PhotochemPub Date : 2024-06-12DOI: 10.3390/photochem4020016
Julia Exeler, T. Jüstel
{"title":"Advances in Functional Ceramics for Water Splitting: A Comprehensive Review","authors":"Julia Exeler, T. Jüstel","doi":"10.3390/photochem4020016","DOIUrl":"https://doi.org/10.3390/photochem4020016","url":null,"abstract":"The global demand for sustainable energy sources has led to extensive research regarding (green) hydrogen production technologies, with water splitting emerging as a promising avenue. In the near future the calculated hydrogen demand is expected to be 2.3 Gt per year. For green hydrogen production, 1.5 ppm of Earth’s freshwater, or 30 ppb of saltwater, is required each year, which is less than that currently consumed by fossil fuel-based energy. Functional ceramics, known for their stability and tunable properties, have garnered attention in the field of water splitting. This review provides an in-depth analysis of recent advancements in functional ceramics for water splitting, addressing key mechanisms, challenges, and prospects. Theoretical aspects, including electronic structure and crystallography, are explored to understand the catalytic behavior of these materials. Hematite photoanodes, vital for solar-driven water splitting, are discussed alongside strategies to enhance their performance, such as heterojunction structures and cocatalyst integration. Compositionally complex perovskite oxides and high-entropy alloys/ceramics are investigated for their potential for use in solar thermochemical water splitting, highlighting innovative approaches and challenges. Further exploration encompasses inorganic materials like metal oxides, molybdates, and rare earth compounds, revealing their catalytic activity and potential for water-splitting applications. Despite progress, challenges persist, indicating the need for continued research in the fields of material design and synthesis to advance sustainable hydrogen production.","PeriodicalId":510825,"journal":{"name":"Photochem","volume":"12 11","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141355063","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
PhotochemPub Date : 2024-06-07DOI: 10.3390/photochem4020015
M. Maafi
{"title":"Excitation Wavelength-Dependent Photochemistry","authors":"M. Maafi","doi":"10.3390/photochem4020015","DOIUrl":"https://doi.org/10.3390/photochem4020015","url":null,"abstract":"The dependence of photochemistry on excitation wavelength is not a recently observed phenomenon; nonetheless, it has, surprisingly enough, been largely ignored in the field. The reasons for this situation are not fully understood but might be related to a provisional extension of Kasha’s rule to photochemistry, or perhaps to a difficulty to justify the kind of short time-scales implied in such photochemistry, that challenges the usually held view giving predominance to fast internal conversion and vibrational relaxation. Regardless of the reasons, it is still a matter of fact that a complete and satisfactory interpretation for experimentally proven wavelength-dependent photochemistry is not yet available and the community endeavor to build a holistic understanding and a comprehensive view of the phenomenon. The present review is a non-exhaustive overview of the published data in the field, reporting on some of the most prominent features, issues, and interpretations.","PeriodicalId":510825,"journal":{"name":"Photochem","volume":" 16","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141371146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
PhotochemPub Date : 2024-05-06DOI: 10.3390/photochem4020014
Alondra A. Lugo-Ruiz, S. Bailón-Ruiz
{"title":"Titanium Nanostructures: Advancing Photocatalysis in Complex Systems","authors":"Alondra A. Lugo-Ruiz, S. Bailón-Ruiz","doi":"10.3390/photochem4020014","DOIUrl":"https://doi.org/10.3390/photochem4020014","url":null,"abstract":"The use of semiconductor materials, specifically TiO2, for photocatalysis of organic pollutants has gained global interest as an effective method for contaminant removal from wastewater. Titanium dioxide (TiO2) is a widely studied photocatalyst and is considered one of the best for wastewater treatments due to its high stability, affordability, and nontoxicity. The discharge of wastewater from the textile industries, which constitutes around 20% of total textile effluent, has become a significant environmental concern, posing a threat to both the aquatic ecosystem and human health. We aimed to investigate the photodegradation of organic dyes like Amaranth (AM), Methyl Orange (MO), and Quinoline Yellow (QY), individually and in combination, in an aqueous suspension with varying concentrations of TiO2. Results indicate a significant degradation of all three dyes in the multicomponent, with approximately 40% degradation in the presence of the 0.050 g/L TiO2 after 360 min. These findings suggest that TiO2 has a significant potential as a nanocatalyst in complex matrices.","PeriodicalId":510825,"journal":{"name":"Photochem","volume":"15 4","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141008607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
PhotochemPub Date : 2023-11-28DOI: 10.3390/photochem3040029
Gordon A. Ochsner, Jaren S. Meikle, Jacob C. Dean
{"title":"Photoprotective Steering of Previtamin D3 Photochemistry by Phenylalanine in Solution","authors":"Gordon A. Ochsner, Jaren S. Meikle, Jacob C. Dean","doi":"10.3390/photochem3040029","DOIUrl":"https://doi.org/10.3390/photochem3040029","url":null,"abstract":"Provitamin D3 is the biological precursor to naturally formed vitamin D3 in humans, and its conversion is initiated via photoexcitation by near ultraviolet light. Following an initial photolysis, the primary intermediate, known as previtamin D3, is prone to light-induced isomerization or recyclization, which creates byproducts that limit the desired final thermal conversion to vitamin D3. The branching of the photochemical reaction is highly wavelength-dependent, whereby excitation toward the blue edge of the provitamin D3 absorption spectrum tends to terminate the reaction with the most undesired tachysterol byproduct and the lowest previtamin D3 concentration. In this work, the influence of introducing the natural amino acid phenyalanine as an excitation energy donor to the photochemical reaction is investigated. We find that the incorporation of phenylalanine into provitamin D3 solution results in greater intermediate concentrations and prolonged lifetimes of the desired previtamin D3 while simultaneously reducing the final concentration of tachysterol when exposing the solution to wavelengths at the blue edge of the provitamin D3 spectrum. The results, coupled with quantum chemical analysis, suggest that phenylalanine indeed helps to funnel energy from shorter wavelengths more effectively into the provitamin D3 precursor, while simultaneously screening those wavelengths from direct excitation, which otherwise leads to enhanced concentrations of tachysterol byproduct at the expense of previtamin D3.","PeriodicalId":510825,"journal":{"name":"Photochem","volume":"22 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139220477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
PhotochemPub Date : 2023-11-25DOI: 10.3390/photochem3040028
J. Hot, Kevin Castelló Lux, Erick Ringot
{"title":"Investigation of the Self-Cleaning Property of Photocatalytic Coatings at a Laboratory Scale","authors":"J. Hot, Kevin Castelló Lux, Erick Ringot","doi":"10.3390/photochem3040028","DOIUrl":"https://doi.org/10.3390/photochem3040028","url":null,"abstract":"Self-cleaning products are commercially available to protect surfaces against soiling and avoid the high consumption of energy and chemical detergents necessary for cleaning. They are based on semiconductor oxides, mostly titanium dioxide (TiO2), which induce photocatalytic oxidation activity and superhydrophilicity. Therefore, we present an experimental procedure at a lab scale to assess the self-cleaning ability of various photocatalytic coatings (five TiO2-based commercial products and one lab-grade zinc oxide (ZnO) product) applied to mortar surfaces. The samples were artificially stained with three types of soiling: Congo red dye, diesel soot, and motor oil. They were exposed to the environmental cycle of UV illumination and water flow for two weeks and the changes in stain colors were first assessed with visual inspection. Then, spectrophotometry measurements were conducted before and after the self-cleaning experiment to calculate the color differences for each stain in the CIELab color space data. In addition, the coatings were characterized via X-ray diffraction analyses and water contact angle measurements. Results highlighted color changes for each stain and higher wettability (induced by OH radicals) of the coated surfaces, which favored surface washing and thus stain removal. Light also had a positive effect on the attenuation of the stains, particularly for the Congo red dye.","PeriodicalId":510825,"journal":{"name":"Photochem","volume":"32 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139236709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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