| 1. |
- Bandyopadhyay, Sulalit, et al.
(författare)
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Synthesis and in vitro cellular interactions of superparamagnetic iron nanoparticles with a crystalline gold shell
- 2014
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Ingår i: Applied Surface Science. - : Elsevier BV. - 0169-4332 .- 1873-5584. ; 316, s. 171-178
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Tidskriftsartikel (refereegranskat)abstract
- Fe@Au core-shell nanoparticles (NPs) exhibit multiple functionalities enabling their effective use in applications such as medical imaging and drug delivery. In this work, a novel synthetic method was developed and optimized for the synthesis of highly stable, monodisperse Fe@Au NPs of average diameter similar to 24 nm exhibiting magneto-plasmonic characteristics. Fe@Au NPs were characterized by a wide range of experimental techniques, including scanning (transmission) electron microscopy (S(T)EM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDX), dynamic light scattering (DLS) and UV-vis spectroscopy. The formed particles comprise an amorphous iron core with a crystalline Au shell of tunable thickness, and retain the superparamagnetic properties at room temperature after formation of a crystalline Au shell. After surface modification, PEGylated Fe@Au NPs were used for in vitro studies on olfactory ensheathing cells (OECs) and human neural stem cells (hNSCs). No adverse effects of the Fe@Au particles were observed post-labeling, both cell types retaining normal morphology, viability, proliferation, and motility. It can be concluded that no appreciable toxic effects on both cell types, coupled with multifunctionality and chemical stability make them ideal candidates for therapeutic as well as diagnostic applications.
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| 2. |
- Lützenkirchen, J, et al.
(författare)
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Adsorption of Al13–Keggin clusters to sapphire c-plane single crystals : Kinetic observations by streaming current measurements
- 2010
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Ingår i: Applied Surface Science. - : Elsevier B V. - 0169-4332 .- 1873-5584. ; 256:17, s. 5406-5411
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Tidskriftsartikel (refereegranskat)abstract
- We have carried out streaming current measurements of sapphire c-plane single crystals in contact with the solutions containing the Al13–-Keggin ions at different pH values. We followed the evolution of the zeta-potential as a function of time and pH. The Keggin ions were synthesised and characterised by ESI-MS in two different laboratories, and the results showed that nearly 100% of Al was in the form of Al13 cluster. The streaming current measurements were carried out to investigate whether Al13 clusters would (i) be adsorbed to the surface and (ii) remain stable. Close to the isoelectric point of the sapphire c-plane (around pH 4) it was found that the Al13 ions were adsorbed and stable in the systems for an extended period. After some time the conductivity of the solution strongly increased and the zeta-potential declined, indicating that the clusters were destroyed (certainly in solution, as indicated by the conductivity reading, but potentially also at the surface). ESI-MS measurements at various dilution factors or decreased pH also showed disintegration of the clusters resulting in a multitude of smaller Al species, in agreement with the conductivity measurements during the streaming current measurements. Additions at higher pH showed clear adsorption of the clusters but resulted in stability over the complete observation period as inferred from the conductivity measurements.
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| 3. |
- Shchukarev, Andrey, et al.
(författare)
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Cryo-XPS analysis reveals surface composition of microalgae
- 2020
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Ingår i: Applied Surface Science. - : Elsevier. - 0169-4332 .- 1873-5584. ; 526
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Tidskriftsartikel (refereegranskat)abstract
- Green microalgae are widely used for wastewater treatment, food/feed and pigment production, as well as for aquaculture. However, very little is known about their surface composition, which can determine algae behavior in nature and influence their processing. In this work, we use cryo-XPS to characterize the surface chemical composition of three different microalgae species. We investigate the applicability of a data treatment method, developed for bacteria, deconvoluting C 1s with respect to protein, lipid and polysaccharide. We discuss how substances unique to algae contribute to the C 1s spectra and how this affects the transferability of the method to microalgae. Two species of green microalgae isolated from Northern Sweden, Chlorella vulgaris 13-1 and Coelastrella sp. 3-4, were compared to reference culture collection strain, Scenedesmus obliquus RISE (UTEX 417). Cryo-XPS data indicate that surfaces of Coelastrella sp. 3-4 and C. vulgaris 13-1 cells are dominated by protein and carbohydrates. However, the carbohydrate content was higher for C. vulgaris. The reference strain shows the highest content of proteins and has an increased amount of lipids compared to the other two. Estimation of the cell surface hydrophobicity suggests that the hydrophobicity increases in the order: C. vulgaris < Coelastrella sp. < S. obliquus.
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| 4. |
- Subramanian, Arunprabaharan, et al.
(författare)
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Effect of tetravalent dopants on hematite nanostructure for enhanced photoelectrochemical water splitting
- 2018
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Ingår i: Applied Surface Science. - : Elsevier. - 0169-4332 .- 1873-5584. ; 427, s. 1203-1212
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Tidskriftsartikel (refereegranskat)abstract
- In this paper, the influence of tetravalent dopants such as Si4+, Sn4+, Ti4+, and Zr4+ on the hematite (alpha-Fe2O3) nanostructure for enhanced photoelectrochemical (PEC) water splitting are reported. The tetravalent doping was performed on hydrothermally grown akaganeite (beta-FeOOH) nanorods on FTO (fluorine-doped tin-oxide) substrates via a simple dipping method for which the respective metal-precursor solution was used, followed by a high-temperature (800 degrees C) sintering in a box furnace. The photocurrent density for the pristine (hematite) photoanode is similar to 0.81 mA/cm(2) at 1.23 V-RHE, with an onset potential of 0.72 V-RHE; however, the tetravalent dopants on the hematite nanostructures alter the properties of the pristine photoanode. The Si4+-doped hematite photoanode showed a slight photocurrent increment without a changing of the onset potential of the pristine photoanode. The Sn4+- and Ti4+-doped hematite photoanodes, however, showed an anodic shift of the onset potential with the photocurrent increment at a higher applied potential. Interestingly, the Zr4+-doped hematite photoanode exhibited an onset potential that is similar to those of the pristine and Si4+-doped hematite, but a larger photocurrent density that is similar to those of the Sn4+- and Ti4+-doped photoanodes was recorded. The photoactivity of the doped photoanodes at 1.23 V-RHE follows the order Zr > Sn > Ti > Si. The onset-potential shifts of the doped photoanodes were investigated using the Ab initio calculations that are well correlated with the experimental data. X-ray diffraction (XRD) and scanning-electron microscopy (FESEM) revealed that both the crystalline phase of the hematite and the nanorod morphology were preserved after the doping procedure. X-ray photoelectron spectroscopy (XPS) confirmed the presence of the tetravalent dopants on the hematite nanostructure. The charge-transfer resistance at the various interfaces of the doped photoanodes was studied using impedance spectroscopy. The doping on the hematite photoanodes was confirmed using the Mott-Schottky (MS) analysis.
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