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11.
Tuning the phase transition of ZnO thin films through lithography: an integrated bottom‐up and top‐down processing
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Luca Malfatti Alessandra Pinna Stefano Enzo Paolo Falcaro Benedetta Marmiroli Plinio Innocenzi 《Journal of synchrotron radiation》2015,22(1):165-171
An innovative approach towards the physico‐chemical tailoring of zinc oxide thin films is reported. The films have been deposited by liquid phase using the sol–gel method and then exposed to hard X‐rays, provided by a synchrotron storage ring, for lithography. The use of surfactant and chelating agents in the sol allows easy‐to‐pattern films made by an organic–inorganic matrix to be deposited. The exposure to hard X‐rays strongly affects the nucleation and growth of crystalline ZnO, triggering the formation of two intermediate phases before obtaining a wurtzite‐like structure. At the same time, X‐ray lithography allows for a fast patterning of the coatings enabling microfabrication for sensing and arrays technology. 相似文献
12.
Plinio Innocenzi Tongjit Kidchob Luca Malfatti Stefano Costacurta Masahide Takahashi Massimo Piccinini Augusto Marcelli 《Journal of Sol-Gel Science and Technology》2008,48(1-2):253-259
Sol–gel processing of thin films involves time dependent phenomena which are basically driven by solvent evaporation. An example is evaporation induced self-assembly that is used to prepare mesoporous ordered films through self-organization of templating micelles. The possibility to follow in situ as a function of time the evolution of the system can give a better knowledge of the process and the physics and chemistry beneath. Time-resolved infrared techniques have been applied to different sol–gel systems to study time-dependent phenomena, in particular rapid scan time resolved infrared spectroscopy has been used to monitor in situ the process and as a tool to design the sol–gel synthesis. 相似文献
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14.
Mazaj M Costacurta S Zabukovec Logar N Mali G Novak Tusar N Innocenzi P Malfatti L Thibault-Starzyk F Amenitsch H Kaucic V Soler-Illia GJ 《Langmuir : the ACS journal of surfaces and colloids》2008,24(12):6220-6225
Mesoporous aluminophosphate thin films with 3D cubic (Im3m) pore arrangement were synthesized for the first time. Thin films were templated with block copolymer nonionic templates Pluronic F127 and F108 and deposited on a glass substrate by dip-coating. In situ SAXS investigations show the formation of a highly ordered mesostructure upon the dip-coating process, which remains stable up to at least 670 K. A cubic mesostructure was observed also by TEM. Template removal process was monitored by TG and FT-IR. A transition from an amorphous aluminophosphate gel to a well-defined aluminophosphate framework was observed by MAS NMR. 相似文献
15.
Ciprian Demeter Francesco Di Plinio 《Journal of Fourier Analysis and Applications》2013,19(4):836-856
It is a result by Lacey and Thiele (Ann. of Math. (2) 146(3):693–724, 1997; ibid. 149(2):475–496, 1999) that the bilinear Hilbert transform maps $L^{p_{1}}(\mathbb{R}) \times L^{p_{2}}(\mathbb{R}) $ into $L^{p_{3}}(\mathbb{R})$ whenever (p 1,p 2,p 3) is a Hölder tuple with p 1,p 2>1 and $p_{3}>\frac{2}{3}$ . We study the behavior of the quartile operator, which is the Walsh model for the bilinear Hilbert transform, when $p_{3}=\frac{2}{3}$ . We show that the quartile operator maps $L^{p_{1}}(\mathbb{R}) \times L^{p_{2}}(\mathbb{R}) $ into $L^{\frac{2}{3},\infty}(\mathbb{R})$ when p 1,p 2>1 and one component is restricted to subindicator functions. As a corollary, we derive that the quartile operator maps $L^{p_{1}}(\mathbb{R}) \times L^{p_{2},\frac{2}{3}}(\mathbb{R}) $ into $L^{\frac{2}{3},\infty}(\mathbb{R})$ . We also provide weak type estimates and boundedness on Orlicz-Lorentz spaces near p 1=1,p 2=2 which improve, in the Walsh case, the results of Bilyk and Grafakos (J. Geom. Anal. 16 (4):563–584, 2006) and Carro et al. (J. Math. Anal. Appl. 357(2):479–497, 2009). Our main tool is the multi-frequency Calderón-Zygmund decomposition from (Nazarov et al. in Math. Res. Lett. 17(3):529–545, 2010). 相似文献
16.
Mesoporous films containing organic or biological functions within an organised array of cavities are produced by combining sol-gel, self-assembly of supramolecular templates and surface chemistry. This paper reviews the essential physics and chemical concepts behind the synthesis of these complex multifunctional materials. 相似文献
17.
Journal of Sol-Gel Science and Technology - 相似文献
18.
Signorini Raffaella Meneghetti Moreno Bozio Renato Brusatin Giovanna Innocenzi Plinio Guglielmi Massimo Negra Federico Della 《Journal of Sol-Gel Science and Technology》2001,22(3):245-253
Hybrid organic-inorganic materials are investigated as suitable materials for inclusion of fullerene derivatives and for fabrication of laser protection devices. A specific synthesis has been developed in order to optimize non-linear optical performances of fullerene derivatives. 3-glicydoxypropyltrymethoxysilane has been used as an inorganic and organic network former to obtain the host material. The sol-gel synthesis consists of the hydrolysis and condensation in acidic conditions of the inorganic network. Epoxy polymerization has been achieved by using zirconium or BF3 alkoxides precursors. Bulk and multilayer materials doped with a fullerene derivative have been fabricated. They show good optical requirements: high fullerenes concentration, high microstructural homogeneity, high laser damage threshold and high optical limiting efficiency. Optical limiting (OL) mechanisms have been investigated. The most effective in the sol-gel materials is the reverse saturable absorption (RSA) one. However, different mechanisms, like non-linear (NL) scattering and NL refraction contribute to a different extent. Open- and closed-aperture OL and z-scan measurements on sol-gel samples show the contribution of NL scattering and NL refraction at 690 nm. Laser damage threshold has been characterized as a function of the structure of the samples and of the optical configurations (f/66 and f/5). 相似文献
19.
Luigi Stagi;Luca Malfatti;Alessia Zollo;Stefano Livraghi;Davide Carboni;Daniele Chiriu;Riccardo Corpino;Pier Carlo Ricci;Antonio Cappai;Carlo Maria Carbonaro;Stefano Enzo;Abbas Khaleel;Abdulmuizz Adamson;Christel Gervais;Andrea Falqui;Plinio Innocenzi; 《Advanced Optical Materials》2024,12(13):2302682
The phosphorescence of boric acid (BA, H3BO3) at room temperature is a puzzling phenomenon subject to controversial interpretations although the role of structural defects has not yet been considered. Heat treatments of boric acid cause its transformation into the metaboric phase and amorphous boron oxide (B2O3). The structural changes after thermal processing can create defects that become centers of luminescence and recombination channels in the visible range. In the present work, commercial boric acid is thermally processed at different temperatures. Samples treated between 200 and 400 °C exhibit remarkable phosphorescence in the visible range. At ≈480 and 528 nm, two distinct phosphorescent emissions occur, associated with trapped charge carriers recombinations identified by thermoluminescence (TL) and electron paramagnetic resonance spectroscopy (EPR). The structural and optical studies suggest that the activation of boric acid phosphorescence after heat treatment is correlated with the presence of defects. The afterglow results from a trapping and detrapping process, which delays the recombination at the active optical centers. Time-dependent density functional study (DFT) of defective BOH molecules and clusters shows the emergence of near UV and blue optical transitions in absorption. These defects trigger the photoluminescence in thermally processed boric acid samples. 相似文献
20.
Augusto Marcelli Wei Xu Dariush Hampai Luca Malfatti Plinio Innocenzi Ulrich Schade Ziyu Wu 《Analytical and bioanalytical chemistry》2010,397(6):2095-2108
Many physical/chemical processes such as metal–insulator transitions or self-assembly phenomena involve correlated changes
of electronic and atomic structure in a wide time range from microseconds to minutes. To investigate these dynamic processes
we not only need a highly brilliant photon source in order to achieve high spatial and time resolution but new experimental
methods have to be implemented. Here we present a new optical layout for performing simultaneous or concurrent infrared and
X-ray measurements. This approach may indeed return unique information for example the interplay between structural changes
and chemical processes occurring in the investigated sample. A beamline combining two X-ray and IR beams may really take advantage
of the unique synchrotron radiation properties: the high brilliance and the broad spectrum. In this contribution we will describe
the conceptual layout and the expected performance of a complex system designed to collect IR and X-ray radiation from the
same bending magnet on a third-generation synchrotron radiation ring. If realized, this beamline will enable time-resolved
spectroscopy experiments offering new scientific opportunities at the frontiers of science. 相似文献