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Sökning: hsv:(NATURVETENSKAP) hsv:(Kemi) hsv:(Materialkemi) > Stockholms universitet

  • Resultat 1-10 av 582
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1.
  • Hagman, Benjamin, et al. (författare)
  • Steps Control the Dissociation of CO2 on Cu(100)
  • 2018
  • Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 140:40, s. 12974-12979
  • Tidskriftsartikel (refereegranskat)abstract
    • CO2 reduction reactions, which provide one route to limit the emission of this greenhouse gas, are commonly performed over Cu-based catalysts. Here, we use ambient pressure X-ray photoelectron spectroscopy together with density functional theory to obtain an atomistic understanding of the dissociative adsorption of CO2 on Cu(100). We find that the process is dominated by the presence of steps, which promote both a lowering of the dissociation barrier and an efficient separation between adsorbed O and CO, reducing the probability for recombination. The identification of steps as sites for efficient CO2 dissociation provides an understanding that can be used in the design of future CO2 reduction catalysts.
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2.
  • Renier, Olivier, et al. (författare)
  • Shape Preserving Single Crystal to Amorphous to Single Crystal Polymorphic Transformation Is Possible
  • 2021
  • Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 143:48, s. 20202-20206
  • Tidskriftsartikel (refereegranskat)abstract
    • Many crystalline materials form polymorphs and undergo solid–solid transitions between different forms as a function of temperature or pressure. However, there is still a poor understanding of the mechanism of transformation. Conclusions about the transformation process are typically drawn by comparing the crystal structures before and after the conversion, but gaining detailed mechanistic knowledge is strongly impeded by the generally fast rate of these transitions. When the crystal morphology does not change, it is assumed that crystallinity is maintained throughout the process. Here we report transformation between polymorphs of ZnCl2(1,3-diethylimidazole-2-thione)2 which are sufficiently slow to allow unambiguous assignment of single crystal to single crystal transformation with shape preservation proceeding through an amorphous intermediate phase. This result fundamentally challenges the commonly accepted views of polymorphic phase transition mechanisms.
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3.
  • Rzepka, Przemyslaw, et al. (författare)
  • CO2-Induced Displacement of Na+ and K+ in Zeolite INaKI-A
  • 2018
  • Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 122:30, s. 17211-17220
  • Tidskriftsartikel (refereegranskat)abstract
    • Adsorption technologies offer opportunities to remove CO2 from gas mixtures, and zeolite A has good properties that include a high capacity for the adsorption of CO2 . It has been argued that its abilities to separate CO2 from N-2 in flue gas and CO2 from CH4 in raw biogas can be further enhanced by replacing Na+ with K+ in the controlling pore window apertures. In this study, several compositions of I Na12-xKxI-A were prepared and studied with respect to the adsorption of CO2 N-2, and CH4, and the detailed structural changes were induced by the adsorption of CO2. The adsorption of CO2 gradually decreased on an increasing content of K+, whereas the adsorption of N-2 and CH4 was completely nulled already at relatively small contents of K. Of the studied samples, INa9K3I-A exhibited the highest CO2 over N-2/CH4 selectivities, with a(CO2/N-2 ) > 21 000 and a(CO2/CH4) > 8000. For samples with and without adsorbed CO2 analyses of powder X-ray diffraction (PXRD) data revealed that K+ preferred to substitute Na+ at the eight-ring sites. The Na(+ )ions at the six-ring sites were gradually replaced by K+ on an increasing content, and these sites split into two positions on both sides of the six-ring mirror plane. It was observed that both the eight-ring and six-ring sites tailored the maximum adsorption capacity for CO2 and possibly also the diffusion of CO2 into the alpha-cavities of INa12-xKxI-A. The adsorption of CH4 and N-2 on the other hand appeared to be controlled by the K+ ions blocking the eight-ring windows. The in situ PXRD study revealed that the positions of the extra-framework cations were displaced into the a-cavities of INa12(_)x,KxI-A on the adsorption of CO2 . For samples with a low content of K+, the repositioning of the cations was consistent with a mutual attraction with the adsorbed CO(2 )molecules.
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4.
  • Seisenbaeva, Gulaim, et al. (författare)
  • Molecular insight into the mode-of-action of phosphonate monolayers as active functions of hybrid metal oxide adsorbents. Case study in sequestration of rare earth elements
  • 2015
  • Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 5:31, s. 24575-24585
  • Tidskriftsartikel (refereegranskat)abstract
    • The insight into the molecular aspects of ligand grafting and potential maximal capacity of hybrid organic-inorganic adsorbents bearing phosphonate ligand monolayers as active functions was obtained by single crystal X-ray studies of ligand-functionalized titanium alkoxide complexes. The attachment of molecules occurs generally in the tripodal vertical fashion with the minimal distance between them being about 8.7 angstrom, resulting in 0.19 nm(2) as the minimal surface area per function. In the present experimental work the theoretical loading capacity could almost be achieved for functionalization of mesoporous nanorods of anatase with imino-bis-methylphosphonic acid (IMPA, NH(CH2PO3H2)(2)) or aminoethylphosphonic acid (AEPA, H2NC2H4PO3H2). The products had the same morphology as the starting material, as was established by SEM and optical microscopy. The size and structure of the individual nanoparticles of the constituting inorganic component of the material were preserved and practically unchanged through the surface modification, as established by powder XRD and EXAFS studies. The surface area of the inorganic-organic hybrids decreased somewhat from the initial similar to 250 m(2) g(-1), on adsorption of AEPA (0.21 mmol g(-1)) to similar to 240 m(2) g(-1), and on adsorption of IMPA (0.17 mmol g(-1)) to similar to 190 m(2) g(-1). The ligands were bound effectively to the surface according to TGA, EDS and FTIR analyses and remained in the mono-deprotonated form. The produced hybrid adsorbents had for the selected pH (3.5) high capacities towards adsorption of Rare Earth Element (REE) cations, but with equilibria achieved relatively slowly. The composition of the surface complexes was determined as M : L = 1 : 1 for IMPA, but varied for the AEPA from 1 : 3 to 1 : 1 dependent on the REE, which can be interpreted in terms of charge compensation as the major driving force behind binding. The cation desorption in strongly acidic media for recuperation of the adsorbed REE and the relative capacity of the re-used adsorbent have been quantified.
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5.
  • Svensson Grape, Erik, et al. (författare)
  • A Robust and Biocompatible Bismuth Ellagate MOF Synthesized Under Green Ambient Conditions
  • 2020
  • Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 142:39, s. 16795-16804
  • Tidskriftsartikel (refereegranskat)abstract
    • The first bioinspired microporous metal-organic framework (MOF) synthesized using ellagic acid, a common natural antioxidant and polyphenol building unit, is presented. Bi2O(H2O)2(C14H2O8)·nH2O (SU-101) was inspired by bismuth phenolate metallodrugs, and could be synthesized entirely from nonhazardous or edible reagents under ambient aqueous conditions, enabling simple scale-up. Reagent-grade and affordable dietary supplement-grade ellagic acid was sourced from tree bark and pomegranate hulls, respectively. Biocompatibility and colloidal stability were confirmed by in vitro assays. The material exhibits remarkable chemical stability for a bioinspired MOF (pH = 2-14, hydrothermal conditions, heated organic solvents, biological media, SO2 and H2S), attributed to the strongly chelating phenolates. A total H2S uptake of 15.95 mmol g-1 was recorded, representing one of the highest H2S capacities for a MOF, where polysulfides are formed inside the pores of the material. Phenolic phytochemicals remain largely unexplored as linkers for MOF synthesis, opening new avenues to design stable, eco-friendly, scalable, and low-cost MOFs for diverse applications, including drug delivery.
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6.
  • Zhang, Chu, et al. (författare)
  • Steps and catalytic reactions : CO oxidation with preadsorbed O on Rh(553)
  • 2022
  • Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 715
  • Tidskriftsartikel (refereegranskat)abstract
    • Industrial catalysts are often comprised of nanoparticles supported on high-surface-area oxides, in order to maximise the catalytically active surface area and thereby utilise the active material better. These nanoparticles expose steps and corners that, due to low coordination to neighboring atoms, are more reactive and, as a consequence, are often assumed to have higher catalytic activity. We have investigated the reaction between CO and preadsorbed O on a stepped Rh(553) surface, and show that CO oxidation indeed occurs faster than on the flat Rh(111) surface at the same temperature. However, we do find that this is not a result of reactions at the step sites but rather at the terrace sites close to the steps, due to in-plane relaxation enabled by the step. This insight can provide ways to optimize the shape of the nanoparticles to further improve the activity of certain reactions.
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7.
  • Asfaw, Habtom Desta, Dr. 1986-, et al. (författare)
  • Facile synthesis of hard carbon microspheres from polyphenols for sodium-ion batteries : insight into local structure and interfacial kinetics
  • 2020
  • Ingår i: Materials Today Energy. - : Elsevier BV. - 2468-6069. ; 18
  • Tidskriftsartikel (refereegranskat)abstract
    • Hard carbons are the most promising negative active materials for sodium ion storage. In this work, a simple synthesis approach is proposed to produce hard carbon microspheres (CMSs) (with a mean diameter of ~1.3 μm) from resorcinol-formaldehyde precursors produced via acid-catalyzed polycondensation reaction. Samples prepared at 1200, 1400, and 1500 oC showed different electrochemical behavior in terms of reversible capacity, initial coulombic efficiency (iCE), and the mechanism of sodium ion storage. The specific capacity contributions from the flat voltage profile (<0.1 V) and the sloping voltage region (0.1–1 V) showed strong correlation to the local structure (and carbonization temperature) determined by the interlayer spacing (d002) and the Raman ID/IG ratio of the hard carbons (HCs) and the rate of cycling. Electrochemical tests indicated that the HC synthesized at 1500 oC performed best with an iCE of 85–89% and a reversible capacity of 300–340 mAh g−1 at 10 mA g−1, with the majority of charge stored below 0.1 V. The d002 and the ID/IG ratio for the sample were ~3.7 Å and ~1.27, respectively, parameters indicative of the ideal local structure in HCs required for optimum performance in sodium-ion cells. In addition, galvanostatic tests on three-electrode half-cells cells revealed that sodium metal plating occurred as cycling rates were increased beyond 80 mA g−1 leading to considerably high capacity and poor coulombic efficiency, a point that must be considered in full-cell batteries. Pairing the hard CMS electrodes with Prussian white positive electrode, a proof-of-concept cell could provide a specific capacity of almost 100 mAh g−1 maintained for more than 50 cycles with a nominal voltage of 3 V.
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8.
  • Celania, Chris, et al. (författare)
  • The Prolific Ternary System Pt/Sn/Nd : Insertion of Pt into the Structures of Sn/Nd Intermetallics Yields Structural Complexity and Wealth
  • 2023
  • Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 62:24, s. 9369-9378
  • Tidskriftsartikel (refereegranskat)abstract
    • The understanding of structure and bonding in intermetallic phases still lags behind that of molecular compounds. For that reason, exploring intermetallic phases and identifying structural patterns and relationships are particularly important for closing this knowledge gap. In particular, here we report on the addition of increasing amounts of platinum to ∼2:1 mixtures of tin and neodymium, which yields eight ternary Pt/Sn/Nd compounds, four of which have not been reported before. Interestingly, except for PtSnNd (1), all observed ternary phases of the system can be derived from the binary compounds Sn2Nd and Sn5Nd2 by adding Pt to the composition(s), as they lie on or close to two lines: Sn2Nd-Pt (Pt0.21(1)Sn2Nd (2), PtSn2Nd (3), Pt1.33Sn2Nd (4), Pt2-xSn2+xNd (x = 0.27(3), 5), and Pt3Sn2Nd (6)) or Sn5Nd2-Pt (Pt1.5Sn5-xNd2 (x = 0.16(2), 7) and Pt3Sn5Nd2-x (x = 0.161(8), 8)). While the introduction of increasing amounts of Pt to the binaries Sn2Nd and Sn5Nd2 leads to stepwise changes in the coordination environment of Nd, Pt preserves its coordination over the entire system in the form of interpenetrating bipyramidal {PtSn5Nd5} clusters.
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9.
  • Gebauer, Denis, et al. (författare)
  • A transparent hybrid of nanocrystalline cellulose and amorphous calcium carbonate nanoparticles
  • 2011
  • Ingår i: NANOSCALE. - : Royal Society of Chemistry (RSC). - 2040-3364 .- 2040-3372. ; 3:9, s. 3563-3566
  • Tidskriftsartikel (refereegranskat)abstract
    • Nanocellulose hybrids are promising candidates for biodegradable multifunctional materials. Hybrids of nanocrystalline cellulose (NCC) and amorphous calcium carbonate (ACC) nanoparticles were obtained through a facile chemical approach over a wide range of compositions. Controlling the interactions between NCC and ACC results in hard, transparent structures with tunable composition, homogeneity and anisotropy.
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10.
  • Marks, Kess, et al. (författare)
  • Investigation of the surface species during temperature dependent dehydrogenation of naphthalene on Ni(111)
  • 2019
  • Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 150:24
  • Tidskriftsartikel (refereegranskat)abstract
    • The temperature dependent dehydrogenation of naphthalene on Ni(111) has been investigated using vibrational sum-frequency generation spectroscopy, X-ray photoelectron spectroscopy, scanning tunneling microscopy, and density functional theory with the aim of discerning the reaction mechanism and the intermediates on the surface. At 110 K, multiple layers of naphthalene adsorb on Ni(111); the first layer is a flat lying chemisorbed monolayer, whereas the next layer(s) consist of physisorbed naphthalene. The aromaticity of the carbon rings in the first layer is reduced due to bonding to the surface Ni-atoms. Heating at 200 K causes desorption of the multilayers. At 360 K, the chemisorbed naphthalene monolayer starts dehydrogenating and the geometry of the molecules changes as the dehydrogenated carbon atoms coordinate to the nickel surface; thus, the molecule tilts with respect to the surface, recovering some of its original aromaticity. This effect peaks at 400 K and coincides with hydrogen desorption. Increasing the temperature leads to further dehydrogenation and production of H-2 gas, as well as the formation of carbidic and graphitic surface carbon. Published under license by AIP Publishing.
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