全文获取类型
收费全文 | 297篇 |
免费 | 14篇 |
国内免费 | 50篇 |
专业分类
化学 | 188篇 |
力学 | 24篇 |
综合类 | 8篇 |
数学 | 31篇 |
物理学 | 110篇 |
出版年
2023年 | 4篇 |
2022年 | 4篇 |
2021年 | 10篇 |
2020年 | 11篇 |
2019年 | 15篇 |
2018年 | 9篇 |
2017年 | 10篇 |
2016年 | 6篇 |
2015年 | 8篇 |
2014年 | 22篇 |
2013年 | 30篇 |
2012年 | 30篇 |
2011年 | 19篇 |
2010年 | 10篇 |
2009年 | 23篇 |
2008年 | 24篇 |
2007年 | 17篇 |
2006年 | 26篇 |
2005年 | 11篇 |
2004年 | 8篇 |
2003年 | 13篇 |
2002年 | 3篇 |
2001年 | 2篇 |
2000年 | 5篇 |
1999年 | 8篇 |
1998年 | 5篇 |
1997年 | 6篇 |
1996年 | 5篇 |
1995年 | 1篇 |
1993年 | 2篇 |
1991年 | 7篇 |
1989年 | 2篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 2篇 |
排序方式: 共有361条查询结果,搜索用时 703 毫秒
41.
Dr. Dong Zhou Yi Chen Prof. Baohua Li Prof. Hongbo Fan Prof. Faliang Cheng Dr. Devaraj Shanmukaraj Prof. Teofilo Rojo Prof. Michel Armand Prof. Guoxiu Wang 《Angewandte Chemie (International ed. in English)》2018,57(32):10168-10172
Ambient‐temperature sodium–sulfur (Na–S) batteries are considered a promising energy storage system due to their high theoretical energy density and low costs. However, great challenges remain in achieving a high rechargeable capacity and long cycle life. Herein we report a stable quasi‐solid‐state Na‐S battery enabled by a poly(S‐pentaerythritol tetraacrylate (PETEA))‐based cathode and a (PETEA‐tris[2‐(acryloyloxy)ethyl] isocyanurate (THEICTA))‐based gel polymer electrolyte. The polymeric sulfur electrode strongly anchors sulfur through chemical binding and inhibits the shuttle effect. Meanwhile, the in situ formed polymer electrolyte with high ionic conductivity and enhanced safety successfully stabilizes the Na anode/electrolyte interface, and simultaneously immobilizes soluble Na polysulfides. The as‐developed quasi‐solid‐state Na‐S cells exhibit a high reversible capacity of 877 mA h g?1 at 0.1 C and an extended cycling stability. 相似文献
42.
A novel and simple t‐BuOLi/I2‐mediated synthesis of 1,2,4‐trisubstituted imidazoles was developed without transition‐metal added. The transition‐metal‐free strategy tolerated a range of substrates and provided products in moderate to good yields with 100% regioselectivity. 相似文献
43.
本文根据各种形态汞氧化还原和溶解性质的差别建立了土壤和沉积物中汞形态分析的系统方法.研究了测定各形态汞的实验条件,考察了各形态汞相互间的干扰情况,并对一些实际样品进行了系统分析.结果表明,所建立的方法可用于土壤和沉积物中汞赋存形态的研究. 相似文献
44.
In this paper, a systematic approach is proposed to obtain the macroscopic elastic-plastic constitutive relation of particle
reinforced composites (PRC). The strain energy density of PRC is analyzed based on the cell model, and the analytical formula
for the macro-constitutive relation of PRC is obtained. The strength effects of volume fraction of the particle and the strain
hardening exponent of matrix material on the macro-constitutive relation are investigated, the relation curve of strain versus
stress of PRC is calculated in detail. The present results are consistent with the results given in the existing references.
The project supported by the National Natural Science Foundation of China (No. 19704100) and National Science Foundation of
Chinese Academy of Sciences (Project KJ951-1-20). 相似文献
45.
一台14.5GHz新型高磁场高电荷态ECR离子源 总被引:3,自引:1,他引:2
自行研制成功一台14.5GHz新型高磁场高电荷态电子回旋共振(ECR)离子源.描述了该离子源结构特点、参数优化及其磁场分布,并给出了调试测量结果.该离子源轴向磁镜场在轴线上的最高磁场可达1.5T,六极永磁体在弧腔内表面磁场可达1.0T.经初步调试,可得到07+140eμA,Ar11+185eμA,Xe26+50eμA.所得结果与1998年国际上最好的ECR离子源进行了比较. 相似文献
46.
Baohua Yue Chien-Yueh Huang Mu-Ping Nieh Charles J. Glinka John Katsaras 《Macromolecular Symposia》2005,219(1):123-134
Unilamellar vesicles (ULV) consisting of a single lipid bilayer are of special interest as drug delivery vehicles. Here, we report on a spontaneously forming ULV system composed of the short- and long-chain phospholipids, dihexanoyl (DHPC) and dimyristoyl (DMPC) phosphorylcholine, respectively, doped with the negatively charged lipid, dimyristoyl phosphorylglycerol (DMPG). Small-angle neutron scattering (SANS) and dynamic light scattering (DLS) were employed to systematically investigate the effects of lipid concentration, salinity, and time on vesicle stability. It is found that ULV size is practically constant over a range of lipid concentration and temperature. The spontaneously formed ULV are stable for periods of four months, or greater, without the use of stabilizers. 相似文献
47.
Baohua Zhang Yi Kong Huijun Liu Bin Chen Bolin Zhao Yelin Luo Lijuan Chen Yuwei Zhang Dongxue Han Zujin Zhao Ben Zhong Tang Li Niu 《Chemical science》2021,12(40):13283
Due to overcoming the limitation of aggregation caused quenching (ACQ) of solid-state emitters, aggregation-induced emission (AIE) organic luminogens have become a promising candidate in aqueous electrochemiluminescence (ECL). However, restricted by the physical nature of fluorescence, current organic AIE luminogen-based ECL (AIECL) faces the bottleneck of low ECL efficiency. Here, we propose to construct de novo aqueous ECL based on aggregation-induced delayed fluorescence (AIDF) luminogens, called AIDF-ECL. Compared with the previous organic AIE luminogens, purely organic AIDF luminogens integrate the superiorities of both AIE and the utilization of dark triplets via thermal-activated spin up-conversion properties, thereby possessing the capability of close-to-unity exciton utilization for ECL. The results show that the ECL characteristics using AIDF luminogens are directly related to their AIDF properties. Compared with an AIECL control sample based on a tetraphenylethylene AIE moiety, the ECL efficiency of our AIDF-ECL model system is improved by 5.4 times, confirming the excellent effectiveness of this innovative strategy.Electrochemiluminescence (ECL) using an aggregation-induced delayed fluorescence (AIDF) organic luminogen, i.e. AIDF-ECL, was reported for the first time, featuring “lighting” dark triplets (ca. 75% in total) for all-exciton-harvesting ECL applications. 相似文献
48.
Transmembrane water pores are crucial for sub-stance transport through cell membranes via membrane fusion, such as in neural communication. However, the molecular mechanism of water pore formation is not clear. In this study, we apply all-atom molecular dynamics and bias-exchange metadynamics simulations to study the pro-cess of water pore formation under an electric field. We show that water molecules can enter a membrane under an electric field and form a water pore of a few nanometers in diame-ter. These water molecules disturb the interactions between lipid head groups and the ordered arrangement of lipids. Fol-lowing the movement of water molecules, the lipid head groups are rotated and driven into the hydrophobic region of the membrane. The reorientated lipid head groups inside the membrane form a hydrophilic surface of the water pore. This study reveals the atomic details of how an electric field influences the movement of water molecules and lipid head groups, resulting in water pore formation. 相似文献
49.
We report a diode-pumped self-Q-switched 1064-nm Cr,Nd:YAG of 16-18 ns. The maximum average output power up to 7 W, 3370, is obtained in a simple and compact linear cavity by using transmittance of 1570. The laser operates at TEM00 mode with a laser with pulse duration in the range corresponding to a slope efficiency of a plane-concave output coupler with a pump power of 14.2 W. 相似文献
50.
本文利用平面角的概念讨论了均匀带电的直线微元和圆弧微元在圆心处的场强等价性,并将结论推广到一些均匀带电的线几何体;然后利用立体角的概念进一步讨论带电的平面微元和球面微元在球心处的场强等价关系,结果表明,只有非均匀的电荷面密度才能使两者等价. 相似文献