79 research outputs found
Synthesis and electrical characterization of monocrystalline nickel nanorods and Ni-CNT composites
Aerospace vessels require electrically conductive, light weight frames to minimize damage from electromagnetic radiation, electrostatic discharge and lightning strikes while economizing fuel. Nickel nanowires and hybrid nickel-carbon nanotube materials are suitable nanostructures to ensure high conductivity at low mass loading. Monocrystalline nickel structures have even better conduction properties than the polycrystalline equivalent due to possessing less particle-particle junctions. We have developed a solutionbased method that produces monocrystalline nickel nanowires via the decomposition of metalorganic precursors in the presence of self-assembled surfactants. The resulting wires are approximately 20 nm wide by 1.5 ”m in length. These wires have a morphology consisting of semi-flattened rods with pyramidal ends. Despite the changing dimensions between the nanorod body and its head, there was no disruption in the crystallographic orientation, as observed with HRTEM and diffraction patterns. The nickel nanostructures were exposed to air for several weeks, but no oxidation was detectable by magnetic measurement, i.e. the saturation magnetization corresponds to Ni0 and no bias is observed in the hysteresis loops. It seems that the long alkyl chain amine surfactant, in addition to being a structuration agent, remains at the surface of the Ni wires after washing and acts as a protective layer. The magnetic field around Ni nanowires was imaged using electron holography. Each Ni wire is a magnetic monodomain. Routes to prepare hybrid nickel-CNT materials were explored using chemical vapor deposition in a fluidized bed, solution chemistry and dry preparation in a Fisher-Porter reactor. Different nickel compositions and material morphologies resulted, depending on the preparation technique. The nickel nanorods and hybrid materials were incorporated into carbon fiber-reinforced polymer composites. The electrical conductivity as a function of wt% loading was measured, showing promise for these materials in discharging electrostatic charges
Magnetically induced CO2 methanation using exchangeâcoupled spinel ferrites in cuboctahedronâshaped nanocrystals
Magnetically induced catalysis can be promoted taking advantage of optimal heating properties from the magnetic nanoparticles to be employed. However, when unprotected, these heating agents that are usually air-sensitive, get sintered under the harsh catalytic conditions. In this context, we present, to the best of our knowledge, the first example of air-stable magnetic nanoparticles that: 1) show excellent performance as heating agents in the CO2 methanation catalyzed by Ni/SiRAlOx, with CH4 yields above 95â%, and 2) do not sinter under reaction conditions. To attain both characteristics we demonstrate, first the exchange-coupled magnetic approach as an alternative and effective way to tune the magnetic response and heating efficiency, and second, the chemical stability of cuboctahedron-shaped coreâshell hard CoFe2O4âsoft Fe3O4 nanoparticles.Xunta de Galicia | Ref. IN607 A 2018/5Xunta de Galicia | Ref. ED431C 2016-034Agencia Estatal de InvestigaciĂłn | Ref. CTM2017-84050-
Ultrastable Magnetic Nanoparticles Encapsulated in Carbon for Magnetically Induced Catalysis
[EN] Magnetically induced catalysis using magnetic nanoparticles (MagNPs) as heating agents is a new efficient method to perform reactions at high temperatures. However, the main limitation is the lack of stability of the catalysts operating in such harsh conditions. Normally, above 500 degrees C, significant sintering of MagNPs takes place. Here we present encapsulated magnetic FeCo and Co NPs in carbon (Co@C and FeCo@C) as an ultrastable heating material suitable for high-temperature magnetic catalysis. Indeed, FeCo@C or a mixture of FeCo@C:Co@C (2:1) decorated with Ni or Pt-Sn showed good stability in terms of temperature and catalytic performances. In addition, consistent conversions and selectivities regarding conventional heating were observed for CO2 methanation (Sabatier reaction), propane dehydrogenation (PDH), and propane dry reforming (PDR). Thus, the encapsulation of MagNPs in carbon constitutes a major advance in the development of stable catalysts for high-temperature magnetically induced catalysis.The authors thank the Instituto de Tecnologia Quimica (ITQ), Consejo Superior de Investigaciones Cientificas (CSIC), Universitat Politecnica de ValĂšncia (UPV) for the facilities and Severo Ochoa programe (SEV-2016-0683), "Juan de la Cierva" by MINECO (IJCI-2016-27966), and Primero Proyectos de InvestigaciĂłn PAID-06-18 (SP20180088) for financial support. The authors acknowledge ERC Advanced Grants (MONACAT-2015-694159 and SynCatMatch-2014671093). We also thank the Electron Microscopy Service of the UPV for TEM facilities.MartĂnez-Prieto, LM.; Marbaix, J.; Asensio, JM.; Cerezo-Navarrete, C.; Fazzini, P.; Soulantica, K.; Chaudret, B.... (2020). Ultrastable Magnetic Nanoparticles Encapsulated in Carbon for Magnetically Induced Catalysis. 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Hydrodeoxygenation Using Magnetic Induction: HighâTemperature Heterogeneous Catalysis in Solution. Angewandte Chemie International Edition, 58(33), 11306-11310. doi:10.1002/anie.201904366Liu, Y., Gao, P., Cherkasov, N., & Rebrov, E. V. (2016). Direct amide synthesis over coreâshell TiO2@NiFe2O4 catalysts in a continuous flow radiofrequency-heated reactor. RSC Advances, 6(103), 100997-101007. doi:10.1039/c6ra22659kLiu, Y., Cherkasov, N., Gao, P., FernĂĄndez, J., Lees, M. R., & Rebrov, E. V. (2017). The enhancement of direct amide synthesis reaction rate over TiO 2 @SiO 2 @NiFe 2 O 4 magnetic catalysts in the continuous flow under radiofrequency heating. Journal of Catalysis, 355, 120-130. doi:10.1016/j.jcat.2017.09.010Meffre, A., Mehdaoui, B., Connord, V., Carrey, J., Fazzini, P. F., Lachaize, S., ⊠Chaudret, B. (2015). Complex Nano-objects Displaying Both Magnetic and Catalytic Properties: A Proof of Concept for Magnetically Induced Heterogeneous Catalysis. 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Generation of subnanometric platinum with high stability during transformation of a 2D zeolite into 3D. Nature Materials, 16(1), 132-138. doi:10.1038/nmat4757Liu, L., Zakharov, D. N., Arenal, R., Concepcion, P., Stach, E. A., & Corma, A. (2018). Evolution and stabilization of subnanometric metal species in confined space by in situ TEM. Nature Communications, 9(1). doi:10.1038/s41467-018-03012-6Liu, L., Gao, F., ConcepciĂłn, P., & Corma, A. (2017). A new strategy to transform mono and bimetallic non-noble metal nanoparticles into highly active and chemoselective hydrogenation catalysts. Journal of Catalysis, 350, 218-225. doi:10.1016/j.jcat.2017.03.014Liu, L., ConcepciĂłn, P., & Corma, A. (2016). Non-noble metal catalysts for hydrogenation: A facile method for preparing Co nanoparticles covered with thin layered carbon. Journal of Catalysis, 340, 1-9. doi:10.1016/j.jcat.2016.04.006Fu, T., Wang, M., Cai, W., Cui, Y., Gao, F., Peng, L., ⊠Ding, W. (2014). 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Bidimensional lamellar assembly by coordination of peptidic homopolymers to platinum nanoparticles
A key challenge for designing hybrid materials is the development of chemical tools to control the organization of inorganic nanoobjects at low scales, from mesoscopic (~”m) to nanometric (~nm). So far, the most efficient strategy to align assemblies of nanoparticles consists in a bottom-up approach by decorating block copolymer lamellae with nanoobjects. This well accomplished procedure is nonetheless limited by the thermodynamic constraints that govern copolymer assembly, the entropy of mixing as described by the FloryâHuggins solution theory supplemented by the critical influence of the volume fraction of the block components. Here we show that a completely different approach can lead to tunable 2D lamellar organization of nanoparticles with homopolymers only, on condition that few elementary rules are respected: 1) the polymer spontaneously allows a structural preorganization, 2) the polymer owns functional groups that interact with the nanoparticle surface, 3) the nanoparticles show a surface accessible for coordination
Synergism of Au and Ru Nanoparticles in Low-Temperature Photoassisted CO2 Methanation
This is the peer reviewed version of the following article:Mateo-Mateo, Diego, De Masi, Deborah , Albero-Sancho, Josep, Lacroix, Lisa-Marie , Fazzini, Pier-Francesco , Chaudret, Bruno , GarcĂa GĂłmez, Hermenegildo. (2018). Synergism of Au and Ru Nanoparticles in Low-Temperature Photoassisted CO2 Methanation.Chemistry - A European Journal, 24, 69, 18436-18443. DOI: 10.1002/chem.201803022, which has been published in final form at http://doi.org/10.1002/chem.201803022. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions[EN] Au and Ru nanoparticles have been deposited on SiraloxÂź substrate by impregnation and chemical reduction, respectively (Au-Ru-S). The as-prepared material has demonstrated to be very active for the selective CO2 metanation to CH4 at temperatures below 250 oC. In addition, Au-Ru-S exhibits CH4 production enhancement upon UV-Vis light irradiation starting at temepratures higher than 200 oC, although the contribution of the photoassisted pathway of CH4 production decreases as temperature increases. Thus, a maximum CH4 production of 204 mmol/gRu at 250 oC upon 100 mW/cm2 irradiation was achieved. Control experiments using Ru-S and Au-S materials revealed that Ru nanoparticles are the CO2 methanation active sites, while Au NPs contribute harvesting light, mainly visible as consequence of the strong Au plasmon band centrered at 529 nm. The visible light absorbed by Au NPs plasmon could act as local heaters of neighbouring Ru NPs, increasing their temperature and enhancing CH4 production.D. M., J.A., and H.G. thank the Spanish Ministry of Economy and Competitiveness (Severo Ochoa SEV2016-0683 and CTQ2015-69563-CO2-1), Generalitat Valenciana (Prometeo 2017-083) for financial support. J.A. and D.M. also thank UPV for a postdoctoral scholarship and the Spanish Ministry of Science for a PhD Scholarship, respectively. This project has received funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement No GA694159 MONACAT).Mateo-Mateo, D.; De Masi, D.; Albero-Sancho, J.; Lacroix, L.; Fazzini, P.; Chaudret, B.; GarcĂa GĂłmez, H. (2018). Synergism of Au and Ru Nanoparticles in Low-Temperature Photoassisted CO2 Methanation. Chemistry - A European Journal. 24(69):18436-18443. https://doi.org/10.1002/chem.201803022S1843618443246
An Improved STEM/EDX Quantitative Method for Dopant Profiling at the Nanoscale
International audienceIn this paper, an improved quantification technique for STEM/EDX measurements of 1D dopant profiles based on the Cliff-Lorimer equation is presented. The technique uses an iterative absorption correction procedure based on density models correlating the local mass density and composition of the specimen. Moreover, a calibration and error estimation procedure based on linear regression and error propagation is proposed in order to estimate the total measurement error in the dopant density. The proposed approach is applied to the measurement of the As profile in a nanodevice test structure. For the calibration, two crystalline Si specimens implanted with different As doses have been used, and the calibration of the Cliff-Lorimer coefficients has been carried out using Rutherford Back Scattering measurements. The As profile measurement has been carried out on an FinFET test structure, showing that quantitative results can be obtained in the nanometer scale and for dopant atomic densities lower than 1%. Using the proposed approach, the measurement error and detection limit for our experimental setup are calculated and the possibility to improve this limit by increasing the observation time is discussed
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