygen reduction reaction (ORR), which makes fuel cell technology possible, is sluggish under normal conditions. Thus, catalysts must be used to allow fuel cells to operate efficiently. Traditionally, platinum (Pt) catalysts are often utilized as they exhibit a highly efficient ORR with low overpotential values. However, Pt is an expensive and precious metal, posing economic problems for commercialization. Herein, advances in carbon-based catalysts are reviewed for their application in ORRs due to their abundance and low-cost syntheses. Various synthetic methods from different renewable sources are presented, and their catalytic properties are compared. Likewise, the effects of heteroatom and non-precious metal doping, surface area, and porosity on their performance are investigated. Carbon-based support materials are discussed in relation to their physical properties and the subsequent effect on Pt ORR performance. Lastly, advances in fuel cell electrolytes for various fuel cell types are presented. This review aims to provide valuable insight into current challenges in fuel cell performance and how they can be overcome using carbon-based materials and next generation electrolytes.

A Comparative Study of the Effect of Graphene Oxide, Graphitic Carbon Nitride, and Their Composite on the Photocatalytic Activity of Cu3SnS4

Photocatalysis has shown high potential in dealing with the ever-broadening problem of wastewater treatment, escalated by the increasing level of recalcitrant chemicals often referred to as emerging contaminants. In this study, the effect of support material on the photocatalytic activity of copper tin sulfide (Cu3SnS4) nanoparticles for the degradation of tetracycline as an emerging contaminant is presented. Graphene oxide, protonated graphitic carbon nitride, and a composite of graphitic carbon nitride and graphene oxide were explored as support materials for Cu3SnS4 nanoparticles. The nanoparticles were incorporated with the different carbonaceous substrates to afford graphene-supported Cu3SnS4 (GO-CTS), protonated graphitic carbon nitride-supported Cu3SnS4 (PCN-CTS), and graphene oxide/protonated graphitic carbon nitride-supported Cu3SnS4 (GO/PCN-CTS). Physicochemical, structural, and optical properties of the prepared nanocomposites were characterized using techniques such as Fourier transform infra-red spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis near infrared, and fluorescence spectrophotometry. The compositing of the Cu3SnS4 nanoparticles on the support materials was confirmed by the characterization techniques, and the optical properties of the composites were found to be influenced by the nature of the support material. The incorporation of CTS into the support materials resulted in a reduction in band gap energy with evaluated band gaps of 1.65, 1.46, 1.43 eV, and 1.16 eV. The reduction in band gap energy suggests the potential of the composites for enhanced photocatalytic activity. From the photocatalytic study, the degradation efficiency of tetracycline by CTS, PCN-CTS, GO-CTS, and PC/GO-CTS was 74.1, 85.2, 90.9, and 96.5%, respectively. All the composites showed enhanced activity compared to pristine CTS, and the existence of a synergy between GO and PCN when both were employed as support materials was observed. Based on the charge carrier recombination characteristics and the band edge potential calculations from the composites, a possible mechanism of action of each composite was proposed. This study therefore confirms the possibility of modulating the mechanism of action and subsequently the efficiency of semiconductor materials by altering the nature of the support material.

Analysis of Preferred Mechanisms of CO Oxidation with Atomically Dispersed Pt1/TiO2 Using the Energetic Span Model

This work examines the mechanisms of low-temperature CO oxidation with atomically dispersed Pt on rutile TiO2 (110) using density functional theory and the energetic span model (ESM). Of the 13 distinct pathways spanning Eley-Rideal (ER), termolecular ER (TER), Langmuir-Hinshelwood(LH), Mars-Van Krevelen (MvK) mechanisms as well as their combinations, TER with CO-assisted CO2 desorption yields the highest turnover frequency (TOF). However, this pathway is ruled out because Pt is dynamically unstable in an intermediate state in the TER cycle, determined in a prior ab initio molecular dynamics study by our group. We instead find that a previously neglected pathway – the ER mechanism – is the most plausible CO oxidation route based on agreement with experimental TOFs and turnover-determining states. The preferred mechanism is sensitive to temperature, with LH becoming more favorable than ER and TER above 750 K. By comparing TOFs for Pt1/TiO2 with prior mechanistic studies of various oxide-supported atomically dispersed catalysts in the literature, we also attempt to identify the most viable metal and support materials for CO oxidation.

Plug-and-Play Heterogeneous Catalysis Enabled by Metal–Organic Cage-Crosslinked Polymers

The immobilization of homogeneous catalysts onto solid supports to improve recyclability while maintaining catalytic efficiency is often a trial-and-error process limited by poor control of the local catalyst environment and a lack of modular strategies to append catalysts to support materials. Here, we introduce a “plug-and-play” heterogenous catalysis platform that overcomes these challenges. Our approach leverages the well-defined interiors of self-assembled Pd12L24 metal–organic cages/polyhedra (MOCs): through a simple combination of catalyst-ligands, polymeric ligands, and spacer ligands, we demonstrate facile self-assembly of a diverse range of polymer gels featuring endohedrally-catalyst-functionalized junctions. Through decoupling catalyst incorporation and environment from the physical properties of the support (polymer matrix), this simple strategy is shown to enhance the recyclability of various catalyst systems (e.g., TEMPO-catalyzed oxidation and Au(I)-catalyzed cyclization) and enable catalysis in environments where homogeneous catalyst analogs are not viable.