首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   1088篇
  免费   169篇
  国内免费   297篇
化学   930篇
晶体学   37篇
力学   8篇
综合类   5篇
数学   3篇
物理学   571篇
  2023年   16篇
  2022年   27篇
  2021年   40篇
  2020年   48篇
  2019年   60篇
  2018年   45篇
  2017年   74篇
  2016年   70篇
  2015年   64篇
  2014年   80篇
  2013年   121篇
  2012年   117篇
  2011年   96篇
  2010年   74篇
  2009年   101篇
  2008年   85篇
  2007年   68篇
  2006年   67篇
  2005年   66篇
  2004年   42篇
  2003年   32篇
  2002年   49篇
  2001年   16篇
  2000年   18篇
  1999年   16篇
  1998年   15篇
  1997年   7篇
  1996年   7篇
  1995年   3篇
  1994年   8篇
  1993年   3篇
  1992年   3篇
  1991年   4篇
  1990年   2篇
  1989年   2篇
  1987年   2篇
  1983年   1篇
  1981年   1篇
  1979年   1篇
  1978年   1篇
  1977年   1篇
  1973年   1篇
排序方式: 共有1554条查询结果,搜索用时 15 毫秒
51.
A simple and efficient nitrile‐directed meta‐C?H olefination, acetoxylation, and iodination of biaryl compounds is reported. Compared to the previous approach of installing a complex U‐shaped template to achieve a molecular U‐turn and assemble the large‐sized cyclophane transition state for the remote C?H activation, a synthetically useful phenyl nitrile functional group could also direct remote meta‐C?H activation. This reaction provides a useful method for the modification of biaryl compounds because the nitrile group can be readily converted to amines, acids, amides, or other heterocycles. Notably, the remote meta‐selectivity of biphenylnitriles could not be expected from previous results with a macrocyclophane nitrile template. DFT computational studies show that a ligand‐containing Pd–Ag heterodimeric transition state (TS) favors the desired remote meta‐selectivity. Control experiments demonstrate the directing effect of the nitrile group and exclude the possibility of non‐directed meta‐C?H activation. Substituted 2‐pyridone ligands were found to be key in assisting the cleavage of the meta‐C?H bond in the concerted metalation–deprotonation (CMD) process.  相似文献   
52.
为优化石墨相氮化碳(g-C3N4)光催化剂的结构,改善其对污染物的降解性能,本文以三聚氰胺为前驱体,通过高温煅烧和热氧化剥离制备了二维石墨相氮化碳(2D-C3N4),并用光还原法一步合成纳米银/二维石墨相氮化碳/还原氧化石墨烯(Ag/2D-C3N4/rGO)复合光催化剂。通过X射线粉末衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外-可见漫反射光谱(UV-Vis DRS)、光致发光光谱(PL)、X射线光电子能谱(XPS)、氮气吸附脱附等温曲线(BET)等对材料进行表征。 以头孢曲松钠为目标污染物,探究pH值、催化剂用量、头孢曲松钠初始浓度等因素对催化剂的吸附、降解性能的影响,并探究降解反应机理。 当pH=6.0,催化剂用量为0.3 g/L,头孢曲松钠初始浓度为10.0 mg/L时,复合材料对头孢曲松钠的降解率可达到89.1%。 催化剂的稳定性较强,具有实际应用价值,可用于处理含头孢类抗生素的废水。  相似文献   
53.
以热氧化剥离法得到的超薄石墨相氮化碳(g-C3N4)纳米片为载体,首次在室温条件下,制备了系列Ag3PO4量子点/g-C3N4纳米片复合光催化剂;通过透射电子显微镜(TEM)、高分辨透射电子显微镜(HRTEM)、X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、紫外-可见漫反射光谱(UV-Vis DRS)、荧光光谱(PL),对复合光催化剂的形貌、结构和光学性质进行了表征,考察了系列光催化剂对苯甲醇的光催化选择性氧化性能。 结果表明,粒径为3~5 nm Ag3PO4颗粒均匀分散g-C3N4纳米片上,结晶度良好。 以乙腈为溶剂时,当m(Ag3PO4)/m(g-C3N4)=0.6时,苯甲醇具有32.1%的最大转化率,对产物苯甲醛具有90%的最高选择性;活性物种捕捉实验结果表明,该催化氧化反应的主要活性物是光生空穴的氧化作用,能带计算结果表明,该复合催化剂结构具有合适的苯甲醇的氧化电位而选择性生成苯甲醛。  相似文献   
54.
采用原位化学反应和热处理相结合的策略,在泡沫铜表面形成丝线状与花瓣状的立体无机物阵列,然后在其表面蒸镀Ag纳米颗粒(NPs),成功制备了基于泡沫铜的Ag/CuO复合光热材料。该复合材料因表面三维立体阵列结构以及Ag NPs而具备较高的太阳光吸收率。故而,Ag/CuO复合光热材料结合三聚氰胺泡沫组成的蒸发器件实现了高效的海水淡化。本研究除了探索光陷阱深度和金属掺杂对吸收体光热转换效率增强之外,还搭建了太阳能驱动界面蒸汽生成测试系统,测试了样品的光热蒸发性能。在1倍太阳(1 kW·m~(-2))辐照下,该器件整体蒸发速率高达1.097 6 kg·m~(-2)·h~(-1),即其蒸发效率可达78.38%。  相似文献   
55.
Graphene-like C3N4/Ag3PO4 photocatalysts are synthesized by calcination and solutions precipitating method.The obtained g-C3N4/Ag3PO4 composites display excellent photocatalytic activity for the degradation of methylene orange(MO),rhodamine B(RhB)and tetracycline(TC)under visible light irradiation.The solutions containing RhB(10 mg/L)and MO(10 mg/L)can be efficiently degraded within15 min and 30 min.Especially,nearly 80%of TC(50 mg/L)is degraded within 20 min.which are much better than those of pure g-C3N4 nanosheets and Ag3PO4,implying that strong interaction and reasonable energy band alignment in the contact interface can effectively transfer the carries.Furthermore,the g-C3N4/Ag3PO4 composites exhibit the improved stability,and only a slight decrease is observed after three recycling runs.Moreover,the impact of inorganic ions and PH values on the degradation performance is rather small.The Z-scheme photocatalytic mechanism of the g-C3N4/Ag3PO4 composites based on the active species trapping experimental is proposed.This work demonstrates the promising applications of the g-C3N4/Ag3PO4 composites in environmental issues.  相似文献   
56.
肖传豪 《分析测试学报》2020,39(12):1544-1547
该文构建了一种基于氯金酸刻蚀球形纳米银检测褪黑激素的简单、高灵敏比色探针。纳米银可被氯金酸氧化刻蚀为Ag+,同时还原生成的纳米金沉积在刻蚀后的纳米银表面,导致其溶液的吸光度降低和颜色增强(由黄色变为橘黄色)。当向体系中加入褪黑激素时,氯金酸被还原,抑制了纳米银的刻蚀,从而使得溶液吸光度增加和颜色变浅。结果显示,在0.1 nmol/L~1.0 mmol/L范围内,褪黑激素浓度对数值(lgC)与其吸光度改变值(ΔA)呈良好的线性关系,线性方程为ΔA=0.049 8+0.516lgC,相关系数(R2)为0.996 4,检出限为0.09 nmol/L。该方法成功应用于人体尿液和葡萄中的褪黑激素的测定。  相似文献   
57.
Using a radio-frequency reactive magnetron sputtering technique, a series of the single-phased Ag20 films are deposited in a mixture of oxygen and argon gas with a flow ratio of 2:3 by changing substrate temperature (Ts). Effects of the Ts on the microstructure and optical properties of the films are investigated by using X-ray diffractometry, scanning electron microscopy and spectrophotometry. The single-phased Ag20 films deposited at values of Ts below 200℃ are (111) preferentially oriented, which may be due to the smallest free energy of the (111) crystalline face. The film crystallization becomes poor as the value of Ts increases from 100℃ to 225℃. In particular, the Ag20 film deposited at Ts=225℃ loses the (111) preferential orientation. Correspondingly, the film surface morphology obviously evolves from a uniform and compact surface structure to a loose and gullied surface structure. With the increase of Ts value, the transmissivity and the reflectivity of the films in the transparent region are gradually reduced, while the absorptivity gradually increases, which may be attributed to an evolution of the crystalline structure and the surface morphology of the films.  相似文献   
58.
The behavior of the flow stress of Al-Cu-Mg-Ag heat-resistant aluminum alloys during hot compression deformation was studied by thermal simulation test. The temperature and the strain rate during hot compression were 340-500 °C, 0.001 s−1 to 10 s−1, respectively. Constitutive equations and an artificial neural network (ANN) model were developed for the analysis and simulation of the flow behavior of the Al-Cu-Mg-Ag alloys. The inputs of the model are temperature, strain rate and strain. The output of the model is the flow stress. Comparison between constitutive equations and ANN results shows that ANN model has a better prediction power than the constitutive equations.  相似文献   
59.
Surface plasmon resonance sensors based on Ag-metalized nanolayer in microstructured optical fibers are theoretically analyzed by using finite element method (FEM). In our simulations we use Drude-Lorentz model to describe the metal dielectric constant. The numerical results show that the sensitivity of Ag-metalized SPR sensor could reach 1167 nm/RIU and corresponding resolution is 8.57×10−5 RIU. Compared to conventional Au-metalized SPR sensors the performance of our device is obviously better.  相似文献   
60.
M.H. Majles Ara  Z. Javadi  R.S. Sirohi 《Optik》2011,122(21):1961-1964
In this paper we have measured second order nonlinear refractive index of Ag and Au nano-particles using the moiré deflectometry with a CW He-Ne laser at wavelength of 632.8 nm. The main advantages of this technique are its extreme experimental simplicity and low sensitivity to external distribution in comparison with other interfrometric methods that need very stable experimental set-up. Because of self-focusing (or self-defocusing) that is due to intensity dependent refractive index, presence of sample in the moiré deflectometry set-up lead to rotation of moiré fringes. By moving the sample in set-up we have measured these rotation angles in different displacements from focus point of lens used in this set-up and then we have calculated the nonlinear refractive index of Ag and Au nano-particles using their values. Also we have obtained the sign of n2 regard to the direction of rotations. Consequently by using the Mathematica software we have exhibited the suitable fitness of theoretical curve with experimental results.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号