ORCID Profile
0000-0001-5971-4292
Current Organisations
CNRS
,
Universität Wien
Does something not look right? The information on this page has been harvested from data sources that may not be up to date. We continue to work with information providers to improve coverage and quality. To report an issue, use the Feedback Form.
Publisher: Wiley
Date: 15-01-2013
Publisher: Springer Science and Business Media LLC
Date: 23-01-2019
DOI: 10.1038/S41598-018-36828-9
Abstract: We demonstrate for the first time the direct stereolithographic 3D printing of an extrinsically self-healing composite, comprised of commercial photocurable resin modified with anisole and PMMA-filled microcapsules. The composites demonstrate solvent-welding based autonomous self-healing to afford 87% recovery of the initial critical toughness. This work illustrates the potential of stereolithographic printing to fabricate self-healing composites with user-defined structures, avoiding the need for extensive rheological optimization of printing inks, like in direct-write 3D printing. Importantly, this work also demonstrates the inclusion of microcapsules into 3D printing resins to incorporate additional functionality into printed composites, which could be adapted for applications beyond self-healing materials.
Publisher: DE GRUYTER
Date: 31-12-2014
Publisher: Wiley
Date: 20-04-2015
Publisher: Royal Society of Chemistry (RSC)
Date: 2011
DOI: 10.1039/C1CC13867G
Abstract: We report here on an efficient one-step-impregnation method to synthesize crystalline mesoporous bimetal oxides (e.g. NiFe(2)O(4), CuFe(2)O(4), Cu/CeO(2)) using mesoporous silicas as hard templates under optimized mixing conditions. This new procedure enables a true replication of the mesostructure with high yield and phase purity, while retaining particle morphology of the template.
Publisher: American Chemical Society (ACS)
Date: 03-05-2010
DOI: 10.1021/JP909836V
Publisher: Elsevier BV
Date: 2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C5NJ03466C
Abstract: The first successful ex le of Hg porosimetry on KIT-6 silicas is demonstrated. This study provides a more thorough understanding of the textural properties of the mesostructures of KIT-6 and SBA-15 silicas.
Publisher: Elsevier
Date: 2008
Publisher: Elsevier BV
Date: 04-2015
Publisher: Wiley
Date: 20-10-2011
Publisher: IOP Publishing
Date: 20-10-2014
Publisher: Royal Society of Chemistry (RSC)
Date: 2010
DOI: 10.1039/B9NJ00478E
Publisher: No publisher found
DOI: 10.1515/SPARK.28.8
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C6CS00391E
Abstract: This review focuses on important aspects of applying physisorption for the pore structural characterization of hierarchical materials such as mesoporous zeolites.
Publisher: American Chemical Society (ACS)
Date: 04-02-2013
DOI: 10.1021/IC3020223
Abstract: A luminescent triarylboron ligand functionalized with three carboxylic groups has been synthesized and fully characterized. Its use in boron-containing metal-organic frameworks (B-MOFs) has been demonstrated by the synthesis and isolation of a Zn(II)B-MOF compound (B-MOF-1). The crystals of B-MOF-1 belong to the cubic space group F432 with 8-fold interpenetrated networks and ∼21% void space. B-MOF-1 exhibits blue fluorescence and is capable of modest gas sorption of N(2), argon, and CO(2).
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3DT33000A
Abstract: Two novel Co-based metal-organic frameworks (MOFs) were synthesised and characterised using an asymmetrically binding ligand, 4-(4'-carboxyphenyl)-1,2,4 triazole (Hcpt). The isolated [Co3(II)(μ3-O)(OH)(cpt)3(H2O)2]n·xH2O·yDMF, Co-MOF1, exhibits a rhombohedral crystal structure (space group, P63/mc), with a trinuclear cobalt core that resembles the MIL88 series. This MOF shows paramagnetic behaviour down to 2 K with no saturation of magnetisation up to 7 T. This is presumably due to a geometrically frustrated triangular arrangement of Co spins. The two-dimensional complex, [Co(II)(cpt)(N3)]n, Co-MOF2, crystallises in a monoclinic crystal system (space group, C2/m). The magnetic measurements reveal metamagnetic behaviour for this complex with a critical field in the range of 700-1000 Oe.
Publisher: American Chemical Society (ACS)
Date: 05-08-2019
DOI: 10.1021/JACS.9B06320
Abstract: Alignment of metal-organic framework (MOF) crystals has previously been performed via careful control of oriented MOF growth on substrates, as well as by dynamic magnetic alignment. We show here that bromobenzene-suspended microrod crystals of the MOF NU-1000 can also be dynamically aligned via electric fields, giving rise to rapid electrooptical responses. This method of dynamic MOF alignment opens up new avenues of MOF control which are important for integration of MOFs into switchable electronic devices as well as in other applications such as reconfigurable sensors or optical systems.
Publisher: Elsevier BV
Date: 2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C2CP22523A
Abstract: The thermoresponsive polymer poly-N-isopropylacrylamide (PNIPAAM) was grafted in mesoporous SBA-15 silica. The grafting process consists of three steps: (i) increasing the amount of surface silanol groups of SBA-15 by hydroxylation, (ii) attachment of an anchor (1-(trichlorosilyl)-2-(m -(chloromethylphenyl)ethane) and finally (iii) the polymerization of the monomers (NIPAAM) onto the anchor. After each step, the materials were characterized regarding the porosity, using inert gas (argon, nitrogen) physisorption measurements. Also, the structure was investigated by small-angle X-ray diffraction analysis and thermogravimetric analysis was used for determination of the amount of grafted material. A total of 17% by weight of organic material was introduced in the porous host and the structure was preserved during the grafting process. Physisorption measurements revealed that the anchor is mainly located in the intrawall pores present in SBA-15. Consequently, the polymer is preferentially located in the intrawall pores or in the vicinity thereof. The final mesopore volume is 0.47 cm(3) g(-1) as compared to 0.96 cm(3) g(-1) for the pure SBA-15. The surprisingly large loss of mesopore volume and an almost constant mesopore diameter is consistent with a partial sealing of the mesopore volume in the composite materials. The potential thermocontrol combined with the large mesoporosity and the possible "storage space" provided by the sealed mesopore volume leads to a material with possibilities for various applications.
Publisher: Wiley
Date: 26-02-2018
Abstract: The term "engineered zeolitic materials" refers to a class of materials with a rationally designed pore system and active-sites distribution. They are primarily made of crystalline microporous zeolites as the main building blocks, which can be accompanied by other secondary components to form composite materials. These materials are of potential importance in many industrial fields like catalysis or selective adsorption. Herein, critical aspects related to the synthesis and modification of such materials are discussed. The first section provides a short introduction on classical zeolite structures and properties, and their conventional synthesis methods. Then, the motivating rationale behind the growing demand for structural alteration of these zeolitic materials is discussed, with an emphasis on the ongoing struggles regarding mass-transfer issues. The state-of-the-art techniques that are currently available for overcoming these hurdles are reviewed. Following this, the focus is set on core-shell composites as one of the promising pathways toward the creation of a new generation of highly versatile and efficient engineered zeolitic substances. The synthesis approaches developed thus far to make zeolitic core-shell materials and their analogues, yolk-shell, and hollow materials, are also examined and summarized. Finally, the last section concisely reviews the performance of novel core-shell, yolk-shell, and hollow zeolitic materials for some important industrial applications.
Publisher: American Chemical Society (ACS)
Date: 17-12-2018
Publisher: Elsevier BV
Date: 11-2020
Publisher: American Chemical Society (ACS)
Date: 17-01-2018
DOI: 10.1021/ACS.LANGMUIR.7B03769
Abstract: Carbon dioxide was shown to identify surface basic properties of nitrogen-substituted microporous and mesoporous silicas, in addition to conventional basic oxides, by a detailed study using isotherm and heat of adsorption measurements as well as by infrared spectroscopy. A hydrogen-bonded weak interaction was primarily observed between CO
Publisher: Wiley
Date: 06-03-2012
Publisher: American Chemical Society (ACS)
Date: 14-05-2020
Publisher: Elsevier BV
Date: 12-2012
Publisher: Wiley
Date: 16-01-2013
Publisher: Elsevier BV
Date: 2016
Publisher: Elsevier BV
Date: 04-2014
Publisher: Elsevier BV
Date: 05-2016
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C8CC10018G
Abstract: Highly catalytic 3D printed UiO-66 composite affords ease of use and clean-up for degradation of nerve agent simulant.
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3NR02969G
Abstract: Mesoporous silica nanoparticles (MSNs) are used in drug delivery and cell tracking applications. As Mn(2+) is already implemented as a "positive" cell contrast agent in preclinical imaging procedures (in the form of MnCl2 for neurological studies), the introduction of Mn in the porous network of MSNs would allow labelling cells and tracking them using MRI. These particles are in general internalized in endosomes, an acidic environment with high saline concentration. In addition, the available MSN porosity could also serve as a carrier to deliver medical/therapeutic substances through the labelled cells. In the present study, manganese oxide was introduced in the porous network of MCM-48 silica nanoparticles (Mn-M48SNs). The particles exhibit a narrow size distribution (~140 nm diam.) and high porosity (~60% vol.), which was validated after insertion of Mn. The resulting Mn-M48SNs were characterized by TEM, N2 physisorption, and XRD. Evidence was found with H2-TPR, and XPS characterization, that Mn(II) is the main oxidation state of the paramagnetic species after suspension in water, most probably in the form of Mn-OOH. The colloidal stability as a function of time was confirmed by DLS in water, acetate buffer and cell culture medium. In NMR data, no significant evidence of Mn(2+) leaching was found in Mn-M48SNs in acidic water (pH 6), up to 96 hours after suspension. High longitudinal relaxivity values of r1 = 8.4 mM(-1) s(-1) were measured at 60 MHz and 37 °C, with the lowest relaxometric ratios (r2/r1 = 2) reported to date for a Mn-MSN system. Leukaemia cells (P388) were labelled with Mn-M48SNs and nanoparticle cell internalization was confirmed by TEM. Finally, MRI contrast enhancement provided by cell labelling with escalated incubation concentrations of Mn-M48SNs was quantified at 1 T. This study confirmed the possibility of efficiently confining Mn into M48SNs using incipient wetness, while maintaining an open porosity and relatively high pore volume. Because these Mn-labelled M48SNs express strong "positive" contrast media properties at low concentrations, they are potentially applicable for cell tracking and drug delivery methodologies.
Publisher: Wiley
Date: 08-03-2011
Abstract: The influence of pore surface functionalities in mesoporous SBA-15 silica on the stability of a model olefin metathesis catalyst, namely Grubbs I, is substantiated. In particular, it is demonstrated that the nature of the interaction between the ruthenium complex and the surface is strongly depending on the presence of surface silanols. For this study, differently functionalized mesoporous SBA-15 silica materials were synthesized according to standard procedures and, subsequently, the Grubbs I catalyst was incorporated into these different host materials. All of the materials were thoroughly characterized by elemental analyses, nitrogen physisorption at -196 °C, thermogravimetric analyses, solid-state NMR spectroscopy, and infrared spectroscopy (ATR-IR). By such in-depth characterization of the materials, it became possible to achieve models for the surface/catalyst interactions as a function of surface functionalities in SBA-15 for ex le, in the case of purely siliceous silanol-rich SBA-15, octenyl-silane modified SBA-15, and silylated equivalents. It was evidenced that large portions of the chemisorbed species that are detected spectroscopically arise from interactions between the tricyclohexylphosphine and the surface silanols. A catalytic study using diethyldiallylmalonate in presence of the various functionalized silicas shows that the presence of surface silanols significantly decreases the longevity of the ring-closing metathesis catalyst, whereas the passivation of the surface by trimethylsilyl groups slows down the catalysis rate, but does not affect significantly the lifetime of the catalyst. This contribution thus provides new insights into the functionalization of SBA-15 materials and the role of surface interactions for the grafting of organometallic complexes.
Publisher: American Chemical Society (ACS)
Date: 27-10-2017
Publisher: MDPI AG
Date: 11-08-2019
DOI: 10.3390/INORGANICS7080098
Abstract: Catalyzed oxygen evolution and oxygen reduction reactions (OER and ORR, respectively) are of particular significance in many energy conversion and storage processes. During the last decade, they emerged as potential routes to sustain the ever-growing needs of the future clean energy market. Unfortunately, the state-of-the-art OER and ORR electrocatalysts, which are based on noble metals, are noticeably limited by a generally high activity towards one type of reaction only, high costs and relatively low abundance. Therefore, the development of (bi)functional low-cost non-noble metal or metal-free electrocatalysts is expected to increase the practical energy density and drastically reduce the production costs. Owing to their pore properties and high surface areas, mesoporous materials show high activity towards electrochemical reactions. Among all synthesis methods available for the synthesis of non-noble mesoporous metal oxides, the hard-templating (or nanocasting) approach is one of the most attractive in terms of achieving variable morphology and porosity of the materials. In this review, we thus focus on the recent advances in the design, synthesis, characterization and efficiency of non-noble metal OER and ORR electrocatalysts obtained via the nanocasting route. Critical aspects of these materials and perspectives for future developments are also discussed.
Publisher: No publisher found
No related grants have been discovered for Remy Guillet-Nicolas.