J. Borkowska-burnecka, W. Żyrnicki, M. Wełna, P. Jamróz
Electron density and ionization temperatures were measured for inductively coupled argon plasma at atmospheric pressure. Different sample introduction systems were investigated. Samples containing Sn, Hg, Mg, and Fe and acidified with hydrochloric or acetic acids were introduced into plasma in the form of aerosol, gaseous mixture produced in the reaction of these solutions with NaBH4 and the mixture of the aerosol and chemically generated gases. The electron densities measured from Hα, Hβ, Hγ, and Hδ lines on the base of Stark broadening were compared. The study of the H Balmer series line profiles showed that the values from Hγ and Hδ were well consistent with those obtained from Hβ which was considered as a common standard line for spectroscopic measurement of electron density. The values varied from to cm−3 and were the highest at loading mixture of chemically generated gases. The ionization temperatures of plasma, determined on the base of the Saha approach from ion-to-atom line intensity ratios, were lower for Sn and Hg (6500–7200 K) than those from Fe and Mg lines (7000–7800 K). The Sn II/Sn I and Hg II/Hg I, Fe II/Fe I, and Mg II/Mg I intensity ratios and the electron densities () were dependent on experimental conditions of plasma generation. Experimental and theoretically calculated ionization degrees were compared.
{"title":"Electron Density from Balmer Series Hydrogen Lines and Ionization Temperatures in Inductively Coupled Argon Plasma Supplied by Aerosol and Volatile Species","authors":"J. Borkowska-burnecka, W. Żyrnicki, M. Wełna, P. Jamróz","doi":"10.1155/2016/7521050","DOIUrl":"https://doi.org/10.1155/2016/7521050","url":null,"abstract":"Electron density and ionization temperatures were measured for inductively coupled argon plasma at atmospheric pressure. Different sample introduction systems were investigated. Samples containing Sn, Hg, Mg, and Fe and acidified with hydrochloric or acetic acids were introduced into plasma in the form of aerosol, gaseous mixture produced in the reaction of these solutions with NaBH4 and the mixture of the aerosol and chemically generated gases. The electron densities measured from Hα, Hβ, Hγ, and Hδ lines on the base of Stark broadening were compared. The study of the H Balmer series line profiles showed that the values from Hγ and Hδ were well consistent with those obtained from Hβ which was considered as a common standard line for spectroscopic measurement of electron density. The values varied from to cm−3 and were the highest at loading mixture of chemically generated gases. The ionization temperatures of plasma, determined on the base of the Saha approach from ion-to-atom line intensity ratios, were lower for Sn and Hg (6500–7200 K) than those from Fe and Mg lines (7000–7800 K). The Sn II/Sn I and Hg II/Hg I, Fe II/Fe I, and Mg II/Mg I intensity ratios and the electron densities () were dependent on experimental conditions of plasma generation. Experimental and theoretically calculated ionization degrees were compared.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"5 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2016-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73245082","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}
This study investigates the level of technological enhancement of normally occurring radioactive materials (TENORM) in the red mud waste due to the production of alumina in Jamaica. Technological enhancements factors (TEF) were determined for the uranium, thorium, actinium series, their progenies, and the nonseries potassium-40 using gamma spectrometry. The study concluded that bauxite production technologically enhances the uranium progenies Th-234, Pb-214, Bi-214, and Pa-234 and the thorium-232 progenies Ac-228, Pb-212, and Bi-212 in red mud. The actinium series was technologically enhanced, but K-40 and the thorium daughter, Tl-208, were reduced. The spectrometric comparison of Tl-208 (at 510 keV) was unexpected since its other photopeaks at 583 keV, 934 keV, and 968 keV were markedly different. An explanation for this anomaly is discussed. An explanation regarding the process of accumulation and fractionation of organically derived phosphate deposits and potassium-feldspar is offered to explain the spectrometric differences between the alumina product and its waste material, red mud.
{"title":"The Technological Enhancement of Normally Occurring Radioactive Materials in Red Mud Due to the Production of Alumina","authors":"M. Miller, D. Miller","doi":"10.1155/2016/4589460","DOIUrl":"https://doi.org/10.1155/2016/4589460","url":null,"abstract":"This study investigates the level of technological enhancement of normally occurring radioactive materials (TENORM) in the red mud waste due to the production of alumina in Jamaica. Technological enhancements factors (TEF) were determined for the uranium, thorium, actinium series, their progenies, and the nonseries potassium-40 using gamma spectrometry. The study concluded that bauxite production technologically enhances the uranium progenies Th-234, Pb-214, Bi-214, and Pa-234 and the thorium-232 progenies Ac-228, Pb-212, and Bi-212 in red mud. The actinium series was technologically enhanced, but K-40 and the thorium daughter, Tl-208, were reduced. The spectrometric comparison of Tl-208 (at 510 keV) was unexpected since its other photopeaks at 583 keV, 934 keV, and 968 keV were markedly different. An explanation for this anomaly is discussed. An explanation regarding the process of accumulation and fractionation of organically derived phosphate deposits and potassium-feldspar is offered to explain the spectrometric differences between the alumina product and its waste material, red mud.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"40 1","pages":"1-6"},"PeriodicalIF":0.0,"publicationDate":"2016-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77951967","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 light induced behaviour of siloxane substituted azobenzene compounds in the presence of alkylene spacers is reported for the first time. Firstly, these photosensitive compounds were synthesized and elucidated the molecular structure by spectral analysis such as NMR, FTIR, and UV/Vis. Photoisomerization effect was evaluated in solution and also in nematic phase. The photosaturation occurred exactly at 29 seconds, whereas thermal back relaxation was observed ranging from 19.8 to 23.8 hours. Long duration of the thermal back relaxation is due to the presence of sterically hindered siloxane group substituted to the azobenzene molecules. Decrease in the duration of cis-trans isomerization was found when the number of alkylene spacers was increased. These siloxane based azobenzene derivatives are useful for the fabrication of optical storage device and molecular switches.
{"title":"Synthesis and Light Induced Characteristics of Siloxane Substituted Azobenzene: An Application for Optical Storage Device","authors":"A. R. Yuvaraj, M. L. Rahman, M. Yusoff","doi":"10.1155/2016/4715230","DOIUrl":"https://doi.org/10.1155/2016/4715230","url":null,"abstract":"The light induced behaviour of siloxane substituted azobenzene compounds in the presence of alkylene spacers is reported for the first time. Firstly, these photosensitive compounds were synthesized and elucidated the molecular structure by spectral analysis such as NMR, FTIR, and UV/Vis. Photoisomerization effect was evaluated in solution and also in nematic phase. The photosaturation occurred exactly at 29 seconds, whereas thermal back relaxation was observed ranging from 19.8 to 23.8 hours. Long duration of the thermal back relaxation is due to the presence of sterically hindered siloxane group substituted to the azobenzene molecules. Decrease in the duration of cis-trans isomerization was found when the number of alkylene spacers was increased. These siloxane based azobenzene derivatives are useful for the fabrication of optical storage device and molecular switches.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"71 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2016-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88255895","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 possibility for double pulse LIBS in the process of a direct layer-by-layer analysis of the titanium-based PVD-coatings on polished flat blank samples of steel and silicon and also of the TiAlN/TiN-coating on a milling cutter is considered. A method is proposed to control thickness of the radiation evaporated layer by defocusing the laser beam with respect to the surface, making it possible to attain the depth resolution of 0.1 μm. The Ti and Ti-Zr-coatings produced using the ion-assisted condensation method and subjected to streams of the nitrogen plasma in a magnetic-plasma compressor are studied.
{"title":"Double Pulse LIBS of Titanium-Based PVD-Coatings with Submicron Resolution","authors":"K. Ermalitskaia, E. Voropay","doi":"10.1155/2016/2504217","DOIUrl":"https://doi.org/10.1155/2016/2504217","url":null,"abstract":"The possibility for double pulse LIBS in the process of a direct layer-by-layer analysis of the titanium-based PVD-coatings on polished flat blank samples of steel and silicon and also of the TiAlN/TiN-coating on a milling cutter is considered. A method is proposed to control thickness of the radiation evaporated layer by defocusing the laser beam with respect to the surface, making it possible to attain the depth resolution of 0.1 μm. The Ti and Ti-Zr-coatings produced using the ion-assisted condensation method and subjected to streams of the nitrogen plasma in a magnetic-plasma compressor are studied.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"53 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2016-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89339275","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 thermal and chain length sensitivity of the infrared spectra of some solid state anhydrous silver(I) salts (n-octanoate to n-eicosanoate, inclusive) are discussed. At ambient temperature, the tilted alkyl chains, anchored to the metal planes via chelating bidentate coordination to the silver ions, are crystallized in the fully extended all-trans conformation. Interestingly, though all compounds are crystallized in a monoclinic crystal system, their lateral chain packing, van der Waals effects, and hence vibrational features are chain length-dependent. This is a direct result of electrostatic effects of the COO group in addition to vibrational coupling between CH2, CH3, and COO modes, an effect which varies significantly with chain length. Variable temperature infrared measurements indicate significant irreversible changes in the metal-carboxyl coordination sphere, most likely due to bond fission. For long chain adducts (), thermally induced crystal system switching, monoclinic to triclinic, indicates greater thermal sensitivity of their alkyl chains. During heating, the regions of the hydrocarbon chains, furthest from the COO, become increasingly molten and mobile as the stepwise melt advances towards the solid COO moieties. This solid-liquid melting behaviour is responsible for mesophase formation in metal carboxylate systems.
{"title":"Chain Length and Thermal Sensitivity of the Infrared Spectra of a Homologous Series of Anhydrous Silver(I) n-Alkanoates","authors":"P. Nelson","doi":"10.1155/2016/3068430","DOIUrl":"https://doi.org/10.1155/2016/3068430","url":null,"abstract":"The thermal and chain length sensitivity of the infrared spectra of some solid state anhydrous silver(I) salts (n-octanoate to n-eicosanoate, inclusive) are discussed. At ambient temperature, the tilted alkyl chains, anchored to the metal planes via chelating bidentate coordination to the silver ions, are crystallized in the fully extended all-trans conformation. Interestingly, though all compounds are crystallized in a monoclinic crystal system, their lateral chain packing, van der Waals effects, and hence vibrational features are chain length-dependent. This is a direct result of electrostatic effects of the COO group in addition to vibrational coupling between CH2, CH3, and COO modes, an effect which varies significantly with chain length. Variable temperature infrared measurements indicate significant irreversible changes in the metal-carboxyl coordination sphere, most likely due to bond fission. For long chain adducts (), thermally induced crystal system switching, monoclinic to triclinic, indicates greater thermal sensitivity of their alkyl chains. During heating, the regions of the hydrocarbon chains, furthest from the COO, become increasingly molten and mobile as the stepwise melt advances towards the solid COO moieties. This solid-liquid melting behaviour is responsible for mesophase formation in metal carboxylate systems.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"30 2 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2016-02-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73188898","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}
A. Gucsik, I. Gyollai, H. Nishido, K. Ninagawa, M. Izawa, C. Jäger, U. Ott, I. Simonia, S. Bérczi, andMasahiro Kayama
The Tagish Lake meteorite is CI/CM2 chondrite, which fell by a fireball event in January 2000. This study emphasizes the cathodoluminescence (CL) and Raman spectroscopical properties of the Tagish Lake meteorite in order to classify the meteoritic forsterite and its relation to the crystallization processes in a parent body. The CL-zoning of Tagish Lake meteorite records the thermal history of chondrules and terrestrial weathering. Only the unweathered olivine is forsterite, which is CL-active. The variation of luminescence in chondrules of Tagish Lake meteorite implies chemical inhomogeneity due to low-grade thermal metamorphism. The blue emission center in forsterite due to crystal lattice defect is proposed as being caused by rapid cooling during the primary crystallization and relatively low-temperature thermal metamorphism on the parent body of Tagish Lake meteorite. This is in a good agreement with the micro-Raman spectroscopical data. A combination of cathodoluminescence and micro-Raman spectroscopies shows some potentials in study of the asteroidal processes of parent bodies in solar system.
{"title":"Cathodoluminescence and Raman Spectromicroscopy of Forsterite in Tagish Lake Meteorite: Implications for Astromineralogy","authors":"A. Gucsik, I. Gyollai, H. Nishido, K. Ninagawa, M. Izawa, C. Jäger, U. Ott, I. Simonia, S. Bérczi, andMasahiro Kayama","doi":"10.1155/2016/1751730","DOIUrl":"https://doi.org/10.1155/2016/1751730","url":null,"abstract":"The Tagish Lake meteorite is CI/CM2 chondrite, which fell by a fireball event in January 2000. This study emphasizes the cathodoluminescence (CL) and Raman spectroscopical properties of the Tagish Lake meteorite in order to classify the meteoritic forsterite and its relation to the crystallization processes in a parent body. The CL-zoning of Tagish Lake meteorite records the thermal history of chondrules and terrestrial weathering. Only the unweathered olivine is forsterite, which is CL-active. The variation of luminescence in chondrules of Tagish Lake meteorite implies chemical inhomogeneity due to low-grade thermal metamorphism. The blue emission center in forsterite due to crystal lattice defect is proposed as being caused by rapid cooling during the primary crystallization and relatively low-temperature thermal metamorphism on the parent body of Tagish Lake meteorite. This is in a good agreement with the micro-Raman spectroscopical data. A combination of cathodoluminescence and micro-Raman spectroscopies shows some potentials in study of the asteroidal processes of parent bodies in solar system.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"60 1","pages":"1-8"},"PeriodicalIF":0.0,"publicationDate":"2016-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82950896","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}
A series of eight water soluble anionic, cationic, and neutral zinc(II) complexes were synthesized and characterized. The interaction of these complexes with bovine serum albumin (BSA), human serum albumin (HSA), lysozyme, and free tryptophan (Trp) was investigated using steady-state fluorescence spectroscopy. Static and dynamic fluorescence quenching analysis based on Stern-Volmer kinetics was conducted, and the decrease in fluorescence intensity of the Trp residue(s) can be ascribed predominantly to static quenching that occurs when the Zn complex binds to the protein and forms a nonfluorescent complex. The role played by the nature of the ligand, the metal, and complex charge in quenching Trp fluorescence was investigated. The binding association constants () ranged from 104 to 1010 M−1 and indicate that complexes with planar aromatic features have the strongest affinity for globular proteins and free Trp. Complexes with nonaromatic features failed to interact with these proteins at or in the vicinity of the Trp residues. These interactions were studied over a range of temperatures, and binding was found to weaken with the increase in temperature and was exothermic with a negative change in entropy. The thermodynamic parameters suggest that binding of Zn complexes to the proteins is a highly spontaneous and favorable process.
{"title":"Interaction of Small Zinc Complexes with Globular Proteins and Free Tryptophan","authors":"J. Butkus, Shelby O’Riley, B. Chohan, Swarna Basu","doi":"10.1155/2016/1378680","DOIUrl":"https://doi.org/10.1155/2016/1378680","url":null,"abstract":"A series of eight water soluble anionic, cationic, and neutral zinc(II) complexes were synthesized and characterized. The interaction of these complexes with bovine serum albumin (BSA), human serum albumin (HSA), lysozyme, and free tryptophan (Trp) was investigated using steady-state fluorescence spectroscopy. Static and dynamic fluorescence quenching analysis based on Stern-Volmer kinetics was conducted, and the decrease in fluorescence intensity of the Trp residue(s) can be ascribed predominantly to static quenching that occurs when the Zn complex binds to the protein and forms a nonfluorescent complex. The role played by the nature of the ligand, the metal, and complex charge in quenching Trp fluorescence was investigated. The binding association constants () ranged from 104 to 1010 M−1 and indicate that complexes with planar aromatic features have the strongest affinity for globular proteins and free Trp. Complexes with nonaromatic features failed to interact with these proteins at or in the vicinity of the Trp residues. These interactions were studied over a range of temperatures, and binding was found to weaken with the increase in temperature and was exothermic with a negative change in entropy. The thermodynamic parameters suggest that binding of Zn complexes to the proteins is a highly spontaneous and favorable process.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"22 1","pages":"1-12"},"PeriodicalIF":0.0,"publicationDate":"2016-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83289296","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}
G. Piga, D. Gonçalves, T. Thompson, A. Brunetti, A. Malgosa, S. Enzo
We have critically investigated the ATR-IR spectroscopy data behavior of burned human teeth as opposed to the generally observed behavior in human bones that were subjected to heat treatment, whether deliberate or accidental. It is shown that the deterioration of the crystallinity index (CI) behavior sometimes observed in bones subjected to high temperature appears to be of higher frequency in the case of bioapatite from teeth. This occurs because the formation of the β-tricalcium phosphate (β-TCP) phase, otherwise known as whitlockite, clearly ascertained by the X-ray diffraction (XRD) patterns collected on the same powdered specimens investigated by ATR-IR. These results point to the need of combining more than one physicochemical technique even if apparently well suitable, in order to verify whether the assumed conditions assessed by spectroscopy are fully maintained in the specimens after temperature and/or mechanical processing.
{"title":"Understanding the Crystallinity Indices Behavior of Burned Bones and Teeth by ATR-IR and XRD in the Presence of Bioapatite Mixed with Other Phosphate and Carbonate Phases","authors":"G. Piga, D. Gonçalves, T. Thompson, A. Brunetti, A. Malgosa, S. Enzo","doi":"10.1155/2016/4810149","DOIUrl":"https://doi.org/10.1155/2016/4810149","url":null,"abstract":"We have critically investigated the ATR-IR spectroscopy data behavior of burned human teeth as opposed to the generally observed behavior in human bones that were subjected to heat treatment, whether deliberate or accidental. It is shown that the deterioration of the crystallinity index (CI) behavior sometimes observed in bones subjected to high temperature appears to be of higher frequency in the case of bioapatite from teeth. This occurs because the formation of the β-tricalcium phosphate (β-TCP) phase, otherwise known as whitlockite, clearly ascertained by the X-ray diffraction (XRD) patterns collected on the same powdered specimens investigated by ATR-IR. These results point to the need of combining more than one physicochemical technique even if apparently well suitable, in order to verify whether the assumed conditions assessed by spectroscopy are fully maintained in the specimens after temperature and/or mechanical processing.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"26 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2016-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79659848","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}
It is usually accepted that most 2D-NMR experiments cannot be approached using classical models. Instructors argue that Product Operators (PO) or density matrix formalisms are the only alternative to get insights into complex spin evolution for experiments involving Multiple-Quantum Coherence, such as the Heteronuclear Multiple-Quantum Correlation (HMQC) technique. Nevertheless, in recent years, several contributions have been published to provide vectorial descriptions for the HMQC taking PO formalism as the starting point. In this work we provide a graphical representation of the HMQC experiment, taking the basic elements of Bloch’s vector model as building blocks. This description bears an intuitive and comfortable understanding of spin evolution during the pulse sequence, for those who are novice in 2D-NMR. Finally, this classical vectorial depiction is tested against the PO formalism and nonclassical vectors, conveying the didactic advantage of shedding light on a single phenomenon from different perspectives. This comparative approach could be useful to introduce PO and nonclassical vectors for advanced upper-division undergraduate and graduate education.
{"title":"The Heteronuclear Multiple-Quantum Correlation Experiment: Perspective from Classical Vectors, Nonclassical Vectors, and Product Operators","authors":"K. Vega-Hernández, M. Antuch","doi":"10.1155/2016/2390109","DOIUrl":"https://doi.org/10.1155/2016/2390109","url":null,"abstract":"It is usually accepted that most 2D-NMR experiments cannot be approached using classical models. Instructors argue that Product Operators (PO) or density matrix formalisms are the only alternative to get insights into complex spin evolution for experiments involving Multiple-Quantum Coherence, such as the Heteronuclear Multiple-Quantum Correlation (HMQC) technique. Nevertheless, in recent years, several contributions have been published to provide vectorial descriptions for the HMQC taking PO formalism as the starting point. In this work we provide a graphical representation of the HMQC experiment, taking the basic elements of Bloch’s vector model as building blocks. This description bears an intuitive and comfortable understanding of spin evolution during the pulse sequence, for those who are novice in 2D-NMR. Finally, this classical vectorial depiction is tested against the PO formalism and nonclassical vectors, conveying the didactic advantage of shedding light on a single phenomenon from different perspectives. This comparative approach could be useful to introduce PO and nonclassical vectors for advanced upper-division undergraduate and graduate education.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"27 1","pages":"1-9"},"PeriodicalIF":0.0,"publicationDate":"2016-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74347055","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}
Core-shell quantum dots CdSe/ZnS and lumogen yellow organic dye are characterized by their inclusion in luminescent downshifting (LDS) layers. Layers were deposited on top of crystalline silicon cell (c-Si), dye synthesized solar cell (DSSC), and cadmium telluride (CdTe) minimodules. External quantum efficiency measurements for the solar cell/LDS devices are discussed. Experimental results were compared with an optical model developed by Rothemund, 2014.
{"title":"External Quantum Efficiency Improvement with Luminescent Downshifting Layers: Experimental and Modelling","authors":"H. Ahmed, S. McCormack, J. Doran","doi":"10.1155/2016/8543475","DOIUrl":"https://doi.org/10.1155/2016/8543475","url":null,"abstract":"Core-shell quantum dots CdSe/ZnS and lumogen yellow organic dye are characterized by their inclusion in luminescent downshifting (LDS) layers. Layers were deposited on top of crystalline silicon cell (c-Si), dye synthesized solar cell (DSSC), and cadmium telluride (CdTe) minimodules. External quantum efficiency measurements for the solar cell/LDS devices are discussed. Experimental results were compared with an optical model developed by Rothemund, 2014.","PeriodicalId":14329,"journal":{"name":"International Journal of Spectroscopy","volume":"5116 1 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"2016-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76908627","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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