全文获取类型
收费全文 | 20350篇 |
免费 | 3028篇 |
国内免费 | 2095篇 |
专业分类
化学 | 11505篇 |
晶体学 | 194篇 |
力学 | 821篇 |
综合类 | 72篇 |
数学 | 1543篇 |
物理学 | 5535篇 |
无线电 | 5803篇 |
出版年
2024年 | 63篇 |
2023年 | 515篇 |
2022年 | 523篇 |
2021年 | 742篇 |
2020年 | 765篇 |
2019年 | 763篇 |
2018年 | 681篇 |
2017年 | 640篇 |
2016年 | 871篇 |
2015年 | 924篇 |
2014年 | 1169篇 |
2013年 | 1462篇 |
2012年 | 1671篇 |
2011年 | 1805篇 |
2010年 | 1303篇 |
2009年 | 1205篇 |
2008年 | 1394篇 |
2007年 | 1277篇 |
2006年 | 1123篇 |
2005年 | 980篇 |
2004年 | 717篇 |
2003年 | 633篇 |
2002年 | 576篇 |
2001年 | 485篇 |
2000年 | 436篇 |
1999年 | 381篇 |
1998年 | 325篇 |
1997年 | 287篇 |
1996年 | 247篇 |
1995年 | 223篇 |
1994年 | 253篇 |
1993年 | 178篇 |
1992年 | 160篇 |
1991年 | 130篇 |
1990年 | 116篇 |
1989年 | 95篇 |
1988年 | 64篇 |
1987年 | 42篇 |
1986年 | 43篇 |
1985年 | 38篇 |
1984年 | 30篇 |
1983年 | 18篇 |
1982年 | 20篇 |
1981年 | 10篇 |
1980年 | 19篇 |
1979年 | 8篇 |
1976年 | 10篇 |
1975年 | 7篇 |
1974年 | 8篇 |
1973年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 226 毫秒
961.
Bilal Ahmed Seung-Bok Lee Rak-Hyun Song Jong-Won Lee Tak-Hyoung Lim Seok-Joo Park 《Journal of Solid State Electrochemistry》2014,18(2):435-443
(La0.8Sr0.2)0.95MnO3?δ (LSM)–Gd0.1Ce0.9O2?δ (gadolinium-doped ceria, GDC) composite cathode material was developed and characterized in terms of chemical stability, sintering behaviour, electrical conductivity, mechanical strength and microstructures to assess its feasibility as cathode support applications in cathode-supported fuel cell configurations. The sintering inhibition effect of LSM, in the presence of GDC, was observed and clearly demonstrated. The mechanical characterization of developed composites revealed that fracture behaviour is directly affected by pore size distribution. The Weibull strength distribution showed that for bimodal pore size distribution, two different fracture rates were present. Furthermore, the contiguity of LSM and GDC grains was calculated with image analysis, and correlation of microstructural features with mechanical and electrical properties was established. Subsequently, an LSM/GDC-based cathode-supported direct carbon fuel cell (DCFC) with Ni/ScSZ (scandia-stabilised zirconia) anode was successfully fabricated via slurry coating and co-firing techniques. The microstructures of electrodes and electrolyte layers were observed to confirm the desired morphology after co-sintering, and a single cell was electrochemically characterized in solid oxide fuel cell (SOFC) and DCFC mode with ambient air as oxidant. The higher values of open-circuit voltage indicated that the electrolyte layer prepared by vacuum slurry coating is dense enough. The corresponding peak power densities at 850 °C were 450 and 225 mW cm?2 in SOFC and DCFC mode, respectively. Electrochemical impedance spectroscopy was carried out to observe electrode polarization and ohmic resistance. 相似文献
962.
Vinod Mathew Jihyeon Gim Eunjoung Kim Muhammad Hilmy Alfaruqi Jinju Song Docheon Ahn Won Bin Im Younkee Paik Jaekook Kim 《Journal of Solid State Electrochemistry》2014,18(6):1557-1567
In the present study, carbon-coated lithium iron phosphate (LiFePO4/C) is prepared directly by a polyol-assisted pyro-synthesis performed under reaction times of a few seconds in open-air conditions. The polyol solvent, tetraethylene glycol (TTEG), acts as a low-cost fuel to facilitate combustion and the released exothermic energy promotes the nucleation and growth processes of the olivine nanoparticles. In addition, phosphoric acid (used as the phosphorous source) acts as a catalyst to accelerate polyol carbonization. The structure analysis of the as-prepared LiFePO4/C using X-ray, neutron diffraction and 7Li NMR studies suggested the efficacy of the rapid technique to produce highly crystalline phase-pure olivine nanocrystals. The electron microscopy and particle-size distribution studies revealed that the average particle diameters lie below 100 nm and confirmed the presence of a surface carbon layer of 2–3 nm thickness. The thermal and elemental studies indicated that the carbon content in the sample was approximately 5 %. The prepared LiFePO4/C cathode delivered capacities of 162 mA h g-1 at 0.1 °C rates with impressive capacity retention for extended cycling. The polyol-assisted pyro-synthesis, which evades the use of external energy sources, is not only a straightforward, simple and timely approach but also offers opportunities for large-scale LiFePO4/C production. 相似文献
963.
Qunfang Gui Dongliang Yu Shaoyu Zhang Huapeng Xiao Chunyan Yang Ye Song Xufei Zhu 《Journal of Solid State Electrochemistry》2014,18(1):141-148
The nanostructure of self-ordered porous anodic TiO2 nanotubes (PATNTs) has extraordinary influence on their physical and chemical properties. For this reason, extensive attention has been paid on pulse anodization to regulate the nanostructure of PATNT. However, the relationships between the nanostructures and current curves still remain unclear. Based on the traditional potentiostatic and pulse anodizations, five different modes (i.e., potentiostatic, pulse, triangle wave, decrease, and increase step by step) of applied voltage and their influences on the nanostructures of PATNT have been investigated in detail. The growing rates of the nanotubes anodized under five different modes were compared for the first time. The results show that the growing rate of pulse voltage anodization is the fastest, reaching 116.4 nm min?1. The slowest is triangle wave voltage anodization, only 59.3 nm min?1. When the applied voltage decreases step-by-step, branched nanotubes can be formed in the bottom of PATNT. Yet, when the applied voltage increases step-by-step, triple-layer nanotubes with different diameters are formed, and the forming mechanism of this special nanostructure is discussed. The present results may be helpful to understand the mechanism of PATNT and facilitate the assembling diverse nanostructures for extensive applications in photocatalysis, dye-sensitized solar cells, and biomedical devices. 相似文献
964.
Tunable Oxygen Activation for Catalytic Organic Oxidation: Schottky Junction versus Plasmonic Effects
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Ming Gong Shan Zhou Jiahua Hu Min Zhi Yang You Song Bai Prof. Jun Jiang Prof. Qun Zhang Prof. Xiaojun Wu Prof. Yujie Xiong 《Angewandte Chemie (International ed. in English)》2014,53(12):3205-3209
The charge state of the Pd surface is a critical parameter in terms of the ability of Pd nanocrystals to activate O2 to generate a species that behaves like singlet O2 both chemically and physically. Motivated by this finding, we designed a metal–semiconductor hybrid system in which Pd nanocrystals enclosed by {100} facets are deposited on TiO2 supports. Driven by the Schottky junction, the TiO2 supports can provide electrons for metal catalysts under illumination by appropriate light. Further examination by ultrafast spectroscopy revealed that the plasmonics of Pd may force a large number of electrons to undergo reverse migration from Pd to the conduction band of TiO2 under strong illumination, thus lowering the electron density of the Pd surface as a side effect. We were therefore able to rationally tailor the charge state of the metal surface and thus modulate the function of Pd nanocrystals in O2 activation and organic oxidation reactions by simply altering the intensity of light shed on Pd–TiO2 hybrid structures. 相似文献
965.
Silver(I)‐Catalyzed Hydroazidation of Ethynyl Carbinols: Synthesis of 2‐Azidoallyl Alcohols
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Zhenhua Liu Jianquan Liu Lin Zhang Dr. Peiqiu Liao Prof. Jinna Song Prof. Xihe Bi 《Angewandte Chemie (International ed. in English)》2014,53(21):5305-5309
The hydroazidation of alkynes is the most straightforward pathway to synthetically useful vinyl azides. However, a general hydroazidation of alkynes remains elusive. Herein, a chemo‐ and regioselective transformation of ethynyl carbinols into vinyl azides is described. This reaction produces a wide variety of 2‐azidoallyl alcohols with high efficiency and in good to excellent yields. These compounds constitute a new class of densely functionalized synthetic intermediates. Their synthetic potential has been demonstrated by further transformations into NH aziridines. The mechanistic aspects of the reaction will attract the attention of chemists working on alkyne chemistry and silver catalysis. The findings that are described in this paper represent significant advances in the regioselective hydroelementation of alkynes and open a new reaction manifold for exploitation. 相似文献
966.
Interaction with the Surrounding Water Plays a Key Role in Determining the Aggregation Propensity of Proteins
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Dr. Song‐Ho Chong Prof. Sihyun Ham 《Angewandte Chemie (International ed. in English)》2014,53(15):3961-3964
Understanding the molecular determinants of the relative propensities of proteins to aggregate in a cellular environment is a central issue for treating protein‐aggregation diseases and developing peptide‐based therapeutics. Despite the expectation that protein aggregation can largely be attributed to direct protein–protein interactions, a crucial role the surrounding water in determining the aggregation propensity of proteins both in vitro and in vivo was identified. The overall protein hydrophobicity, defined solely by the hydration free energy of a protein in its monomeric state sampling its equilibrium structures, was shown to be the predominant determinant of protein aggregation propensity in aqueous solution. Striking discrimination of positively and negatively charged residues by the surrounding water was also found. This effect depends on the protein net charge and plays a crucial role in regulating the solubility of the protein. These results pave the way for the design of aggregation‐resistant proteins as biotherapeutics. 相似文献
967.
Inside Back Cover: Patternable Large‐Scale Molybdenium Disulfide Atomic Layers Grown by Gold‐Assisted Chemical Vapor Deposition (Angew. Chem. Int. Ed. 5/2014)
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
968.
Hexafluoroantimonic Acid Catalysis: Formal [3+2+2] Cycloaddition of Aziridines with Two Alkynes
下载免费PDF全文
![点击此处可从《Angewandte Chemie (International ed. in English)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Ming‐Bo Zhou Ren‐Jie Song Prof. Dr. Jin‐Heng Li 《Angewandte Chemie (International ed. in English)》2014,53(16):4196-4199
A practical method for the synthesis of azepine derivatives, a typical seven‐membered heterocyclic ring system, was developed and involves the use of hexafluoroantimonic acid to catalyze a formal [3+2+2] cycloaddition of aziridines with two alkynes. This method was applicable to two of the same or different terminal alkynes for the [3+2+2] cycloaddition with unactivated aziridines, and furnished the corresponding azepine derivatives in good yields with good levels of chemo‐ and regioselectivity. The mechanism was also discussed according to the results of the in situ HRMS and 1H NMR analysis. 相似文献
969.
Self‐Assembly of Pyridinium‐Functionalized Anthracenes: Molecular‐Skeleton‐Directed Formation of Microsheets and Microtubes
下载免费PDF全文
![点击此处可从《Chemistry (Weinheim an der Bergstrasse, Germany)》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Dr. Jun Hu Peiyi Wang Prof. Yuan Lin Prof. Jidong Zhang Dr. Mark Smith Dr. Perry J. Pellechia Prof. Song Yang Prof. Baoan Song Prof. Qian Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(25):7603-7607
Two amphiphilic regioisomers, 9‐AP (1‐[11‐(9‐anthracenylmethoxy)‐11‐oxoundecyl]pyridinium bromide), and 2‐AP (1‐[11‐(2‐anthracenyl methoxy)‐11‐oxoundecyl]pyridinium bromide), were synthesized and their assembly behaviors were studied. Due to the anisotropic features of the anthracene structure, different substituted positions on the anthracene ring lead 9‐AP and 2‐AP to adapt “shaver” and “spatula”‐like molecular shapes, respectively, which consequently dictate the structure of their final assemblies. While “shaver”‐shaped 9‐AP assembled into microsheets, driven by π–π interactions, “spatula”‐shaped 2‐AP assembled into microtubular structures, promoted primarily by charge‐transfer interactions. 相似文献
970.
Shasha Song Haiqiao Wang Prof. Dr. Aixin Song Prof. Dr. Shuli Dong Prof. Dr. Jingcheng Hao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(29):9063-9072
The aggregation behavior of mixtures of the alkaline amino acid L ‐Arginine (L ‐Arg) and bis(2‐ethylhexyl)phosphoric acid (DEHPA) in water was studied in detail. At a fixed L ‐Arg concentration, a phase sequence of micellar phase (L1 phase), vesicle phase (Lαv phase), planar lamellar phase (Lαl phase), and sponge phase (L3 phase) was obtained with increasing DEHPA concentration due to changes in the packing parameter. The phase transition of the lamellar structures was determined by freeze‐fracture TEM and 2H NMR spectroscopy. Rheological measurements reflected the phase transition through significant variations of both the elastic modulus and the viscous modulus. Porous CeO2 materials were produced by utilizing the L3 phase as template, and the porous CeO2 exhibited excellent catalytic oxidation activity toward CO due to its high surface area, which provides more active sites for CO conversion. 相似文献