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181.
刘艳  贾成  郭福明  杨玉军 《物理学报》2016,65(3):33201-033201
理论上研究了中红外强激光分别与长程库仑原子和短程势模型原子相互作用产生的高次谐波辐射.发现在相同激光参数条件下,与长程库仑原子的谐波辐射相比,短程原子具有更低的辐射效率,但在高频区域(接近cutoff位置),二者效率相似.通过对谐波辐射的时间频率分析发现,在短程模型原子谐波辐射中,长轨道发挥更重要的作用.利用其产生的高次谐波辐射,可以产生孤立阿秒脉冲.  相似文献   
182.
运用数学解析法导出了关于拉曼增益与自陡峭综合效应的光脉冲传输方程,在此基础上引入洛伦兹模型将拉曼增益整合到非线性系数中来研究光脉冲中拉曼增益对自陡峭效应的作用,重点分析了高斯脉冲在各向同性光纤中传播时,拉曼增益对其自陡峭效应具体影响方式,结果表明拉曼增益会减弱自陡峭中后沿偏移程度,减小脉冲展宽,但不会影响其峰值大小.  相似文献   
183.
刘佳  解洪文  严卿  张恒  崔毅楠 《应用声学》2015,23(12):90-90
试验总控软件是应用于半实物仿真中对参试系统进行管理和控制的一种软件,它可以对半实物仿真中的参试系统进行配置,实现对整个试验仿真的管理和监控。解析各参试系统的数据交互协议是试验总控软件对参试系统进行监控和管理的关键功能。通常试验总控软件解析功能代码完全按照各参试系统数据交互协议开发,这样一旦数据交互协议发生更改,解析功能代码需要根据新协议重新开发导致软件重复开发,影响软件开发效率和通用性。为了解决这个问题,文中提出一种试验总控软件设计框架并采用动态解析数据帧技术将解析代码与数据交互协议隔离,不仅提高软件通用性,同时缩短半实物仿真开发周期,减少人力财力开支。  相似文献   
184.
Absolute rate constants for hydroxyl radical, azide radical, and hydrated electron reactions with a sulfa drug 4,4'‐diamino diphenyl sulfone (dapsone) in water have been evaluated using electron pulse radiolysis technique. Absolute rate constants for hydroxyl radical and azide radical were determined as (8.4 ± 0.3) × 109 and (5.6 ± 0.5) × 109 M?1 s?1, respectively. The reduction of dapsone with the hydrated electron occurred with rate constant of (9.2 ± 0.1) × 109 M?1 s?1. Hydroxyl radical reactions result in the synchronous formation of adduct as well as anilino radical. The interesting observation is that the yield of the anilino radical increases with increase in pH. Contrary to this, the yield of the adduct decreases with pH. We propose that hydroxyl radical adds predominantly to the aniline. In contrast, the reaction of azide radical with the dapsone suggests that the reaction occurs at the –NH2 moiety of the aniline ring. The free radical electron transfer from dapsone to parent radical cation of non‐polar solvent also results in the formation of anilino radical only suggesting that the radical cation of dapsone has a short lifetime. The reaction of hydrated electrons with the dapsone suggests that the reaction occurs at different reaction site. The experimental results supported by theoretical calculations of this study provide fundamental mechanistic parameters that probably decide the fate of the radical cation of aniline derivatives. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   
185.
董磊  刘欣悦  陈浩 《中国光学》2015,8(5):800-805
为了研制激光干涉成像所需的主振荡功率放大(MOPA)结构脉冲单频激光器,本文完成MOPA激光器的种子源即声光调Q脉冲单频1 064 nm激光器的特性研究,同时完成种子源腔外倍频绿光特性研究。脉冲单频激光器采用声光调Q模块实现脉宽约20 ns的1 064 nm脉冲激光输出,采用环形腔设计并采用一组不同厚度的标准具实现单纵模运转。实验研究基频1 064nm和倍频532 nm激光脉冲的线宽,得出在全脉宽范围内都具有较高时间相干性的结论。实验分别获得脉宽约28 ns峰值功率约6.5 kW的1 064 nm脉冲单频激光和脉宽约20 ns、峰值功率约0.5 kW的532 nm脉冲单频激光,腔外倍频效率为5.6%。实验同时也验证了腔外倍频的激光脉宽压缩效应。  相似文献   
186.
Since the proof-of-principle demonstration of optical parametric amplification to efficiently amplify chirped laser pulses in 1992,optical parametric chirped pulse amplification(OPCPA)became the most promising method for the amplification of broadband optical pulses.In the meantime,we are witnessing an exciting progress in the development of powerful and ultrashort pulse laser systems that employ chirped pulse parametric amplifiers.The output power and pulse duration of these systems have ranged from a few gigawatts to hundreds of terawatts with a potential of tens of petawatts power level.Meanwhile,the output pulse duration based on optical parametric amplification has entered the range of fewoptical-cycle field.In this paper,we overview the basic principles,trends in development,and current state of the ultrashort and laser systems based on OPCPA,respectively.  相似文献   
187.
188.
This paper describes the preparation of a new sensor based on Zn‐ferrite modified glassy carbon paste electrode and its electrochemical application for the determination of trace Cd(II) ions in waste waters using differential pulse anodic stripping voltammetry (DPASV). Different Zn/Ni ferrite nanoparticles were synthesized and characterized using scanning electron microscopy (SEM) and X‐ray powder diffraction (XRPD). The prepared ferrite nanoparticles were used for the preparation of Zn‐ferrite‐modified glassy carbon paste electrode (ZnMGCPE) for determination of Cd(II) at nanomolar levels in waste water at pH 5. The different parameters such as conditions of preparation, Zn2+/Ni2+/Fe2+ ratio and electrochemical parameters, percentage of modifier, accumulation time, pH and accumulation potential were investigated. Besides, interference measurements were also evaluated under optimized parameters. The best voltammetric response was observed for ZnFe2O4 modifier, when the percentage of modifier was 3 %, accumulation time 9 min, pH of supporting electrolyte 5 and accumulation potential ?1.05 V. Thus prepared electrode displays excellent response to Cd(II) with a detection limit of 0.38 ppb, and selective detection toward Cd(II) was achieved.  相似文献   
189.
Mycotoxins are highly toxic compounds often found in the food. It is of paramount importance to have analytical technique for point‐of‐care on‐spot detection for authorised personnel to immediately take the action required. Electrochemistry offers the portability for miniaturized sensor of mycotoxins. Here we show that edge‐plane pyrolytic electrode offers excellent selectivity and sensitivity towards simultaneous detection of zearalenone and citrinin. This will have a great impact for point‐of‐care mycotoxin detection.  相似文献   
190.
Simultaneous electropolymerization of 3‐methylthiophene and incorporation of Laccase (LAC) was carried out in the presence of propylene carbonate as a medium by amperometric method. This enzyme modified electrode was used for the sensing of polyphenol. Catechol is taken as a model compound for the study. UV‐Vis spectral studies suggest no denaturation of LAC in presence of propylene carbonate. The SEM studies reveal the surface morphology and incorporation of LAC in P3MT with agglomerated flaky masses are observed in with and without enzyme micrographs. The cyclic voltammograms were recorded for 0.01 mM catechol on plain glassy carbon, polymer and enzyme incorporated electrodes at pH 6.0 and scan rate 50 mV s?1. The fabricated electrochemical biosensor was used for the determination of catechol in aqueous solution by Differential Pulse Voltammetry (DPV) technique. The concentration linear range of 8×10?8 to 1.4×10?5 M a value of Michealis? Menten constant Km=7.67 µmol dm?3 and activation energy is 32.75 kJ mol?1. It retains 83 % of the original activity after 60 days which is much higher than that of other biosensors. The developed biosensor was used to quantify catechol in the determination in real samples.  相似文献   
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