Florinel Sava, I. Simandan, A. Buruiana, Amelia-Elena Bocirnea, Outman El Khouja, Teddy Tite, M. Zaki, C. Mihai, A. Velea
In the quest for advanced materials suitable for next-generation electronic and optoelectronic applications, tungsten disulfide (WS2) ultrathin films have emerged as promising candidates due to their unique properties. However, obtaining WS2 directly on the desired substrate, eliminating the need for transfer, which produces additional defects, poses many challenges. This paper aims to explore the synthesis of WS2 ultrathin films via physical vapor deposition (PVD) followed by sulfurization in a confined space, addressing the challenge of film formation for practical applications. Precursor layers of tungsten and WS2 were deposited by RF magnetron sputtering. Subsequent sulfurization treatments were conducted in a small, closed, graphite box to produce WS2 films. The physical and chemical properties of these precursor and sulfurized layers were thoroughly characterized using techniques such as X-ray reflectometry (XRR), X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The findings reveal notable distinctions in film thickness, structural orientation, and chemical composition, attributable to the different precursor used. Particularly, the sulfurized layers from the tungsten precursor exhibited a preferred orientation of WS2 crystallites with their (00L) planes parallel to the substrate surface, along with a deviation from parallelism in a small angular range. This study highlights the necessity of precise control over deposition and sulfurization parameters to tailor the properties of WS2 films for specific technological applications.
{"title":"Synthesis of WS2 Ultrathin Films by Magnetron Sputtering Followed by Sulfurization in a Confined Space","authors":"Florinel Sava, I. Simandan, A. Buruiana, Amelia-Elena Bocirnea, Outman El Khouja, Teddy Tite, M. Zaki, C. Mihai, A. Velea","doi":"10.3390/surfaces7010008","DOIUrl":"https://doi.org/10.3390/surfaces7010008","url":null,"abstract":"In the quest for advanced materials suitable for next-generation electronic and optoelectronic applications, tungsten disulfide (WS2) ultrathin films have emerged as promising candidates due to their unique properties. However, obtaining WS2 directly on the desired substrate, eliminating the need for transfer, which produces additional defects, poses many challenges. This paper aims to explore the synthesis of WS2 ultrathin films via physical vapor deposition (PVD) followed by sulfurization in a confined space, addressing the challenge of film formation for practical applications. Precursor layers of tungsten and WS2 were deposited by RF magnetron sputtering. Subsequent sulfurization treatments were conducted in a small, closed, graphite box to produce WS2 films. The physical and chemical properties of these precursor and sulfurized layers were thoroughly characterized using techniques such as X-ray reflectometry (XRR), X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The findings reveal notable distinctions in film thickness, structural orientation, and chemical composition, attributable to the different precursor used. Particularly, the sulfurized layers from the tungsten precursor exhibited a preferred orientation of WS2 crystallites with their (00L) planes parallel to the substrate surface, along with a deviation from parallelism in a small angular range. This study highlights the necessity of precise control over deposition and sulfurization parameters to tailor the properties of WS2 films for specific technological applications.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"26 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139845160","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}
Florinel Sava, I. Simandan, A. Buruiana, Amelia-Elena Bocirnea, Outman El Khouja, Teddy Tite, M. Zaki, C. Mihai, A. Velea
In the quest for advanced materials suitable for next-generation electronic and optoelectronic applications, tungsten disulfide (WS2) ultrathin films have emerged as promising candidates due to their unique properties. However, obtaining WS2 directly on the desired substrate, eliminating the need for transfer, which produces additional defects, poses many challenges. This paper aims to explore the synthesis of WS2 ultrathin films via physical vapor deposition (PVD) followed by sulfurization in a confined space, addressing the challenge of film formation for practical applications. Precursor layers of tungsten and WS2 were deposited by RF magnetron sputtering. Subsequent sulfurization treatments were conducted in a small, closed, graphite box to produce WS2 films. The physical and chemical properties of these precursor and sulfurized layers were thoroughly characterized using techniques such as X-ray reflectometry (XRR), X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The findings reveal notable distinctions in film thickness, structural orientation, and chemical composition, attributable to the different precursor used. Particularly, the sulfurized layers from the tungsten precursor exhibited a preferred orientation of WS2 crystallites with their (00L) planes parallel to the substrate surface, along with a deviation from parallelism in a small angular range. This study highlights the necessity of precise control over deposition and sulfurization parameters to tailor the properties of WS2 films for specific technological applications.
{"title":"Synthesis of WS2 Ultrathin Films by Magnetron Sputtering Followed by Sulfurization in a Confined Space","authors":"Florinel Sava, I. Simandan, A. Buruiana, Amelia-Elena Bocirnea, Outman El Khouja, Teddy Tite, M. Zaki, C. Mihai, A. Velea","doi":"10.3390/surfaces7010008","DOIUrl":"https://doi.org/10.3390/surfaces7010008","url":null,"abstract":"In the quest for advanced materials suitable for next-generation electronic and optoelectronic applications, tungsten disulfide (WS2) ultrathin films have emerged as promising candidates due to their unique properties. However, obtaining WS2 directly on the desired substrate, eliminating the need for transfer, which produces additional defects, poses many challenges. This paper aims to explore the synthesis of WS2 ultrathin films via physical vapor deposition (PVD) followed by sulfurization in a confined space, addressing the challenge of film formation for practical applications. Precursor layers of tungsten and WS2 were deposited by RF magnetron sputtering. Subsequent sulfurization treatments were conducted in a small, closed, graphite box to produce WS2 films. The physical and chemical properties of these precursor and sulfurized layers were thoroughly characterized using techniques such as X-ray reflectometry (XRR), X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The findings reveal notable distinctions in film thickness, structural orientation, and chemical composition, attributable to the different precursor used. Particularly, the sulfurized layers from the tungsten precursor exhibited a preferred orientation of WS2 crystallites with their (00L) planes parallel to the substrate surface, along with a deviation from parallelism in a small angular range. This study highlights the necessity of precise control over deposition and sulfurization parameters to tailor the properties of WS2 films for specific technological applications.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"106 10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139785495","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}
In this research, the pure fatigue behaviors of AM60 magnesium alloy with polylactic acid (PLA) coating (PF-AM60-PLA) and the corrosion fatigue behaviors of magnesium alloy with PLA coating (CF-AM60-PLA) were evaluated. Polymer coating was made by fused deposition modeling (FDM) with a 3D printer and attached to standard fatigue test specimens with glue. Then, after 27 days of immersion in the simulated body fluid (SBF), the high-cycle bending fatigue test was performed on samples. Due to corrosion, the weight of the specimens was reduced by an average of 35%. The corrosion rate decreased in the first 7 days and then increased. PF samples with a coating had an average 49% increase in fatigue lifetime. Regarding the CF samples, despite the use of a 10-times stronger solution, the fatigue lifetime of these samples decreased by only 35%. The field-emission scanning electron microscopy (FESEM) results also showed cleavage plates and striations. In addition, the separation of the glue from the coating and Mg was observed. Corrosion products, in addition to microcracks and holes, were seen on the fracture surface of CF specimens, which caused the stress concentration and the crack initiation. Holes caused by the release of gases were also observed in polymer coatings, which were fabricated by 3D printing.
{"title":"Impact of Corrosion in Simulated Body Fluid on Fatigue Characteristics of 3D-Printed Polylactic Acid-Coated AM60 Magnesium Alloys","authors":"Seyed Ali Ashraf Talesh, Mohammad Azadi","doi":"10.3390/surfaces7010007","DOIUrl":"https://doi.org/10.3390/surfaces7010007","url":null,"abstract":"In this research, the pure fatigue behaviors of AM60 magnesium alloy with polylactic acid (PLA) coating (PF-AM60-PLA) and the corrosion fatigue behaviors of magnesium alloy with PLA coating (CF-AM60-PLA) were evaluated. Polymer coating was made by fused deposition modeling (FDM) with a 3D printer and attached to standard fatigue test specimens with glue. Then, after 27 days of immersion in the simulated body fluid (SBF), the high-cycle bending fatigue test was performed on samples. Due to corrosion, the weight of the specimens was reduced by an average of 35%. The corrosion rate decreased in the first 7 days and then increased. PF samples with a coating had an average 49% increase in fatigue lifetime. Regarding the CF samples, despite the use of a 10-times stronger solution, the fatigue lifetime of these samples decreased by only 35%. The field-emission scanning electron microscopy (FESEM) results also showed cleavage plates and striations. In addition, the separation of the glue from the coating and Mg was observed. Corrosion products, in addition to microcracks and holes, were seen on the fracture surface of CF specimens, which caused the stress concentration and the crack initiation. Holes caused by the release of gases were also observed in polymer coatings, which were fabricated by 3D printing.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"4 11","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139802681","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}
In this research, the pure fatigue behaviors of AM60 magnesium alloy with polylactic acid (PLA) coating (PF-AM60-PLA) and the corrosion fatigue behaviors of magnesium alloy with PLA coating (CF-AM60-PLA) were evaluated. Polymer coating was made by fused deposition modeling (FDM) with a 3D printer and attached to standard fatigue test specimens with glue. Then, after 27 days of immersion in the simulated body fluid (SBF), the high-cycle bending fatigue test was performed on samples. Due to corrosion, the weight of the specimens was reduced by an average of 35%. The corrosion rate decreased in the first 7 days and then increased. PF samples with a coating had an average 49% increase in fatigue lifetime. Regarding the CF samples, despite the use of a 10-times stronger solution, the fatigue lifetime of these samples decreased by only 35%. The field-emission scanning electron microscopy (FESEM) results also showed cleavage plates and striations. In addition, the separation of the glue from the coating and Mg was observed. Corrosion products, in addition to microcracks and holes, were seen on the fracture surface of CF specimens, which caused the stress concentration and the crack initiation. Holes caused by the release of gases were also observed in polymer coatings, which were fabricated by 3D printing.
{"title":"Impact of Corrosion in Simulated Body Fluid on Fatigue Characteristics of 3D-Printed Polylactic Acid-Coated AM60 Magnesium Alloys","authors":"Seyed Ali Ashraf Talesh, Mohammad Azadi","doi":"10.3390/surfaces7010007","DOIUrl":"https://doi.org/10.3390/surfaces7010007","url":null,"abstract":"In this research, the pure fatigue behaviors of AM60 magnesium alloy with polylactic acid (PLA) coating (PF-AM60-PLA) and the corrosion fatigue behaviors of magnesium alloy with PLA coating (CF-AM60-PLA) were evaluated. Polymer coating was made by fused deposition modeling (FDM) with a 3D printer and attached to standard fatigue test specimens with glue. Then, after 27 days of immersion in the simulated body fluid (SBF), the high-cycle bending fatigue test was performed on samples. Due to corrosion, the weight of the specimens was reduced by an average of 35%. The corrosion rate decreased in the first 7 days and then increased. PF samples with a coating had an average 49% increase in fatigue lifetime. Regarding the CF samples, despite the use of a 10-times stronger solution, the fatigue lifetime of these samples decreased by only 35%. The field-emission scanning electron microscopy (FESEM) results also showed cleavage plates and striations. In addition, the separation of the glue from the coating and Mg was observed. Corrosion products, in addition to microcracks and holes, were seen on the fracture surface of CF specimens, which caused the stress concentration and the crack initiation. Holes caused by the release of gases were also observed in polymer coatings, which were fabricated by 3D printing.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"211 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139862524","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}
Rachele Sciotto, I. A. Ruiz Alvarado, W. G. Schmidt
Density-functional theory calculations on P-rich InP(001):H surfaces are presented. Depending on temperature, pressure and substrate doping, hydrogen desorption or adsorption will occur and influence the surface electronic properties. For p-doped samples, the charge transition levels of the P dangling bond defects resulting from H desorption will lead to Fermi level pinning in the lower half of the band gap. This explains recent experimental data. For n-doped substrates, H-deficient surfaces are the ground-state structure. This will lead to Fermi level pinning below the bulk conduction band minimum. Surface defects resulting from the adsorption of additional hydrogen can be expected as well, but affect the surface electronic properties less than H desorption.
本文介绍了富含 P 的 InP(001):H 表面的密度泛函理论计算。根据温度、压力和衬底掺杂情况，氢会发生解吸或吸附，并影响表面电子特性。对于掺杂 p 的样品，氢解吸导致的 P 悬空键缺陷的电荷转移水平将导致费米级钉死在带隙的下半部分。这解释了最近的实验数据。对于 n 掺杂基底，缺 H 表面是基态结构。这将导致费米级钉扎在体导带最小值以下。由于吸附了额外的氢而导致的表面缺陷也是可以预期的，但对表面电子特性的影响要小于氢的解吸。
{"title":"Substrate Doping and Defect Influence on P-Rich InP(001):H Surface Properties","authors":"Rachele Sciotto, I. A. Ruiz Alvarado, W. G. Schmidt","doi":"10.3390/surfaces7010006","DOIUrl":"https://doi.org/10.3390/surfaces7010006","url":null,"abstract":"Density-functional theory calculations on P-rich InP(001):H surfaces are presented. Depending on temperature, pressure and substrate doping, hydrogen desorption or adsorption will occur and influence the surface electronic properties. For p-doped samples, the charge transition levels of the P dangling bond defects resulting from H desorption will lead to Fermi level pinning in the lower half of the band gap. This explains recent experimental data. For n-doped substrates, H-deficient surfaces are the ground-state structure. This will lead to Fermi level pinning below the bulk conduction band minimum. Surface defects resulting from the adsorption of additional hydrogen can be expected as well, but affect the surface electronic properties less than H desorption.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":" 30","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139624070","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}
Afonso Henrique da Silva Júnior, Carlos Rafael Silva de Oliveira, Tarcisio Wolff Leal, Leandro Pellenz, Selene de Souza, Antônio de Souza, A. Mapossa, Robert Tewo, Hilary Rutto, Luciano da Silva, Adriano da Silva
Society confronts the pressing environmental challenges posed by the pervasive presence of toxic pollutants in aquatic ecosystems. The repercussions of contaminant release extend far and wide, endangering marine life and human well-being. While various techniques such as bioremediation, filtration, and adsorption have been employed for wastewater treatment, they grapple with cost effectiveness and overall efficiency issues. Advanced oxidative processes, including photocatalysis and Fenton, have emerged as viable solutions in response to the emerging contaminants. However, the efficacy of photocatalysis largely hinges on the choice of catalyst. Their distinctive attributes, such as chemical defects and exceptional stability, make perovskite oxides a promising catalyst. These materials can be synthesized through diverse methods, rendering them versatile and adaptable for widespread applications. Ongoing research endeavors are diligently focused on enhancing the performance of perovskite oxides, optimizing their integration into catalytic processes, and exploring innovative approaches for material immobilization. This comprehensive review seeks to elucidate the most pivotal advances in perovskite oxides and their composites within the wastewater treatment domain. Additionally, it sheds light on burgeoning research trends and multifaceted challenges confronting this field, which present insights into techniques for treating the antibiotic-contaminated environment, delving into innovative strategies, green technologies, challenges, and emerging trends.
{"title":"Reviewing Perovskite Oxide-Based Materials for the Effective Treatment of Antibiotic-Polluted Environments: Challenges, Trends, and New Insights","authors":"Afonso Henrique da Silva Júnior, Carlos Rafael Silva de Oliveira, Tarcisio Wolff Leal, Leandro Pellenz, Selene de Souza, Antônio de Souza, A. Mapossa, Robert Tewo, Hilary Rutto, Luciano da Silva, Adriano da Silva","doi":"10.3390/surfaces7010005","DOIUrl":"https://doi.org/10.3390/surfaces7010005","url":null,"abstract":"Society confronts the pressing environmental challenges posed by the pervasive presence of toxic pollutants in aquatic ecosystems. The repercussions of contaminant release extend far and wide, endangering marine life and human well-being. While various techniques such as bioremediation, filtration, and adsorption have been employed for wastewater treatment, they grapple with cost effectiveness and overall efficiency issues. Advanced oxidative processes, including photocatalysis and Fenton, have emerged as viable solutions in response to the emerging contaminants. However, the efficacy of photocatalysis largely hinges on the choice of catalyst. Their distinctive attributes, such as chemical defects and exceptional stability, make perovskite oxides a promising catalyst. These materials can be synthesized through diverse methods, rendering them versatile and adaptable for widespread applications. Ongoing research endeavors are diligently focused on enhancing the performance of perovskite oxides, optimizing their integration into catalytic processes, and exploring innovative approaches for material immobilization. This comprehensive review seeks to elucidate the most pivotal advances in perovskite oxides and their composites within the wastewater treatment domain. Additionally, it sheds light on burgeoning research trends and multifaceted challenges confronting this field, which present insights into techniques for treating the antibiotic-contaminated environment, delving into innovative strategies, green technologies, challenges, and emerging trends.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"9 10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139438334","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}
Mikhail Lomaev, V. Tarasenko, Dmitry Sorokin, D. Beloplotov
Many scientific teams are currently studying the effects of plasma generated by nanosecond diffuse discharges on the surfaces of various materials in order to modify their properties. To achieve this, uniform plasma is required to act on the target being treated, which is often an electrode in a discharge system. Previously, the surface treatment uniformity of flat electrodes during a nanosecond discharge in a point-to-plane gap was studied by applying a carbon black layer, and a discharge mode was identified in which there was no erosion on the treated electrode. In this study, it was established that during a nanosecond discharge in air at atmospheric pressure in a non-uniform electric field, carbon black deposited on the surface of a flat anode can ignite. The conditions and dynamics of carbon black ignition during the nanosecond discharge were determined. It was observed that the carbon black is ignited on the surface and continues to combust in the gap in the form of flame plumes for tens of milliseconds. It was also found that the combustion of carbon black can occur in both diffuse and spark discharges.
{"title":"Ignition of Carbon Black during Nanosecond Diffuse and Spark Discharges in Air at Atmospheric Pressure","authors":"Mikhail Lomaev, V. Tarasenko, Dmitry Sorokin, D. Beloplotov","doi":"10.3390/surfaces7010004","DOIUrl":"https://doi.org/10.3390/surfaces7010004","url":null,"abstract":"Many scientific teams are currently studying the effects of plasma generated by nanosecond diffuse discharges on the surfaces of various materials in order to modify their properties. To achieve this, uniform plasma is required to act on the target being treated, which is often an electrode in a discharge system. Previously, the surface treatment uniformity of flat electrodes during a nanosecond discharge in a point-to-plane gap was studied by applying a carbon black layer, and a discharge mode was identified in which there was no erosion on the treated electrode. In this study, it was established that during a nanosecond discharge in air at atmospheric pressure in a non-uniform electric field, carbon black deposited on the surface of a flat anode can ignite. The conditions and dynamics of carbon black ignition during the nanosecond discharge were determined. It was observed that the carbon black is ignited on the surface and continues to combust in the gap in the form of flame plumes for tens of milliseconds. It was also found that the combustion of carbon black can occur in both diffuse and spark discharges.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"66 10","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139441039","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}
The removal of air pollutants is an important research topic in order to improve the environment. In addition, many common pollutants can affect human health to varying degrees. In this work, we investigate NO and SO2 conversion by reaction with a commonly used metal oxide catalyst, TiO2. Rutile TiO2(110) single crystals and industrial powder samples used in sunscreen are studied using near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) as a main tool. This allows in situ monitoring of the gas conversion process. We find Ti3+ defects (oxygen vacancies) or Mn oxides/cations (MnO) at the TiO2 surfaces can improve the conversion of NO and SO2 to surface-bound species. MnO and Ti3+ defects at the surface of rutile TiO2(110) exhibit a synergistic effect on the conversion of NO and SO2 that is significantly improved by nearly an order of magnitude. The by-products are mainly in the form of NO3−, SO32−, and SO42−. We find the main oxidation products formed on the single crystals are subtly different from those on the industrial powder samples. For TiO2 nanopowders (undoped and Mndoped), the presence of Mn also shows improvement in toxic gas adsorption capacity. Overall, it is believed that the outcome obtained from NAP-XPS in this research provides useful insights for the future use of TiO2 in pollutant gas capture.
为了改善环境，清除空气污染物是一个重要的研究课题。此外，许多常见污染物会对人体健康造成不同程度的影响。在这项工作中，我们研究了 NO 和 SO2 与常用金属氧化物催化剂 TiO2 反应转化的问题。我们使用近常压 X 射线光电子能谱 (NAP-XPS) 作为主要工具，对金红石 TiO2(110) 单晶和防晒霜中使用的工业粉末样品进行了研究。这样就可以对气体转换过程进行原位监测。我们发现，TiO2 表面的 Ti3+ 缺陷（氧空位）或锰氧化物/阳离子（MnO）可提高 NO 和 SO2 向表面结合物种的转化率。金红石型二氧化钛（110）表面的 MnO 和 Ti3+ 缺陷对 NO 和 SO2 的转化具有协同作用，可显著提高近一个数量级。副产物主要以 NO3-、SO32- 和 SO42- 的形式存在。我们发现在单晶体上形成的主要氧化产物与在工业粉末样品上形成的主要氧化产物有细微差别。对于二氧化钛纳米粉体（未掺杂和掺杂锰）来说，锰的存在也显示出其对有毒气体的吸附能力有所提高。总之，本研究从 NAP-XPS 中获得的结果为今后将二氧化钛用于污染物气体捕集提供了有益的启示。
{"title":"The Effect of Mn Doping and Ti3+ Defects at TiO2 Surfaces in NO and SO2 Gas Capture Investigated Using Near-Ambient Pressure X-ray Photoelectron Spectroscopy","authors":"J. C. Ke, A. Thomas, Joseph Peake, Robert Sayer","doi":"10.3390/surfaces7010003","DOIUrl":"https://doi.org/10.3390/surfaces7010003","url":null,"abstract":"The removal of air pollutants is an important research topic in order to improve the environment. In addition, many common pollutants can affect human health to varying degrees. In this work, we investigate NO and SO2 conversion by reaction with a commonly used metal oxide catalyst, TiO2. Rutile TiO2(110) single crystals and industrial powder samples used in sunscreen are studied using near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) as a main tool. This allows in situ monitoring of the gas conversion process. We find Ti3+ defects (oxygen vacancies) or Mn oxides/cations (MnO) at the TiO2 surfaces can improve the conversion of NO and SO2 to surface-bound species. MnO and Ti3+ defects at the surface of rutile TiO2(110) exhibit a synergistic effect on the conversion of NO and SO2 that is significantly improved by nearly an order of magnitude. The by-products are mainly in the form of NO3−, SO32−, and SO42−. We find the main oxidation products formed on the single crystals are subtly different from those on the industrial powder samples. For TiO2 nanopowders (undoped and Mndoped), the presence of Mn also shows improvement in toxic gas adsorption capacity. Overall, it is believed that the outcome obtained from NAP-XPS in this research provides useful insights for the future use of TiO2 in pollutant gas capture.","PeriodicalId":508474,"journal":{"name":"Surfaces","volume":"33 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139383724","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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