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Pump−probe experiments at the TEMPO beamline using the low‐α operation mode of Synchrotron SOLEIL 下载免费PDF全文
Mathieu G. Silly Tom Ferté Marie Agnes Tordeux Debora Pierucci Nathan Beaulieu Christian Chauvet Federico Pressacco Fausto Sirotti Horia Popescu Victor Lopez-Flores Marina Tortarolo Maurizio Sacchi Nicolas Jaouen Philippe Hollander Jean Paul Ricaud Nicolas Bergeard Christine Boeglin Bharati Tudu Renaud Delaunay Jan Luning Gregory Malinowski Michel Hehn Cédric Baumier Franck Fortuna Damjan Krizmancic Luigi Stebel Rudi Sergo Giuseppe Cautero 《Journal of synchrotron radiation》2017,24(4):886-897
The SOLEIL synchrotron radiation source is regularly operated in special filling modes dedicated to pump–probe experiments. Among others, the low‐α mode operation is characterized by shorter pulse duration and represents the natural bridge between 50 ps synchrotron pulses and femtosecond experiments. Here, the capabilities in low‐α mode of the experimental set‐ups developed at the TEMPO beamline to perform pump–probe experiments with soft X‐rays based on photoelectron or photon detection are presented. A 282 kHz repetition‐rate femtosecond laser is synchronized with the synchrotron radiation time structure to induce fast electronic and/or magnetic excitations. Detection is performed using a two‐dimensional space resolution plus time resolution detector based on microchannel plates equipped with a delay line. Results of time‐resolved photoelectron spectroscopy, circular dichroism and magnetic scattering experiments are reported, and their respective advantages and limitations in the framework of high‐time‐resolution pump–probe experiments compared and discussed. 相似文献
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Naturally occurring saponins are attractive candidates or lead compounds for new drug design and development and thus have become important synthetic targets. This short account reviews the recent progress in the chemical synthesis and structure-activity relationship (SAR) studies of naturally occurring saponins and their derivatives. 相似文献
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Dr. Xiulin Fan Dr. Fei Wang Dr. Xiao Ji Ruixing Wang Dr. Tao Gao Singyuk Hou Dr. Ji Chen Tao Deng Dr. Xiaogang Li Dr. Long Chen Dr. Chao Luo Luning Wang Prof. Chunsheng Wang 《Angewandte Chemie (International ed. in English)》2018,57(24):7146-7150
Low‐cost multivalent battery chemistries (Mg2+, Al3+) have been extensively investigated for large‐scale energy storage applications. However, their commercialization is plagued by the poor power density and cycle life of cathodes. A universal polyimides@CNT (PI@CNT) cathode is now presented that can reversibly store various cations with different valences (Li+, Mg2+, Al3+) at an extremely fast rate. The ion‐coordination charge storage mechanism of PI@CNT is systemically investigated. Full cells using PI@CNT cathodes and corresponding metal anodes exhibit long cycle life (>10000 cycles), fast kinetics (>20 C), and wide operating temperature range (?40 to 50 °C), making the low‐cost industrial polyimides universal cathodes for different multivalent metal batteries. The stable ion‐coordinated mechanism opens a new foundation for the development of high‐energy and high‐power multivalent batteries. 相似文献
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The problem of determining the motion of a rotating inextensible string of length l, free at one end and fixed at the other can, under certain assumptions, be treated by solving a non-linear boundary value problem. p]In this paper, two Picard-type iterative schemes are constructed and the sequences generated are proved to converge to a positive solution of that non-linear boundary value problem. Additionally, one sequence converges to the solution from above, the other from below. Moreover, the iterative scheme can be used to solve the inverse problem of determining the angular velocity of the rotating string, given two observations (at one point in time) of position of the string. 相似文献
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Marie Labat Jean-Blaise Brubach Alessandra Ciavardini Marie-Emmanuelle Couprie Erik Elkaim Pierre Fertey Tom Ferte Philippe Hollander Nicolas Hubert Emmanuelle Jal Claire Laulhé Jan Luning Olivier Marcouillé Thierry Moreno Paul Morin Francois Polack Pascale Prigent Sylvain Ravy Jean-Paul Ricaud Pascale Roy Mathieu Silly Fausto Sirotti Amina Taleb Marie-Agnès Tordeux Amor Nadji 《Journal of synchrotron radiation》2018,25(2):385-398
The investigation of ultrafast dynamics, taking place on the few to sub‐picosecond time scale, is today a very active research area pursued in a variety of scientific domains. With the recent advent of X‐ray free‐electron lasers (XFELs), providing very intense X‐ray pulses of duration as short as a few femtoseconds, this research field has gained further momentum. As a consequence, the demand for access strongly exceeds the capacity of the very few XFEL facilities existing worldwide. This situation motivates the development of alternative sub‐picosecond pulsed X‐ray sources among which femtoslicing facilities at synchrotron radiation storage rings are standing out due to their tunability over an extended photon energy range and their high stability. Following the success of the femtoslicing installations at ALS, BESSY‐II, SLS and UVSOR, SOLEIL decided to implement a femtoslicing facility. Several challenges were faced, including operation at the highest electron beam energy ever, and achievement of slice separation exclusively with the natural dispersion function of the storage ring. SOLEIL's setup also enables, for the first time, delivering sub‐picosecond pulses simultaneously to several beamlines. This last feature enlarges the experimental capabilities of the facility, which covers the soft and hard X‐ray photon energy range. In this paper, the commissioning of this original femtoslicing facility is reported. Furthermore, it is shown that the slicing‐induced THz signal can be used to derive a quantitative estimate for the degree of energy exchange between the femtosecond infrared laser pulse and the circulating electron bunch. 相似文献
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We have employed 800 nm 150 fs laser pulses to carry out photoionization (PI) time-of-flight mass spectrometric detection
of intermediates following corona discharges on aromatic molecules (alkylbenzenes and pyridine) in He, stabilized by subsequent
supersonic gas expansions. Observed product peaks appear to be at least roughly in proportion to actual number densities;
PI induced fragmentation of parent ions appears not to be excessive. Consequently, 800 nm fs PI should be useful for general
product analysis applications in plasma chemistry. For most alkylbenzenes subjected to corona discharges in rare gas, the
overall trends in product chemistry are similar in many respects to observed flame and pyrolysis chemistry in rare gases for
the same species. Following discharge, as in those other cases, H deficient carbon radical fragments initially produced react
in turn to form larger aromatic species. However, compared with flame/pyrolysis, discharge produced a larger number of fragment
species, which can lead to a wider and somewhat different range of higher mass aromatic products. Co-addition of even a small
component of O2 to the discharge mixes has a potent effect in inhibiting formation of higher mass aromatic products in alkylbenzenes. 相似文献
10.
Luning Tian Hanping Chen Zhenhui Chen Xianhua Wang Shihong Zhang 《Journal of Thermal Analysis and Calorimetry》2014,115(1):45-53
The non-isothermal experiments of limestone decomposition at multi-heating rates in O2/N2 and O2/CO2 atmospheres were studied using thermogravimetry. The limestone decomposition kinetic model function, kinetic parameters of apparent activation energy (E), and pre-exponential factor (A) were evaluated by Bagchi and Malek method. The results shown that in 20 % O2/80 % N2 atmosphere, the limestone decomposed slowly following the contracting sphere volume model controlled by boundary reaction (spherical symmetry) in two stages, and the E increased by about 50 kJ mol?1 in the second decomposition stage. But in 20 % O2/80 % CO2 atmosphere, the presence of high-concentration CO2 significantly inhibited the limestone decomposition, and made the decomposition process occur at high temperature with a rapid rate; the decomposition kinetics was divided into three stages, the first stage was an accelerated decomposition process following the Mampel Power law model with the exponential law equation, the second stage followed the nth order chemical reaction model as an α–t deceleration process, and the third stage belonged to the random nucleation and nuclei growth model with the Avrami–Erofeev equation. And with the heating rate increasing, the reaction order n showed a slight rise tendency. The E was about 1,245 kJ mol?1 in 20 % O2/80 % CO2 atmosphere, but was only about 175 kJ mol?1 in 20 % O2/80 % N2 atmosphere. The E and A increased markedly in the O2/CO2 atmosphere. 相似文献