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81.
We have found that polymer poly (sodium 4‐styrenesulfonate) (PSS) is a facile and effective polymer to assist in the dispersion of MWCNTs in aqueous solutions. With the increase of the concentration of PSS solutions, the dispersibility of MWCNTs in PSS solution increases. Cast films of MWCNTs/PSS (2 wt.%) on GC electrode show a typical redox couple at scan rate of 1 V/s in phosphate buffer solution, indicating good electrical conductivity.  相似文献   
82.
Zhan L  Gu Z  Zhang J  Xia Y 《Optics letters》2007,32(16):2276-2278
The critical behavior of passive mode locking has been demonstrated in a figure-eight fiber laser that performs rational harmonic mode locking (RHML). On both the repetition rate and the pulse amplitude distribution, the observed pulse trains near the threshold exhibit the same regulations as the rational harmonic mode-locked ones. The theory also shows that there should be a middle status of RHML before achieving normal mode locking. It is important to note that the results provide what we believe to be the first confirmed attempt to address a fundamental question: how does a laser become mode locking with an increase of pump power?  相似文献   
83.
通过运用扰动向量场的Hodge分解理论来构造适当的检验函数,得到非齐次A-调和方程Dirichlet问题-divA(x,(△)u)=f(x)在Grand-Sobolev空间很弱解的唯一性理论.  相似文献   
84.
Nano-carbon connections among carbon-coated LiFe0.8Mn0.2PO4 grains are successfully constructed using polyacrylic acid and sucrose as carbon sources by sol-gel method, which can improve the electrochemical performance of LiFe0.8Mn0.2PO4. Samples were characterised by X-ray diffraction, scanning electron microscopy and electrochemical tests. The electrochemical tests show LiFe0.8Mn0.2PO4 grains connected by nano-carbon networks obtain the discharge specific capacity of 165 mA h g?1 at 0.1 C rate and excellent rate capability. Its specific capacity reaches 122 mA h g?1 at 5 C rate. Its capacity retention at 5 C rate attains 97% cycled 100 cycles. Therefore the construction of nano-carbon networks offers an effective and convenient technique to improve the specific capacities and rate capabilities of electrode materials of low electronic conductivity.  相似文献   
85.
Epitope mapping is an important tool for the development of monoclonal antibodies, mAbs, as therapeutic drugs. Recently, a class of therapeutic mAb alternatives, adnectins, has been developed as targeted biologics. They are derived from the 10th type III domain of human fibronectin (10Fn3). A common approach to map the epitope binding of these therapeutic proteins to their binding partners is X-ray crystallography. Although the crystal structure is known for Adnectin 1 binding to human epidermal growth factor receptor (EGFR), we seek to determine complementary binding in solution and to test the efficacy of footprinting for this purpose. As a relatively new tool in structural biology and complementary to X-ray crystallography, protein footprinting coupled with mass spectrometry is promising for protein–protein interaction studies. We report here the use of fast photochemical oxidation of proteins (FPOP) coupled with MS to map the epitope of EGFR-Adnectin 1 at both the peptide and amino-acid residue levels. The data correlate well with the previously determined epitopes from the crystal structure and are consistent with HDX MS data, which are presented in an accompanying paper. The FPOP-determined binding interface involves various amino-acid and peptide regions near the N terminus of EGFR. The outcome adds credibility to oxidative labeling by FPOP for epitope mapping and motivates more applications in the therapeutic protein area as a stand-alone method or in conjunction with X-ray crystallography, NMR, site-directed mutagenesis, and other orthogonal methods. Figure
?  相似文献   
86.
Li  Kun  Wu  Yishi  Li  Xuemei  Fu  Hongbing  Zhan  Chuanlang 《中国科学:化学(英文版)》2020,63(4):490-496
Quaternary blended organic solar cells utilize four blended material components(one donor plus three acceptors, two donors and two acceptors, or three donors plus one acceptor) as the active layer materials. The use of four material components allows us to have more material selections and more mechanism choices to improve the photon-to-electron conversion efficiency. In this contribution, we present a new case of quaternary material system, that shows 17.1% efficiency obtained by adding IDIC and PC_(71)BM as the guest acceptors of the host binary of PM6:Y6. The lowest unoccupied molecular orbital(LUMO) levels of IDIC and PC_(71)BM are both higher than that of Y6, which is one reason to obtain increased open-circuit voltage(V_(oc)) in the quaternary device. Upon introduction of IDIC and PC_(71)BM as the acceptor guests, the hole and electron mobilities are both increased, which contributes to the increased short-circuit current-density(J_(sc)). Effects of the weight ratios of the three acceptor components are investigated, which demonstrates that the increased hole and electron mobilities, the accelerated hole-transfer, and the reduced monomolecular recombination are the factors contributing to the increased J_(sc)and fill-factor. This case of quaternary device demonstrates the applicability of the quaternary strategy in increasing the device functions and hence the efficiencies in the field of organic photovoltaic cells.  相似文献   
87.
Wang  Guowei  Yang  Lijian  Zhan  Xuan  Li  Anbang  Jia  Ya 《Nonlinear dynamics》2022,107(4):3945-3962
Nonlinear Dynamics - Chaotic resonance (CR) is the response of a nonlinear system to weak signals enhanced by internal or external chaotic activity (such as the signal derived from Lorenz system)....  相似文献   
88.
针对独立学院创业教育的现状、优势和存在的问题,提出在大学生创业观上必须正确处理好自身条件与社会需求、个人就业观与家庭期望、学校创业教育与个人专业学习三大关系。  相似文献   
89.
竖向地震加速度对堤坝抗震性能影响分析   总被引:3,自引:0,他引:3  
将堤坝地震动力响应的有限元效值分析方法与坝坡地震滑移量的Newmark估算方法相结合,通过效值计算探讨了水平与竖向加速度组合作用下堤坝的抗震稳定性.首先以堤坝地震动力响应的二维平面应变有限元分析为基础,按照Makdisi与Seed所建议的计算方法估算堤坝安全系效的变化过程,依此对地震过程中堤坝的瞬态稳定性进行评价.对瞬时安全系效小于1的时段,采用Newmark方法估算滑坡体的可能滑移量,进而由此评判堤坝的抗震安全性.最后,针对一座高度为100m的堤坝,分别采用正弦波和实际El-Centro地震加速度记录作为激励,通过具体效值计算讨论了竖向地震加速度对堤坝抗震稳定性的影响.研究表明竖向加速度对堤坝瞬态稳定性及地震滑移量均具有显著影响,在堤坝抗震设计中应合理地予以考虑.  相似文献   
90.
Recently molecular dynamics simulations were performed for polyethylene in the inclusion complex with perhydrotriphenylene. The system contained ninety molecules of perhydrotriphenylene, arranged in six stacks of fifteen molecules each, and one molecule of n-tetracontane, C40H82. The internal CH2-CH2 bonds in n-tetracontane have a very strong preference for the trans state. Nevertheless, the chain exhibits a high degree of internal flexibility. This motion produces a characteristic pattern in δ|ψ N + i ψi| vs. N, where ψi describes the instantaneous angle of a C-H bond vector at carbon atom i about the axis defined by the channel, and δ denotes the fluctuation. The pattern expected for δ|ψ N + i ψi| vs. N is derived for the case where the rapid internal motion is produced by a twiston. It is compared with the results from the simulation and from the expectation for the case where the rapid motion arises from uncorrelated internal fluctuations within the trans state at each CH2-CH2 bond.  相似文献   
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