全文获取类型
收费全文 | 89934篇 |
免费 | 16885篇 |
国内免费 | 9184篇 |
专业分类
化学 | 61504篇 |
晶体学 | 916篇 |
力学 | 5747篇 |
综合类 | 512篇 |
数学 | 10091篇 |
物理学 | 37233篇 |
出版年
2024年 | 344篇 |
2023年 | 2045篇 |
2022年 | 3298篇 |
2021年 | 3389篇 |
2020年 | 3928篇 |
2019年 | 3509篇 |
2018年 | 3217篇 |
2017年 | 2867篇 |
2016年 | 4584篇 |
2015年 | 4362篇 |
2014年 | 5322篇 |
2013年 | 6765篇 |
2012年 | 8209篇 |
2011年 | 8403篇 |
2010年 | 5548篇 |
2009年 | 5381篇 |
2008年 | 5782篇 |
2007年 | 5065篇 |
2006年 | 4766篇 |
2005年 | 3821篇 |
2004年 | 2940篇 |
2003年 | 2299篇 |
2002年 | 2109篇 |
2001年 | 1817篇 |
2000年 | 1606篇 |
1999年 | 1840篇 |
1998年 | 1597篇 |
1997年 | 1580篇 |
1996年 | 1569篇 |
1995年 | 1322篇 |
1994年 | 1152篇 |
1993年 | 996篇 |
1992年 | 859篇 |
1991年 | 783篇 |
1990年 | 643篇 |
1989年 | 502篇 |
1988年 | 371篇 |
1987年 | 308篇 |
1986年 | 324篇 |
1985年 | 261篇 |
1984年 | 152篇 |
1983年 | 118篇 |
1982年 | 101篇 |
1981年 | 57篇 |
1980年 | 42篇 |
1979年 | 15篇 |
1976年 | 1篇 |
1974年 | 1篇 |
1957年 | 31篇 |
1922年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
941.
942.
Pamela M. Aker Jian-Xiang Zhang 《Journal of photochemistry and photobiology. A, Chemistry》1994,80(1-3):381-388
A novel non-linear Raman spectroscopic technique, which can be used to characterize the chemical composition of the interface region of volatile aerosol particles, is described. The technique is morphology-dependent stimulated Raman scattering (MDSRS). We discuss the phenomenology behind this new optical probe, and present experimental results which show that this technique can be used as quantitative spectroscopic tool. We outline the potential application of MDSRS to in situ gas—aerosol kinetics and dynamics studies. 相似文献
943.
石墨炉原子吸收光谱无标样分析法的研究:Ⅰ.消除基体干扰 总被引:1,自引:0,他引:1
实现石墨炉原子吸收光谱绝对分析必须消除基体干扰,本研究采用有机基体改进剂,管壁原子化、热解涂层石墨管,峰面积积分吸收信号,D2灯或Zeeman效应扣除背景,有效地控制和消除了海水基体对As,Cd,Co,Cr,Cu,Mn,Ni,Pb和V等元素的干扰,实现了无干扰测定。 相似文献
944.
Ultra-long single-crystalline trigonal selenium submicrotubes were synthesized using a facile one-step solution-phase approach with the assistance of nonionic surfactant Polyoxyethylene(20)sorbitan monolaurate (Tween-20), which turned out to be significant for the formation of ultra-long Se submicrotubes. XRD, Raman, SEM, and TEM were adopted to characterize the morphology, structure and phase composition of the as-prepared Se products. It was found that the length of the obtained Se submicrotubes was over 100 microm. By variation of the experimental parameters, the t-Se spheres, nanowires, and broken microtubes can be prepared. The possible growth mechanism of the ultra-long selenium submicrotubes was explained. In addition, we have also demonstrated that the synthesized ultra-long t-Se submicrotubes using the Tween-20-assisted approach can electrochemically charge and discharge with the high capacity of 265 mAh/g (corresponding to 0.97 wt % hydrogen in SWNTs) under normal atmosphere at room temperature. Cyclic voltammetry was adopted to investigate the adsorption-oxidation behavior of ultra-long selenium submicrotubes. It was observed that the morphology of the synthesized selenium products had a remarkable influence on their capacity of electrochemical hydrogen storage. These differences in hydrogen storage capacity are likely due to the size and density of tubes as well as the microcosmic morphology of different Se samples. The as-obtained ultra-long Se submicrotubes are expected to find wide applications in hydrogen storage, high-energy batteries, and optoelectronic, biologic, and catalytic fields as well as in the studies of structure-property relationships. This simple Tween-assisted approach might be extended to the preparations of one-dimensional nanostructures of tellurium and other anisotropic materials. 相似文献
945.
Simultaneous determination of carbohydrates and organic acids in beer and wine by ion chromatography 总被引:3,自引:0,他引:3
The simultaneous determination of mono-organic acids and carbohydrates by ion chromatography with both conductometric and pulsed amperometric detection is described. The carbohydrates, such as mannitol, arabinose, glucose, fructose, lactose, sucrose, raffinose, and maltose, as well as monoorganic acids including acetate, glycolate, formate, pyruvate, and fluoride are separated as anions by ion-exchange chromatography with 0.080 mol/L sodium hydroxide eluent at 1 mL/min within 12 min. Carbohydrates are determined by pulsed amperometric detection and mono-organic acids are determined by suppressed conductivity detection. The species in beverages are determined. 相似文献
946.
947.
络合物晶体的电子吸收光谱作为研究晶体的电子结构的基础内容,很早以前就得到人们注意,虽然对Cu~(2+)、Ni~(2+)等络合物电子光谱的能级的经验指认已是一项较为成熟的工作,但对吸收光谱的系统的理论计算和定量解释在以前的文献中尚不多见.近年来,我们对多种晶体的电子吸收光谱进行了定量的解释,结果表明理论计算值总是能很好地符合于实验测定值。一般说来,吸收峰位的波数误差在8%以内. 早在本世纪四十年代就奠定了乙二胺四乙酸(EDTA)在分析化学中的应用基础。 相似文献
948.
949.
根据CR传输线模型和QR电路之间的关系,建立了拟合其初值的计算方法,借助Z-View软件,可求得各元件精确值.根据电容(Ci)和电阻(Ri)随特征频率(f*)的分布,推导了元件相对增量与恒相位角元件(Q)指数参数n的关系. 结果表明, 当n小于0.5时,Ci比Ri增加得更快,从新的角度说明了n的物理意义及其和界面脱层之间的关系.作为应用实例,拟合了不同特征的电化学阻抗谱,分析了有机涂层/金属腐蚀体系阻抗变化的具体过程,区分了点蚀和脱层因素对阻抗谱的影响,从高阻抗体系同时得到了与不同空隙率有关的涂层电容和电阻值,并根据涂层体系的不均匀特征探讨了模型结构的物理意义. 相似文献
950.
Ming-Liang Zhang Yu-Peng Tian Xuan-Jun Zhang Jie-Ying Wu Sheng-Yi Zhang Dong Wang Min-Hua Jiang Suchada Chantrapromm Hoong-Kun Fun 《Transition Metal Chemistry》2004,29(6):596-602
A new Schiff base ligand derived from S-benzyldithiocarbazate and 4-[N-hydroxy ethyl-N-(methyl)amino]benzaldehyde (HL, where H is a dissociable proton) and its NiII, CuII, ZnII and PdII complexes were prepared and fully characterized. The structures of HL and Ni(L)2 were determined by X-ray diffraction analysis, which revealed that the geometry of the NiII ion is square-planar with two equivalent Ni=N and Ni=S bonds, and that the two neighboring molecules in two layers have weak contact. The electronic spectra and solution fluorescence of the ligand and the complexes were studied, and the quantum yields of single-photon fluorescence for the compounds were determined. The compounds possess two-photon absorption (t.p.a.) character and the t.p.a. coefficient and t.p.a. cross-section were determined by the Z-scan technique. Especially, the Zn(L)2complex and the HL ligand exhibit intensive two-photon fluorescence (t.p.f.) at 800 nm laser pulses in the femtosecond regime. 相似文献