排序方式: 共有23条查询结果,搜索用时 62 毫秒
1.
Dr. Zhengxing Qin Dr. Georgian Melinte Prof. Jean‐Pierre Gilson Prof. Maguy Jaber Prof. Krassimir Bozhilov Dr. Philippe Boullay Dr. Svetlana Mintova Prof. Ovidiu Ersen Dr. Valentin Valtchev 《Angewandte Chemie (International ed. in English)》2016,55(48):15049-15052
Zeolites are widely used in many commercial processes, mostly as catalysts or adsorbents. Understanding their intimate structure at the nanoscale is the key to control their properties and design the best materials for their ever increasing uses. Herein, we report a new and controllable fluoride treatment for the non‐discriminate extraction of zeolite framework cations. This sheds new light on the sub‐structure of commercially relevant zeolite crystals: they are segmented along defect zones exposing numerous nanometer‐sized crystalline domains, separated by low‐angle boundaries, in what were apparent single‐crystals. The concentration, morphology, and distribution of such domains analyzed by electron tomography indicate that this is a common phenomenon in zeolites, independent of their structure and chemical composition. This is a milestone to better understand their growth mechanism and rationally design superior catalysts and adsorbents. 相似文献
2.
Tutuc E Melinte S De Poortere EP Pillarisetty R Shayegan M 《Physical review letters》2003,91(7):076802
We study interacting GaAs hole bilayers in the limit of zero interlayer tunneling. When the layers have equal density, we observe a phase-coherent bilayer quantum Hall state (QHS) at a total filling factor nu=1, flanked by a reentrant insulating phase at nearby fillings which suggests the formation of a pinned, bilayer Wigner crystal. As we transfer charge from one layer to another, the phase-coherent QHS becomes stronger, evincing its robustness against charge imbalance, but the insulating phase disappears, suggesting that its stability requires the commensurability of the two layers. 相似文献
3.
Moldovan L Melinte S Bayot V Papadakis SJ De Poortere EP Shayegan M 《Physical review letters》2000,85(20):4369-4372
We report very low temperature ( T) thermopower and resistivity ( rho) measurements on variable-density, two-dimensional hole systems confined to GaAs quantum wells. As the hole density is lowered from 1.49x10(11) cm(-2) to 0.14x10(11) cm(-2), the system crosses from an insulating ( drho / dT less, similar0) to a metallic regime ( drho / dT>0) and finally displays insulating behavior ( drho / dT<0). Diffusion thermopower shows a striking sign reversal in a narrow range of density in the metallic regime, suggesting a qualitative change in the conduction or the scattering mechanism. 相似文献
4.
Dr. Georgian Melinte Dr. Veselina Georgieva Dr. Marie‐Anne Springuel‐Huet Dr. Andreï Nossov Prof. Ovidiu Ersen Dr. Flavien Guenneau Prof. Antoine Gedeon Dr. Ana Palčić Dr. Krassimir N. Bozhilov Dr. Cuong Pham‐Huu Prof. Shilun Qiu Dr. Svetlana Mintova Dr. Valentin Valtchev 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(50):18316-18327
The principle aspects and constraints of the dynamics and kinetics of zeolite nucleation in hydrogel systems are analyzed on the basis of a model Na‐rich aluminosilicate system. A detailed time‐series EMT‐type zeolite crystallization study in the model hydrogel system was performed to elucidate the topological and temporal aspects of zeolite nucleation. A comprehensive set of analytical tools and methods was employed to analyze the gel evolution and complement the primary methods of transmission electron microscopy (TEM) and nuclear magnetic resonance (NMR) spectroscopy. TEM tomography reveals that the initial gel particles exhibit a core–shell structure. Zeolite nucleation is topologically limited to this shell structure and the kinetics of nucleation is controlled by the shell integrity. The induction period extends to the moment when the shell is consumed and the bulk solution can react with the core of the gel particles. These new findings, in particular the importance of the gel particle shell in zeolite nucleation, can be used to control the growth process and properties of zeolites formed in hydrogels. 相似文献
5.
S. Faniel E. Tutuc E.P. De Poortere C. Gustin A. Vlad L. Moldovan S. Melinte M. Shayegan V. Bayot 《Physica E: Low-dimensional Systems and Nanostructures》2006,34(1-2):120
We report on low-temperature thermopower measurements of interacting GaAs bilayer hole systems in the limit of no interlayer tunneling. These systems exhibit a reentrant insulating phase near the many-body quantum Hall state (QHS) at total filling factor ν=1, when both layers have the same density. The diffusion thermopower is expected to diverge as T-1 in the presence of an energy gap (Wigner crystal) or to vanish in the case of a disordered induced mobility gap. Our results show that, as the temperature is decreased, the diffusion thermopower exhibits a T-1 dependence in the insulating phase around ν=1. This behavior clearly indicates the opening of an energy gap at low temperature, in agreement with the formation of a pinned Wigner solid. Finally, we report on the T-dependence of the thermopower at ν=1. 相似文献
6.
Dr. Artur Ciesielski Jürgen Weippert Dr. Artur Böttcher Yuyoung Shin Georgian Melinte Prof. Dr. Ovidiu Ersen Dr. Cinzia Casiraghi Prof. Dr. Xinliang Feng Prof. Dr. Klaus Müllen Prof. Dr. Manfred M. Kappes Prof. Dr. Paolo Samorì Dr. Marco Cecchini 《Chemphyschem》2016,17(3):352-357
Providing a quantitative understanding of the thermodynamics involved in molecular adsorption and self‐assembly at a nanostructured carbon material is of fundamental importance and finds outstanding applications in the graphene era. Here, we study the effect of edge perchlorination of coronene, which is a prototypical polyaromatic hydrocarbon, on the binding affinity for the basal planes of graphite. First, by comparing the desorption barrier of hydrogenated versus perchlorinated coronene measured by temperature‐programmed desorption, we quantify the enhancement of the strength of physisorption at the single‐molecule level though chlorine substitution. Then, by a thermodynamic analysis of the corresponding monolayers based on force‐field calculations and statistical mechanics, we show that perchlorination decreases the free energy of self‐assembly, not only enthalpically (by enhancing the strength of surface binding), but also entropically (by decreasing the surface concentration). The functional advantage of a chemically modulated 2D self‐assembly is demonstrated in the context of the molecule‐assisted liquid‐phase exfoliation of graphite into graphene. 相似文献
7.
Melinte Violeta Chibac Andreea Buruiana Tinca Hitruc Gabriela Buruiana Emil C. 《Journal of nanoparticle research》2015,17(10):1-15
Journal of Nanoparticle Research - Synthesis of yttrium oxide nanoparticles in a specially designed radio frequency thermal plasma reactor is reported. Good crystallinity, narrow size distribution,... 相似文献
8.
Dr. Georgian Melinte Dr. Veselina Georgieva Dr. Marie‐Anne Springuel‐Huet Dr. Andreï Nossov Prof. Ovidiu Ersen Dr. Flavien Guenneau Prof. Antoine Gedeon Dr. Ana Palčić Dr. Krassimir N. Bozhilov Dr. Cuong Pham‐Huu Prof. Shilun Qiu Dr. Svetlana Mintova Dr. Valentin Valtchev 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(6):1881-1881
9.
Preparation of photocrosslinked sol‐gel composites based on urethane‐acrylic matrix,silsesquioxane sequences,TiO2, and Ag/Au Nanoparticles for use in photocatalytic applications
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Andreea L. Chibac Violeta Melinte Tinca Buruiana Ionel Mangalagiu Emil C. Buruiana 《Journal of polymer science. Part A, Polymer chemistry》2015,53(10):1189-1204
An acid urethane oligodimethacrylate based on poly(ethylene glycol) was synthesized and used in the preparation of hybrid composites containing silsesquioxane sequences and titania domains formed through sol‐gel reactions along with silver/gold nanoparticles (Ag/Au NPs) in situ photogenerated during the UV‐curing process. The photopolymerization kinetics studied by Fourier transform infrared spectroscopy and photoDSC showed that the photoreactivity of the investigated formulations depends on the amount of titanium butoxide (5–20 wt %) added in the system subjected to UV irradiation. The introduction of 1 wt % AgNO3/AuBr3 in formulations slightly improved the degree of conversion but diminished the polymerization rates. The formation of hybrid materials comprising predominantly amorphous TiO2/SiO2 NPs, with or without Ag/Au NPs, was confirmed through specific analyses. The evaluation of photocatalytic activity demonstrated that the synthesized hybrid films are suitable for the complete removal of organic pollutants (phenolic compounds) from water under UV irradiation (200–350 min) at low intensity (found in the solar radiation). © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1189–1204 相似文献
10.
Andreea L. Chibac Violeta Melinte Tinca Buruiana Emil C. Buruiana 《Journal of polymer science. Part A, Polymer chemistry》2014,52(5):728-738
Urethane–urea dimethacrylates were synthesized and used in the preparation of nanocomposites containing gold nanoparticles (Au NPs) in situ photogenerated during the UV‐curing process in the absence of reducing agent. A study of the photopolymerization kinetics showed that the photoreactivity of the monomers alone or in combination with a dual urethane benzophenone (BP) macromer is dependent on the nature of photoinitiator (Irgacure819, BP/amine) and the formulation composition. It was found that the addition of 1 wt % AuBr3 in monomers slightly improved the polymerization rate and the degree of conversion. The formation of Au NPs into the network was confirmed through UV–vis, XRD, EDX, SAXS, and TEM analyses, the last indicating the existence of NPs with size around 8.5 nm and spherical/triangle shapes. On addition of 10 wt % 2[N‐methacryloyloxyethyl‐(N'‐2‐thioethyl)] (urea) in formulation, the Au NPs (200 nm) became predominantly cubic/hexagonal in shape. The composite films emit fluorescence at 575 nm, and this property could be exploited in the field of fluorescent bio/sensors. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 728–738 相似文献