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991.
992.
Dielectric constant(ε)is an important parameter affecting the power conversion efficiency of organic solar cells(OSC).Increasingεof bulk heterojunctions in general can benefit the performance of OSCs,as an increasedεwill reduce the influence of Coulomb interaction between weakly bound electron-hole pairs on charge-transfer states or bimolecular recombination involving mobile carriers to reduce geminate and nongeminate losses.In this review,we overview the current understandings on dielectric constant and its impacts on exciton dissociation and voltage losses in OSCs and summarize recent efforts attempting to modify the dielectric properties of OSC materials through synthetic approaches.We further discuss the commonly adopted techniques for determining the parameter ofεwith stressing the testing conditions that may affect the accuracy of results.At last,we suggest that novel experimental methods to improve the dielectric constant and resultant physical processes in OSCs will be appreciated,which helps enrich the existing strategy reservoir toward enhancement of photovoltaic efficiencies. 相似文献
993.
针对货车运行故障动态图像检测,提出无故障目标识别工作模式,解决货车枕簧丢失故障的自动识别问题。利用Haar特征提取枕簧特征信息,基于AdaBoost算法选取特征并构建层叠分类器,等比缩放搜索窗口检测货车图像,最终分选出无故障的枕簧图像,从而大大地减少了待识别图像的数量,显著地提高了人工识别效率。实验表明,该算法使用的特征简单,搜索策略高效,不受枕簧位置、缩放和旋转的影响,抗噪能力强,对分辨率低、局部遮挡、光照不足或过度曝光等质量较差的图像仍具有很强的适应性,所提出的方案能够满足全天候条件下的货车枕簧目标识别,为货车故障动态图像检测的工程化应用奠定了基础。 相似文献
994.
995.
通过对共享保护算法的深入分析,使用K条最短路和迭代思想的方法,提出了两种共享风险链路组不相关的共享保护算法,并在仿真平台上对两种算法的性能进行了仿真.KWFF算法借鉴了传统的K条最短路策略,并且在每一个波长平面上,都对新到业务进行了K条工作路由的计算,极大挖掘了网络中潜在的波长资源.而IFF算法由于引入了迭代的思想,避免了共享风险链路组问题中,所特别有“陷阱”问题的出现,并且利用两套权重计算公式,在计算工作路由和保护路由的时候,充分考虑了网络资源的实时变化情况.通过仿真数据可以看到,与以往算法相比,KWFF和IFF算法大大降低了网络阻塞率,并且提高了网络资源的使用效率. 相似文献
996.
Transition metal-catalyzed carbene transfer reaction is one of the most notable advances for C-C bond formation reactionsduring the past decade,which has been widely employed in the preparation of C3-substituted indoles,Here,we described an efficient exa mple of catalyst-and metal-free aminobo ration of alkynes and C—C bond formation with diazo compounds to produce C3-substituted indoles,Diverse alkynyla nilines and diazo compounds ca n be utilized for this tandem transfo rmation under mild reaction conditions,re sulting in broad functional group co mpatibility.Additionally,this metal-free strategy can be extended to construct substituted benzofurans. 相似文献
997.
998.
Efficient and selective removal of 90Sr is an important process for the safe use of nuclear energy. Herein, we investigate and assess the Sr2+ adsorption properties of a metal-organic framework UiO-66-(COOH)2 functionalized by non-bonded carboxylic groups. This MOF is an exciting class of free carboxylic functionalized MOFs that combine chemical stability with gas sorption, dye elimination, and conductivity. Specifically, we show that uniformly distributed carboxyl and water stability make it accessible for loading Sr2+ without structural changes. The FTIR spectroscopy, PXRD analysis, XPS, and SEM-EDS studies show excellent stability as well as the strong affinity between -COOH active site and Sr2+. This strong coordination interaction guarantees a high adsorption capacity of 114 mg g−1 within 5 h (pH 5 and 298 K). Combined kinetic and thermodynamic studies show that the surface complexation is strong chemisorption and cost-effective spontaneous process (ΔG = −5.49 kJ mol−1~−2.16 kJ mol−1). The fact that UiO-66-(COOH)2 not only possesses a high adsorption capacity, but also enables selectivity to Sr2+ in the presence of similar radius ions Na+ and K+, prefigures its great potential for the practical treatment of radioactive Sr2+ in polluted water. 相似文献
999.
<正>有机发光材料由于分子结构多样、发光颜色可调、加工简便等优点受到广泛关注。经典有机发光分子往往含有大的π共轭结构,并由此产生充分的电子离域。然而,此类有机发光分子往往含有稠环或芳杂环结构,具有潜在的细胞毒性[1];且在调节发光颜色时往往需要增加分子共轭、改变取代基或引入不同的推拉电子结构,合成步骤较为繁琐。与之相比,不含大型共轭单元而仅含N、O、S、P等杂原子及C=O、C=N、C≡N、C=C等富电子单元的非典型发光化合物结构简单,可通过商购或简单反应获得。且许多非典型发光分子与生物体系密切相关,生物相容性良好,有利于后续应用[2]。 相似文献
1000.
Developing an ideal and cheap adsorbent for adsorbing heavy metals from aqueous solution has been urgently need. In this study, a novel, effective and low-cost method was developed to prepare the biochar from lettuce waste with H3PO4 as an acidic activation agent at a low-temperature (circa 200 °C) hydrothermal carbonization process. A batch adsorption experiment demonstrated that the biochar reaches the adsorption equilibrium within 30 min, and the optimal adsorption capacity of Cd(II) is 195.8 mg∙g−1 at solution pH 6.0, which is significantly improved from circa 20.5 mg∙g−1 of the original biochar without activator. The fitting results of the prepared biochar adsorption data conform to the pseudo-second-order kinetic model (PSO) and the Sips isotherm model, and the Cd(II) adsorption is a spontaneous and exothermic process. The hypothetical adsorption mechanism is mainly composed of ion exchange, electrostatic attraction, and surface complexation. This work offers a novel and low-temperature strategy to produce cheap and promising carbon-based adsorbents from organic vegetation wastes for removing heavy metals in aquatic environment efficiently. 相似文献